Screening for hemochromatosis - A public health perspective

Context: The discovery of the HFE gene in 1996 has introduced DNA testing a s a possible tool for screening and diagnosis of homochromatosis and increa sed interest in the disorder. Population screening using transferrin satura tion has been advocated by experts to permit early detection and treatment with phlebotomy before the onset of clinical disease. Methods: Based on a liter atl:re review, we consider the relative risks and merits of two screening tests as part of a broader look at the evidence re quired for the recommendation of universal screening for hemochromatosis. Results: Several questions must be answered before universal screening can be recommended. Uncertainties remain about the penetrance and preventable d isease burden, laboratory standardization, and optimal strategies to minimi ze potential risks of screening for hemochromatosis. Conclusions: As a common genetic disorder with simple, effective therapy, h emochromatosis offers a model for other genetically influenced chronic dise ases that some day may have interventions to improve prognosis. Resolution of questions related to prevention of chronic diseases from hemochromatosis , therefore, will have broad usefulness in the future.