Evidence map›Paper›PMID 18683048›Full record

ArticleDigestive diseases and sciences2009

HFE gene mutations, serum ferritin level, transferrin saturation, and their clinical correlates in a Korean population.

Sang Hyub Lee, Jin-Wook Kim, So Hyun Shin, Kyoung Phil Kang, Hyun Cheol Choi, Sung Hee Choi, Kyoung Un Park, Hyun Young Kim, Weechang Kang, Sook-Hyang Jeong

Abstract read
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In one paragraph

Article in Digestive diseases and sciences, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

9 citing papers in PubMed, 24 citations in OpenAlex.

  1. Article
  2. Ethnic Differences in Iron Status.Advances in nutrition (Bethesda, Md.) · 2021
    Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Salt-Dependent Aggregation and Assembly of E coli-Expressed Ferritin.Dose-response : a publication of International Hormesis Society
    Article
  9. 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

10 authors at 2 institutions in 1 country.

Sang Hyub LeeDepartment of Internal Medicine, Seoul National University College of Medicine, Seoul National University Bundang Hospital, 300 Gumi-dong, Bundang-gu, Seongnam-si, Gyeonggi-do, 463-707, South Korea.
Jin-Wook Kim
So Hyun Shin
Kyoung Phil Kang
Hyun Cheol Choi
Sung Hee Choi
Kyoung Un Park
Hyun Young Kim
Weechang Kang
Sook-Hyang Jeong
Seoul National University Bundang Hospital · KRDaejeon University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The aim of this study was to investigate HFE gene mutations, blood iron indices, and their clinical correlates in a Korean population. In 484 prospectively enrolled health-check examinees, HFE gene mutations and iron indices with clinical and laboratory variables were analyzed. Although neither the C282Y nor S65C gene mutation were found, the H63D heterozygote was detected in 41 subjects (8.5%). The mean serum ferritin and transferrin saturation (TS) were 136.2 +/- 129.8 microg/dl and 39.2 +/- 15.7%, respectively. The H63D genotype was not significantly associated with iron indices. High serum ferritin was associated with old age, the male gender, high body mass index (BMI), and the presence of nonalcoholic fatty liver disease (NAFLD). High TS was associated with the male gender and alcohol drinking. HFE gene mutation is rare; however, TS seems to be higher in Koreans compared to Caucasians or other ethnic groups. Serum ferritin reflects iron store as well as the presence of NAFLD.

Indexed as

AdultAge FactorsAsian PeopleFemaleFerritinsGenotypeHemochromatosis ProteinHistocompatibility Antigens Class IHumansIronKoreaMaleMembrane ProteinsMiddle AgedMutation, MissensePolymorphism, Restriction Fragment LengthFerritinsHemochromatosis ProteinHFE protein, humanHistocompatibility Antigens Class IIronMembrane ProteinsTransferrin

Identifiers

PMID18683048
OpenAlexW2047749133

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.