找回密码
 注册

肠易激综合症

作者:大江 | 时间:2020-6-6 00:01:44 | 阅读:544| 显示全部楼层
肠易激综合症(IBS)是一组症状-包括腹痛和肠蠕动方式的改变,而没有任何潜在损害的证据。这些症状会持续很长时间(通常为数年)。根据腹泻是常见病,便秘是常见病,两者都是常见病还是很少发生(分别是IBS-D,IBS-C,IBS-M或IBS-U),它已被分为四种主要类型。 IBS对生活质量有负面影响,并可能导致失学或工作。 IBS患者常见焦虑症,重度抑郁症和慢性疲劳综合症。

IBS的病因尚不清楚。理论包括肠脑轴问题,肠蠕动障碍,疼痛敏感性,包括小肠细菌过度生长,神经递质,遗传因素和食物敏感性在内的感染。发病可能由肠道感染或压力性生活事件触发。 IBS是一种功能性胃肠疾病。诊断的依据是缺乏令人担忧的特征的症状,并且一旦排除了其他潜在的状况。令人不安的特征包括超过50岁的发作,体重减轻,大便中有血或发炎性肠病的家族史。可能类似地出现的其他疾病包括乳糜泻,微观结肠炎,炎症性肠病,胆汁酸吸收不良和结肠癌。

没有已知的治疗IBS的方法。进行治疗以改善症状。这可能包括饮食变化,药物治疗,益生菌和咨询。饮食措施包括增加可溶性纤维的摄入量,无麸质饮食或可发酵低聚糖,二糖,单糖和多元醇(FODMAP)含量低的短期饮食。洛哌丁胺药物可用于帮助腹泻,而泻药可用于帮助便秘。抗抑郁药可以改善整体症状并减轻疼痛。患者教育和良好的医患关系是护理的重要组成部分。

据信,发达国家约有10%到15%的人受到IBS的影响。据估计,全球有45%的人受到IBS的影响。它在南美更为常见,而在东南亚则较不常见。它是女性的两倍,是男性的两倍,通常发生在45岁之前。这种病随着年龄的增长而变得越来越少。 IBS不会影响预期寿命或导致其他严重疾病。对这种疾病的首次描述是在1820年,而目前的术语肠易激综合征是在1944年开始使用的。


画示IBS的痛苦

内容
1 分类
2 体征和症状
2.1 食物不耐受
3 原因
3.1 压力
3.2 感染后
3.3 细菌
3.4 真菌
3.5 原生动物
3.6 维生素D
3.7 遗传学
4 机制
5 诊断
5.1 罗马标准
5.2 鉴别诊断
5.3 调查
5.4 误诊
5.5 合并症
6 管理
6.1 饮食
6.2 用药
6.3 心理疗法
6.4 替代药物
7 流行病学
7.1 性别
8 历史
9 社会与文化
9.1 名称
9.2 经济学
10 研究
11 参考

分类
IBS可分为腹泻型(IBS-D),便秘型(IBS-C),粪便交替型(IBS-A)或疼痛型。 在某些个体中,IBS可能是急性发作,并在以以下两种或多种特征为特征的感染性疾病后发展:发烧,呕吐,腹泻或粪便培养阳性。 因此,这种感染后综合症被称为“感染后IBS”(IBS-PI)。

体征和症状
IBS的主要症状是腹痛或不适,伴有频繁的腹泻或便秘以及大便习惯的改变。症状通常表现为在一天之内消退的急性发作,但可能会反复发作。排便,紧迫感(里急后重)或腹胀的感觉也很紧迫。在某些情况下,肠蠕动可缓解症状。患有IBS的人比其他人更常见,有胃食管反流,与泌尿生殖系统有关的症状,慢性疲劳综合症,纤维肌痛,头痛,腰酸以及精神病症状,如抑郁和焦虑。患有IBS的男人和女人中约有三分之一也报告性功能障碍,通常表现为性欲降低。

食物不耐受
多达90%的人的症状是由食物不耐受引起的。这些通常包括可发酵的寡糖,二糖,单糖和多元醇(FODMAP)。

原因
尽管IBS的病因尚不清楚,但据信整个肠脑轴都受到了影响。

急性胃肠道感染后发生IBS的风险增加了六倍。感染后,其他危险因素是年轻,长期发烧,焦虑和抑郁。尚未显示出诸如抑郁或焦虑之类的心理因素会导致或影响IBS的发作,但可能在症状的持续性和感知严重性中起作用。但是,它们可能会使IBS症状和生活质量恶化。抗生素的使用也似乎增加了患IBS的风险。研究发现,先天免疫和上皮稳态的遗传缺陷增加了感染后以及其他形式的IBS发生的风险。

压力
暗示脑肠轴作用的出版物出现在1990年代,儿童的身心虐待通常与IBS的发展有关。据认为,心理压力可能触发易感人群中的IBS。

鉴于IBS患者经历的焦虑程度很高,并且与诸如纤维肌痛和慢性疲劳综合症等疾病重叠,IBS的潜在解释涉及压力系统的破坏。体内的压力反应涉及下丘脑-垂体-肾上腺轴(HPA)和交感神经系统,这两种疾病在IBS患者中均显示异常。在三分之二的IBS患者中,精神疾病或焦虑先于IBS症状出现,并且心理特征使先前健康的人易患胃肠炎。

感染后
大约10%的IBS病例是由急性胃肠炎感染引起的。 CdtB毒素是由引起肠胃炎的细菌产生的,当宿主的CdtB抗体与纽蛋白交叉反应时,宿主可能会产生自身免疫。与先天免疫系统和上皮屏障有关的遗传缺陷,以及高压力和焦虑水平似乎增加了感染后IBS发生的风险。感染后IBS通常表现为以腹泻为主的亚型。有证据表明,急性肠感染期间高水平促炎细胞因子的释放导致肠道通透性增加,导致共生细菌跨过上皮屏障移位。这反过来会导致对局部组织的显着损害,并可能在敏感个体中发展成慢性肠道异常。但是,无论IBS是否是由感染引起的,肠道通透性的增加都与IBS密切相关。小肠细菌过度生长与热带灌浆之间的联系已被认为是导致IBS感染的原因。

细菌
与健康对照相比,被诊断患有IBS的人小肠细菌过度生长(SIBO)的发生频率更高。 SIBO在以腹泻为主的IBS中最常见,但在以便秘为主的IBS中也比健康对照组更常见。 SIBO的症状包括腹胀,腹痛,腹泻或便秘。 IBS可能是免疫系统与肠道菌群异常相互作用导致细胞因子信号传导异常的结果。

与健康个体相比,发现某些细菌的丰度较低或较高。通常,拟杆菌,硬毛菌和变形杆菌增加,放线菌,双歧杆菌和乳杆菌减少。在人的肠道内,有常见的门。最常见的是Firmicutes。其中包括发现患有IBS的人减少的乳杆菌和表现出丰度增加的链球菌。在这个门中,梭状芽胞杆菌属的物种显示增加,特别是Ruminococcus和Dorea。唇螺科家族的IBS-D患者增加。第二个最常见的门是拟杆菌。在患有IBS的人中,门生细菌已显示出总体减少,但细菌种增加了。 IBS-D显示放线菌门的减少和变形杆菌的增加,特别是肠杆菌科。

细菌
越来越多的证据表明,肠道微生物群的改变(营养不良)与IBS的肠道表现有关,但也与多达80%的IBS患者共存的精神病发病率有关。截至2005年,肠道菌群的作用,特别是某些IBS患者中白色念珠菌酵母的异常增殖的作用正在调查中。

原生动物

21世纪工业化国家(美国和加拿大)的原生动物感染率
原生动物感染可引起反映特定IBS亚型的症状,例如,被人型芽孢杆菌的某些亚型感染(囊胚病)。

截至2017年,有证据表明胚泡定植定植在受IBS影响的个体中更为普遍,并且是发展IBS的可能危险因素。尽管在没有IBS的人中也发现了脆弱的Dientamoeba fragilis,但它也被认为是一种可能的生物。

维生素D
维生素D缺乏症在肠易激综合症患者中更为常见。维生素D参与调节IBS的触发因素,包括肠道微生物组,炎症过程和免疫反应以及社会心理因素。

遗传学
在少数患有IBS的人群中发现了SCN5A突变,尤其是在以便秘为主的变异人群(IBS-C)中。所产生的缺陷会影响结肠和起搏器细胞的平滑肌中的Nav1.5通道,从而导致肠功能中断。

机制
遗传,环境和心理因素在IBS的发展中似乎很重要。研究表明,即使主要受环境因素影响,IBS仍具有遗传成分。

有证据表明,患有IBS的个体的肠道菌群中出现异常,例如多样性降低,属于拟杆菌科的细菌减少以及属于刚毛门的细菌的增多。在以腹泻为主的IBS患者中,肠道菌群的变化最为深刻。针对共肠肠道菌群的常见成分(即鞭毛蛋白)的抗体在受IBS影响的个体中很常见。

慢性低度炎症通常发生在受IBS感染的个体中,发现异常包括肠嗜铬细胞,上皮内淋巴细胞和肥大细胞增多,导致肠道粘膜的慢性免疫介导炎症。据报道,IBS的多代家庭中IBS的数量要多于正常人群。据认为,心理压力可引起炎症增加,从而引起IBS在易感个体中发展。

诊断
没有专门的实验室或影像学检查可以诊断肠易激综合症。诊断应基于症状,排除令人担忧的特征以及进行特定调查以排除可能表现出相似症状的器质性疾病。

给医生的建议是尽量减少医学检查的使用。通常使用罗马标准。它们允许诊断仅基于症状,但没有任何仅基于症状的标准足以准确地诊断IBS。令人担忧的特征包括超过50岁的发作,体重减轻,大便中的血液,铁缺乏性贫血或结肠癌,腹腔疾病或炎性肠病的家族病史。选择测试和研究的标准还取决于可用医疗资源的水平。

罗马标准
Rome IV标准包括最近3个月平均每周至少1天/每周的复发性腹痛,并伴有以下两个或多个标准:

有关排便
与大便次数的变化有关
与大便形式(外观)的变化有关。
医生可以选择使用这些指南之一,也可以仅选择依靠自己对过去患者的轶事经验。该算法可能包括其他测试,以防止其他疾病如IBS的误诊。此类“危险信号”症状可能包括体重减轻,胃肠道出血,贫血或夜间症状。但是,红旗状况可能并不总是有助于诊断的准确性;例如,多达31%的IBS患者的粪便中有血液,其中许多可能是痔疮出血引起的。

