دانلود مقاله ISI انگلیسی شماره 76012
ترجمه فارسی عنوان مقاله

شناسایی زنان بعد از یائسگی در معرض خطر کاهش شناختی در یک گروه همسال سالم با استفاده از پانل شاخص های بالینی متابولیکی: پتانسیل تشخیص فنوتیپ متابولیک خطر ابتلا به آلزایمر

عنوان انگلیسی
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
کد مقاله سال انتشار تعداد صفحات مقاله انگلیسی
76012 2016 9 صفحه PDF
منبع

Publisher : Elsevier - Science Direct (الزویر - ساینس دایرکت)

Journal : Neurobiology of Aging, Volume 40, April 2016, Pages 155–163

ترجمه کلمات کلیدی
پیری شناختی، متابولیسم، بیومارکر، بیماری آلزایمر، یائسگی، هورمون درمانی
کلمات کلیدی انگلیسی
Cognitive aging; Metabolism; Biomarker; Alzheimer's disease; Menopause; Hormone therapy

چکیده انگلیسی

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.