The association between subclinical thyroid dysfunction and dementia: The Health, Aging and Body Composition (Health ABC) Study

被引:73
作者
Aubert, Carole E. [1 ]
Bauer, Douglas C. [2 ,3 ]
da Costa, Bruno R. [4 ]
Feller, Martin [1 ,4 ]
Rieben, Carole [5 ]
Simonsick, Eleanor M. [6 ]
Yaffe, Kristine [3 ,7 ,8 ]
Rodondi, Nicolas [1 ,4 ]
机构
[1] Univ Bern, Univ Hosp Bern, Dept Gen Internal Med, Inselspital, Bern, Switzerland
[2] Univ Calif San Francisco, Dept Med, San Francisco, CA USA
[3] Univ Calif San Francisco, Dept Epidemiol & Biostat, San Francisco, CA 94143 USA
[4] Univ Bern, Inst Primary Hlth Care BIHAM, Bern, Switzerland
[5] Univ Bern, Univ Hosp Bern, Dept Diabet Endocrinol Clin Nutr & Metab, Inselspital, Bern, Switzerland
[6] NIA, Intramural Res Program, Baltimore, MD 21224 USA
[7] Univ Calif San Francisco, Dept Psychiat, San Francisco, CA USA
[8] Univ Calif San Francisco, Dept Neurol, San Francisco, CA USA
基金
瑞士国家科学基金会;
关键词
cognitive ageing; cognitive decline; dementia; thyroid dysfunction; COGNITIVE FUNCTION; HYPOTHYROIDISM; DISEASE; RISK; PEOPLE; IMPAIRMENT; PREVALENCE; DECLINE;
D O I
10.1111/cen.13458
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective: Data on the association between subclinical thyroid dysfunction and dementia are limited and conflicting. We aimed to determine whether subclinical thyroid dysfunction was associated with dementia and cognitive decline. Design: Population-based prospective cohort study. Patients: Adults aged 70-79years with measured thyroid function, but no dementia at baseline, and Modified Mini-Mental State (3MS) at baseline and follow-up. Measurements: Primary outcome was incident-adjudicated dementia, based on 3MS, hospital records and dementia drugs. Secondary outcome was change in 3MS. Models were adjusted for age, sex, race, education and baseline 3MS, and then further for cardiovascular risk factors. Results: Among 2558 adults, 85% were euthyroid (TSH 0.45-4.49mIU/L), 2% had subclinical hyperthyroidism with mildly decreased TSH (TSH 0.10-0.44mIU/L), 1% subclinical hyperthyroidism with suppressed TSH (TSH<0.10mIU/L with normal free thyroxine [FT4]) and 12% subclinical hypothyroidism (TSH 4.50-19.99mIU/L with normal FT4). Over 9years, 22% developed dementia. Compared to euthyroidism, risk of dementia was higher in participants with subclinical hyperthyroidism with suppressed TSH (HR 2.38, 95% CI=1.13;5.04), while we found no significant association in those with mildly decreased TSH (HR 0.79, 95% CI=0.45;1.38) or with subclinical hypothyroidism (HR 0.91, 95% CI=0.70;1.19). Participants with subclinical hyperthyroidism with suppressed TSH had a larger decline in 3MS (-3.89, 95% CI=-7.62; -0.15). Conclusions: Among older adults, subclinical hyperthyroidism with a TSH<0.10mIU/L was associated with a higher risk of dementia and a larger cognitive decline, while subclinical hyperthyroidism with mildly decreased TSH or subclinical hypothyroidism were not.
引用
收藏
页码:617 / 626
页数:10
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