Evidence map›Paper›PMID 19095725›Full record

ArticleClinical chemistry2009

Relation of genetic variation in the gene coding for C-reactive protein with its plasma protein concentrations: findings from the Women's Health Initiative Observational Cohort.

Cathy C Lee, Nai-chieh Yuko You, Yiqing Song, Yi-Hsiang Hsu, JoAnn Manson, Lauren Nathan, Lesley Tinker, Simin Liu

Open access · bronzeAbstract read
In one paragraph

Article in Clinical chemistry, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
2.8field-weighted citation impact, top 10% 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

25 citing papers in PubMed, 47 citations in OpenAlex.

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  4. C-reactive protein in adult Samoans: Population variation and physiological correlates.American journal of human biology : the official journal of the Human Biology Council · 2022
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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

8 authors at 6 institutions in 1 country.

Cathy C LeeDepartment of Medicine, David Geffen School of Medicine, UCLA, Los Angeles, CA 90095, USA.
Nai-chieh Yuko You
Yiqing Song
Yi-Hsiang Hsu
JoAnn Manson
Lauren Nathan
Lesley Tinker
Simin Liu
Harvard University · USUniversity of California, Los Angeles · USBrigham and Women's Hospital · USFred Hutch Cancer Center · USUCLA Health · USVA Greater Los Angeles Healthcare System · US

Funding

Genetic and Biochemical Predictors of Type 2 DM in WomenR01DK062290 · NIDDK · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI LIU, SIMIN · 2002 to 2006
$2.6M
Magnesium Intake, Gene Variants, and Type 2 DiabetesK01DK078846 · NIDDK · BRIGHAM AND WOMEN'S HOSPITAL · PI SONG, YIQING · 2008 to 2010
$409k
NIDDK NIH HHS K01 DK078846NIDDK NIH HHS R01 DK062290
6 · The paper itself

Abstract

backgroundAlthough common genetic variants of the CRP gene (C-reactive protein, pentraxin related) have been associated with plasma concentrations of high-sensitivity CRP (hsCRP) in several cohorts of European Americans, relatively few studies have comprehensively assessed this association in well-characterized multiethnic populations.

methodsIn a case-control study of diabetes nested in the Women's Health Initiative Observational Cohort, we comprehensively evaluated the association of genetic variation in CRP with plasma hsCRP concentrations. Thirteen haplotype-tagging single-nucleotide polymorphisms (tSNPs) were identified and subsequently genotyped in 3782 postmenopausal women.

resultsThe allele frequencies for these tSNPs and the haplotype blocks defined by these tSNPs varied significantly by ethnic group (P < 0.0001). Consistent with prior studies of whites, rs3093068, rs1130864, and rs1417938 were significantly associated with higher hsCRP concentrations (geometric-mean increase per minor-allele change, 1.20-1.25 mg/L), and rs1205 and rs1800947 were significantly associated with lower hsCRP values (decrease of 1.28-1.48 mg/L). The associations with rs3093068 and rs1205 appeared to be stronger in Asians/Pacific Islanders than in whites (geometric-mean increase, 1.65 mg/L vs 1.25 mg/L, respectively). Minor alleles at rs3093075 and rs3093059 were associated with substantially increased hsCRP concentrations, whereas rs1800947 was associated with lower hsCRP values. All haplotype-based association results tended to be consistent with the associations seen with single CRP SNPs.

conclusionsOur large multiethnic case-control study of postmenopausal women provides evidence that common genetic variants in the CRP gene are substantially associated with plasma hsCRP concentrations in this case-control subcohort. The data also suggest ethnic variations in these associations.

Indexed as

C-Reactive ProteinPolymorphism, Single NucleotideCase-Control StudiesCohort StudiesDiabetes MellitusEthnicityFemaleHaplotypesHumansPostmenopauseUnited StatesC-Reactive Protein

Identifiers

PMID19095725
PMCPMC2856608
OpenAlexW1992486326

What OpenQuestion holds

Textmetadata
LicenceTDM
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.