诊断算法会根据腹泻,腹痛和便秘的症状来识别可应用于患者状况的名称。例如,声明“ 50%的返回旅行者发生了功能性腹泻,而25%的患者发生了IBS”,则意味着一半的旅行者出现了腹泻而四分之一的患者则出现了腹痛。尽管一些研究人员认为这种分类系统将有助于医生了解IBS,但其他人则质疑该系统的价值,并建议所有患有IBS的人都具有相同的潜在疾病,但具有不同的症状。

鉴别诊断
结肠癌,炎性肠病,甲状腺疾病(甲状腺功能亢进症或甲状腺功能减退症)和贾第鞭毛虫病都可能以排便异常和腹痛为特征。这种症状的较不常见原因是类癌综合征,微观结肠炎,细菌过度生长和嗜酸性胃肠炎。但是,IBS是一种常见的表示方式,对这些条件的测试将产生少量的积极结果,因此认为很难证明费用合理。可能类似出现的疾病包括乳糜泻,胆汁酸吸收不良,结肠癌和排尿障碍。

在做出肠易激综合征的诊断之前,建议排除寄生虫感染,乳糖不耐症,小肠细菌过度生长和乳糜泻。需进行小肠活检的上镜检查才能确定是否存在腹腔疾病。回肠结肠镜检查活检可用于排除克罗恩氏病和溃疡性结肠炎(炎症性肠病)。

一些因IBS治疗多年的人可能具有非芹菜麸质敏感性(NCGS)。 IBS的胃肠道症状在临床上与NCGS的症状无法区分,但以下任何非肠道表现均表明可能存在NCGS:头痛或偏头痛,“精神模糊”,慢性疲劳,纤维肌痛,关节和肌肉疼痛,腿部或手臂麻木,四肢发麻,皮炎(湿疹或皮疹),特应性疾病,对一种或多种吸入剂,食物或金属(如螨虫,禾本科,披肩草,猫或狗毛,贝类或镍)过敏,焦虑症,贫血,缺铁性贫血,叶酸缺乏症,哮喘,炎,进食障碍,神经精神疾病(例如精神分裂症,自闭症,周围神经病,共济失调,注意力缺陷多动障碍)或自身免疫性疾病。曾经合理地排除了乳糜泻和小麦过敏的无麸质饮食可以改善免疫介导的症状,包括自身免疫性疾病,这是实现鉴别诊断的另一种方法。

调查
进行调查以排除其他情况:

粪便显微镜和培养(排除传染病)
血液检查:全血检查,肝功能检查,红细胞沉降率以及乳糜泻的血清学检查
腹部超声检查(排除胆结石和其他胆道疾病)
内窥镜检查和活检(排除消化性溃疡病,腹腔疾病,炎症性肠病和恶性肿瘤
氢呼气测试(排除果糖和乳糖吸收不良)
误诊
由于被误诊为其他疾病,IBS患者接受阑尾切除术,胆囊切除术和子宫切除术等不适当手术的风险增加。误诊的一些常见示例包括传染病,腹腔疾病,幽门螺杆菌,寄生虫(非原生动物)。美国胃肠病学院建议对所有患有IBS症状的人进行乳糜泻检查。

在以腹泻为主的IBS患者中,胆汁酸吸收不良有时也被遗漏。 SeHCAT测试表明,约30%的D-IBS患者患有此病,并且大多数人对胆汁酸螯合剂有反应。

合并症
患有IBS的人出现几种疾病或合并症的频率更高。

神经科/精神科:一项针对97593名IBS患者的研究确定了合并症,例如头痛,纤维肌痛和抑郁症。 IBS发生在51%的慢性疲劳综合症患者和49%的纤维肌痛患者中,而精神疾病发生在94%的IBS患者中。
炎症性肠病:IBS可能与炎症性肠病略相关。研究人员发现IBS和IBD之间存在一定的相关性,并指出IBD患者在IBD缓解后会出现类似IBS的症状。一项为期三年的研究发现,在研究期间,被诊断为IBS的患者被诊断为IBD的可能性是16.3倍,尽管这可能是由于最初的误诊所致。
腹部手术:IBS患者发生不必要的胆囊切除手术的风险增加,不是由于胆结石的风险增加,而是由于腹痛,对胆结石的认识以及不适当的手术适应症。这些人进行腹部和骨盆手术的可能性也要高出87%,而胆囊手术的可能性要高出三倍。此外,IBS患者接受子宫切除术的可能性是后者的两倍。
子宫内膜异位症:一项研究报告偏头痛,IBS和子宫内膜异位之间存在统计学上的显着联系。
其他慢性疾病:间质性膀胱炎可能与其他慢性疼痛综合征有关,例如肠易激综合征和纤维肌痛。这些综合症之间的联系是未知的。
管理
已经发现许多有效的治疗方法,包括纤维,谈话疗法,解痉和抗抑郁药以及薄荷油。

饮食
FODMAP
一项2018年的系统评价发现,尽管有证据表明低FODMAP饮食可改善IBS症状;证据质量很差。最有可能改善的症状包括尿急,肠胃气胀,腹胀,腹痛和粪便排出量改变。一项国家指南建议,如果其他饮食和生活方式措施不成功,则应采用低FODMAP饮食来管理IBS。饮食中限制了各种在小肠中吸收不良的碳水化合物,以及果糖和乳糖,这些糖同样在那些对它们不耐受的人中吸收不良。在果糖吸收不良和IBS患者中,减少果糖和果聚糖可降低IBS症状,并呈剂量依赖性。

FODMAP是可发酵的寡糖,二糖,单糖和多元醇,它们在小肠中吸收差,随后在小肠远端和大肠近端被细菌发酵。这是每个人都常见的正常现象。产生的气体可能会导致腹胀和肠胃气胀。尽管FODMAPs可能在某些人中引起某些消化系统不适,但它们不仅不会引起肠道炎症,而且有助于避免炎症,因为它们会在肠道菌群中产生有益的改变,从而有助于保持结肠的良好健康。 FODMAP并非肠易激综合症或其他功能性胃肠道疾病的病因,而是当潜在的肠反应被夸大或异常时,人会出现症状。

低FODMAP饮食包括限制饮食。它们是全局修剪的,而不是单独修剪的,这比例如仅限制果糖和果糖类(也是FODMAPs)成功得多,这对于果糖吸收不良的人是建议的。

FODMAP含量低的饮食可能有助于改善肠易激综合症的成年人的短期消化系统症状,但长期随访可能会产生负面影响,因为它会对肠道菌群和代谢组产生不利影响。它只能在专家的建议下短时间使用。低FODMAP饮食对各种营养素都有严格的限制,因此从长远来看可能不切实际。需要更多的研究来评估这种饮食对健康的真正影响。

此外,使用低FODMAP饮食而不验证IBS的诊断可能会导致其他疾病(如乳糜泻)的误诊。由于低FODMAP饮食可以抑制或减少麸质的消耗,因此,这种饮食的消化系统症状的改善可能与FODMAP的撤除无关,而与麸质无关,这表明存在无法识别的乳糜泻,应避免它的诊断和正确治疗,随之而来的是发生多种严重健康并发症(包括各种类型的癌症)的风险。

纤维
一些证据表明可溶性纤维补充剂(例如洋车前子/木瓜皮)是有效的。它可以作为填充剂,对于许多患有IBS-D的人来说,可以使粪便更加均匀。对于患有IBS-C的人来说,它似乎可以使凳子更柔软,更湿润,更容易通过。

然而,尚未发现不溶性纤维(例如麸皮)对IBS有效。在某些人中,补充不溶性纤维可能会加重症状。

纤维可能对便秘占多数的人有益。在患有IBS-C的人中,可溶性纤维可以减轻总体症状,但不会减轻疼痛。支持膳食纤维的研究包含相互矛盾的小型研究,这些研究因纤维类型和使用剂量的异质性而变得复杂。

一项荟萃分析发现,仅可溶性纤维可改善肠易激综合症状,但两种纤维均不能减轻疼痛。同一作者的最新荟萃分析还发现,可溶性纤维减轻了症状,而在某些情况下,可溶性纤维却加重了症状。积极研究每天使用10-30克伊斯普拉(欧车前)。一项研究专门检查了剂量的影响,发现20克ispaghula(车前子)优于10克,相当于每天30克。

药物
可能有用的药物包括解痉药,例如二环明和抗抑郁药。关于抗抑郁药,选择性5-羟色胺再摄取抑制剂和三环抗抑郁药似乎都是有用的。 H1-抗组胺药和肥大细胞稳定剂也已显示出减轻IBS内脏超敏反应相关疼痛的功效。

泻药
对于不能对膳食纤维做出充分反应的人,渗透性泻药,例如聚乙二醇,眼眼醇和乳果糖可以帮助避免与兴奋性泻药相关的“泻药结肠”。鲁比前列酮是一种用于治疗便秘为主的IBS的胃肠道药物。

解痉药
使用解痉药物(例如,抗胆碱药,例如hyoscyamine或dicyclomine)可能会帮助抽筋或腹泻的人。 Cochrane合作组织的荟萃分析得出的结论是,如果有7个人接受解痉药物治疗,其中一个人将受益。解痉药可以分为两类:神经营养药和肌肉营养药。促肌药,例如美贝维林,直接作用于胃肠道的平滑肌,缓解痉挛而不影响正常的肠蠕动。由于这种作用不是由植物神经系统介导的,因此不存在通常的抗胆碱能副作用。解痉性奥替铵也可能是有用的。

停止质子泵抑制剂
用于抑制胃酸产生的质子泵抑制剂(PPI)可能导致细菌过度生长,从而导致IBS症状。已建议中止在选定个体中使用PPI,因为这可能导致IBS症状改善或缓解。

抗抑郁药
有充分的证据表明,低剂量的三环类抗抑郁药可以有效治疗IBS。但是,关于其他抗抑郁药如选择性5-羟色胺再摄取抑制剂抗抑郁药(SSRIs)的有效性的证据不充分。抗抑郁药对抑郁症患者的IBS无效,这可能是因为缓解IBS所需的抗抑郁药剂量低于治疗抑郁症所需的剂量。

