Key result
Aging is associated with a non-linear increase in spontaneous platelet aggregation (from 3.3% to 10.9%) and a decrease in maximum induced aggregation for ristocetin, ADP, and collagen.
Why the study?
Data on platelet function in relation to age are limited, particularly among healthy elderly subjects aged 80-98 years, despite the importance of understanding thrombotic processes in older populations.
How does spontaneous and induced platelet aggregation change with age in apparently healthy subjects?
Cross-Sectional
How does spontaneous and induced platelet aggregation change with age in apparently healthy subjects?
Aging is associated with increased spontaneous platelet activation but decreased aggregatory potential ('platelet exhaustion'), indicating that platelet function data from middle-aged subjects cannot be directly extrapolated to the elderly.
Supports age-adjusted platelet aggregation reference ranges; hypothesis-generating for age-related thrombotic risk and antiplatelet response.
Thrombotic disorders remain the leading cause of mortality and morbidity, despite the fact that anti-platelet therapies and vascular implants are successfully used today. As life expectancy is increasing in western societies, the specific knowledge about processes leading to thrombosis in elderly is essential for an adequate therapeutic management of platelet dysfunction and for tailoring blood contacting implants. This study addresses the limited available data on platelet function in apparently healthy subjects in relation to age, particularly in view of subjects of old age (80-98 years). Apparently healthy subjects between 20 and 98 years were included in this study. Platelet function was assessed by light transmission aggregometry and comprised experiments on spontaneous as well as ristocetin-, ADP- and collagen-induced platelet aggregation. The data of this study revealed a non-linear increase in the maximum spontaneous platelet aggregation (from 3.3% ±3.3% to 10.9% ±5.9%). The maximum induced aggregation decreased with age for ristocetin (from 85.8% ±7.2% to 75.0% ±7.8%), ADP (from 88.5% ±4.6% to 64.8% ±7.3%) and collagen (from 89.5% ±3.0% to 64.0% ±4.0%) in a non-linear manner (linear regression analysis). These observations indicate that during aging, circulating platelets become increasingly activated but lose their full aggregatory potential, a phenomenon that was earlier termed "platelet exhaustion". In this study we extended the limited existing data for spontaneous and induced platelet aggregation of apparently healthy donors above the age of 75 years. The presented data indicate that the extrapolation of data from a middle age group does not necessarily predict platelet function in apparently healthy subjects of old age. It emphasizes the need for respective studies to improve our understanding of thrombotic processes in elderly humans.
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Kuhnla et al. (2019) conducted a cross-sectional in Apparently healthy. Aging was evaluated on Maximum spontaneous and induced platelet aggregation. Aging is associated with a non-linear increase in spontaneous platelet aggregation (from 3.3% to 10.9%) and a decrease in maximum induced aggregation for ristocetin, ADP, and collagen.
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