Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Stockholm, Sweden.
Massachusetts General Hospital, Crohn's and Colitis Center and Harvard Medical School, Boston, Massachusetts, USA.
United European Gastroenterol J. 2023 Mar;11(2):189-201. doi: 10.1002/ueg2.12374. Epub 2023 Mar 20.
An association has been reported between celiac disease (CD) and microscopic colitis (MC). However, large, population-based cohort studies are rare.
To systematically examine the association between CD and MC in a large, nationwide cohort.
We conducted a nationwide population-based matched cohort study in Sweden of 45,138 patients with biopsy-verified CD (diagnosed in 1990-2016), 223,149 reference individuals, and 51,449 siblings of CD patients. Data on CD and MC were obtained from all (n = 28) pathology departments in Sweden. Adjusted hazard ratios (aHRs) were calculated using Cox regression.
During follow-up, 452 CD patients and 197 reference individuals received an MC diagnosis (86.1 vs. 7.5 per 100,000 person-years). This difference corresponded to an aHR of 11.6 (95% confidence interval [CI] = 9.8-13.8) or eight extra MC cases in 1000 CD patients followed up for 10 years. Although the risk of MC was highest during the first year of follow-up (aHR 35.2; 95% CI = 20.1-61.6), it remained elevated even after 10 years (aHR 8.1; 95% CI = 6.0-10.9). Examining MC subtypes lymphocytic colitis (LC) and collagenous colitis (CC) separately, the aHR was 12.4 (95% CI = 10.0-15.3) for LC and 10.2 (95% CI = 7.7-13.6) for CC. MC was also more common before CD (adjusted odds ratio [aOR] = 52.7; 95% CI = 31.4-88.4). Compared to siblings, risk estimates decreased but remained elevated (CD and later MC: HR = 6.2; CD and earlier MC: aOR = 7.9).
Our study demonstrated a very strong association of MC with CD with an increased risk of future and previous MC in CD patients. The magnitude of the associations underscores the need to consider the concomitance of these diagnoses in cases in which gastrointestinal symptoms persist or recur despite a gluten-free diet or conventional MC treatment. The comparatively lower risk estimates in sibling comparisons suggest that shared genetic and early environmental factors may contribute to the association between CD and MC.
已有研究报告显示,乳糜泻(CD)与显微镜下结肠炎(MC)之间存在关联。然而,基于人群的大型队列研究较为罕见。
在一个大型全国性队列中,系统地研究 CD 与 MC 之间的关联。
我们在瑞典进行了一项基于人群的全国性匹配队列研究,纳入了 45138 例经活检证实的 CD 患者(1990-2016 年确诊)、223149 名对照者和 51449 名 CD 患者的同胞。所有(n=28)瑞典病理学部门均获取 CD 和 MC 数据。采用 Cox 回归计算校正后危险比(aHR)。
在随访期间,452 例 CD 患者和 197 名对照者被诊断为 MC(86.1 比 7.5/100000 人年)。这一差异对应于 aHR 为 11.6(95%CI 9.8-13.8),即在 1000 例接受 10 年随访的 CD 患者中,每 1000 例患者中会多发生 8 例 MC。尽管 MC 的风险在随访的第一年最高(aHR 35.2;95%CI 20.1-61.6),但即使在 10 年后,风险仍居高不下(aHR 8.1;95%CI 6.0-10.9)。分别对淋巴细胞性结肠炎(LC)和胶原性结肠炎(CC)两种 MC 亚型进行分析,LC 的 aHR 为 12.4(95%CI 10.0-15.3),CC 的 aHR 为 10.2(95%CI 7.7-13.6)。MC 在 CD 之前也更为常见(校正比值比[aOR]52.7;95%CI 31.4-88.4)。与同胞相比,风险估计值降低,但仍处于升高状态(CD 伴随后 MC:HR 6.2;CD 伴早期 MC:aOR 7.9)。
本研究显示 MC 与 CD 之间存在极强的关联,CD 患者发生未来和既往 MC 的风险增加。关联的强度表明,在接受无麸质饮食或常规 MC 治疗后,胃肠道症状持续或复发的情况下,应考虑这些诊断同时存在的可能性。同胞比较中的风险估计值较低提示,共同的遗传和早期环境因素可能促成了 CD 与 MC 之间的关联。