由于SSRI具有血清素能作用,因此已对其进行了研究,以了解它们是否对IBS有帮助,尤其是在便秘占主导地位的人群,但截至2015年,有证据表明SSRI没有帮助。

其他代用
硅酸铝镁和柠檬酸小白药可以有效治疗IBS。

有关IBS中抗抑郁药益处的证据存在矛盾。一些荟萃分析发现了好处,而另一些则没有。使用TCA,大约有三分之一的人在进步。

利福昔明可用于治疗IBS症状,包括腹胀和肠胃气胀,尽管延迟了腹胀的缓解。在涉及小肠细菌过度生长的地方,此功能特别有用。

对于IBS和维生素D水平低的个体,建议补充。一些证据表明,补充维生素D可能会改善IBS的症状,但在将其推荐为IBS的特殊治疗方法之前,还需要进一步的研究。

多潘立酮是一种多巴胺受体阻滞剂和拟交感神经药,已被证明可减少结肠扩张时间和粪便负荷,从而减轻腹胀和腹痛,从而减轻“隐藏的便秘”。排便同样得到改善。

抗生素治疗小肠细菌过度生长后,IBS症状减轻。但是,最近的研究表明,乳果糖氢呼气试验实际上并不能测量SIBO,SIBO不太可能是IBS的病因。

心理疗法
从方法学质量较差的研究中得出的证据不足,表明心理疗法可以有效治疗IBS;然而,心理疗法对IBS并没有明显的不利影响。对于IBS,已经提出了心身或脑-肠相互作用,并且正在获得越来越多的研究关注。催眠可以改善心理健康,认知行为疗法可以为应对令人痛苦的症状提供心理应对策略,并有助于抑制增加IBS症状的思想和行为。尽管心理疗法和催眠疗法的有效性的证据基础薄弱,一般不建议使用此类疗法,但在耐药性病例中,至少12个月以上的药物疗法未能缓解,NICE临床指南建议应考虑给予心理治疗策略,例如认知行为治疗[CBT],催眠治疗和/或心理治疗。

减轻压力可能会降低IBS症状的频率和严重程度。可能有用的技术包括:

冥想等放松技巧
体育锻炼,例如瑜伽或太极拳
定期运动,例如游泳,散步或跑步
替代药物
荟萃分析发现,与安慰剂相比,针灸对于IBS症状严重程度或与IBS相关的生活质量无益处。

益生菌
益生菌可能对IBS的治疗有益。建议每天服用100亿到1000亿有益细菌以取得有益效果。但是,需要对有益细菌的各个菌株进行进一步研究,以获得更完善的建议。益生菌具有积极作用,例如增强肠粘膜屏障,提供物理屏障,产生细菌素(导致减少病原菌和产气细菌的数量),降低肠道通透性和细菌易位性,以及在局部和全身性调节免疫系统其他有益效果。益生菌还可以通过抵消压力对肠道免疫力和肠道功能的影响而对肠脑轴产生积极作用。

已经发现许多益生菌是有效的,包括植物乳杆菌和婴儿双歧杆菌。但一项评论发现只有婴儿双歧杆菌才显示疗效。婴儿双歧杆菌可能通过肠道产生超出肠道的作用,导致促炎细胞因子活性降低和血色氨酸水平升高,从而可能导致抑郁症状的改善。一些酸奶是使用益生菌制成的,可以帮助缓解IBS的症状。益生菌酵母(Saccharomyces boulardii)具有治疗肠易激综合症的有效证据。

某些益生菌对IBS的某些症状有不同的作用。例如,已发现短双歧杆菌,长双歧杆菌和嗜酸乳杆菌可减轻腹痛。短双歧杆菌,婴儿双歧杆菌,干酪乳杆菌或植物乳杆菌物种缓解了扩张症状。短双歧杆菌,婴儿双歧杆菌,干酪乳杆菌,植物乳杆菌,长双歧杆菌,嗜酸乳杆菌,保加利亚乳杆菌和唾液链球菌ssp。已经发现嗜热菌会影响肠胃气胀水平。大多数临床研究表明,益生菌并不能改善劳损,不完全疏散感,粪便稠度,粪便紧迫性或大便次数,尽管一些临床研究确实发现了益生菌疗法的一些益处。益生菌是否能改善整体生活质量得分的证据是矛盾的。

益生菌可通过保存肠道菌群,使细胞因子血液水平正常化,改善肠道运输时间,降低小肠通透性以及治疗发酵细菌引起的小肠细菌过度繁殖,对IBS症状发挥有益作用。截至2019年,粪便移植似乎不再有用。

草药
薄荷油似乎很有用。在荟萃分析中,发现改善IBS症状至少在短期内优于安慰剂。较早的一项荟萃​​分析表明,薄荷油的结果是试验性的,因为研究的人数很少,不清楚接受治疗的人的盲目性。但是,尚未确定怀孕期间的安全性,因此请注意不要咀嚼或破坏肠溶衣;否则,由于食管括约肌松弛,胃食管反流可能发生。有时,恶心和肛周灼伤会产生副作用。发现伊贝罗司特(一种多草药提取物)在功效上优于安慰剂。

对于IBS的其他草药疗法的有效性,只有有限的证据。与所有草药一样,明智的选择是注意可能的药物相互作用和不良反应。

流行病学

在不同国家的各种研究中报告的患有IBS的人口百分比
IBS的患病率因国家和所检查的年龄范围而异。 右侧的条形图显示了来自不同地理区域的研究中报告IBS症状的人口百分比(请参阅下表以供参考)。

性别
女性被诊断出患有IBS的可能性是男性的两倍到三倍,而寻求特殊护理的可能性是男性的四到五倍。这些差异可能反映了生物学(性)和社会(性别)因素的结合。被诊断患有IBS的人通常不到45岁。对患有IBS的女性进行的研究表明,症状严重程度通常会随着月经周期而变化,这表明荷尔蒙的差异可能起到了作用。认可与性别有关的特征与IBS的生活质量和心理调节有关。寻求医疗保健方面的性别差异也可能起作用。特质焦虑的性别差异可能有助于降低女性的疼痛阈值,使她们更有可能罹患多种慢性疼痛疾病。最后,性创伤是IBS的主要危险因素,多达33%的受影响者报告了这种虐待。由于女性遭受性虐待的风险比男性高,因此与性别相关的性虐待风险可能导致女性IBS发生率更高。

历史
1950年,在《落基山医学杂志》中出现了“肠易激”的概念。该术语用于对出现腹泻,腹痛和便秘症状的人进行分类,但是找不到公认​​的感染原因。早期的理论表明,肠易激是由心身或精神疾病引起的。

社会与文化
名字
过去所用疾病的其他名称包括肠易激,痉挛性结肠,神经结肠,结肠炎,粘液性结肠炎和痉挛性肠。

由于结肠疾病不仅限于消化道的这一部分,因此提及结肠的术语不准确且不建议使用。类似地,术语“结肠炎”也不准确,因为不存在炎症。放弃这些用语的其他原因是为了反映对这种障碍不是一个人的想象力的嘲弄的理解。

经济学
地球图标。
本节中的示例和观点可能并不代表该主题的全球视野。您可以根据需要改进本节,在讨论页上讨论问题,或创建新的节。 (2011年7月)(了解如何以及何时删除此模板消息)
美国
在美国,肠易激综合症的总费用估计为直接医疗费用17至100亿美元,另外还有200亿美元的间接费用,总计21.7至300亿美元。一家管理式护理公司进行的一项研究比较了IBS患者和非IBS对照者的医疗费用,发现与IBS诊断相关的医疗费用每年增加49%。患有IBS的人在2007年的平均年度直接费用为$ 5,049,自付费用为$ 406。对IBS工人的研究发现,他们报告的生产率下降了34.6%,相当于每40小时每周损失13.8小时。一项根据1990年代的数据对《财富》 100强公司进行的与雇主相关的健康费用的研究发现,患有IBS的人的索赔费用为4527美元,而对照组为3276美元。乔治亚大学药房学院和诺华公司在2003年进行的医疗补助费用研究发现,IBS与加利福尼亚州医疗补助费用增加962美元和北卡罗莱纳州增加2191美元有关。患有IBS的人的医师就诊,门诊就诊和处方药费用较高。研究表明,与IBS相关的费用与哮喘患者的费用相当。

研究
已经发现患有IBS的个体的细菌群落的多样性和数目减少。粪便微生物群移植治疗IBS的有效性的初步研究非常有利,其“治愈”率在36%至60%之间,随访9、19个月仍持续缓解IBS核心症状。益生菌菌株的治疗已证明是有效的,尽管并非所有微生物菌株都具有相同的益处,并且在少数情况下已记录了不良副作用。

越来越多的证据表明美沙拉嗪(5-氨基水杨酸)可有效治疗IBS。美沙拉嗪是一种具有抗炎特性的药物,据报道可通过美沙拉嗪治疗显着减少IBS感染个体的肠道中免疫介导的炎症,从而改善IBS症状以及IBS感染者的总体健康感觉。还已经观察到,美沙拉嗪治疗有助于使肠道菌群正常化,这在患有IBS的人中通常是异常的。美沙拉嗪的治疗益处可能是改善上皮屏障功能的结果。不推荐基于“异常”高IgG抗体的治疗。

在IBS中已经注意到内脏敏感性和肠道生理的差异。与对照组相比,IBS中没有响应口服5-HTP的粘膜屏障增强。与上功能性胃肠疾病和健康人群相比,IBS / IBD患者的HLA DQ2 / 8阳性率较低。

