Late-Onset T1DM and Older Age Predict Risk of Additional Autoimmune Disease.


Journal

Diabetes care
ISSN: 1935-5548
Titre abrégé: Diabetes Care
Pays: United States
ID NLM: 7805975

Informations de publication

Date de publication:
01 2019
Historique:
received: 26 05 2018
accepted: 02 10 2018
pubmed: 27 10 2018
medline: 3 5 2019
entrez: 27 10 2018
Statut: ppublish

Résumé

Type 1 diabetes (T1DM) is associated with other autoimmune diseases (AIDs), which may have serious health consequences. The epidemiology of AIDs in T1DM is not well defined in adults with T1DM. In this cross-sectional cohort study, we sought to characterize the incident ages and prevalence of AIDs in adults with T1DM across a wide age spectrum. A total of 1,212 adults seen at the Washington University Diabetes Center from 2011 to 2018 provided informed consent for the collection of their age, sex, race, and disease onset data. We performed paired association analyses based on age at onset of T1DM. Multivariate logistic regression was used to evaluate the independent effects of sex, race, T1DM age of onset, and T1DM duration on the prevalence of an additional AID. Mean ± SD age of T1DM onset was 21.2 ± 14.4 years. AID incidence and prevalence increased with age. Female sex strongly predicted AID risk. The most prevalent T1DM-associated AIDs were thyroid disease, collagen vascular diseases, and pernicious anemia. T1DM age of onset and T1DM duration predicted AID risk. Patients with late-onset T1DM after 30 years of age had higher risks of developing additional AIDs compared with patients with younger T1DM onset. The prevalence of AIDs in patients with T1DM increases with age and female sex. Later onset of T1DM is an independent and significant risk factor for developing additional AIDs. Individuals who are diagnosed with T1DM at older ages, particularly women, should be monitored for other autoimmune conditions.

Identifiants

pubmed: 30361208
pii: dc18-1157
doi: 10.2337/dc18-1157
pmc: PMC6300704
doi:

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

32-38

Subventions

Organisme : NIDDK NIH HHS
ID : P30 DK020579
Pays : United States
Organisme : NIDDK NIH HHS
ID : T32 DK007120
Pays : United States

Informations de copyright

© 2018 by the American Diabetes Association.

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Auteurs

Jing W Hughes (JW)

Division of Endocrinology, Metabolism and Lipid Research, Washington University School of Medicine in St. Louis, St. Louis, MO jing.hughes@wustl.edu jmcgill@wustl.edu.

Yicheng K Bao (YK)

Division of Endocrinology, Metabolism and Lipid Research, Washington University School of Medicine in St. Louis, St. Louis, MO.
University of Missouri-Kansas City School of Medicine, Kansas City, MO.

Maamoun Salam (M)

Division of Endocrinology, Metabolism and Lipid Research, Washington University School of Medicine in St. Louis, St. Louis, MO.

Prajesh Joshi (P)

Division of Endocrinology, Metabolism and Lipid Research, Washington University School of Medicine in St. Louis, St. Louis, MO.
Mercy Hospital Northwest Arkansas and University of Arkansas for Medical Sciences Northwest Regional Campus, Fayetteville, AR.

C Rachel Kilpatrick (CR)

Division of Endocrinology, Metabolism and Lipid Research, Washington University School of Medicine in St. Louis, St. Louis, MO.
Washington Regional Medical Center, Fayetteville, AR.

Kavita Juneja (K)

Division of Endocrinology, Metabolism and Lipid Research, Washington University School of Medicine in St. Louis, St. Louis, MO.
Gilead Sciences, Foster City, CA.

David Nieves (D)

Division of Endocrinology, Metabolism and Lipid Research, Washington University School of Medicine in St. Louis, St. Louis, MO.
Northwell Health Lenox Hill Hospital, New York, NY.

Victoria Bouhairie (V)

Division of Endocrinology, Metabolism and Lipid Research, Washington University School of Medicine in St. Louis, St. Louis, MO.
Novant Health, Charlotte, NC.

Olivia J Jordan (OJ)

Division of Endocrinology, Metabolism and Lipid Research, Washington University School of Medicine in St. Louis, St. Louis, MO.
Pritzker School of Medicine, The University of Chicago, Chicago, IL.

Erica C Blustein (EC)

Division of Endocrinology, Metabolism and Lipid Research, Washington University School of Medicine in St. Louis, St. Louis, MO.
John Peter Smith Hospital, Fort Worth, TX.

Garry S Tobin (GS)

Division of Endocrinology, Metabolism and Lipid Research, Washington University School of Medicine in St. Louis, St. Louis, MO.

Janet B McGill (JB)

Division of Endocrinology, Metabolism and Lipid Research, Washington University School of Medicine in St. Louis, St. Louis, MO jing.hughes@wustl.edu jmcgill@wustl.edu.

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