Impact of Type 2 Diabetes and Postmenopausal Hormone Therapy on Incidence of Cognitive Impairment in Older Women.

TitleImpact of Type 2 Diabetes and Postmenopausal Hormone Therapy on Incidence of Cognitive Impairment in Older Women.
Publication TypeJournal Article
Year of Publication2015
AuthorsEspeland MA, Brinton RDiaz, Hugenschmidt C, Manson JAE, Craft S, Yaffe K, Weitlauf J, Vaughan L, Johnson KC, Padula CB, Jackson RD, Resnick SM
Corporate AuthorsWHIMS Study Group
JournalDiabetes Care
Volume38
Issue12
Pagination2316-24
Date Published2015 Dec
ISSN1935-5548
KeywordsAged, Aged, 80 and over, Brain, Cognition, Cognition Disorders, Dementia, Diabetes Mellitus, Type 2, Estrogen Replacement Therapy, Estrogens, Estrogens, Conjugated (USP), Female, Glucose, Humans, Incidence, Medroxyprogesterone Acetate, Postmenopause, Randomized Controlled Trials as Topic, Risk
Abstract

OBJECTIVE: In older women, higher levels of estrogen may exacerbate the increased risk for cognitive impairment conveyed by diabetes. We examined whether the effect of postmenopausal hormone therapy (HT) on cognitive impairment incidence differs depending on type 2 diabetes.

RESEARCH DESIGN AND METHODS: The Women's Health Initiative (WHI) randomized clinical trials assigned women to HT (0.625 mg/day conjugated equine estrogens with or without [i.e., unopposed] 2.5 mg/day medroxyprogesterone acetate) or matching placebo for an average of 4.7-5.9 years. A total of 7,233 women, aged 65-80 years, were classified according to type 2 diabetes status and followed for probable dementia and cognitive impairment (mild cognitive impairment or dementia).

RESULTS: Through a maximum of 18 years of follow-up, women with diabetes had increased risk of probable dementia (hazard ratio [HR] 1.54 [95% CI 1.16-2.06]) and cognitive impairment (HR 1.83 [1.50-2.23]). The combination of diabetes and random assignment to HT increased their risk of dementia (HR 2.12 [1.47-3.06]) and cognitive impairment (HR 2.20 [1.70-2.87]) compared with women without these conditions, interaction P = 0.09 and P = 0.08. These interactions appeared to be limited to women assigned to unopposed conjugated equine estrogens.

CONCLUSIONS: These analyses provide additional support to a prior report that higher levels of estrogen may exacerbate risks that type 2 diabetes poses for cognitive function in older women. The role estrogen plays in suppressing non-glucose-based energy sources in the brain may explain this interaction.

DOI10.2337/dc15-1385
Alternate JournalDiabetes Care
PubMed ID26486190
PubMed Central IDPMC4657616
Grant ListP30 CA015704 / CA / NCI NIH HHS / United States
HHSN-271-2011-00004C / / PHS HHS / United States
Faculty Member Reference: 
Roberta Diaz Brinton, Ph.D