参考
"Definition and Facts for Irritable Bowel Syndrome". NIDDKD. February 23, 2015. Archived from the original on April 2, 2016. Retrieved March 29, 2016.
"Symptoms and Causes of Irritable Bowel Syndrome". NIDDK. February 23, 2015. Archived from the original on April 5, 2016. Retrieved March 29, 2016.
Chey WD, Kurlander J, Eswaran S (March 2015). "Irritable bowel syndrome: a clinical review". JAMA. 313 (9): 949–58. doi:10.1001/jama.2015.0954. PMID 25734736.
Levy J, Bernstein L, Silber N (December 2014). "Celiac disease: an immune dysregulation syndrome". Current Problems in Pediatric and Adolescent Health Care. 44 (11): 324–7. doi:10.1016/j.cppeds.2014.10.002. PMID 25499458.
"Treatment for Irritable Bowel Syndrome". NIDDK. February 23, 2015. Archived from the original on April 6, 2016. Retrieved March 29, 2016.
Quigley, Eamonn M.M. (2013). "Treatment level 1". Irritable Bowel Syndrome: Diagnosis and Clinical Management (First ed.). Chichester, West Sussex: Wiley-Blackwell. ISBN 9781118444740. Archived from the original on September 8, 2017.
Maxion-Bergemann S, Thielecke F, Abel F, Bergemann R (2006). "Costs of irritable bowel syndrome in the UK and US". PharmacoEconomics. 24 (1): 21–37. doi:10.2165/00019053-200624010-00002. PMID 16445300.
Alexandros Hadjivasilis, Constantinos Tsioutis, Adamantios Michalinos, Dimitrios Ntourakis, Dimitrios K. Christodoulou, and Aris P. Agouridis (2019). "New insights into irritable bowel syndrome: from pathophysiology to treatment". Ann Gastroenterol. 32 (6): 554–564. doi:10.20524/aog.2019.0428. PMC 6826071. PMID 31700231.
Hulisz D (2004). "The burden of illness of irritable bowel syndrome: current challenges and hope for the future". Journal of Managed Care Pharmacy. 10 (4): 299–309. doi:10.18553/jmcp.2004.10.4.299. PMID 15298528.
Whitehead WE, Palsson O, Jones KR (April 2002). "Systematic review of the comorbidity of irritable bowel syndrome with other disorders: what are the causes and implications?". Gastroenterology. 122 (4): 1140–56. doi:10.1053/gast.2002.32392. PMID 11910364.
Spiller R, Garsed K (May 2009). "ostinfectious irritable bowel syndrome". Gastroenterology. 136 (6): 1979–88. doi:10.1053/j.gastro.2009.02.074. PMID 19457422.
Chang L (March 2011). "The role of stress on physiologic responses and clinical symptoms in irritable bowel syndrome". Gastroenterology. 140 (3): 761–5. doi:10.1053/j.gastro.2011.01.032. PMC 3039211. PMID 21256129.
Moayyedi P, Quigley EM, Lacy BE, Lembo AJ, Saito YA, Schiller LR, Soffer EE, Spiegel BM, Ford AC (September 2014). "The effect of fiber supplementation on irritable bowel syndrome: a systematic review and meta-analysis". The American Journal of Gastroenterology. 109 (9): 1367–74. doi:10.1038/ajg.2014.195. PMID 25070054.
Rao SS, Yu S, Fedewa A (June 2015). "Systematic review: dietary fibre and FODMAP-restricted diet in the management of constipation and irritable bowel syndrome". Alimentary Pharmacology & Therapeutics. 41 (12): 1256–70. doi:10.1111/apt.13167. PMID 25903636.
Mayer EA (April 2008). "Clinical practice. Irritable bowel syndrome". The New England Journal of Medicine. 358 (16): 1692–9. doi:10.1056/NEJMcp0801447. PMC 3816529. PMID 18420501.
Hatch, Maureen C. (2000). Women and Health. San Diego, Calif: Academic Press. p. 1098. ISBN 9780122881459. Archived from the original on September 8, 2017.
Holten KB, Wetherington A, Bankston L (May 2003). "Diagnosing the patient with abdominal pain and altered bowel habits: is it irritable bowel syndrome?". American Family Physician. 67 (10): 2157–62. PMID 12776965. Archived from the original on May 15, 2008.
Schmulson MW, Chang L (November 1999). "Diagnostic approach to the patient with irritable bowel syndrome". The American Journal of Medicine. 107 (5A): 20S–26S. doi:10.1016/S0002-9343(99)00278-8. PMID 10588169.
Tamparo C (2011). Fifth Edition: Diseases of the Human Body. Philadelphia, PA: F.A. Davis Company. p. 407. ISBN 978-0-8036-2505-1.
Talley NJ (November 2006). "Irritable bowel syndrome". Internal Medicine Journal. 36 (11): 724–8. doi:10.1111/j.1445-5994.2006.01217.x. PMC 1761148. PMID 17040359.
Sperber AD, Dekel R (April 2010). "Irritable Bowel Syndrome and Co-morbid Gastrointestinal and Extra-gastrointestinal Functional Syndromes". Journal of Neurogastroenterology and Motility. 16 (2): 113–9. doi:10.5056/jnm.2010.16.2.113. PMC 2879857. PMID 20535341.
Wouters MM, Vicario M, Santos J (January 2016). "The role of mast cells in functional GI disorders". Gut. 65 (1): 155–68. doi:10.1136/gutjnl-2015-309151. PMID 26194403.
Ohman L, Simrén M (March 2010). "athogenesis of IBS: role of inflammation, immunity and neuroimmune interactions". Nature Reviews. Gastroenterology & Hepatology. 7 (3): 163–73. doi:10.1038/nrgastro.2010.4. PMID 20101257.
Thabane M, Kottachchi DT, Marshall JK (August 2007). "Systematic review and meta-analysis: The incidence and prognosis of post-infectious irritable bowel syndrome". Alimentary Pharmacology & Therapeutics. 26 (4): 535–44. doi:10.1111/j.1365-2036.2007.03399.x. PMID 17661757. Archived from the original on July 13, 2013.
"World Gastroenterology Organisation Global Guidelines. Irritable Bowel Syndrome: a Global Perspective" (PDF). World Gastroenterology Organisation. September 2015. Archived (PDF) from the original on May 27, 2016. Retrieved April 24, 2016.
Shanahan F, Quigley EM (May 2014). "Manipulation of the microbiota for treatment of IBS and IBD-challenges and controversies". Gastroenterology. 146 (6): 1554–63. doi:10.1053/j.gastro.2014.01.050. PMID 24486051.
Beatty JK, Bhargava A, Buret AG (April 2014). "ost-infectious irritable bowel syndrome: mechanistic insights into chronic disturbances following enteric infection". World Journal of Gastroenterology. 20 (14): 3976–85. doi:10.3748/wjg.v20.i14.3976. PMC 3983453. PMID 24744587.
Fukudo S, Nomura T, Muranaka M, Taguchi F (September 1993). "Brain-gut response to stress and cholinergic stimulation in irritable bowel syndrome. A preliminary study". Journal of Clinical Gastroenterology. 17 (2): 133–41. doi:10.1097/00004836-199309000-00009. PMID 8031340.
Barreau F, Ferrier L, Fioramonti J, Bueno L (September 2007). "New insights in the etiology and pathophysiology of irritable bowel syndrome: contribution of neonatal stress models". Pediatric Research. 62 (3): 240–5. doi:10.1203/PDR.0b013e3180db2949. PMID 17622962.
Li J, Zhu W, Liu W, Wu Y, Wu B (January 2016). "Rifaximin for Irritable Bowel Syndrome: A Meta-Analysis of Randomized Placebo-Controlled Trials". Medicine. 95 (4): e2534. doi:10.1097/MD.0000000000002534. PMC 5291563. PMID 26825893.
Spiller R, Aziz Q, Creed F, Emmanuel A, Houghton L, Hungin P, Jones R, Kumar D, Rubin G, Trudgill N, Whorwell P (December 2007). "Guidelines on the irritable bowel syndrome: mechanisms and practical management". Gut. 56 (12): 1770–98. doi:10.1136/gut.2007.119446. PMC 2095723. PMID 17488783.
Fukudo S (January 2007). "Role of corticotropin-releasing hormone in irritable bowel syndrome and intestinal inflammation". Journal of Gastroenterology. 42 (Suppl 17): 48–51. doi:10.1007/s00535-006-1942-7. PMID 17238026.
Barbara G, Grover M, Bercik P, Corsetti M, Ghoshal UC, Ohman L, Rajilić-Stojanović M (January 2019). "Rome Foundation Working Team Report on Post-Infection Irritable Bowel Syndrome". Gastroenterology. 156 (1): 46–58.e7. doi:10.1053/j.gastro.2018.07.011. PMC 6309514. PMID 30009817.
Ghoshal UC, Gwee KA (July 2017). "ost-infectious IBS, tropical sprue and small intestinal bacterial overgrowth: the missing link". Nature Reviews. Gastroenterology & Hepatology. 14 (7): 435–441. doi:10.1038/nrgastro.2017.37. PMID 28513629.
Chen, B; Kim, JJ; Zhang, Y; Du, L; Dai, N (July 2018). "revalence and predictors of small intestinal bacterial overgrowth in irritable bowel syndrome: a systematic review and meta-analysis". Journal of Gastroenterology. 53 (7): 807–818. doi:10.1007/s00535-018-1476-9. PMID 29761234.
Ghoshal UC, Srivastava D (March 2014). "Irritable bowel syndrome and small intestinal bacterial overgrowth: meaningful association or unnecessary hype". World Journal of Gastroenterology. 20 (10): 2482–91. doi:10.3748/wjg.v20.i10.2482. PMC 3949258. PMID 24627585.
Bennet SM, Ohman L, Simren M (May 2015). "Gut microbiota as potential orchestrators of irritable bowel syndrome". Gut and Liver. 9 (3): 318–31. doi:10.5009/gnl14344. PMC 4413965. PMID 25918261.
Collins SM (August 2014). "A role for the gut microbiota in IBS". Nature Reviews. Gastroenterology & Hepatology. 11 (8): 497–505. doi:10.1038/nrgastro.2014.40. PMID 24751910.
Santelmann H, Howard JM (January 2005). "Yeast metabolic products, yeast antigens and yeasts as possible triggers for irritable bowel syndrome". European Journal of Gastroenterology & Hepatology. 17 (1): 21–6. CiteSeerX 10.1.1.567.6030. doi:10.1097/00042737-200501000-00005. PMID 15647635.
Lagacé-Wiens PR, VanCaeseele PG, Koschik C (August 2006). "Dientamoeba fragilis: an emerging role in intestinal disease". CMAJ. 175 (5): 468–9. doi:10.1503/cmaj.060265. PMC 1550747. PMID 16940260.
Amin OM (June 2002). "Seasonal prevalence of intestinal parasites in the United States during 2000". The American Journal of Tropical Medicine and Hygiene. 66 (6): 799–803. doi:10.4269/ajtmh.2002.66.799. PMID 12224595.
