Literature DB >> 17976429

Biological variability of transferrin saturation and unsaturated iron-binding capacity.

Paul C Adams1, David M Reboussin, Richard D Press, James C Barton, Ronald T Acton, Godfrey C Moses, Catherine Leiendecker-Foster, Gordon D McLaren, Fitzroy W Dawkins, Victor R Gordeuk, Laura Lovato, John H Eckfeldt.   

Abstract

BACKGROUND: Transferrin saturation is widely considered the preferred screening test for hemochromatosis. Unsaturated iron-binding capacity has similar performance at lower cost. However, the within-person biological variability of both these tests may limit their ability at commonly used cut points to detect HFE C282Y homozygous patients.
METHODS: The Hemochromatosis and Iron Overload Screening Study screened 101,168 primary care participants for iron overload using transferrin saturation, unsaturated iron-binding capacity, ferritin, and HFE C282Y and H63D genotyping. Transferrin saturation and unsaturated iron-binding capacity were performed at initial screening and again when selected participants and controls returned for a clinical examination several months later. A missed case was defined as a C282Y homozygote who had transferrin saturation below the cut point (45% for women, 50% for men) or unsaturated iron-binding capacity above the cut point (150 micromol/L for women, 125 micromol/L for men) at the initial screening or the clinical examination, or both, regardless of serum ferritin.
RESULTS: There were 209 C282Y previously undiagnosed homozygotes with transferrin saturation and unsaturated iron-binding capacity testing performed at the initial screening and clinical examination. Sixty-eight C282Y homozygotes (33%) would have been missed at these transferrin saturation cut points (19 men, 49 women; median serum ferritin level of 170 microg/L; first and third quartiles, 50 and 474 microg/L), and 58 homozygotes (28%) would have been missed at the unsaturated iron-binding capacity cut points (20 men, 38 women; median serum ferritin level of 168 microg/L; first and third quartiles, 38 and 454 microg/L). There was no advantage to using fasting samples.
CONCLUSIONS: The within-person biological variability of transferrin saturation and unsaturated iron-binding capacity limits their usefulness as an initial screening test for expressing C282Y homozygotes.

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Year:  2007        PMID: 17976429      PMCID: PMC2151312          DOI: 10.1016/j.amjmed.2007.02.027

Source DB:  PubMed          Journal:  Am J Med        ISSN: 0002-9343            Impact factor:   4.965


  26 in total

1.  Diagnosis and management of hemochromatosis.

Authors:  A S Tavill
Journal:  Hepatology       Date:  2001-05       Impact factor: 17.425

2.  Diurnal variation of serum iron, iron-binding capacity, transferrin saturation, and ferritin levels.

Authors:  Jane C Dale; Mary F Burritt; Alan R Zinsmeister
Journal:  Am J Clin Pathol       Date:  2002-05       Impact factor: 2.493

3.  Insurance, employment, and psychosocial consequences of a diagnosis of hereditary hemochromatosis in subjects without end organ damage.

Authors:  Nicholas J Shaheen; Laura B Lawrence; Bruce R Bacon; James C Barton; Nancy H Barton; Joseph Galanko; Christopher F Martin; Charles K Burnett; Robert S Sandler
Journal:  Am J Gastroenterol       Date:  2003-05       Impact factor: 10.864

4.  Psychosocial impact of C282Y mutation testing for hemochromatosis.

Authors:  T E Power; P C Adams
Journal:  Genet Test       Date:  2001

5.  Genetic discrimination and screening for hemochromatosis: then and now.

Authors:  C I Barash
Journal:  Genet Test       Date:  2000

6.  Penetrance of 845G--> A (C282Y) HFE hereditary haemochromatosis mutation in the USA.

Authors:  Ernest Beutler; Vincent J Felitti; James A Koziol; Ngoc J Ho; Terri Gelbart
Journal:  Lancet       Date:  2002-01-19       Impact factor: 79.321

7.  Hemochromatosis and Iron Overload Screening (HEIRS) study design for an evaluation of 100,000 primary care-based adults.

Authors:  Christine E McLaren; James C Barton; Paul C Adams; Emily L Harris; Ronald T Acton; Nancy Press; David M Reboussin; Gordon D McLaren; Phyliss Sholinsky; Ann P Walker; Victor R Gordeuk; Catherine Leiendecker-Foster; Fitzroy W Dawkins; John H Eckfeldt; Beverly G Mellen; Mark Speechley; Elizabeth Thomson
Journal:  Am J Med Sci       Date:  2003-02       Impact factor: 2.378

Review 8.  Nonexpressing homozygotes for C282Y hemochromatosis: minority or majority of cases?

