m+Medelevator.RU
← Поиск публикаций
The Journal of clinical investigation · 2011

FGF23 induces left ventricular hypertrophy.

СтатьяМногоцентровое исследованиеПоддержка NIH: внешняя программаПоддержка исследования: вне правительства СШАПоддержка правительства СШАНазвание и аннотация: Перевод пока не подготовлен
Обработка статьи · этапы, ошибки и управление
Загрузка состояния…

История · было → стало

Состояние обновляется каждые 5 секунд, пока блок открыт. Процент показывается только там, где известен объём работы. Пауза останавливает продолжение этапа; текущий запрос к источнику может завершиться.

Faul Christian, Amaral Ansel P, Oskouei Behzad, Hu Ming-Chang, Sloan Alexis, Isakova Tamara, Gutiérrez Orlando M, Aguillon-Prada Robier, Lincoln Joy, Hare Joshua M, Mundel Peter, Morales Azorides, Scialla Julia, Fischer Michael, Soliman Elsayed Z, Chen Jing, Go Alan S, Rosas Sylvia E, Nessel Lisa, Townsend Raymond R, Feldman Harold I, St John Sutton Martin, Ojo Akinlolu, Gadegbeku Crystal, Di Marco Giovana Seno, Reuter Stefan, Kentrup Dominik, Tiemann Klaus, Brand Marcus, Hill Joseph A, Moe Orson W, Kuro-O Makoto, Kusek John W, Keane Martin G, Wolf Myles

Аннотация

Chronic kidney disease (CKD) is a public health epidemic that increases risk of death due to cardiovascular disease. Left ventricular hypertrophy (LVH) is an important mechanism of cardiovascular disease in individuals with CKD. Elevated levels of FGF23 have been linked to greater risks of LVH and mortality in patients with CKD, but whether these risks represent causal effects of FGF23 is unknown. Here, we report that elevated FGF23 levels are independently associated with LVH in a large, racially diverse CKD cohort. FGF23 caused pathological hypertrophy of isolated rat cardiomyocytes via FGF receptor-dependent activation of the calcineurin-NFAT signaling pathway, but this effect was independent of klotho, the coreceptor for FGF23 in the kidney and parathyroid glands. Intramyocardial or intravenous injection of FGF23 in wild-type mice resulted in LVH, and klotho-deficient mice demonstrated elevated FGF23 levels and LVH. In an established animal model of CKD, treatment with an FGF-receptor blocker attenuated LVH, although no change in blood pressure was observed. These results unveil a klotho-independent, causal role for FGF23 in the pathogenesis of LVH and suggest that chronically elevated FGF23 levels contribute directly to high rates of LVH and mortality in individuals with CKD.

Предметные рубрики MeSH

ИП Урсолов Владлен Сергеевич

ИНН 500118482352 · ОГРНИП 314500117700049

Реквизиты и контакты