Stark D, van Hal S, Marriott D, Ellis J, Harkness J (January 2007). "Irritable bowel syndrome: a review on the role of intestinal protozoa and the importance of their detection and diagnosis". International Journal for Parasitology. 37 (1): 11–20. doi:10.1016/j.ijpara.2006.09.009. PMID 17070814.
Wawrzyniak I, Poirier P, Viscogliosi E, Dionigia M, Texier C, Delbac F, Alaoui HE (October 2013). "Blastocystis, an unrecognized parasite: an overview of pathogenesis and diagnosis". Therapeutic Advances in Infectious Disease. 1 (5): 167–78. doi:10.1177/2049936113504754. PMC 4040727. PMID 25165551. Recent in vitro and in vivo studies have shed new light on the pathogenic power of this parasite, suggesting that Blastocystis sp. infection is associated with a variety of gastrointestinal disorders, may play a significant role in irritable bowel syndrome, and may be linked with cutaneous lesions (urticaria).
Roberts T, Stark D, Harkness J, Ellis J (2014). "Update on the pathogenic potential and treatment options for Blastocystis sp". Gut Pathogens. 6: 17. doi:10.1186/1757-4749-6-17. PMC 4039988. PMID 24883113.
Rostami A, Riahi SM, Haghighi A, Saber V, Armon B, Seyyedtabaei SJ (September 2017). "The role of Blastocystis sp. and Dientamoeba fragilis in irritable bowel syndrome: a systematic review and meta-analysis". Parasitology Research. 116 (9): 2361–2371. doi:10.1007/s00436-017-5535-6. PMID 28668983.
Windsor JJ, Macfarlane L (May 2005). "Irritable bowel syndrome: the need to exclude Dientamoeba fragilis". The American Journal of Tropical Medicine and Hygiene. 72 (5): 501, author reply 501–2. doi:10.4269/ajtmh.2005.72.5.0720501. PMID 15891119. Archived from the original on July 17, 2010.
Williams CE, Williams EA, Corfe BM (October 2018). "Vitamin D status in irritable bowel syndrome and the impact of supplementation on symptoms: what do we know and what do we need to know?" (PDF). European Journal of Clinical Nutrition. 72 (10): 1358–1363. doi:10.1038/s41430-017-0064-z. PMID 29367731.
Ferguson LR, Laing B, Marlow G, Bishop K (January 2016). "The role of vitamin D in reducing gastrointestinal disease risk and assessment of individual dietary intake needs: Focus on genetic and genomic technologies". Molecular Nutrition & Food Research. 60 (1): 119–33. doi:10.1002/mnfr.201500243. PMID 26251177.
Barbalho SM, Goulart RA, Araújo AC, Guiguer éL, Bechara MD (April 2019). "Irritable bowel syndrome: a review of the general aspects and the potential role of vitamin D". Expert Rev Gastroenterol Hepatol. 13 (4): 345–359. doi:10.1080/17474124.2019.1570137. PMID 30791775.
Beyder A, Farrugia G (2016). "Ion channelopathies in functional GI disorders". American Journal of Physiology. Gastrointestinal and Liver Physiology. 311 (4): G581–G586. doi:10.1152/ajpgi.00237.2016. PMC 5142191. PMID 27514480.
Verstraelen TE, Ter Bekke RM, Volders PG, Masclee AA, Kruimel JW (2015). "The role of the SCN5A-encoded channelopathy in irritable bowel syndrome and other gastrointestinal disorders". Neurogastroenterology & Motility. 27 (7): 906–13. doi:10.1111/nmo.12569. PMID 25898860.
Talley NJ (December 2006). "Genes and environment in irritable bowel syndrome: one step forward". Gut. 55 (12): 1694–6. doi:10.1136/gut.2006.108837. PMC 1856457. PMID 17124153.
Cremon C, Carini G, De Giorgio R, Stanghellini V, Corinaldesi R, Barbara G (May 2010). "Intestinal dysbiosis in irritable bowel syndrome: etiological factor or epiphenomenon?". Expert Review of Molecular Diagnostics. 10 (4): 389–93. doi:10.1586/erm.10.33. PMID 20465494.
Schmulson M, Bielsa MV, Carmona-Sánchez R, Hernández A, López-Colombo A, López Vidal Y, Peláez-Luna M, Remes-Troche JM, Tamayo JL, Valdovinos MA (2014). "Microbiota, gastrointestinal infections, low-grade inflammation, and antibiotic therapy in irritable bowel syndrome: an evidence-based review". Revista de Gastroenterologia de Mexico (in Spanish). 79 (2): 96–134. doi:10.1016/j.rgmx.2014.01.004. PMID 24857420.
Saito YA (March 2011). "The role of genetics in IBS". Gastroenterology Clinics of North America. 40 (1): 45–67. doi:10.1016/j.gtc.2010.12.011. PMC 3056499. PMID 21333900.
Yawn BP, Lydick E, Locke GR, Wollan PC, Bertram SL, Kurland MJ (2001). "Do published guidelines for evaluation of irritable bowel syndrome reflect practice?". BMC Gastroenterology. 1: 11. doi:10.1186/1471-230X-1-11. PMC 59674. PMID 11701092.
Irvine AJ, Chey WD, Ford AC (January 2017). "Screening for Celiac Disease in Irritable Bowel Syndrome: An Updated Systematic Review and Meta-analysis" (PDF). The American Journal of Gastroenterology (Review). 112 (1): 65–76. doi:10.1038/ajg.2016.466. PMID 27753436. Although IBS is not a diagnosis of exclusion, with physicians advised to minimize the use of investigations, the gastrointestinal (GI) tract has a limited repertoire of symptoms, meaning that abdominal pain and a change in bowel habit is not specific to the disorder.
Drossman DA (February 2016). "Functional Gastrointestinal Disorders: History, Pathophysiology, Clinical Features and Rome IV". Gastroenterology. 150 (6): 1262–1279.e2. doi:10.1053/j.gastro.2016.02.032. PMID 27144617.
Saha L (June 2014). "Irritable bowel syndrome: pathogenesis, diagnosis, treatment, and evidence-based medicine". World Journal of Gastroenterology (Review). 20 (22): 6759–73. doi:10.3748/wjg.v20.i22.6759. PMC 4051916. PMID 24944467.
Fass R, Longstreth GF, Pimentel M, Fullerton S, Russak SM, Chiou CF, Reyes E, Crane P, Eisen G, McCarberg B, Ofman J (September 2001). "Evidence- and consensus-based practice guidelines for the diagnosis of irritable bowel syndrome". Archives of Internal Medicine. 161 (17): 2081–8. doi:10.1001/archinte.161.17.2081. PMID 11570936.
Talley NJ (2006). "A unifying hypothesis for the functional gastrointestinal disorders: really multiple diseases or one irritable gut?". Reviews in Gastroenterological Disorders. 6 (2): 72–8. PMID 16699476.
C. Hauser (2005). Mayo Clinic Gastroenterology and Hepatology Board Review. CRC Press. p. 225–. ISBN 978-0-203-50274-7. Archived from the original on May 10, 2013. Retrieved October 24, 2010.
El-Salhy M (October 2012). "Irritable bowel syndrome: diagnosis and pathogenesis". World Journal of Gastroenterology. 18 (37): 5151–63. doi:10.3748/wjg.v18.i37.5151 (inactive May 21, 2020). PMC 3468846. PMID 23066308.
Fasano A, Sapone A, Zevallos V, Schuppan D (May 2015). "Nonceliac gluten sensitivity". Gastroenterology (Review). 148 (6): 1195–204. doi:10.1053/j.gastro.2014.12.049. PMID 25583468.
Volta U, Caio G, De Giorgio R, Henriksen C, Skodje G, Lundin KE (June 2015). "Non-celiac gluten sensitivity: a work-in-progress entity in the spectrum of wheat-related disorders". Best Practice & Research. Clinical Gastroenterology. 29 (3): 477–91. doi:10.1016/j.bpg.2015.04.006. PMID 26060112.
Rossi A, Di Lollo AC, Guzzo MP, Giacomelli C, Atzeni F, Bazzichi L, Di Franco M (2015). "Fibromyalgia and nutrition: what news?". Clinical and Experimental Rheumatology. 33 (1 Suppl 88): S117-25. PMID 25786053.
San Mauro Martín I, Garicano Vilar E, Collado Yurrutia L, Ciudad Cabañas MJ (December 2014). "[Is gluten the great etiopathogenic agent of disease in the XXI century?]". Nutricion Hospitalaria. 30 (6): 1203–10. doi:10.3305/nh.2014.30.6.7866. PMID 25433099.
Catassi C, Bai JC, Bonaz B, Bouma G, Calabrò A, Carroccio A, Castillejo G, Ciacci C, Cristofori F, Dolinsek J, Francavilla R, Elli L, Green P, Holtmeier W, Koehler P, Koletzko S, Meinhold C, Sanders D, Schumann M, Schuppan D, Ullrich R, Vécsei A, Volta U, Zevallos V, Sapone A, Fasano A (September 2013). "Non-Celiac Gluten sensitivity: the new frontier of gluten related disorders". Nutrients (Review). 5 (10): 3839–53. doi:10.3390/nu5103839. PMC 3820047. PMID 24077239.
Lebwohl B, Ludvigsson JF, Green PH (October 2015). "Celiac disease and non-celiac gluten sensitivity". BMJ (Review). 351: h4347. doi:10.1136/bmj.h4347. PMC 4596973. PMID 26438584.
Bixquert Jiménez M (August 2009). "Treatment of irritable bowel syndrome with probiotics. An etiopathogenic approach at last?". Revista Espanola de Enfermedades Digestivas. 101 (8): 553–64. doi:10.4321/s1130-01082009000800006. PMID 19785495. Archived from the original on October 6, 2014.
Spiegel BM, DeRosa VP, Gralnek IM, Wang V, Dulai GS (June 2004). "Testing for celiac sprue in irritable bowel syndrome with predominant diarrhea: a cost-effectiveness analysis". Gastroenterology. 126 (7): 1721–32. doi:10.1053/j.gastro.2004.03.012. PMID 15188167.
Su YC, Wang WM, Wang SY, Lu SN, Chen LT, Wu DC, Chen CY, Jan CM, Horowitz M (August 2000). "The association between Helicobacter pylori infection and functional dyspepsia in patients with irritable bowel syndrome". The American Journal of Gastroenterology. 95 (8): 1900–5. PMID 10950033.
Gerards C, Leodolter A, Glasbrenner B, Malfertheiner P (2001). "H. pylori infection and visceral hypersensitivity in patients with irritable bowel syndrome". Digestive Diseases. 19 (2): 170–3. doi:10.1159/000050673. PMID 11549828.
Grazioli B, Matera G, Laratta C, Schipani G, Guarnieri G, Spiniello E, Imeneo M, Amorosi A, Focà A, Luzza F (March 2006). "Giardia lamblia infection in patients with irritable bowel syndrome and dyspepsia: a prospective study". World Journal of Gastroenterology. 12 (12): 1941–4. doi:10.3748/wjg.v12.i12.1941. PMC 4087522. PMID 16610003. Archived from the original on August 15, 2009.
