Type 1 diabetes and multiple sclerosis - A Danish population-based cohort study

被引:97
作者
Nielsen, Nete M.
Westergaard, Tine
Frisch, Morten
Rostgaard, Klaus
Wohlfahrt, Jan
Koch-Henriksen, Nils
Melbye, Mads
Hjalgrim, Henrik
机构
[1] Statens Serum Inst, Dept Epidemiol Res, DK-2300 Copenhagen S, Denmark
[2] Natl Inst Publ Hlth, Copenhagen, Denmark
[3] Aarhus Univ Hosp, Dept Neurol, Aalborg, Denmark
[4] Natl Univ Hosp, Danish Register Multiple Sclerosis, Copenhagen, Denmark
关键词
D O I
10.1001/archneur.63.7.1001
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background: Type 1 diabetes mellitus (T1D) and multiple sclerosis (MS) contribute considerably to the burden of autoimmune diseases in young adults. Although HLA patterns of T1D and MS are considered mutually exclusive, individual and familial co-occurrence of the 2 diseases has been reported. Objective: To assess the co-occurrence of T1D and MS by estimating the risk for MS in patients with T1D and the risk for T1D in first-degree relatives of patients with MS. Design, Setting, and Participants: Two populationbased disease registers, the Danish Hospital Discharge Register and the Danish Multiple Sclerosis Register were used to identify patients with T1D, defined as patients in whom diabetes was diagnosed before age 20 years (N = 6078), and patients with MS (N = 11 862). Firstdegree relatives (N = 14 771) of patients with MS were identified from family information in the Danish Civil Registration System. Main Outcome Measure: Patients with T1D and first-degree relatives of patients with MS were followed up for occurrence of MS and T1D, respectively, and the relative risks were expressed as standardized incidence ratios, that is, ratios of observed to expected numbers of outcomes based on national age, sex, and period-specific MS and T1D incidence rates. Results: Patients with T1D were at more than 3-fold increased risk for development of MS (relative risk, 3.26; 95% confidence interval, 1.80-5.88; n = 11). First-degree relatives of patients with MS were at 63% increased risk (relative risk, 1.63; 95% confidence interval, 1.26-2.12; n = 56) for development of T1D. However, adjusting for familial relationship to patients with T1D reduced the excess risk to 44% (relative risk, 1.44; 95% confidence interval, 1.11-1.88; n = 56). Conclusion: The present nationwide cohort study demonstrates an intraindividual and, to a lesser degree, an intrafamilial co-occurrence of MS and T1D.
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页码:1001 / 1004
页数:4
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