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DOI 10.1016/j.neurobiolaging.2016.01.011

Медицинская библиотека · Neurobiology of aging · 2016

Identifying postmenopausal women at risk for cognitive decline within a healthy cohort using a panel of clinical metabolic indicators: potential for detecting an at-Alzheimer's risk metabolic phenotype.

Rettberg Jamaica R, Dang Ha, Hodis Howard N, Henderson Victor W, St John Jan A, Mack Wendy J, Brinton Roberta Diaz

СтатьяПоддержка NIH: внешняя программаПеревод пока не подготовлен

Аннотация

Detecting at-risk individuals within a healthy population is critical for preventing or delaying Alzheimer's disease. Systems biology integration of brain and body metabolism enables peripheral metabolic biomarkers to serve as reporters of brain bioenergetic status. Using clinical metabolic data derived from healthy postmenopausal women in the Early versus Late Intervention Trial with Estradiol (ELITE), we conducted principal components and k-means clustering analyses of 9 biomarkers to define metabolic phenotypes. Metabolic clusters were correlated with cognitive performance and analyzed for change over 5 years. Metabolic biomarkers at baseline generated 3 clusters, representing women with healthy, high blood pressure, and poor metabolic phenotypes. Compared with healthy women, poor metabolic women had significantly lower executive, global and memory cognitive performance. Hormone therapy provided metabolic benefit to women in high blood pressure and poor metabolic phenotypes. This panel of well-established clinical peripheral biomarkers represents an initial step toward developing an affordable, rapidly deployable, and clinically relevant strategy to detect an at-risk phenotype of late-onset Alzheimer's disease.

Для цитирования: Rettberg Jamaica R, Dang Ha, Hodis Howard N, Henderson Victor W, St John Jan A, Mack Wendy J, Brinton Roberta Diaz. Identifying postmenopausal women at risk for cognitive decline within a healthy cohort using a panel of clinical metabolic indicators: potential for detecting an at-Alzheimer's risk metabolic phenotype.. Neurobiology of aging. 2016. DOI: 10.1016/j.neurobiolaging.2016.01.011.

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