Vernia P, Ricciardi MR, Frandina C, Bilotta T, Frieri G (April 1995). "Lactose malabsorption and irritable bowel syndrome. Effect of a long-term lactose-free diet". The Italian Journal of Gastroenterology. 27 (3): 117–21. PMID 7548919.
Brandt LJ, Chey WD, Foxx-Orenstein AE, Schiller LR, Schoenfeld PS, Spiegel BM, Talley NJ, Quigley EM (January 2009). "An evidence-based position statement on the management of irritable bowel syndrome" (PDF). The American Journal of Gastroenterology. 104 (Suppl 1): S1-35. doi:10.1038/ajg.2008.122. PMID 19521341. Archived (PDF) from the original on December 5, 2010.
Wedlake L, A'Hern R, Russell D, Thomas K, Walters JR, Andreyev HJ (October 2009). "Systematic review: the prevalence of idiopathic bile acid malabsorption as diagnosed by SeHCAT scanning in patients with diarrhoea-predominant irritable bowel syndrome". Alimentary Pharmacology & Therapeutics. 30 (7): 707–17. doi:10.1111/j.1365-2036.2009.04081.x. PMID 19570102.
Cole JA, Rothman KJ, Cabral HJ, Zhang Y, Farraye FA (September 2006). "Migraine, fibromyalgia, and depression among people with IBS: a prevalence study". BMC Gastroenterology. 6: 26. doi:10.1186/1471-230X-6-26. PMC 1592499. PMID 17007634.
Bercik P, Verdu EF, Collins SM (June 2005). "Is irritable bowel syndrome a low-grade inflammatory bowel disease?". Gastroenterology Clinics of North America. 34 (2): 235–45, vi–vii. doi:10.1016/j.gtc.2005.02.007. PMID 15862932.
Quigley EM (2005). "Irritable bowel syndrome and inflammatory bowel disease: interrelated diseases?". Chinese Journal of Digestive Diseases. 6 (3): 122–32. doi:10.1111/j.1443-9573.2005.00202.x. PMID 16045602.
Simrén M, Axelsson J, Gillberg R, Abrahamsson H, Svedlund J, Björnsson ES (February 2002). "Quality of life in inflammatory bowel disease in remission: the impact of IBS-like symptoms and associated psychological factors". The American Journal of Gastroenterology. 97 (2): 389–96. doi:10.1016/S0002-9270(01)04037-0. PMID 11866278.
Minderhoud IM, Oldenburg B, Wismeijer JA, van Berge Henegouwen GP, Smout AJ (March 2004). "IBS-like symptoms in patients with inflammatory bowel disease in remission; relationships with quality of life and coping behavior". Digestive Diseases and Sciences. 49 (3): 469–74. doi:10.1023/BDAS.0000020506.84248.f9. PMID 15139501.
García Rodríguez LA, Ruigómez A, Wallander MA, Johansson S, Olbe L (March 2000). "Detection of colorectal tumor and inflammatory bowel disease during follow-up of patients with initial diagnosis of irritable bowel syndrome". Scandinavian Journal of Gastroenterology. 35 (3): 306–11. doi:10.1080/003655200750024191. PMID 10766326.
Corazziari E, Attili AF, Angeletti C, De Santis A (December 2008). "Gallstones, cholecystectomy and irritable bowel syndrome (IBS) MICOL population-based study". Digestive and Liver Disease. 40 (12): 944–50. doi:10.1016/j.dld.2008.02.013. PMID 18406218.
Cole JA, Yeaw JM, Cutone JA, Kuo B, Huang Z, Earnest DL, Walker AM (December 2005). "The incidence of abdominal and pelvic surgery among patients with irritable bowel syndrome". Digestive Diseases and Sciences. 50 (12): 2268–75. doi:10.1007/s10620-005-3047-1. PMID 16416174.
Longstreth GF, Yao JF (June 2004). "Irritable bowel syndrome and surgery: a multivariable analysis". Gastroenterology. 126 (7): 1665–73. doi:10.1053/j.gastro.2004.02.020. PMID 15188159.
Tietjen GE, Bushnell CD, Herial NA, Utley C, White L, Hafeez F (2007). "Endometriosis is associated with prevalence of comorbid conditions in migraine". Headache. 47 (7): 1069–78. doi:10.1111/j.1526-4610.2007.00784.x. PMID 17635599.
"Interstitial cystitis: Risk factors". Mayo Clinic. January 20, 2009. Archived from the original on May 16, 2008.
Ford AC, Talley NJ, Spiegel BM, Foxx-Orenstein AE, Schiller L, Quigley EM, Moayyedi P (November 2008). "Effect of fibre, antispasmodics, and peppermint oil in the treatment of irritable bowel syndrome: systematic review and meta-analysis". BMJ. 337: a2313. doi:10.1136/bmj.a2313. PMC 2583392. PMID 19008265.
Ford AC, Quigley EM, Lacy BE, Lembo AJ, Saito YA, Schiller LR, Soffer EE, Spiegel BM, Moayyedi P (September 2014). "Effect of antidepressants and psychological therapies, including hypnotherapy, in irritable bowel syndrome: systematic review and meta-analysis". The American Journal of Gastroenterology. 109 (9): 1350–65, quiz 1366. doi:10.1038/ajg.2014.148. PMID 24935275.
Khanna R, MacDonald JK, Levesque BG (July 2014). "eppermint oil for the treatment of irritable bowel syndrome: a systematic review and meta-analysis". Journal of Clinical Gastroenterology. 48 (6): 505–12. doi:10.1097/MCG.0b013e3182a88357. PMID 24100754.
Dionne J, Ford AC, Yuan Y, Chey WD, Lacy BE, Saito YA, Quigley EM, Moayyedi P (September 2018). "A Systematic Review and Meta-Analysis Evaluating the Efficacy of a Gluten-Free Diet and a Low FODMAPs Diet in Treating Symptoms of Irritable Bowel Syndrome". The American Journal of Gastroenterology. 113 (9): 1290–1300. doi:10.1038/s41395-018-0195-4. PMID 30046155.
Staudacher HM, Irving PM, Lomer MC, Whelan K (April 2014). "Mechanisms and efficacy of dietary FODMAP restriction in IBS". Nature Reviews. Gastroenterology & Hepatology (Review). 11 (4): 256–66. doi:10.1038/nrgastro.2013.259. PMID 24445613. An emerging body of research now demonstrates the efficacy of fermentable carbohydrate restriction in IBS. [...] However, further work is urgently needed both to confirm clinical efficacy of fermentable carbohydrate restriction in a variety of clinical subgroups and to fully characterize the effect on the gut microbiota and the colonic environ¬ment. Whether the effect on luminal bifidobacteria is clinically relevant, preventable, or long lasting, needs to be investigated. The influence on nutrient intake, dietary diversity, which might also affect the gut microbiota,137 and quality of life also requires further exploration as does the possible economic effects due to reduced physician contact and need for medication. Although further work is required to confirm its place in IBS and functional bowel disorder clinical pathways, fermentable carbohydrate restriction is an important consideration for future national and international IBS guidelines.
Fedewa A, Rao SS (January 2014). "Dietary fructose intolerance, fructan intolerance and FODMAPs". Current Gastroenterology Reports. 16 (1): 370. doi:10.1007/s11894-013-0370-0. PMC 3934501. PMID 24357350.
Gibson PR, Shepherd SJ (February 2010). "Evidence-based dietary management of functional gastrointestinal symptoms: The FODMAP approach". Journal of Gastroenterology and Hepatology. 25 (2): 252–8. doi:10.1111/j.1440-1746.2009.06149.x. PMID 20136989.
Makharia A, Catassi C, Makharia GK (December 2015). "The Overlap between Irritable Bowel Syndrome and Non-Celiac Gluten Sensitivity: A Clinical Dilemma". Nutrients (Review). 7 (12): 10417–26. doi:10.3390/nu7125541. PMC 4690093. PMID 26690475.
Greer JB, O'Keefe SJ (2011). "Microbial induction of immunity, inflammation, and cancer". Frontiers in Physiology (Review). 1: 168. doi:10.3389/fphys.2010.00168. PMC 3059938. PMID 21423403.
Andoh A, Tsujikawa T, Fujiyama Y (2003). "Role of dietary fiber and short-chain fatty acids in the colon". Current Pharmaceutical Design (Review). 9 (4): 347–58. doi:10.2174/1381612033391973. PMID 12570825.
Turco R, Salvatore S, Miele E, Romano C, Marseglia GL, Staiano A (May 2018). "Does a low FODMAPs diet reduce symptoms of functional abdominal pain disorders? A systematic review in adult and paediatric population, on behalf of Italian Society of Pediatrics". Italian Journal of Pediatrics (Systematic Review). 44 (1): 53. doi:10.1186/s13052-018-0495-8. PMC 5952847. PMID 29764491.
Marsh A, Eslick EM, Eslick GD (April 2016). "Does a diet low in FODMAPs reduce symptoms associated with functional gastrointestinal disorders? A comprehensive systematic review and meta-analysis". European Journal of Nutrition. 55 (3): 897–906. doi:10.1007/s00394-015-0922-1. PMID 25982757.
Tuck CJ, Muir JG, Barrett JS, Gibson PR (September 2014). "Fermentable oligosaccharides, disaccharides, monosaccharides and polyols: role in irritable bowel syndrome". Expert Review of Gastroenterology & Hepatology. 8 (7): 819–34. doi:10.1586/17474124.2014.917956. PMID 24830318.
Heiman ML, Greenway FL (May 2016). "A healthy gastrointestinal microbiome is dependent on dietary diversity". Molecular Metabolism (Review). 5 (5): 317–320. doi:10.1016/j.molmet.2016.02.005. PMC 4837298. PMID 27110483.
Staudacher HM, Whelan K (August 2017). "The low FODMAP diet: recent advances in understanding its mechanisms and efficacy in IBS". Gut (Review). 66 (8): 1517–1527. doi:10.1136/gutjnl-2017-313750. PMID 28592442.
Hou JK, Lee D, Lewis J (October 2014). "Diet and inflammatory bowel disease: review of patient-targeted recommendations". Clinical Gastroenterology and Hepatology (Review). 12 (10): 1592–600. doi:10.1016/j.cgh.2013.09.063. PMC 4021001. PMID 24107394. Even less evidence exists for the efficacy of the SCD, FODMAP, or Paleo diet. Furthermore, the practicality of maintaining these interventions over long periods of time is doubtful. At a practical level, adherence to defined diets may result in an unnecessary financial burden or reduction in overall caloric intake in people who are already at risk for protein-calorie malnutrition.
