Evidence map›Paper›PMID 19002551›Full record

ArticleIrish journal of medical science2009

Haemochromatosis gene frequency in a control and diabetic Irish population.

L Kirk, J Bird, S Ramadan, A Samad, G Adebayo, W Lourens, J Williams

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Article in Irish journal of medical science, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
–field-weighted citation impact
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

7 citing papers in PubMed.

  1. Genes · 2026
    Article
  2. Article
  3. Hemochromatosis osteoarthritis.Frontiers in endocrinology · 2026
    Review
  4. Article
  5. Review
  6. Haemochromatosis.Nature reviews. Disease primers · 2018
    Review
  7. 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

7 authors.

L KirkPathology Department, Sligo General Hospital, Sligo, Ireland.
J Bird
S Ramadan
A Samad
G Adebayo
W Lourens
J Williams

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundHereditary haemochromatosis is inherited in an autosomal recessive manner. Two major mutations have been identified and the condition is emerging as one of the most common recessive mutations among subjects of Northern European descendants.

aimThis study investigated the prevalence of C282Y, H63D and S65C (three mutations of clinical significance for haemochromatosis), in a diabetic and control population from the North West of Ireland.

methodsDNA was extracted from whole blood samples of 249 known diabetics and 249 controls and assayed for the three genetic variants (C282Y, H63D and S65C).

resultsThe incidence for C282Y homozygosity is higher in the control population (1 in 83) when compared to the diabetic group (1 in 249). However, this is not statistically significant. S65C heterozygosity occurs with an incidence of 1 in 32 in control individuals and 1 in 124 in the diabetic population. The prevalence of the H63D mutation was similar in both populations.

conclusionFor the three haemochromatosis mutations, there was no significant difference between the control group and the diabetic populations.

Indexed as

AdolescentAdultAgedAged, 80 and overCase-Control StudiesDiabetes MellitusFemaleGenotypeHemochromatosisHemochromatosis ProteinHistocompatibility Antigens Class IHumansIrelandMaleMembrane ProteinsMiddle AgedHemochromatosis ProteinHFE protein, humanHistocompatibility Antigens Class IMembrane Proteins

Identifiers

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Textmetadata
Read underepoch 390

Registered trials

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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.