Julien Kirchgesner , Jeremy Augustin , Thomas Bazin , Pamela Freiha , Alexandre Nuzzo , Philippe Seksik , Iradj Sobhani , Pablo Bartolucci , Mathieu Uzzan
{"title":"一系列镰状细胞病相关的炎症性肠病:结肠累及和原发性硬化性胆管炎的高患病率","authors":"Julien Kirchgesner , Jeremy Augustin , Thomas Bazin , Pamela Freiha , Alexandre Nuzzo , Philippe Seksik , Iradj Sobhani , Pablo Bartolucci , Mathieu Uzzan","doi":"10.1016/j.clinre.2025.102615","DOIUrl":null,"url":null,"abstract":"<div><h3>Objective</h3><div>Co-occurrence of Sickle Cell Disease (SCD) and Inflammatory Bowel Diseases (IBD) has been scarcely reported. Our aim was to explore the intersection between SCD and IBD, focusing on the impact of SCD on the natural course of IBD and drug safety.</div></div><div><h3>Methods</h3><div>We conducted a multicenter retrospective case-control study including consecutive patients diagnosed with IBD and SCD. Each IBD patient with SCD was matched with up to 4 IBD patients without SCD. Matching criteria were IBD type, sex, date of birth, length of follow-up and year of diagnosis. The primary outcome was a complicated IBD course.</div></div><div><h3>Results</h3><div>125 IBD patients were studied, including 24 SCD. 23/24 SCD patients had colonic involvement. 33.3 % had concomitant primary sclerosing cholangitis (PSC) compared to 1 % of controls (<em>p</em> < 0.001). Survival without a complicated IBD course was estimated at 58.7 % (CI95[49.6–69.5]) at 5 years for non-SCD patients, as compared to 63.3 % (CI95[45.7–87.6]) for SCD patients SCD (<em>p</em> = 0.36). The survival without the need of advanced therapy was estimated at 66.1 % (CI95[57.3–76.2]) at 5 years for non-SCD patient, and at 78.2 % (CI95[63–97.2]) in SCD patients (<em>p</em> = 0.45) Regarding treatment safety, 26.3 % of patients with SCD and 13.5 % of controls experienced adverse events with biologics (<em>p</em> = 0.17). There was one reported vaso-occlusive crisis associated with thiopurines.</div></div><div><h3>Conclusion</h3><div>Patients with SCD and IBD displayed a distinctive phenotype with constant colonic involvement and high prevalence of PSC.</div></div>","PeriodicalId":10424,"journal":{"name":"Clinics and research in hepatology and gastroenterology","volume":"49 7","pages":"Article 102615"},"PeriodicalIF":2.6000,"publicationDate":"2025-05-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"A series of Sickle cell disease-associated inflammatory bowel diseases: high prevalence of colonic involvement and primary sclerosing cholangitis\",\"authors\":\"Julien Kirchgesner , Jeremy Augustin , Thomas Bazin , Pamela Freiha , Alexandre Nuzzo , Philippe Seksik , Iradj Sobhani , Pablo Bartolucci , Mathieu Uzzan\",\"doi\":\"10.1016/j.clinre.2025.102615\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>Objective</h3><div>Co-occurrence of Sickle Cell Disease (SCD) and Inflammatory Bowel Diseases (IBD) has been scarcely reported. Our aim was to explore the intersection between SCD and IBD, focusing on the impact of SCD on the natural course of IBD and drug safety.</div></div><div><h3>Methods</h3><div>We conducted a multicenter retrospective case-control study including consecutive patients diagnosed with IBD and SCD. Each IBD patient with SCD was matched with up to 4 IBD patients without SCD. Matching criteria were IBD type, sex, date of birth, length of follow-up and year of diagnosis. The primary outcome was a complicated IBD course.</div></div><div><h3>Results</h3><div>125 IBD patients were studied, including 24 SCD. 23/24 SCD patients had colonic involvement. 33.3 % had concomitant primary sclerosing cholangitis (PSC) compared to 1 % of controls (<em>p</em> < 0.001). Survival without a complicated IBD course was estimated at 58.7 % (CI95[49.6–69.5]) at 5 years for non-SCD patients, as compared to 63.3 % (CI95[45.7–87.6]) for SCD patients SCD (<em>p</em> = 0.36). The survival without the need of advanced therapy was estimated at 66.1 % (CI95[57.3–76.2]) at 5 years for non-SCD patient, and at 78.2 % (CI95[63–97.2]) in SCD patients (<em>p</em> = 0.45) Regarding treatment safety, 26.3 % of patients with SCD and 13.5 % of controls experienced adverse events with biologics (<em>p</em> = 0.17). There was one reported vaso-occlusive crisis associated with thiopurines.</div></div><div><h3>Conclusion</h3><div>Patients with SCD and IBD displayed a distinctive phenotype with constant colonic involvement and high prevalence of PSC.</div></div>\",\"PeriodicalId\":10424,\"journal\":{\"name\":\"Clinics and research in hepatology and gastroenterology\",\"volume\":\"49 7\",\"pages\":\"Article 102615\"},\"PeriodicalIF\":2.6000,\"publicationDate\":\"2025-05-23\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Clinics and research in hepatology and gastroenterology\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S2210740125000932\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"GASTROENTEROLOGY & HEPATOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Clinics and research in hepatology and gastroenterology","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2210740125000932","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"GASTROENTEROLOGY & HEPATOLOGY","Score":null,"Total":0}
A series of Sickle cell disease-associated inflammatory bowel diseases: high prevalence of colonic involvement and primary sclerosing cholangitis
Objective
Co-occurrence of Sickle Cell Disease (SCD) and Inflammatory Bowel Diseases (IBD) has been scarcely reported. Our aim was to explore the intersection between SCD and IBD, focusing on the impact of SCD on the natural course of IBD and drug safety.
Methods
We conducted a multicenter retrospective case-control study including consecutive patients diagnosed with IBD and SCD. Each IBD patient with SCD was matched with up to 4 IBD patients without SCD. Matching criteria were IBD type, sex, date of birth, length of follow-up and year of diagnosis. The primary outcome was a complicated IBD course.
Results
125 IBD patients were studied, including 24 SCD. 23/24 SCD patients had colonic involvement. 33.3 % had concomitant primary sclerosing cholangitis (PSC) compared to 1 % of controls (p < 0.001). Survival without a complicated IBD course was estimated at 58.7 % (CI95[49.6–69.5]) at 5 years for non-SCD patients, as compared to 63.3 % (CI95[45.7–87.6]) for SCD patients SCD (p = 0.36). The survival without the need of advanced therapy was estimated at 66.1 % (CI95[57.3–76.2]) at 5 years for non-SCD patient, and at 78.2 % (CI95[63–97.2]) in SCD patients (p = 0.45) Regarding treatment safety, 26.3 % of patients with SCD and 13.5 % of controls experienced adverse events with biologics (p = 0.17). There was one reported vaso-occlusive crisis associated with thiopurines.
Conclusion
Patients with SCD and IBD displayed a distinctive phenotype with constant colonic involvement and high prevalence of PSC.
期刊介绍:
Clinics and Research in Hepatology and Gastroenterology publishes high-quality original research papers in the field of hepatology and gastroenterology. The editors put the accent on rapid communication of new research and clinical developments and so called "hot topic" issues. Following a clear Editorial line, besides original articles and case reports, each issue features editorials, commentaries and reviews. The journal encourages research and discussion between all those involved in the specialty on an international level. All articles are peer reviewed by international experts, the articles in press are online and indexed in the international databases (Current Contents, Pubmed, Scopus, Science Direct).
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