Barrett JS (March 2017). "How to institute the low-FODMAP diet". Journal of Gastroenterology and Hepatology (Review). 32 (Suppl 1): 8–10. doi:10.1111/jgh.13686. PMID 28244669. Common symptoms of IBS are bloating, abdominal pain, excessive flatus, constipation, diarrhea, or alternating bowel habit. These symptoms, however, are also common in the presentation of coeliac disease, inflammatory bowel disease, defecatory disorders, and colon cancer. Confirming the diagnosis is crucial so that appropriate therapy can be undertaken. Unfortunately, even in these alternate diagnoses, a change in diet restricting FODMAPs may improve symptoms and mask the fact that the correct diagnosis has not been made. This is the case with coeliac disease where a low-FODMAP diet can concurrently reduce dietary gluten, improving symptoms, and also affecting coeliac diagnostic indices.3,4 Misdiagnosis of intestinal diseases can lead to secondary problems such as nutritional deficiencies, cancer risk, or even mortality in the case of colon cancer.
"Celiac disease". World Gastroenterology Organisation Global Guidelines. July 2016. Archived from the original on 17 March 2017. Retrieved 4 June 2018.
Francis CY, Whorwell PJ (July 1994). "Bran and irritable bowel syndrome: time for reappraisal". Lancet. 344 (8914): 39–40. doi:10.1016/S0140-6736(94)91055-3. PMID 7912305.
Shen YH, Nahas R (February 2009). "Complementary and alternative medicine for treatment of irritable bowel syndrome". Canadian Family Physician. 55 (2): 143–8. PMC 2642499. PMID 19221071.
Bijkerk CJ, de Wit NJ, Muris JW, Whorwell PJ, Knottnerus JA, Hoes AW (August 2009). "Soluble or insoluble fibre in irritable bowel syndrome in primary care? Randomised placebo controlled trial". BMJ. 339 (b3154): b3154. doi:10.1136/bmj.b3154. PMC 3272664. PMID 19713235.
Ducrotté P (November 2007). "[Irritable bowel syndrome: current treatment options]". Presse Médicale. 36 (11 Pt 2): 1619–26. doi:10.1016/j.lpm.2007.03.008. PMID 17490849.
Bijkerk CJ, Muris JW, Knottnerus JA, Hoes AW, de Wit NJ (February 2004). "Systematic review: the role of different types of fibre in the treatment of irritable bowel syndrome". Alimentary Pharmacology & Therapeutics. 19 (3): 245–51. doi:10.1111/j.0269-2813.2004.01862.x. PMID 14984370.
Bijkerk CJ, de Wit NJ, Muris JW, Whorwell PJ, Knottnerus JA, Hoes AW (August 2009). "Soluble or insoluble fibre in irritable bowel syndrome in primary care? Randomised placebo controlled trial". BMJ. 339 (b): b3154. doi:10.1136/bmj.b3154. PMC 3272664. PMID 19713235.
Prior A, Whorwell PJ (November 1987). "Double blind study of ispaghula in irritable bowel syndrome". Gut. 28 (11): 1510–3. doi:10.1136/gut.28.11.1510. PMC 1433676. PMID 3322956.
Jalihal A, Kurian G (1990). "Ispaghula therapy in irritable bowel syndrome: improvement in overall well-being is related to reduction in bowel dissatisfaction". Journal of Gastroenterology and Hepatology. 5 (5): 507–13. doi:10.1111/j.1440-1746.1990.tb01432.x. PMID 2129822.
Kumar A, Kumar N, Vij JC, Sarin SK, Anand BS (February 1987). "Optimum dosage of ispaghula husk in patients with irritable bowel syndrome: correlation of symptom relief with whole gut transit time and stool weight". Gut. 28 (2): 150–5. doi:10.1136/gut.28.2.150. PMC 1432983. PMID 3030900.
Ruepert L, Quartero AO, de Wit NJ, van der Heijden GJ, Rubin G, Muris JW (August 2011). "Bulking agents, antispasmodics and antidepressants for the treatment of irritable bowel syndrome". The Cochrane Database of Systematic Reviews (8): CD003460. doi:10.1002/14651858.CD003460.pub3. PMID 21833945.
Ford, AC; Lacy, BE; Harris, LA; Quigley, EMM; Moayyedi, P (January 2019). "Effect of Antidepressants and Psychological Therapies in Irritable Bowel Syndrome: An Updated Systematic Review and Meta-Analysis" (PDF). The American Journal of Gastroenterology. 114 (1): 21–39. doi:10.1038/s41395-018-0222-5. PMID 30177784.
Joo JS, Ehrenpreis ED, Gonzalez L, Kaye M, Breno S, Wexner SD, Zaitman D, Secrest K (June 1998). "Alterations in colonic anatomy induced by chronic stimulant laxatives: the cathartic colon revisited". Journal of Clinical Gastroenterology. 26 (4): 283–6. doi:10.1097/00004836-199806000-00014. PMID 9649012.
Paul Barber; Joy Parkes; Diane Blundell (June 1, 2012). Further Essentials of Pharmacology for Nurses. McGraw-Hill Education (UK). pp. 34–. ISBN 978-0-335-24398-3. Archived from the original on February 16, 2017.
Annaházi A, Róka R, Rosztóczy A, Wittmann T (May 2014). "Role of antispasmodics in the treatment of irritable bowel syndrome". World Journal of Gastroenterology. 20 (20): 6031–43. doi:10.3748/wjg.v20.i20.6031. PMC 4033443. PMID 24876726.
Simrén M, Barbara G, Flint HJ, Spiegel BM, Spiller RC, Vanner S, Verdu EF, Whorwell PJ, Zoetendal EG (January 2013). "Intestinal microbiota in functional bowel disorders: a Rome foundation report". Gut. 62 (1): 159–76. doi:10.1136/gutjnl-2012-302167. PMC 3551212. PMID 22730468.
Song KH, Jung HK, Kim HJ, Koo HS, Kwon YH, Shin HD, Lim HC, Shin JE, Kim SE, Cho DH, Kim JH, Kim HJ (April 2018). "Clinical Practice Guidelines for Irritable Bowel Syndrome in Korea, 2017 Revised Edition". Journal of Neurogastroenterology and Motility. 24 (2): 197–215. doi:10.5056/jnm17145. PMC 5885719. PMID 29605976.
Xie C, Tang Y, Wang Y, Yu T, Wang Y, Jiang L, Lin L (August 7, 2015). "Efficacy and Safety of Antidepressants for the Treatment of Irritable Bowel Syndrome: A Meta-Analysis". PLOS ONE. 10 (8): e0127815. Bibcode:2015PLoSO..1027815X. doi:10.1371/journal.pone.0127815. PMC 4529302. PMID 26252008.
Lee KJ (October 2015). "harmacologic Agents for Chronic Diarrhea". Intestinal Research. 13 (4): 306–12. doi:10.5217/ir.2015.13.4.306. PMC 4641856. PMID 26576135.
Arnold Wald. Nicholas J Talley; Shilpa Grover (eds.). "Treatment of irritable bowel syndrome in adults". UpToDate Inc.
Jackson JL, O'Malley PG, Tomkins G, Balden E, Santoro J, Kroenke K (January 2000). "Treatment of functional gastrointestinal disorders with antidepressant medications: a meta-analysis". The American Journal of Medicine. 108 (1): 65–72. doi:10.1016/S0002-9343(99)00299-5. PMID 11059442.
Ford AC, Harris LA, Lacy BE, Quigley EM, Moayyedi P (November 2018). "Systematic review with meta-analysis: the efficacy of prebiotics, probiotics, synbiotics and antibiotics in irritable bowel syndrome". Alimentary Pharmacology & Therapeutics. 48 (10): 1044–1060. doi:10.1111/apt.15001. PMID 30294792.
Raahave D, Christensen E, Loud FB, Knudsen LL. "Correlation of bowel symptoms with colonic transit, length, and faecal load in functional faecal retention" 2009; 56: 83–8
Lin HC (August 2004). "Small intestinal bacterial overgrowth: a framework for understanding irritable bowel syndrome". JAMA. 292 (7): 852–8. doi:10.1001/jama.292.7.852. PMID 15316000.
Spiegel BM (June 2011). "Questioning the bacterial overgrowth hypothesis of irritable bowel syndrome: an epidemiologic and evolutionary perspective". Clinical Gastroenterology and Hepatology. 9 (6): 461–9, quiz e59. doi:10.1016/j.cgh.2011.02.030. PMID 21397724.
Irritable Bowel Syndrome in Adults Archived May 26, 2014, at the Wayback Machine: Diagnosis and management of irritable bowel syndrome in primary care; NICE clinical guideline 61, Issue Feb 2008
"Irritable Bowel Syndrome (IBS) – Treatment". NHS Choices. National Health Service. Archived from the original on October 18, 2012. Retrieved October 21, 2012.
Manheimer E, Cheng K, Wieland LS, Min LS, Shen X, Berman BM, Lao L (May 2012). "Acupuncture for treatment of irritable bowel syndrome". The Cochrane Database of Systematic Reviews. 5 (5): CD005111. doi:10.1002/14651858.CD005111.pub3. PMC 3718572. PMID 22592702.
Nikfar S, Rahimi R, Rahimi F, Derakhshani S, Abdollahi M (December 2008). "Efficacy of probiotics in irritable bowel syndrome: a meta-analysis of randomized, controlled trials". Diseases of the Colon and Rectum. 51 (12): 1775–80. doi:10.1007/s10350-008-9335-z. PMID 18465170.
Konturek PC, Brzozowski T, Konturek SJ (December 2011). "Stress and the gut: pathophysiology, clinical consequences, diagnostic approach and treatment options". Journal of Physiology and Pharmacology. 62 (6): 591–9. PMID 22314561.
"New Studies Examine the Evidence on Probiotics in IBS" (PDF) (Press release). American College of Gastroenterology. October 31, 2005. Archived from the original (PDF) on February 10, 2006.
Brenner DM, Moeller MJ, Chey WD, Schoenfeld PS (April 2009). "The utility of probiotics in the treatment of irritable bowel syndrome: a systematic review". The American Journal of Gastroenterology. 104 (4): 1033–49, quiz 1050. doi:10.1038/ajg.2009.25. PMID 19277023.
Aragon G, Graham DB, Borum M, Doman DB (January 2010). "robiotic therapy for irritable bowel syndrome". Gastroenterology & Hepatology. 6 (1): 39–44. PMC 2886445. PMID 20567539.
"IBS diet: Can yogurt ease symptoms?". Mayo Clinic. May 21, 2008. Archived from the original on February 9, 2010.
McFarland LV (May 2010). "Systematic review and meta-analysis of Saccharomyces boulardii in adult patients". World Journal of Gastroenterology. 16 (18): 2202–22. doi:10.3748/wjg.v16.i18.2202. PMC 2868213. PMID 20458757.
