The effect of plasma donation frequency on total serum protein, immunoglobulin G and donor safety: A non-inferiority randomized controlled trial.

IF 1.6 4区 医学 Q3 HEMATOLOGY
Vox Sanguinis Pub Date : 2025-08-28 DOI:10.1111/vox.70105
Morten Haugen, Lise Sofie Haug Nissen-Meyer, Tor A Strand, Karin Magnussen
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引用次数: 0

Abstract

Background and objectives: The safety of varying plasma donation frequencies remains unclear. This non-inferiority randomized controlled trial investigated the effect of plasma donation frequency on total serum protein (TSP), immunoglobulin G (IgG) concentrations, additional biomarkers, adverse events (AEs) and psychological distress.

Materials and methods: In this trial, 120 male donors were randomized into three groups: high-frequency plasma donors (HFPDs, three times every 2 weeks), regular-frequency plasma donors (RFPDs, once every 2 weeks) and a control group (whole blood donation every 3 months). Blood samples were collected biweekly from baseline until the last donation in Week 16 and 4 weeks after the last donation.

Results: HFPDs completed median (range) 21.5 (1-24), RFPDs 8 (1-8) and controls 2 (1-2) donations. HFPDs had lower concentrations of TSP and IgG compared to controls, with a mean difference (95% confidence interval [CI]) of -5.5 g/L (-7.4, -3.6) and -2.8 g/L (-3.8, -1.8), respectively. Within-group analysis revealed significant reductions, which increased with the frequency of donations, in TSP, IgG, IgG subclasses, immunoglobulin M (IgM), immunoglobulin A (IgA), ferritin and haemoglobin. Many of the biomarkers required more than 4 weeks to return to baseline levels. Only mild AEs were reported, and plasma donation frequency had no effect on psychological distress.

Conclusion: High- and regular-frequency plasmapheresis substantially reduces concentrations of TSP, IgG and other biomarkers, with greater reductions at higher donation frequencies. Further research is needed to assess the long-term health implications of frequent plasma donation.

血浆捐献频率对血清总蛋白、免疫球蛋白G和献血者安全性的影响:一项非劣效性随机对照试验。
背景和目的:不同血浆捐献频率的安全性尚不清楚。这项非劣效性随机对照试验研究了血浆捐献频率对血清总蛋白(TSP)、免疫球蛋白G (IgG)浓度、其他生物标志物、不良事件(ae)和心理困扰的影响。材料与方法:本试验将120名男性献血者随机分为三组:高频献血者(HFPDs,每2周3次)、高频献血者(RFPDs,每2周1次)和对照组(每3个月全血一次)。从基线开始每两周采集一次血样,直到第16周和最后一次献血后4周。结果:HFPDs完成中位(范围)21.5 (1-24),RFPDs完成8(1-8),对照组完成2(1-2)。与对照组相比,HFPDs的TSP和IgG浓度较低,平均差异(95%置信区间[CI])分别为-5.5 g/L(-7.4, -3.6)和-2.8 g/L(-3.8, -1.8)。组内分析显示,随着献血频率的增加,TSP、IgG、IgG亚类、免疫球蛋白M (IgM)、免疫球蛋白A (IgA)、铁蛋白和血红蛋白的含量显著降低。许多生物标志物需要超过4周的时间才能恢复到基线水平。只有轻度不良反应被报道,血浆捐献频率对心理困扰没有影响。结论:高频和高频血浆置换可显著降低血清TSP、IgG等生物标志物的浓度,且频率越高,降低幅度越大。需要进一步的研究来评估频繁献血对健康的长期影响。
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来源期刊
Vox Sanguinis
Vox Sanguinis 医学-血液学
CiteScore
4.40
自引率
11.10%
发文量
156
审稿时长
6-12 weeks
期刊介绍: Vox Sanguinis reports on important, novel developments in transfusion medicine. Original papers, reviews and international fora are published on all aspects of blood transfusion and tissue transplantation, comprising five main sections: 1) Transfusion - Transmitted Disease and its Prevention: Identification and epidemiology of infectious agents transmissible by blood; Bacterial contamination of blood components; Donor recruitment and selection methods; Pathogen inactivation. 2) Blood Component Collection and Production: Blood collection methods and devices (including apheresis); Plasma fractionation techniques and plasma derivatives; Preparation of labile blood components; Inventory management; Hematopoietic progenitor cell collection and storage; Collection and storage of tissues; Quality management and good manufacturing practice; Automation and information technology. 3) Transfusion Medicine and New Therapies: Transfusion thresholds and audits; Haemovigilance; Clinical trials regarding appropriate haemotherapy; Non-infectious adverse affects of transfusion; Therapeutic apheresis; Support of transplant patients; Gene therapy and immunotherapy. 4) Immunohaematology and Immunogenetics: Autoimmunity in haematology; Alloimmunity of blood; Pre-transfusion testing; Immunodiagnostics; Immunobiology; Complement in immunohaematology; Blood typing reagents; Genetic markers of blood cells and serum proteins: polymorphisms and function; Genetic markers and disease; Parentage testing and forensic immunohaematology. 5) Cellular Therapy: Cell-based therapies; Stem cell sources; Stem cell processing and storage; Stem cell products; Stem cell plasticity; Regenerative medicine with cells; Cellular immunotherapy; Molecular therapy; Gene therapy.
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