Multiple substance use and the risk of pancreatitis: a systematic review.

IF 3.4 3区 医学 Q1 GASTROENTEROLOGY & HEPATOLOGY
Therapeutic Advances in Gastroenterology Pub Date : 2025-08-25 eCollection Date: 2025-01-01 DOI:10.1177/17562848251365030
Esther A Adeniran, Yi Jiang, Dhiraj Yadav, Judy Tan, Samuel Han, Simon K Lo, Stephen J Pandol, Christie Y Jeon
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引用次数: 0

Abstract

Background: The impact of multiple substance use on the risk of pancreatitis remains underexplored.

Objective: To systematically review peer-reviewed observational studies assessing the association of multiple substance use with the risk of acute pancreatitis (AP) or chronic pancreatitis (CP) in adults.

Design: We conducted a systematic review informed by the Preferred Reporting Items for Systematic Review and Meta-Analyses guideline.

Data sources and methods: EMBASE, MEDLINE, and PsycINFO were searched up to March 2024. Reference lists of included studies were reviewed. From 5205 records identified, 181 relevant records were evaluated in full text. Studies evaluating the association of ⩾2 substances, including tobacco, alcohol, cannabis, and illicit substances, with AP or CP were included. Data were extracted by one reviewer, with quality control by a second reviewer. Quality assessments were independently conducted by two reviewers, with differences resolved by a third.

Results: Of 11 included studies, 6 investigated AP as the outcome and 5 examined CP. Among AP studies, 5 comparing smoking and alcohol to alcohol-only use showed high heterogeneity (I 2 = 90.9%), with relative risks (RRs) from 1.40 to 11.40. One study examining cannabis and alcohol versus alcohol found a lower risk of AP in cannabis users. Among CP studies, four comparing smoking and alcohol to alcohol-only use were heterogeneous (I 2 = 81%) with odds ratios 1.21-31.50. Where examined, smoking increases the risk of AP and CP in a dose-dependent fashion. Heavy alcohol users demonstrated a significant increase in CP risk across all smoking categories in one study.

Conclusion: Combined alcohol and tobacco use increases pancreatitis risk compared to single substance use, despite heterogeneity in RRs and exposure definitions. Evidence suggests a dose-dependent impact of smoking on pancreatitis risk when added to alcohol. Studies on the impact of a combination of other substance use on pancreatitis risk are needed.

Trial registration prospero: CRD42024503677.

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多种物质使用与胰腺炎的风险:一项系统综述。
背景:多种药物使用对胰腺炎风险的影响尚不清楚。目的:系统回顾同行评议的观察性研究,评估多种药物使用与成人急性胰腺炎(AP)或慢性胰腺炎(CP)风险的关系。设计:我们根据系统评价和荟萃分析指南的首选报告项目进行了系统评价。数据来源和方法:检索截止到2024年3月EMBASE、MEDLINE和PsycINFO。回顾了纳入研究的参考文献。从确定的5205条记录中,对181条相关记录进行了全文评价。包括评估与AP或CP相关的小于或等于2物质(包括烟草、酒精、大麻和非法物质)的研究。数据由一名审稿人提取,另一名审稿人负责质量控制。质量评估由两名评审员独立进行,差异由第三名评审员解决。结果:在纳入的11项研究中,6项研究将AP作为结局,5项研究将CP作为结局。在AP研究中,5项比较吸烟和饮酒与仅饮酒的研究显示出高度异质性(i2 = 90.9%),相对危险度(RRs)从1.40到11.40。一项关于大麻和酒精与酒精的研究发现,大麻使用者患AP的风险较低。在CP研究中,有4项比较吸烟和饮酒与仅饮酒的研究是异质的(I 2 = 81%),比值比为1.21-31.50。在检查中,吸烟以剂量依赖的方式增加AP和CP的风险。在一项研究中,重度饮酒者在所有吸烟类别中都显示出CP风险的显著增加。结论:与单一物质使用相比,酒精和烟草联合使用增加了胰腺炎的风险,尽管危险比和暴露定义存在异质性。有证据表明,当吸烟与酒精混合时,对胰腺炎风险的影响呈剂量依赖性。需要对其他药物联合使用对胰腺炎风险的影响进行研究。试验注册prospero: CRD42024503677。
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来源期刊
Therapeutic Advances in Gastroenterology
Therapeutic Advances in Gastroenterology GASTROENTEROLOGY & HEPATOLOGY-
CiteScore
6.70
自引率
2.40%
发文量
103
审稿时长
15 weeks
期刊介绍: Therapeutic Advances in Gastroenterology is an open access journal which delivers the highest quality peer-reviewed original research articles, reviews, and scholarly comment on pioneering efforts and innovative studies in the medical treatment of gastrointestinal and hepatic disorders. The journal has a strong clinical and pharmacological focus and is aimed at an international audience of clinicians and researchers in gastroenterology and related disciplines, providing an online forum for rapid dissemination of recent research and perspectives in this area. The editors welcome original research articles across all areas of gastroenterology and hepatology. The journal publishes original research articles and review articles primarily. Original research manuscripts may include laboratory, animal or human/clinical studies – all phases. Letters to the Editor and Case Reports will also be considered.
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