Morbidity and Mortality Among Older Individuals With Undiagnosed Celiac Disease
Background & Aims
Outcomes of undiagnosed celiac disease (CD) are unclear. We evaluated the morbidity and mortality of undiagnosed CD in a population-based sample of individuals 50 years of age and older.
Methods
Stored sera from a population-based sample of 16,886 Olmsted County, Minnesota, residents 50 years of age and older were tested for CD based on analysis of tissue transglutaminase and endomysial antibodies. A nested case-control study compared serologically defined subjects with CD with age- and sex-matched, seronegative controls. Medical records were reviewed for comorbid conditions.
Results
We identified 129 (0.8%) subjects with undiagnosed CD in a cohort of 16,847 older adults. A total of 127 undiagnosed cases (49% men; median age, 63.0 y) and 254 matched controls were included in a systematic evaluation for more than 100 potentially coexisting conditions. Subjects with undiagnosed CD had increased rates of osteoporosis and hypothyroidism, as well as lower body mass index and levels of cholesterol and ferritin. Overall survival was not associated with CD status. During a median follow-up period of 10.3 years after serum samples were collected, 20 cases but no controls were diagnosed with CD (15.2% Kaplan–Meier estimate at 10 years).
Conclusions
With the exception of reduced bone health, older adults with undiagnosed CD had limited comorbidity and no increase in mortality compared with controls. Some subjects were diagnosed with CD within a decade of serum collection, indicating that although most cases of undiagnosed CD are clinically silent, some result in symptoms. Undiagnosed CD can confer benefits and liabilities to older individuals.
Keywords: Prevalence, Epidemiology, Autoantibodies, Outcomes of Undiagnosed Celiac Disease
Abbreviations used in this paper: CD, celiac disease, CI, confidence interval, EMA, endomysial antibody, Ig, immunoglobulin, tTGA, tissue transglutaminase
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Conflicts of interest The authors disclose no conflicts.
Funding This work was supported by research grants R01-DK57892, P01 CA62242, R01-AR30582, and T-32 AI07047 (A.R.-T.) from the National Institutes of Health, U.S. Public Health Service. The project described was supported by grant number 1 UL1 RR024150 from the National Center for Research Resources, a component of the National Institutes of Health, and the National Institutes of Health Roadmap for Medical Research. Its contents are solely the responsibility of the authors and do not necessarily represent the official view of the National Center for Research Resources or the National Institutes of Health. Information on the National Center for Research Resources is available at http://www.ncrr.nih.gov/. Information on Reengineering the Clinical Research Enterprise can be obtained from http://nihroadmap.nih.gov.
PII: S0016-5085(10)00802-4
doi:10.1053/j.gastro.2010.05.041
© 2010 AGA Institute. Published by Elsevier Inc. All rights reserved.

