Subclinical Hypothyroidism and Cognitive Impairment: Systematic Review and Meta-Analysis

痴呆 亚临床感染 优势比 医学 荟萃分析 置信区间 内科学 韦氏成人智力量表 甲状腺功能 入射(几何) 认知 心理学 儿科 甲状腺 精神科 疾病 光学 物理
作者
Giuseppe Pasqualetti,Gennaro Pagano,Giuseppe Rengo,Nicola Ferrara,Fabio Monzani
出处
期刊:The Journal of Clinical Endocrinology and Metabolism [Oxford University Press]
卷期号:100 (11): 4240-4248 被引量:179
标识
DOI:10.1210/jc.2015-2046
摘要

BACKGROUND: The association between subclinical hypothyroidism (sHT) and cognitive impairment or risk of dementia is not well-defined, especially in the elderly, where the assessment of central nervous system function is challenging. The aim of this systematic review and meta-analysis was to evaluate the possible effect of sHT on cognitive decline and the risk of dementia. METHODS: Cognitive function was the primary outcome, evaluated as composite endpoint of incidence or prevalence of dementia or difference of Mini Mental State Examination, Wechsler Adult Intelligence Scale, and Wechsler Memory Scale-Revised scores. RESULTS: Thirteen studies were included in the meta-analysis. A significant risk of cognitive alteration was observed only in sHT individuals younger than age 75 years: composite endpoint odds ratio (OR) 1.56 (95% confidence interval [CI] 1.07-2.27, P = .02, I(2) = 82.5%), risk of dementia OR 1.81 (95% CI 1.43-2.28, P < .01, I(2) = 35%). Mean serum thyroid-stimulating hormone (TSH) levels and the OR of composite endpoint were positively correlated. No significant effect of sHT was found when considering all the studies as a whole: composite endpoint OR 1.26 (95% CI 0.96-1.66, P = .09, I(2) = 87.2%), risk of dementia OR 1.42 (95% CI, 0.97-2.07, P = .07, I(2) = 66.8%), Mini Mental State Examination mean difference -0.059 (95% CI -0.464 to 0.346 P = .78, I(2) = 51.8%). CONCLUSIONS: This meta-analysis demonstrates a relationship between sHT and cognitive impairment only in individuals younger than 75 years of age and those with higher TSH concentrations. No correlation was found while considering all the studies as a whole. The lack of utilization of age-related serum TSH reference ranges and consequent potential misdiagnosis of sHT in older people may account for this.

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