Ortiz-Lucas M, Tobías A, Saz P, Sebastián JJ (January 2013). "Effect of probiotic species on irritable bowel syndrome symptoms: A bring up to date meta-analysis" (PDF). Revista Espanola de Enfermedades Digestivas. 105 (1): 19–36. doi:10.4321/s1130-01082013000100005. PMID 23548007.
Xu, D; Chen, VL; Steiner, CA; Berinstein, JA; Eswaran, S; Waljee, AK; Higgins, PDR; Owyang, C (July 2019). "Efficacy of Fecal Microbiota Transplantation in Irritable Bowel Syndrome: A Systematic Review and Meta-Analysis". The American Journal of Gastroenterology. 114 (7): 1043–1050. doi:10.14309/ajg.0000000000000198. PMID 30908299.
Wilkins T, Pepitone C, Alex B, Schade RR (September 2012). "Diagnosis and management of IBS in adults". American Family Physician. 86 (5): 419–26. PMID 22963061.
Rösch W, Liebregts T, Gundermann KJ, Vinson B, Holtmann G (2006). "hytotherapy for functional dyspepsia: a review of the clinical evidence for the herbal preparation STW 5". Phytomedicine. 13 (Suppl 5): 114–21. doi:10.1016/j.phymed.2006.03.022. PMID 16978851.
Boivin M (October 2001). "Socioeconomic impact of irritable bowel syndrome in Canada". Canadian Journal of Gastroenterology. 15 (Suppl B): 8B–11B. doi:10.1155/2001/401309. PMID 11694908.
Quigley EM, Locke GR, Mueller-Lissner S, Paulo LG, Tytgat GN, Helfrich I, Schaefer E (July 2006). "revalence and management of abdominal cramping and pain: a multinational survey". Alimentary Pharmacology & Therapeutics. 24 (2): 411–9. doi:10.1111/j.1365-2036.2006.02989.x. PMID 16842469.
Ehlin AG, Montgomery SM, Ekbom A, Pounder RE, Wakefield AJ (August 2003). "Prevalence of gastrointestinal diseases in two British national birth cohorts". Gut. 52 (8): 1117–21. doi:10.1136/gut.52.8.1117. PMC 1773740. PMID 12865268.
Wilson S, Roberts L, Roalfe A, Bridge P, Singh S (July 2004). "Prevalence of irritable bowel syndrome: a community survey". The British Journal of General Practice. 54 (504): 495–502. PMC 1324800. PMID 15239910.
Hungin AP, Chang L, Locke GR, Dennis EH, Barghout V (June 2005). "Irritable bowel syndrome in the United States: prevalence, symptom patterns and impact". Alimentary Pharmacology & Therapeutics. 21 (11): 1365–75. doi:10.1111/j.1365-2036.2005.02463.x. PMID 15932367.
Jafri W, Yakoob J, Jafri N, Islam M, Ali QM (June 2007). "Irritable bowel syndrome and health seeking behaviour in different communities of Pakistan". JPMA. The Journal of the Pakistan Medical Association. 57 (6): 285–7. PMID 17629228.
Jafri W, Yakoob J, Jafri N, Islam M, Ali QM (2005). "Frequency of irritable bowel syndrome in college students". Journal of Ayub Medical College, Abbottabad. 17 (4): 9–11. PMID 16599025.
Schmulson M, Ortíz O, Santiago-Lomeli M, Gutiérrez-Reyes G, Gutiérrez-Ruiz MC, Robles-Díaz G, Morgan D (2006). "Frequency of functional bowel disorders among healthy volunteers in Mexico City". Digestive Diseases. 24 (3–4): 342–7. doi:10.1159/000092887. PMID 16849861.
Payne S (August 2004). "Sex, gender, and irritable bowel syndrome: making the connections". Gender Medicine. 1 (1): 18–28. doi:10.1016/S1550-8579(04)80007-X. PMID 16115580.
Jackson NA, Houghton LA, Whorwell PJ, Currer B (December 1994). "Does the menstrual cycle affect anorectal physiology?". Digestive Diseases and Sciences. 39 (12): 2607–11. doi:10.1007/bf02087697. PMID 7995186.
Voci SC, Cramer KM (November 2009). "Gender-related traits, quality of life, and psychological adjustment among women with irritable bowel syndrome". Quality of Life Research. 18 (9): 1169–76. doi:10.1007/s11136-009-9532-9. PMID 19728159.
Drossman DA, Li Z, Andruzzi E, Temple RD, Talley NJ, Thompson WG, Whitehead WE, Janssens J, Funch-Jensen P, Corazziari E (September 1993). "U.S. householder survey of functional gastrointestinal disorders. Prevalence, sociodemography, and health impact". Digestive Diseases and Sciences. 38 (9): 1569–80. doi:10.1007/bf01303162. PMID 8359066.
Goffaux P, Michaud K, Gaudreau J, Chalaye P, Rainville P, Marchand S (September 2011). "Sex differences in perceived pain are affected by an anxious brain". Pain. 152 (9): 2065–73. doi:10.1016/j.pain.2011.05.002. PMID 21665365.
Walker EA, Katon WJ, Roy-Byrne PP, Jemelka RP, Russo J (October 1993). "Histories of sexual victimization in patients with irritable bowel syndrome or inflammatory bowel disease". The American Journal of Psychiatry. 150 (10): 1502–6. doi:10.1176/ajp.150.10.1502. PMID 8379554.
Brown PW (May 1950). "The irritable bowel syndrome". Rocky Mountain Medical Journal. 47 (5): 343–6. PMID 15418074.
"Definition & Facts for Irritable Bowel Syndrome. What is IBS? | NIDDK". National Institute of Diabetes and Digestive and Kidney Diseases. February 2015. Archived from the original on 4 October 2017. Retrieved 15 March 2018.
Spiller R, Aziz Q, Creed F, Emmanuel A, Houghton L, Hungin P, Jones R, Kumar D, Rubin G, Trudgill N, Whorwell P (December 2007). "Guidelines on the irritable bowel syndrome: mechanisms and practical management". Gut (Practice Guideline. Review). 56 (12): 1770–98. doi:10.1136/gut.2007.119446. PMC 2095723. PMID 17488783.
Camilleri M (November 2012). "Irritable bowel syndrome: how useful is the term and the 'diagnosis'?". Therapeutic Advances in Gastroenterology. 5 (6): 381–6. doi:10.1177/1756283X12442223. PMC 3491678. PMID 23152731.
García MD, García JI, Pereda A (2002). "Trastornos intestinales funcionales (equivalentes del colon irritable)". Sociedad Española de Gastroenterología, Hepatología y Nutrición Pediátrica (Review) (in Spanish). 57 (3): 253–63. doi:10.1016/S1695-4033(02)77914-9.
Levy RL, Von Korff M, Whitehead WE, Stang P, Saunders K, Jhingran P, Barghout V, Feld AD (November 2001). "Costs of care for irritable bowel syndrome patients in a health maintenance organization". The American Journal of Gastroenterology. 96 (11): 3122–9. PMID 11721759.
Nyrop KA, Palsson OS, Levy RL, Von Korff M, Feld AD, Turner MJ, Whitehead WE (July 2007). "Costs of health care for irritable bowel syndrome, chronic constipation, functional diarrhoea and functional abdominal pain". Alimentary Pharmacology & Therapeutics. 26 (2): 237–48. doi:10.1111/j.1365-2036.2007.03370.x. PMID 17593069. Archived from the original on July 13, 2013.
Paré P, Gray J, Lam S, Balshaw R, Khorasheh S, Barbeau M, Kelly S, McBurney CR (October 2006). "Health-related quality of life, work productivity, and health care resource utilization of subjects with irritable bowel syndrome: baseline results from LOGIC (Longitudinal Outcomes Study of Gastrointestinal Symptoms in Canada), a naturalistic study". Clinical Therapeutics. 28 (10): 1726–35, discussion 1710–1. doi:10.1016/j.clinthera.2006.10.010. PMID 17157129.
Leong SA, Barghout V, Birnbaum HG, Thibeault CE, Ben-Hamadi R, Frech F, Ofman JJ (April 2003). "The economic consequences of irritable bowel syndrome: a US employer perspective". Archives of Internal Medicine. 163 (8): 929–35. doi:10.1001/archinte.163.8.929. PMID 12719202.
Martin BC, Ganguly R, Pannicker S, Frech F, Barghout V (2003). "Utilization patterns and net direct medical cost to Medicaid of irritable bowel syndrome". Current Medical Research and Opinion. 19 (8): 771–80. doi:10.1185/030079903125002540. PMID 14687449. Archived from the original on December 20, 2003.
Aroniadis OC, Brandt LJ (January 2013). "Fecal microbiota transplantation: past, present and future". Current Opinion in Gastroenterology. 29 (1): 79–84. doi:10.1097/MOG.0b013e32835a4b3e. PMID 23041678.
Smits LP, Bouter KE, de Vos WM, Borody TJ, Nieuwdorp M (November 2013). "Therapeutic potential of fecal microbiota transplantation". Gastroenterology. 145 (5): 946–53. doi:10.1053/j.gastro.2013.08.058. PMID 24018052.
Ford AC, Quigley EM, Lacy BE, Lembo AJ, Saito YA, Schiller LR, Soffer EE, Spiegel BM, Moayyedi P (October 2014). "Efficacy of prebiotics, probiotics, and synbiotics in irritable bowel syndrome and chronic idiopathic constipation: systematic review and meta-analysis". The American Journal of Gastroenterology. 109 (10): 1547–61, quiz 1546, 1562. doi:10.1038/ajg.2014.202. PMID 25070051.
Klotz U (February 2012). "The pharmacological profile and clinical use of mesalazine (5-aminosalicylic acid)". Arzneimittel-Forschung. 62 (2): 53–8. doi:10.1055/s-0031-1299685. PMID 22344548.
Barbara G, et al. (2009). "Aminosalicylates and other anti-inflammatory compounds for irritable bowel syndrome". Digestive Diseases. 27 (Suppl 1): 115–21. doi:10.1159/000268131. PMID 20203507.
Philpott H, Nandurkar S, Lubel J, Gibson PR (January 2013). "Alternative investigations for irritable bowel syndrome". Journal of Gastroenterology and Hepatology. 28 (1): 73–7. doi:10.1111/j.1440-1746.2012.07291.x. PMID 23033865.
Keszthelyi D, Troost FJ, Jonkers DM, van Eijk HM, Lindsey PJ, Dekker J, Buurman WA, Masclee AA (August 2014). "Serotonergic reinforcement of intestinal barrier function is impaired in irritable bowel syndrome". Alimentary Pharmacology & Therapeutics. 40 (4): 392–402. doi:10.1111/apt.12842. PMID 24943480.
DiGiacomo D, Santonicola A, Zingone F, Troncone E, Caria MC, Borgheresi P, Parrilli G, Ciacci C (April 2013). "Human leukocyte antigen DQ2/8 prevalence in non-celiac patients with gastrointestinal diseases". World Journal of Gastroenterology. 19 (16): 2507–13. doi:10.3748/wjg.v19.i16.2507. PMC 3646141. PMID 23674852.
您需要登录后才可以回帖 登录 | 注册
Copyright © 2011-2024 东莞市珍屯医疗科技有限公司Powered by zhentun.com
返回顶部