Adams P C
Western University, London, ON, Canada.
Int J Lab Hematol. 2015 May;37 Suppl 1:25-30. doi: 10.1111/ijlh.12347.
Hemochromatosis is the most common genetic disease in northern European populations. Body iron stores progressively increase in most patients, which can lead to cirrhosis of the liver, hepatocellular carcinoma, heart failure, arthritis, and pigmentation. Simple blood tests such as the serum ferritin and transferrin saturation are useful to suggest the diagnosis which can be confirmed in most cases with a simple genetic test for the C282Y mutation of the HFE gene. However, these blood tests are often misinterpreted and there are rare patients with iron overload without HFE mutations. A diagnostic approach is presented based on a large referral practice and a population-based study (HEIRS) which screened for iron overload in 101,168 participants.
血色素沉着症是北欧人群中最常见的遗传性疾病。大多数患者体内的铁储存会逐渐增加,这可能导致肝硬化、肝细胞癌、心力衰竭、关节炎和色素沉着。诸如血清铁蛋白和转铁蛋白饱和度等简单的血液检测有助于提示诊断,在大多数情况下,通过对HFE基因的C282Y突变进行简单的基因检测即可确诊。然而,这些血液检测常常被误解,并且存在罕见的无HFE突变但铁过载的患者。本文基于一项大型转诊实践和一项针对101168名参与者进行铁过载筛查的人群研究(HEIRS),提出了一种诊断方法。