Patients With Microscopic Colitis Are at Higher Risk of Major Adverse Cardiovascular Events: A Matched Cohort Study

被引:10
|
作者
Forss, Anders [1 ,2 ,12 ]
Bergman, David [1 ]
Roelstraete, Bjorn [1 ]
Sundstroem, Johan [3 ,4 ]
Mahdi, Ali [5 ]
Khalili, Hamed [6 ,7 ,8 ,9 ]
Ludvigsson, Jonas F. [1 ,10 ,11 ]
机构
[1] Karolinska Inst, Dept Med Epidemiol & Biostat, Stockholm, Sweden
[2] Karolinska Univ Hosp, Dept Gastroenterol Dermatovenereol & Rheumatol, Gastroenterol Unit, Stockholm, Sweden
[3] Uppsala Univ, Dept Med Sci, Uppsala, Sweden
[4] Univ New South Wales, George Inst Global Hlth, Sydney, NSW, Australia
[5] Karolinska Inst, Karolinska Univ Hosp, Dept Med Solna, Div Cardiol, Stockholm, Sweden
[6] Massachusetts Gen Hosp, Mongan Inst, Clin & Translat Epidemiol Unit, Boston, MA USA
[7] Harvard Med Sch, Massachusetts Gen Hosp, Gastroenterol Unit, Boston, MA USA
[8] Karolinska Inst, Inst Environm Med, Stockholm, Sweden
[9] Broad Inst MIT & Harvard, Cambridge, MA USA
[10] Orebro Univ Hosp, Dept Paediat, Orebro, Sweden
[11] Columbia Univ Coll Phys & Surg, Dept Med, New York, NY USA
[12] Karolinska Inst, Dept Med Epidemiol & Biostat, Box 281, SE-17177 Stockholm, Sweden
关键词
Biopsy; Epidemiology; Inflammatory Bowel Disease; Register-Based; DISEASE; ATHEROSCLEROSIS; INFLAMMATION; REGISTER;
D O I
10.1016/j.cgh.2023.05.014
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
BACKGROUND AND AIMS: Inflammatory diseases are associated with an increased risk of incident major adverse cardiovascular events (MACE). However, data on MACE are lacking in large population-based histopathology cohorts of microscopic colitis (MC).METHODS: This study included all Swedish adults with MC without previous cardiovascular disease (1990- 2017; N = 11,018). MC and subtypes (collagenous colitis and lymphocytic colitis) were defined from prospectively recorded intestinal histopathology reports from all pathology departments (n = 28) in Sweden. MC patients were matched for age, sex, calendar year, and county with up to 5 reference individuals (N = 48,371) without MC or cardiovascular disease. Sensitivity analyses included full sibling comparisons, and adjustment for cardiovascular medication and healthcare utilization. Multivariable-adjusted hazard ratios for MACE (any of ischemic heart disease, congestive heart failure, stroke, and cardiovascular mortality) were calculated using Cox proportional hazards modelling. RESULTS: Over a median of 6.6 years of follow-up, 2181 (19.8%) incident cases of MACE were confirmed in MC patients and 6661 (13.8%) in reference individuals. MC patients had a higher overall risk of MACE outcomes compared with reference individuals (adjusted hazard ratio [aHR], 1.27; 95% confidence interval [CI], 1.21-1.33) and higher risk of its components: ischemic heart disease (aHR, 1.38; 95% CI, 1.28-1.48), congestive heart failure (aHR, 1.32; 95% CI, 1.22-1.43), and stroke (aHR, 1.12; 95% CI, 1.02-1.23) but not cardiovascular mortality (aHR, 1.07; 95% CI, 0.98-1.18). The results remained robust in the sensitivity analyses.CONCLUSIONS: Compared with reference individuals, MC patients had a 27% higher risk of incident MACE, equal to 1 extra case of MACE for every 13 MC patients followed for 10 years.
引用
收藏
页码:3356 / 3364.e9
页数:18
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