کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
8262304 | 1534836 | 2018 | 7 صفحه PDF | دانلود رایگان |
عنوان انگلیسی مقاله ISI
High levels of an endothelial dysfunction marker (sVCAM-1) are associated with injurious and recurrent falls and mortality over a 5-year interval in an older population
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کلمات کلیدی
موضوعات مرتبط
علوم زیستی و بیوفناوری
بیوشیمی، ژنتیک و زیست شناسی مولکولی
سالمندی
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چکیده انگلیسی
We investigated the association between elevated plasma concentrations of circulating soluble Vascular Cell Adhesion Molecule-1 (sVCAM-1) and injurious falls and mortality over a 5-year period. We studied the prospective relationship between levels of circulating adhesion molecules and falls in 680 community-dwelling participants in the MOBILIZE Boston Study. The mean sVCAM-1 (±SD) concentration was 1192â¯Â±â¯428â¯ng/mL. Over 5-years of follow-up, 10.2% of participants died. The baseline sVCAM-1 (±SD) concentration was 1434â¯Â±â¯511â¯ng/mL in those who died vs. 1162â¯Â±â¯402â¯ng/mL in those who survived (Pâ¯<â¯0.0001). sVCAM-1 level was associated with recurrent falls (Pâ¯<â¯0.01); compared to the lowest quintile, the highest quintile of sVCAM-1 was associated with increased risk of injurious falls [multivariable adjusted Incidence Rate Ratioâ¯=â¯1.9, 95% CI (1.2-2.9), Pâ¯=â¯0.009]. On survival analysis, the highest sVCAM-1 quintile was associated with the greatest mortality over 5â¯years (log-rank test, Pâ¯<â¯0.0001). The adjusted hazard ratio was 2.4 [95% CI (2.1-2.7), Pâ¯=â¯0.002]. High sVCAM-1 blood concentration was strongly associated with recurrent falls, injurious falls, and mortality in older adults.
ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Experimental Gerontology - Volume 106, June 2018, Pages 1-7
Journal: Experimental Gerontology - Volume 106, June 2018, Pages 1-7
نویسندگان
Achille Tchalla, Gregory A. Wellenius, Sophie Boyer, Thomas G. Travison, Daniel Habtemariam, Margaret Gagnon, Ikechukwu Iloputaife, Farzaneh A. Sorond, Thierry Dantoine, Lewis A. Lipsitz,