Genetics in Medicine

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Genetics in Medicine:
November 2006 - Volume 8 - Issue 11 - pp 681-687
doi: 10.1097/01.gim.0000245631.07117.ac
Original Articles: Article

Impact of hemochromatosis screening in patients with indeterminate results: The hemochromatosis and iron overload screening study

Anderson, Roger T. PhD; Wenzel, Lari PhD; Walker, Ann P. MA, CGC; Ruggiero, Andrea MS; Acton, Ronald T. PhD; Hall, Mark A. JD; Tucker, Diane C. PhD; Thomson, Elizabeth MS, RN; Harrison, Barbara MS; Howe, Edmund III MD, JD; Holup, Joan MA; Leiendecker-Foster, Catherine MS; Power, Tara PhD; Adams, Paul MD

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Abstract

Purpose: Assess the quality of life impact of receiving indeterminate test results for hemochromatosis, a disorder involving HFE genetic mutations and/or elevated serum transferrin saturation and ferritin.

Methods: The study sample was from the Hemochromatosis and Iron Overload Screening Study, a large observational study of hemochromatosis among primary care patients in the US and Canada using HFE genotype and serum transferrin saturation and ferritin screening. Study subjects included 2,304 patients found with hemochromatosis risk of uncertain clinical significance. Assessed was SF-36 general health and emotional well-being before screening and six weeks after participants received their test results. Health worries were assessed after screening.

Results: Of the study subjects, 1,268 participants (51.5%) completed both assessments. Compared to normal controls, those with HFE mutations or elevated serum transferrin saturation and ferritin levels of uncertain significance were more likely to report diminished general health and mental well-being, and more health worries. These effects were associated with participants' belief of having tested positive for hemochromatosis or iron overload.

Conclusion: Notification of indeterminate results from screening may be associated with mild negative effects on well-being, and might be a potential participant risk in screening programs for disorders with uncertain genotype-phenotype.

©2006The American College of Medical Genetics

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