Pathiyil Mythili Menon, Jena Anuraag, Venkataramana Raju Arvind Kumar, Omprakash Tina Aswani, Sharma Vishal, Sebastian Shaji
Department of Internal Medicine, Saint Vincent Hospital, Worcester, MA, USA.
Department of Gastroenterology, Topiwala National Medical College and BYL Nair Hospital, Mumbai, India.
Lancet Gastroenterol Hepatol. 2023 Dec;8(12):1143-1151. doi: 10.1016/S2468-1253(23)00193-0. Epub 2023 Oct 10.
Inflammatory bowel disease (IBD) is now recognised as a global disease, with incidence rapidly increasing in newly industrialised countries in South America, Asia, and Africa. Trials in IBD, therefore, should adequately represent diverse groups with respect to gender, age, place of residence, race, and ethnicity to ensure the global applicability and generalisability of their findings. In this systematic review, we searched PubMed and Embase for randomised controlled trials (RCTs) published in English from Jan 1, 1995, to Jan 13, 2023, evaluating the efficacy of any pharmacological intervention in patients with IBD. Of 7543 records yielded in the search, we included 617 records reporting data from 627 RCTs and 108 986 participants. The results show a paucity of adequate representation of diverse groups in these RCTs. This finding was true for various groups, including racially and ethnically diverse populations, older (aged >65 years) and younger (aged <18 years) populations, those who identify outside of the gender binary, and people from South America and Africa. Also, some regions had an apparent scarcity of funding sources for trials. Pharmaceutical companies and clinical trial organisations should aim to ensure adequate representation of such under-represented groups in future IBD trials.
炎症性肠病(IBD)现已被公认为一种全球性疾病,在南美洲、亚洲和非洲的新兴工业化国家发病率迅速上升。因此,IBD试验应在性别、年龄、居住地、种族和民族方面充分代表不同群体,以确保其研究结果具有全球适用性和普遍性。在这项系统评价中,我们检索了PubMed和Embase数据库,以查找1995年1月1日至2023年1月13日期间发表的英文随机对照试验(RCT),评估任何药物干预对IBD患者的疗效。在检索到的7543条记录中,我们纳入了617条记录,这些记录报告了来自627项RCT和108986名参与者的数据。结果显示,这些RCT中缺乏对不同群体的充分代表性。这一发现适用于各个群体,包括不同种族和族裔的人群、老年人(年龄>65岁)和年轻人(年龄<18岁)、非二元性别者以及来自南美洲和非洲的人群。此外,一些地区的试验资金来源明显短缺。制药公司和临床试验组织应致力于确保在未来的IBD试验中充分代表这些代表性不足的群体。