Waalen Jill, Felitti Vincent, Gelbart Terri, Ho Ngoc J, Beutler Ernest
Department of Molecular and Experimental Medicine, Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, CA 92037, USA.
Blood Cells Mol Dis. 2002 Nov-Dec;29(3):418-32. doi: 10.1006/bcmd.2002.0596.
We undertook a three-year screening program for mutations of the HFE gene among 41,000 subjects attending the Kaiser Permanente Health Appraisal Center in San Diego, California. Our results show that the C282Y and H63D mutations of the HFE gene associated with hemochromatosis have measurable and consistent effects on iron indicators and are associated with liver disorders, but have no measurable effect on other iron overload-related symptoms and life-expectancy. The very low clinical penetrance of the HFE mutations must be taken into account in calculating cost/benefit and risk/benefit ratios in screening for hemochromatosis.
我们在加利福尼亚州圣地亚哥的凯撒医疗机构健康评估中心,对41000名受试者开展了一项为期三年的HFE基因突变筛查项目。我们的结果显示,与血色素沉着症相关的HFE基因C282Y和H63D突变,对铁指标有可测量且一致的影响,并与肝脏疾病相关,但对其他与铁过载相关的症状和预期寿命没有可测量的影响。在计算血色素沉着症筛查的成本/效益和风险/效益比时,必须考虑HFE突变极低的临床外显率。