Stored platelet hemostatic phenotype and function is not altered when donors are on testosterone replacement therapy

• Published in: Transfusion (Philadelphia, Pa.) Vol. 64; no. 8; pp. 1520 - 1532
• Main Authors: Chitrakar, Alisha, Bean, Scott‐Wesley M., Kanias, Tamir, Thomas, Kimberly A.
• Format: Journal Article
• Language: English
• Published: Hoboken, USA John Wiley & Sons, Inc 01.08.2024; Wiley Subscription Services, Inc
• Subjects: Adult; Blood clots; blood component preparations; Blood Donors; Blood platelets; Blood Platelets - drug effects; Blood Platelets - metabolism; Blood Preservation; Erythrocytes; Female; Genotype & phenotype; hemostasis; Hemostasis - drug effects; Hormone Replacement Therapy; Humans; Male; Metabolism; Middle Aged; Phenotype; Phenotypes; Phlebotomy; Platelets; Room temperature; Stored products; Testosterone; Testosterone - blood; Testosterone - pharmacology; therapeutic apheresis; Thrombin; Thrombosis; therapeutic apheresis; blood component preparations; hemostasis
• ISSN: 0041-1132; 1537-2995; 1537-2995
• DOI: 10.1111/trf.17926

Background Critical shortages in the national blood supply have led to a re‐evaluation of previously overlooked donor sources for blood products. As a part of that effort, red blood cells collected from therapeutic phlebotomy of donors on testosterone replacement therapy (TRT) have been conditionally approved for transfusion. However, platelets from TRT donors are not currently approved for use due to limited data on effects of supraphysiologic testosterone on recipient safety and platelet function. The objective of this study was to provide a comprehensive profile of phenotype and function in platelets from TRT and control donors. Study Design and Methods Platelets in plasma were collected from TRT and control donors (N = 10 per group; age‐ and sex‐matched) and stored at room temperature for 7 days. On storage Day 1 (D1) and Day 7 (D7), platelet products were analyzed for platelet count, metabolic parameters (i.e., glucose, lactate, mitochondrial function), surface receptor expression, aggregation, thrombin generation, and thrombus formation under physiological flow conditions. Results TRT donor platelets were not significantly different than control donor platelets in terms of count, surface phenotype, metabolic function, ability to aggregate, thrombin generation, or ability to form occlusive thrombus under arterial flow regimes. Both groups were similar to each other by D7, but had significantly lost hemostatic function compared to D1. Discussion Platelets derived from donors undergoing TRT have similar phenotypic and functional profiles compared to those derived from control donors. This suggests that therapeutic phlebotomy of TRT donors may provide a useful source for platelet products.