Evidence map›Paper›PMID 20095037›Full record

ArticleAmerican journal of hematology2010

Heritability of serum iron measures in the hemochromatosis and iron overload screening (HEIRS) family study.

Christine E McLaren, James C Barton, John H Eckfeldt, Gordon D McLaren, Ronald T Acton, Paul C Adams, Leora F Henkin, Victor R Gordeuk, Chris D Vulpe, Emily L Harris and 3 more

Open access · bronzeAbstract readMulticenter Study
In one paragraph

Article in American journal of hematology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
0.9field-weighted citation impact, top 25% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

8 citing papers in PubMed, 1 synthesis or guideline pooled it, 17 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors at 10 institutions in 2 countries.

Christine E McLarenDepartment of Epidemiology, University of California, Irvine, California 92697-7550, USA. cmclaren@uci.edu
James C Barton
John H Eckfeldt
Gordon D McLaren
Ronald T Acton
Paul C Adams
Leora F Henkin
Victor R Gordeuk
Chris D Vulpe
Emily L Harris
Barbara W Harrison
Jacob A Reiss
Beverly M Snively
Howard University · USUniversity of California, Irvine · USWake Forest University · USIron Disorders Institute · USKaiser Permanente · USNational Institutes of Health · USUniversity of Alabama at Birmingham · USUniversity of California, Berkeley · USUniversity of Minnesota · USWestern University · CA

Funding

ZOVIRAX CREAM TO TREAT HERPES LABIALIS IN ADOLESCENTSM01RR000827 · NCRR · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI CHANG, R JEFFREY · 1985 to 2010
$74.3M
Univ.of Calif., Irvine Cancer Center Support GrantP30CA062203 · NCI · UNIVERSITY OF CALIFORNIA-IRVINE · PI Melanie Funes · 1994 to 2026
$57.9M
Zevalin Radioimmunotherapy Using a Modified TreatmentM01RR000032 · NCRR · UNIVERSITY OF SOUTHERN CALIFORNIA · PI RICH, ROBERT R. · 1985 to 2008
$23.6M
UVDM01RR010284 · NCRR · HOWARD UNIVERSITY · PI TAYLOR, ROBERT E. · 1996 to 2010
$17.4M
Labile Iron Pools In Hempglobin S ErythmocytesUH1HL003679 · NHLBI · HOWARD UNIVERSITY · PI GORDEUK, VICTOR R · 1996 to 2004
$3.5M
Role of cGMP in Ventilator-Induced Lung Endothelial Barrier DysfunctionR01HL067189 · NHLBI · JOHNS HOPKINS UNIVERSITY · PI PEARSE, DAVID B · 2002 to 2013
$3.1M
Iron Status: A Pathway Analysis in Multiple EthnicitiesR01HL083328 · NHLBI · UNIVERSITY OF CALIFORNIA-IRVINE · PI MCLAREN, CHRISTINE E. · 2006 to 2009
$2.6M
IRON OVERLOAD AND HEREDITARY HEMOCHROMATOSISN01HC005185 · HC · UNIVERSITY OF MINNESOTA TWIN CITIES · PI ECKFELDT, JOHN H · 2000 to 2000
$1.1M
IRON OVERLOAD AND HEREDITARY HEMOCHROMATOSIS-N01HC5192-268005192-268005192N01HC005192 · HC · WAKE FOREST UNIVERSITY · PI REBOUSSIN, DAVID M · 2000 to 2006
$867k
IRON OVERLOAD AND HEREDITARY HEMOCHROMOTOSISN01HC005189 · HC · KAISER FOUNDATION RESEARCH INSTITUTE · PI HARRIS, EMILY L · 2000 to 2000
$500k
IRON OVERLOAD AND HEREDITARY HEMOCHROMATOSIS STUDYN01HC005190 · HC · UNIVERSITY OF CALIFORNIA IRVINE · PI MCLAREN, CHRISTINE E · 2000 to 2000
$338k
IRON OVERLOAD AND HEREDITARY HEMOCHROMOTOSIS STUDYN01HC005188 · HC · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI ACTON, RONALD T. · 2000 to 2000
$256k
NCI NIH HHS P30 CA062203NCRR NIH HHS M01 RR000032NCRR NIH HHS M01-RR00032NCRR NIH HHS M01 RR000827NCRR NIH HHS M01-RR00827-29NCRR NIH HHS M01 RR010284NCRR NIH HHS M01-RR10284NHLBI NIH HHS N01 HB067189NHLBI NIH HHS N01 HC005185NHLBI NIH HHS N01 HC005186NHLBI NIH HHS N01 HC005188NHLBI NIH HHS N01 HC005189NHLBI NIH HHS N01 HC005190NHLBI NIH HHS N01 HC005191NHLBI NIH HHS N01 HC005192NHLBI NIH HHS N01-HC-05185NHLBI NIH HHS N01-HC-05186NHLBI NIH HHS N01-HC-05188NHLBI NIH HHS N01-HC-05189NHLBI NIH HHS N01-HC-05190NHLBI NIH HHS N01-HC-05191NHLBI NIH HHS R01 HL083328NHLBI NIH HHS R01 HL083328-01A1NHLBI NIH HHS UH1 HL003679NHLBI NIH HHS UH1-HL03679-05
6 · The paper itself

Abstract

Heritability is the proportion of observed variation in a trait among individuals in a population that is attributable to hereditary factors. The Hemochromatosis and Iron Overload Screening family study estimated heritability of serum iron measures. Probands were HFE C282Y homozygotes or non-C282Y homozygotes with elevated transferrin saturation (TS > 50%, men; TS > 45%, women) and serum ferritin concentration (SF > 300 microg/L, men; SF > 200 microg/L, women). Heritability (h(2)) was estimated by variance component analysis of TS, natural logarithm (ln) of SF, and unsaturated iron-binding capacity (UIBC). Participants (N = 942) were 77% Caucasians, 10% Asians, 8% Hispanics, and 5% other race/ethnicities. Average age (SD) was 49 (16) years; 57% were female. For HFE C282Y homozygote probands and their family members, excluding variation due to HFE C282Y and H63D genotype and measured demographic and environmental factors, the residual h(2) (SE) was 0.21 (0.07) for TS, 0.37 (0.08) for ln SF, and 0.34 (0.08) for UIBC (all P < 0.0004 for comparisons with zero). For the non-C282Y homozygote proband group, residual h(2) was significant with a value of 0.64 (0.26) for ln SF (P = 0.0096). In conclusion, serum iron measures have significant heritability components, after excluding known genetic and nongenetic sources of variation.

Indexed as

AdultAgedFamilyFemaleFerritinsHemochromatosisHemochromatosis ProteinHistocompatibility Antigens Class IHomozygoteHumansIronIron OverloadMaleMembrane ProteinsMiddle AgedMutation, MissenseFerritinsHemochromatosis ProteinHFE protein, humanHistocompatibility Antigens Class IIronMembrane Proteins

Identifiers

PMID20095037
PMCPMC3816512
OpenAlexW2039127104

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.