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遗传性血色素沉着症中的红细胞增多症和贫血症

Polycythemia and Anemia in Hereditary Hemochromatosis.

作者信息

Khan Adnan Aman, Hadi Yousaf, Hassan Ayesha, Kupec Justin

机构信息

Medicine, West Virginia University School of Medicine, Morgantown, USA.

Gastroenterology and Hepatology, West Virginia University School of Medicine, Morgantown, USA.

出版信息

Cureus. 2020 Apr 9;12(4):e7607. doi: 10.7759/cureus.7607.

Abstract

Introduction Hereditary hemochromatosis is a syndrome of dysregulated iron homeostasis resulting in the excessive deposition of iron. Hemochromatosis causes pulmonary, pancreatic, and hepatic dysfunction, all of which are risk factors for anemia in the general population. Conversely, iron overload states are thought to predispose to polycythemia. The effect of the homozygosity and heterozygosity of hereditary hemochromatosis-associated genes on hemoglobin levels has not been sufficiently studied. Materials and methods We conducted a retrospective cohort study at West Virginia University of all patients who underwent HFE gene analysis and carried the diagnosis of hemochromatosis. Charts were reviewed to identify relevant variables and the patients' clinical course. Results A total of 213 patients were included with 143 male participants (67.13%). The mean age was 53.6 years (SD: 15.2). A total of 108 patients were homozygous for the C282Y mutation. The prevalence of baseline characteristics are as follows: tobacco use 46.3%, chronic obstructive pulmonary disease 16.4%, malignancy 20.1%, cirrhosis 16.8%, anticoagulant use 6.5%, and chronic renal insufficiency 13.1%. The mean hemoglobin of the population was 15.0 mg/dL (SD 2.21). Anemia was seen in 23 patients (10.80%) and 59 patients (27.6%) had polycythemia. Concurrent malignancy and the presence of chronic renal insufficiency were significantly associated with anemia in both the univariate and multivariate analysis (p-values < 0.001). Patients with homozygosity for C282Y were more likely to receive phlebotomy as compared to other patients. Serum ferritin was not associated with anemia or polycythemia on multivariate analyses (p-values 0.197 and 0.105, respectively). Conclusion Despite the high prevalence of comorbidities that are known risk factors for anemia in the general population, few patients with hereditary hemochromatosis develop anemia. Female patients with hereditary hemochromatosis are relatively protected against polycythemia, affecting only one-fourth of all patients with hemochromatosis, with most patients' serum hemoglobin reported within normal limits.

摘要

引言

遗传性血色素沉着症是一种铁稳态失调导致铁过度沉积的综合征。血色素沉着症会引起肺部、胰腺和肝脏功能障碍,所有这些都是普通人群贫血的危险因素。相反,铁过载状态被认为易引发红细胞增多症。遗传性血色素沉着症相关基因的纯合性和杂合性对血红蛋白水平的影响尚未得到充分研究。

材料与方法

我们在西弗吉尼亚大学对所有接受HFE基因分析并被诊断为血色素沉着症的患者进行了一项回顾性队列研究。查阅病历以确定相关变量和患者的临床病程。

结果

共纳入213例患者,其中男性参与者143例(67.13%)。平均年龄为53.6岁(标准差:15.2)。共有108例患者C282Y突变纯合。基线特征的患病率如下:吸烟46.3%,慢性阻塞性肺疾病16.4%,恶性肿瘤20.1%,肝硬化16.8%,使用抗凝剂6.5%,慢性肾功能不全13.1%。该人群的平均血红蛋白为15.0mg/dL(标准差2.21)。23例患者(10.80%)出现贫血,59例患者(27.6%)患有红细胞增多症。在单因素和多因素分析中,并发恶性肿瘤和慢性肾功能不全的存在均与贫血显著相关(p值<0.001)。与其他患者相比,C282Y纯合的患者更有可能接受放血治疗。多因素分析中,血清铁蛋白与贫血或红细胞增多症均无关联(p值分别为0.197和0.105)。

结论

尽管已知普通人群中作为贫血危险因素的合并症患病率很高,但遗传性血色素沉着症患者中很少有人发生贫血。遗传性血色素沉着症女性患者相对不易患红细胞增多症,仅影响所有血色素沉着症患者的四分之一,大多数患者的血清血红蛋白报告在正常范围内。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/24f0/7213665/296d09af3c74/cureus-0012-00000007607-i01.jpg

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