Evidence map›Paper›PMID 17490902›Full record

ArticleBlood cells, molecules & diseases

SLC40A1 Q248H allele frequencies and Q248H-associated risk of non-HFE iron overload in persons of sub-Saharan African descent.

James C Barton, Ronald T Acton, Pauline L Lee, Carol West

Open access · greenAbstract read
In one paragraph

Article in Blood cells, molecules & diseases. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.3field-weighted citation impact, top 20% 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

6 citing papers in PubMed, 34 citations in OpenAlex.

  1. Diagnosis and Management of Genetic Iron Overload Disorders.Journal of general internal medicine · 2018
    Review
  2. Review
  3. Review
  4. A comparison between whites and blacks with severe multi-organ iron overload identified in 16,152 autopsies.Clinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association · 2009
    Article
  5. Article
  6. Reasons why West Africa continues to be a hotbed for hepatocellular carcinoma.Nigerian medical journal : journal of the Nigeria Medical Association
    Review
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

4 authors at 3 institutions in 1 country.

James C BartonSouthern Iron Disorders Center, G105, 2022 Brookwood Medical Center Drive, Birmingham, AL 35209, USA. ironmd@dnamail.com
Ronald T Acton
Pauline L Lee
Carol West
Scripps Research Institute · USIron Mountain (United States) · USUniversity of Alabama at Birmingham · US

Funding

HEMOCHROMATOSIS--EPIDEMIOLOGY AND MOLECULAR MECHANISMSR01DK053505 · NIDDK · SCRIPPS RESEARCH INSTITUTE, THE · PI LEE, PAULINE L · 1998 to 2010
$7.8M
NIDDK NIH HHS DK53505NIDDK NIH HHS R01 DK053505
6 · The paper itself

Abstract

The ferroportin polymorphism SLC40A1 Q248H (exon 6, cDNA 744G-->T; Gln248His) occurs in persons of sub-Saharan African descent with and without iron overload, and is associated with elevated serum ferritin concentrations (SF). However, the risk of iron overload associated with Q248H has not been defined. We tabulated previously reported Q248H allele frequency estimates in African-Americans and Native Africans, and computed the risk of iron overload associated with Q248H in subjects who lacked HFE C282Y. The aggregate Q248H allele frequency in 1038 African-Americans in two cohorts from Alabama and one cohort each from Washington, DC and California was 0.0525 (95% CI: 0.0451, 0.0652); there was no significant difference in frequencies across these cohorts. The aggregate frequency in 259 Natives from southeast Africa in two cohorts was 0.0946 (95% CI: 0.0694, 0.1198); the difference between the frequencies of these cohorts was not significant. The aggregate Q248H frequencies in African-Americans and Native Africans differed significantly (0.0525 vs. 0.0946, respectively; p=0.0021). There were reports of 24 unrelated African-Americans and 15 unrelated Native Africans without HFE C282Y who had iron overload. In African-Americans, the odds ratio (OR) of Q248H-associated risk of iron overload using 610 C282Y-negative control subjects unselected for SF was 1.57 (95% CI: 0.52, 4.72; p=0.29). In Native Africans, the OR using 208 control subjects unselected for SF was 1.05 (95% CI: 0.28, 3.90; p=0.58). We conclude that the frequency of SLC40A1 Q248H is significantly lower in African-Americans than in Native Africans. Although OR estimates of iron overload in African-Americans and Native Africans with Q248H were greater than unity, the increased OR were not statistically significant.

Indexed as

Gene FrequencyAfrica South of the SaharaBlack or African AmericanCation Transport ProteinsFerroportinGenetic Predisposition to DiseaseHumansIron OverloadMolecular EpidemiologyCation Transport ProteinsFerroportin

Identifiers

PMID17490902
PMCPMC1986732
OpenAlexW2041030349

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.