Authors:  P C Adams
Journal:  Mol Genet Metab       Date:  2000 Sep-Oct       Impact factor: 4.797

9.  Screening for hemochromatosis: high prevalence and low morbidity in an unselected population of 65,238 persons.

Authors:  A Asberg; K Hveem; K Thorstensen; E Ellekjter; K Kannelønning; U Fjøsne; T B Halvorsen; H B Smethurst; E Sagen; K S Bjerve
Journal:  Scand J Gastroenterol       Date:  2001-10       Impact factor: 2.423

10.  Circadian variations of transferrin saturation levels in iron-overloaded patients: implications for the screening of C282Y-linked haemochromatosis.

Authors:  Anne Guillygomarc'h; Jacquelinet Christian; Moirand Romain; Quentin Vincent; David Véronique; Yves Deugnier
Journal:  Br J Haematol       Date:  2003-01       Impact factor: 6.998

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  20 in total

1.  The diagnosis and management of hereditary haemochromatosis.

Authors:  Paul Clark; Laurence J Britton; Lawrie W Powell
Journal:  Clin Biochem Rev       Date:  2010-02

2.  Management of Iron Deficiency Anemia in Pregnancy in India.

Authors:  Rimpy Tandon; Arihant Jain; Pankaj Malhotra
Journal:  Indian J Hematol Blood Transfus       Date:  2018-03-14       Impact factor: 0.900

3.  Management of elevated serum ferritin levels.

Authors:  Paul Adams
Journal:  Gastroenterol Hepatol (N Y)       Date:  2008-05

4.  Predicting C282Y homozygote genotype for hemochromatosis using serum ferritin and transferrin saturation values from 44,809 participants of the HEIRS study.

Authors:  Andrew Lim; Mark Speechley; Paul C Adams
Journal:  Can J Gastroenterol Hepatol       Date:  2014-10

5.  Should we screen for hereditary hemochromatosis in healthy Lebanese: a pilot study.

Authors:  Rami A R Mahfouz; Doja S Sarieddine; Khalil M Charafeddine; Rabab N Abdul Khalik; Najwa K Cortas; Rose T Daher
Journal:  Mol Biol Rep       Date:  2011-05-07       Impact factor: 2.316

Review 6.  Markers of iron status in chronic kidney disease.

Authors:  Adam E Gaweda
Journal:  Hemodial Int       Date:  2017-03-22       Impact factor: 1.812

7.  Hereditary hemochromatosis: insights from the Hemochromatosis and Iron Overload Screening (HEIRS) Study.

Authors:  Gordon D McLaren; Victor R Gordeuk
Journal:  Hematology Am Soc Hematol Educ Program       Date:  2009

8.  HFE mutations in Caucasian participants of the Hemochromatosis and Iron Overload Screening study with serum ferritin level <1000 µg/L.

Authors:  Paul C Adams; Christine E McLaren; Mark Speechley; Gordon D McLaren; James C Barton; John H Eckfeldt
Journal:  Can J Gastroenterol       Date:  2013-07       Impact factor: 3.522

9.  HFE C282Y homozygotes have reduced low-density lipoprotein cholesterol: the Atherosclerosis Risk in Communities (ARIC) Study.

Authors:  James S Pankow; Eric Boerwinkle; Paul C Adams; Eliseo Guallar; Catherine Leiendecker-Foster; Jason Rogowski; John H Eckfeldt
Journal:  Transl Res       Date:  2008-06-13       Impact factor: 7.012

Review 10.  Screening for iron overload: lessons from the hemochromatosis and iron overload screening (HEIRS) study.

Authors:  Paul Adams; James C Barton; Gordon D McLaren; Ronald T Acton; Mark Speechley; Christine E McLaren; David M Reboussin; Catherine Leiendecker-Foster; Emily L Harris; Beverly M Snively; Thomas Vogt; Phyliss Sholinsky; Elizabeth Thomson; Fitzroy W Dawkins; Victor R Gordeuk; John H Eckfeldt
Journal:  Can J Gastroenterol       Date:  2009-11       Impact factor: 3.522

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