Evidence map›Paper›PMID 17032446›Full record

ArticleBMC medical genetics2006

Triglyceride associated polymorphisms of the APOA5 gene have very different allele frequencies in Pune, India compared to Europeans.

Giriraj R Chandak, Kirsten J Ward, Chittaranjan S Yajnik, Anand N Pandit, Ashish Bavdekar, Charu V Joglekar, Caroline H D Fall, P Mohankrishna, Terence J Wilkin, Bradley S Metcalf and 3 more

Open access · goldAbstract readComparative Study
In one paragraph

Article in BMC medical genetics, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed, 3 pooled it
2.1field-weighted citation impact, top 13% 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

31 citing papers in PubMed, 3 syntheses or guidelines pooled it, 52 citations in OpenAlex.

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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

13 authors at 4 institutions in 2 countries.

Giriraj R ChandakGenome Research Group, Centre for Cellular and Molecular Biology, Hyderabad, India. chandakgrc@ccmb.res.in
Kirsten J Ward
Chittaranjan S Yajnik
Anand N Pandit
Ashish Bavdekar
Charu V Joglekar
Caroline H D Fall
P Mohankrishna
Terence J Wilkin
Bradley S Metcalf
Michael N Weedon
Timothy M Frayling
Andrew T Hattersley
Peninsula College of Medicine and Dentistry · GBKing Edward Memorial Hospital Research Centre · INCentre for Cellular and Molecular Biology · INSouthampton City Council · GB

Funding

Medical Research Council G0400519Medical Research Council G0400519(71108)Medical Research Council MC_U147574246Medical Research Council MC_U147585821Medical Research Council U.1475.00.004.00005.01(74246)Medical Research Council U.1475.00.004.00005.01 (85821)Wellcome Trust 059609Wellcome Trust 079877
6 · The paper itself

Abstract

backgroundThe APOA5 gene variants, -1131T>C and S19W, are associated with altered triglyceride concentrations in studies of subjects of Caucasian and East Asian descent. There are few studies of these variants in South Asians. We investigated whether the two APOA5 variants also show similar association with various lipid parameters in Indian population as in the UK white subjects.

methodsWe genotyped 557 Indian adults from Pune, India, and 237 UK white adults for -1131T>C and S19W variants in the APOA5 gene, compared their allelic and genotype frequency and determined their association with fasting serum triglycerides, total cholesterol, HDL and LDL cholesterol levels using univariate general linear analysis. APOC3 SstI polymorphism was also analyzed in 175 Pune Indian subjects for analysis of linkage disequilibrium with the APOA5 variants.

resultsThe APOA5 -1131C allele was more prevalent in Indians from Pune (Pune Indians) compared to UK white subjects (allele frequency 20% vs. 4%, p = 0.00001), whereas the 19W allele was less prevalent (3% vs. 6% p = 0.0015). Patterns of linkage disequilibrium between the two variants were similar between the two populations and confirmed that they occur on two different haplotypes. In Pune Indians, the presence of -1131C allele and the 19W allele was associated with a 19% and 15% increase respectively in triglyceride concentrations although only -1131C was significant (p = 0.0003). This effect size was similar to that seen in the UK white subjects. Analysis of the APOC3 SstI polymorphism in 175 Pune Indian subjects showed that this variant is not in appreciable linkage disequilibrium with the APOA5 -1131T>C variant (r2 = 0.07).

conclusionThis is the first study to look at the role of APOA5 in Asian Indian subjects that reside in India. The -1131C allele is more prevalent and the 19W allele is less prevalent in Pune Indians compared to UK Caucasians. We confirm that the APOA5 variants are associated with triglyceride levels independent of ethnicity and that this association is similar in magnitude in Asian Indians and Caucasians. The -1131C allele is present in 36% of the Pune Indian population making it a powerful marker for looking at the role of elevated triglycerides in important conditions such as pancreatitis, diabetes and coronary heart disease.

Indexed as

Gene FrequencyPolymorphism, Single NucleotideAdultApolipoprotein A-VApolipoproteinsApolipoproteins AAsian PeopleFemaleGenotypeHumansIndiaLipidsMalePhenotypeTriglyceridesUnited KingdomAPOA5 protein, humanApolipoprotein A-VApolipoproteinsApolipoproteins ALipidsTriglycerides

Identifiers

PMID17032446
PMCPMC1618828
OpenAlexW2109190686

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Textmetadata
LicenceCC BY
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.