Evidence map›Paper›PMID 16042809›Full record

ArticleBMC blood disorders2005

Total blood lymphocyte counts in hemochromatosis probands with HFE C282Y homozygosity: relationship to severity of iron overload and HLA-A and -B alleles and haplotypes.

James C Barton, Howard W Wiener, Ronald T Acton, Rodney Cp Go

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In one paragraph

Article in BMC blood disorders, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.5field-weighted citation impact, top 19% 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

10 citing papers in PubMed, 30 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Iron and immunity: immunological consequences of iron deficiency and overload.Archivum immunologiae et therapiae experimentalis · 2010
    Review
  7. Article
  8. Hereditary hemochromatosis in the post-HFE era.Hepatology (Baltimore, Md.) · 2008
    Article
  9. Iron overload and immunity.World journal of gastroenterology · 2007
    Review
  10. Article
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 1 institution in 1 country.

James C Barton *Southern Iron Disorders Center, Birmingham, Alabama, USA.
Howard W WienerDepartment of Epidemiology and International Health, University of Alabama at Birmingham, Birmingham, Alabama, USA.
Ronald T Acton *Department of Medicine, University of Alabama at Birmingham, Birmingham, Alabama, USA.
Rodney Cp GoDepartment of Epidemiology and International Health, University of Alabama at Birmingham, Birmingham, Alabama, USA.
University of Alabama at Birmingham · US

Funding

Schizophrenia Liability Genes among African AmericansR01MH066181 · NIMH · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI GO, RODNEY CHUN PUNG · 2002 to 2006
$4.7M
Search for AD Genes in the NIMH Sibling DatasetR01NS045934 · NINDS · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI GO, RODNEY CHUN PUNG · 2002 to 2004
$981k
NIMH NIH HHS R01 MH066181NINDS NIH HHS R01 NS045934
6 · The paper itself

Abstract

backgroundIt has been reported that some persons with hemochromatosis have low total blood lymphocyte counts, but the reason for this is unknown.

methodsWe measured total blood lymphocyte counts using an automated blood cell counter in 146 hemochromatosis probands (88 men, 58 women) with HFE C282Y homozygosity who were diagnosed in medical care. Univariate and multivariate analyses of total blood lymphocyte counts were evaluated using these variables: sex; age, transferrin saturation, and serum ferritin concentration at diagnosis; units of blood removed by phlebotomy to achieve iron depletion; and human leukocyte antigen (HLA)-A and -B alleles and haplotypes.

resultsThe mean age at diagnosis was 49 +/- 14 years (range 18 - 80 years) in men and 50 +/- 13 years (range 22-88 years) in women. The correlations of total blood lymphocyte counts with sex, age, transferrin saturation, and serum ferritin concentration at diagnosis, and units of blood removed by phlebotomy to achieve iron depletion were not significant at the 0.05 level. Univariate analyses revealed significant associations between total blood lymphocyte counts and presence of the HLA-A*01, -B*08, and -B*14 alleles, and the A*01-B*08 haplotype. Presence of the A*01 allele, B*08 allele, or A*01-B*08 haplotype were associated with a lower total blood lymphocyte count, whereas presence of the B*14 allele was associated with a greater total blood lymphocyte count. There was an inverse association of total blood lymphocyte count with units of phlebotomy to achieve iron depletion, serum ferritin concentration, and with presence of the A*01-B*08 haplotype.

conclusionWe conclude that there is a significant inverse relationship of total blood lymphocyte counts and severity of iron overload in hemochromatosis probands with HFE C282Y homozygosity. The presence of the HLA-A*01 allele or the -B*08 allele was also associated with significantly lower total blood lymphocyte counts, whereas presence of the -B*14 allele was associated with significantly higher total blood lymphocyte counts. In univariate and multivariate analyses, total blood lymphocyte counts were significantly lower in probands with the HLA-A*01-B*08 haplotype than in probands without this haplotype.

Identifiers

PMID16042809
PMCPMC1198220
OpenAlexW1606274933

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LicenceCC BY
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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.