Journal of the American Heart Association · 2025
Dual Contrast-Enhanced Microcomputed Tomography Uncovers Leaflet-Dependent Patterns of Macrocalcification, Fibrous Extracellular Matrix Remodeling, and Adipocyte Degeneration in Calcific Aortic Stenosis.
СтатьяПоддержка NIH: внешняя программаНазвание и аннотация: Перевод пока не подготовлен
Обработка статьи · этапы, ошибки и управление
Загрузка состояния…
Ошибки и ограничения
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.
El Zeini Mustapha, Tacco Ines Ross, Jimenez John I, Kabiri Angela, Vailionis Arturas, Perrino John, Burns Dale, Jensen Kristin C, Burdon Thomas A, Shudo Yasuhiro, Woo Y Joseph, Liang Tie, Alexander Kevin M, Joubert Lydia-Marie, Chen Ian Y
Аннотация
BACKGROUND: Clinical imaging studies of calcific aortic stenosis have suggested interleaflet pathological differences in patients. In this cross-sectional study, we sought to investigate interleaflet differences in calcification, fibrous extracellular matrix remodeling, and adipocyte degeneration in explanted human aortic valves.
METHODS: Diseased (n=45) and control (n=39) tricuspid aortic valve leaflets obtained from patients with aortic stenosis and normal aortic valves on echocardiography were assessed for calcification, fibrous extracellular matrix remodeling, and adipocyte degeneration using contrast-enhanced microcomputed tomography in conjunction with scanning and transmission electron microscopy, with interleaflet differences analyzed by fractional response regression.
RESULTS: In diseased leaflets, the calcification volume fraction was significantly greater in the noncoronary cusp than the left coronary cusp (LCC; β=0.313 [95% CI, 0.048-0.579], P=0.021) but not than the right coronary cusp (RCC; β=0.196 [95% CI, -0.107 to 0.499], P=0.204), with no difference between the RCC and LCC (β=0.117 [95% CI, -0.150 to 0.385], P=0.390). However, the fibrous extracellular matrix volume fraction was significantly greater in the RCC and LCC than the noncoronary cusp (β=0.502 [95% CI, 0.300-0.704], P<0.001; β=0.388 [95% CI, 0.188-0.589], P<0.001), with the RCC also greater than the LCC (β=0.114 [95% CI, 0.065-0.163], P<0.001). The volume fraction of osmium-labeled inclusions observed on microcomputed tomography-confirmed to be predominantly adipocytes (95.4 [IQR, 72.4-99.0]%) and occasionally membranous fat necrosis (4.6 [IQR, 1.0-27.6]%) on electron microscopy-was significantly less in the noncoronary cusp than the LCC (β=-0.269 [95% CI, -0.441 to -0.096], P=0.002) but not than the RCC (β=-0.185 [95% CI, -0.409 to 0.038], P=0.104), with no difference between the RCC and LCC (β=-0.083 [95% CI, -0.348 to 0.182], P=0.538).
CONCLUSIONS: Valvular calcification diverges from fibrous extracellular matrix remodeling but converges with adipocyte degeneration in terms of preferential impact on the noncoronary cusp versus, in particular, the LCC. Future mechanistic studies to elucidate the intimate relationship between adipocyte degeneration and valvular calcification may provide opportunities for further therapeutic development.
METHODS: Diseased (n=45) and control (n=39) tricuspid aortic valve leaflets obtained from patients with aortic stenosis and normal aortic valves on echocardiography were assessed for calcification, fibrous extracellular matrix remodeling, and adipocyte degeneration using contrast-enhanced microcomputed tomography in conjunction with scanning and transmission electron microscopy, with interleaflet differences analyzed by fractional response regression.
RESULTS: In diseased leaflets, the calcification volume fraction was significantly greater in the noncoronary cusp than the left coronary cusp (LCC; β=0.313 [95% CI, 0.048-0.579], P=0.021) but not than the right coronary cusp (RCC; β=0.196 [95% CI, -0.107 to 0.499], P=0.204), with no difference between the RCC and LCC (β=0.117 [95% CI, -0.150 to 0.385], P=0.390). However, the fibrous extracellular matrix volume fraction was significantly greater in the RCC and LCC than the noncoronary cusp (β=0.502 [95% CI, 0.300-0.704], P<0.001; β=0.388 [95% CI, 0.188-0.589], P<0.001), with the RCC also greater than the LCC (β=0.114 [95% CI, 0.065-0.163], P<0.001). The volume fraction of osmium-labeled inclusions observed on microcomputed tomography-confirmed to be predominantly adipocytes (95.4 [IQR, 72.4-99.0]%) and occasionally membranous fat necrosis (4.6 [IQR, 1.0-27.6]%) on electron microscopy-was significantly less in the noncoronary cusp than the LCC (β=-0.269 [95% CI, -0.441 to -0.096], P=0.002) but not than the RCC (β=-0.185 [95% CI, -0.409 to 0.038], P=0.104), with no difference between the RCC and LCC (β=-0.083 [95% CI, -0.348 to 0.182], P=0.538).
CONCLUSIONS: Valvular calcification diverges from fibrous extracellular matrix remodeling but converges with adipocyte degeneration in terms of preferential impact on the noncoronary cusp versus, in particular, the LCC. Future mechanistic studies to elucidate the intimate relationship between adipocyte degeneration and valvular calcification may provide opportunities for further therapeutic development.