用血清铁蛋白测量日本全血捐献者的铁缺乏症。

IF 1.8 4区 医学 Q3 HEMATOLOGY Vox Sanguinis Pub Date : 2024-09-01 Epub Date: 2024-06-14 DOI:10.1111/vox.13688
Takeshi Odajima, Nelson H Tsuno, Fumihiko Ishimaru, Rie Okubo, Junko Murakami, Kaori Kitsukawa, Katsuya Ikuta, Koji Matsuzaki, Kazuo Muroi, Masahiro Satake, Shuichi Kino
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引用次数: 0

摘要

背景和目的:日本采用了更严格的献血标准,全血(WB)最大献血量为 400 毫升,女性献血者每年可献血两次,男性献血者每年可献血三次。然而,女性献血者在献血前缺铁率高达 20.5%,献血后缺铁率增至 37.7%。从那时起已经过去了 20 多年,因此我们开始调查目前的情况:我们共招募了 2659 名(男性/女性:1496/1163)400 毫升白细胞的献血者,这些献血者均在知情同意的情况下参加了研究。根据性别和年龄,比较了首次/再活化(FT/RA)捐献者与重复捐献者的血清铁蛋白(sFer);还对研究期间返回进行后续捐献的捐献者进行了随访:结果:约三分之一的 FT/RA 女性捐献者患有缺铁症,这可能反映了缺铁症在普通人群中的高发病率。有趣的是,虽然绝经前 FT/RA 女性捐献者的 sFer 水平较低,但这些值在重复捐献者中差别不大,而在绝经后女性捐献者中,FT/RA 与重复捐献者之间存在显著差异,在男性捐献者的大多数年龄组中也存在显著差异。正如预期的那样,初始 sFer 正常(≥26 纳克/毫升)的供体比初始 sFer 低的供体恢复得更快:结论:尤其是女性献血者,在献血前就存在缺铁问题,且缺铁率较之前有所上升。结论:尤其是女性献血者,在献血前就已经缺铁,而且缺铁率与以前相比有所增加。
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Iron deficiency among Japanese whole-blood donors measured by serum ferritin.

Background and objectives: A more restrictive blood donation criterion has been applied in Japan, with a maximum volume of whole blood (WB) donation of 400 mL, allowing twice a year for female donors and thrice a year for male donors. However, iron deficiency was as high as 20.5% among female donors prior to donation, increasing to 37.7% after blood donation. More than 20 years have passed since then, so we set out to investigate the present situation.

Materials and methods: A total of 2659 (male/female: 1496/1163) donors of 400 mL WB who gave informed consent to join the study were enrolled. Serum ferritin (sFer) of first-time/reactivated (FT/RA) donors were compared with those of repeat donors, according to gender and age; those who returned for subsequent donations during the study period were also followed up.

Results: About one-third of FT/RA female donors had iron deficiency, possibly reflecting its high incidence among the general population. Interestingly, although sFer levels were low among pre-menopausal FT/RA female donors, these values were not much different in repeat donors, whereas significant differences were observed between FT/RA and repeat donors among post-menopausal females and in most age groups among males. As expected, donors with a normal initial sFer (≥26 ng/mL) recovered faster than those with a low initial sFer.

Conclusion: Female donors, especially, have iron deficiency even before donation, and the rate increased compared to what was found previously. Measures to prevent iron deficiency of blood donors is required, and studies are going on in Japan.

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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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