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奥美沙坦相关肠病:一项全国性调查的结果。

Olmesartan-associated enteropathy: results of a national survey.

机构信息

Kremlin Bicêtre University Hospital, Assistance Publique-Hopitaux de Paris (AP-HP), Paris-Sud University, Le Kremlin Bicêtre; Antoine Béclère University Hospital, AP-HP, Paris-Sud University, Clamart, France.

出版信息

Aliment Pharmacol Ther. 2014 Nov;40(9):1103-9. doi: 10.1111/apt.12937. Epub 2014 Sep 9.

Abstract

BACKGROUND

Recently, a new enteropathy has been described: olmesartan-associated enteropathy. However, the association has been questioned: a phase 3 trial and a cohort study found no association between gastrointestinal events and olmesartan.

AIM

To collect French cases of sartan-associated enteropathy to describe further this entity, confirm or refute causality, and determine if the association exists with other sartans.

METHODS

French gastroenterologists were invited to report cases of sartan-associated enteropathy and collect clinical, biological and histological data. Patients with diarrhoea and histological duodenal abnormalities were included.

RESULTS

Thirty-six patients with olmesartan-associated enteropathy were reported, including 32 with villous atrophy and four without. There was only one patient with irbesartan-associated enteropathy. None of the patients died. Patients with villous atrophy had diarrhoea, vomiting, renal failure, hypokalaemia, body weight loss and hypoalbuminaemia. Thirty-one patients were hospitalised; four required intensive care. Anti-transglutaminase and anti-enterocyte antibodies were negative; anti-nuclear antibodies were positive (9/11). Endoscopic duodenal biopsies showed villous atrophy (32/32) and polyclonal intra-epithelial CD3+CD8+ lymphocytosis (11/11). Exactly, 14/15 patients responded to steroids and/or immunosuppressants, prescribed because of suspected autoimmune enteropathy. Ten olmesartan interruptions were followed by reintroductions before steroids or immunosuppressants. Interruptions were followed by remissions (9/10), but reintroductions were followed by relapses (9/9). Twenty-nine patients were in remission since olmesartan interruption, including 26 without immunosuppressants. Patients with normal villi had similar clinical characteristics, but mild histological abnormalities (intra-epithelial lymphocytosis and lamina propria lymphocytic infiltration).

CONCLUSIONS

Olmesartan causes a severe and immune-mediated enteropathy, with or without villous atrophy. Enteropathy associated with other sartans seems to be very rare.

摘要

背景

最近,一种新的肠病已经被描述:奥美沙坦相关肠病。然而,这种关联受到了质疑:一项 3 期试验和一项队列研究发现奥美沙坦与胃肠道事件之间没有关联。

目的

收集法国的沙坦类相关肠病病例,进一步描述这种疾病,确认或反驳因果关系,并确定这种关联是否与其他沙坦类药物有关。

方法

邀请法国胃肠病学家报告沙坦类相关肠病病例,并收集临床、生物学和组织学数据。纳入有腹泻和组织学十二指肠异常的患者。

结果

报告了 36 例奥美沙坦相关肠病患者,其中 32 例有绒毛萎缩,4 例无绒毛萎缩。仅有 1 例与依普罗沙坦相关的肠病患者。无患者死亡。绒毛萎缩患者有腹泻、呕吐、肾衰竭、低钾血症、体重减轻和低白蛋白血症。31 例患者住院治疗;4 例需要重症监护。抗转谷氨酰胺酶和抗肠细胞抗体阴性;抗核抗体阳性(9/11)。内镜十二指肠活检显示绒毛萎缩(32/32)和多克隆上皮内 CD3+CD8+淋巴细胞浸润(11/11)。确切地说,14/15 例患者对类固醇和/或免疫抑制剂有反应,这些药物是因为疑似自身免疫性肠病而开的。在类固醇或免疫抑制剂之前,10 例奥美沙坦停药后重新开始使用。停药后缓解(9/10),但重新开始后复发(9/9)。29 例患者在奥美沙坦停药后处于缓解期,其中 26 例未使用免疫抑制剂。绒毛正常的患者具有相似的临床特征,但组织学异常较轻(上皮内淋巴细胞增多和固有层淋巴细胞浸润)。

结论

奥美沙坦可引起严重的免疫介导的肠病,伴有或不伴有绒毛萎缩。与其他沙坦类药物相关的肠病似乎非常罕见。

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