Background: The distribution of C282Y and H63D variants of the HFE gene was determined in donors with evidence of phenotypical hemochromatosis. The ferritin level and the effect of a donation on iron status in the different HFE genotypes were studied.
Study Design And Methods: Forty women and 107 men with hemochromatosis were compared to HFE wild-type donors. The influence of a blood donation was assessed by the change in ferritin between two consecutive donations.
Results: In women and men, 85 and 59%, respectively, were C282Y homozygote. None of the women had H63D alleles. There was no significant difference in the donation history or the ferritin level between the HFE genotypes. Donation frequencies were, respectively, 3.3 and 3.7 per year for women and men. The ferritin level was significantly higher in women with hemochromatosis, while in men it was similar compared to the respective wild types. The negative influence of a donation on iron status was similar in hemochromatotic and wild-type women, while men with hemochromatosis were significantly less vulnerable to a blood donation than genetically wild-type men.
Conclusion: Subjects with hemochromatosis are valuable as blood donors independent of their HFE genotype. In general, the ferritin level tended to be higher in those with hemochromatosis than in wild types. The negative influence of a blood donation on iron status was less in male donors with hemochromatosis than in wild types.
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http://dx.doi.org/10.1111/j.1537-2995.2010.02627.x | DOI Listing |
Int J Gen Med
January 2025
Department of Infectious Diseases, Tongji Hospital Affiliated to Tongji Medical College, Huazhong University of Science and Technology, Wuhan, People's Republic of China.
Purpose: Hemophagocytic lymphohistiocytosis (HLH) is a critical syndrome with a high mortality rate. In clinical practice, some patients with fever of unknown origin (FUO) can develop HLH, further complicating the diagnosis and treatment. However, studies on HLH in adults with FUO are limited.
View Article and Find Full Text PDFis a major contributor to infections in humans and is widely distributed in the environment. It is capable of aerobic and anaerobic growth, providing adaptability to environmental changes and in confronting immune responses. We applied high-throughput native 2-dimensional metalloproteomics to under oxic and anoxic conditions.
View Article and Find Full Text PDFPak J Med Sci
January 2025
Rong Zou Department of Nephrology, The Affiliated Nanhua Hospital, Hengyang Medical School, University of South China, Hengyang, Hunan Province 421002, P.R. China.
Objective: To explore the effects of hybrid blood purification on nutritional status and cardiovascular events in patients with end-stage renal disease (ESRD).
Methods: A total of 135 patients with ESRD who received treatment in The Affiliated Nanhua Hospital of Hengyang Medical School from March 2021 to June 2023 were included in this retrospective study. Of them, 66 patients were treated with hemodialysis purification (hemodialysis group), and 69 patients underwent hybrid blood purification (hybrid group).
Pak J Med Sci
January 2025
Dr. Rubeena Zakar, MBBS, PhD Public Health, Department of Public Health, Institute of Social and Cultural Studies, University of Punjab, Lahore, Pakistan.
Background & Objectives: Hypoferritinemia without anemia (HWA) is an under-recognized public health concern. Early identification and targeted treatment of HWA can prevent unnecessary medication use and potential drug abuse. This study aims to establish clearer guidelines for recognizing and managing HWA, improving patient's outcome.
View Article and Find Full Text PDFFront Pediatr
January 2025
Key Laboratory of Birth Defects and Related Diseases of Women and Children of Ministry of Education (MOE), West China Institute of Women and Children's Health, Key Laboratory of Development and Diseases of Women and Children of Sichuan Province, Department of Pediatrics, Department of Pediatric Cardiology, West China Second University Hospital, Sichuan University, Chengdu, Sichuan, China.
Background: Cardiovascular involvement is a rare but severe complication of Epstein-Barr virus (EBV) infections. Patients with chronic active EBV (CAEBV) are at increased risk of developing cardiovascular complications and have a poor prognosis. Here, we report the rare case of a pediatric patient with CAEBV and EBV- hemophagocytic lymphohistiocytosis (HLH) complicated with a giant coronary artery aneurysm (CAA) and thrombosis, a giant Valsalva sinus aneurysm, and ascending aorta dilation seven years after the disease onset.
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