Evidence map›Paper›PMID 37738238›Full record

ArticlePloS one2023

Genetic associations of TMEM154, PRC1 and ZFAND6 loci with type 2 diabetes in an endogamous business community of North India.

Gagandeep Kaur Walia, Pratiksha Sharma, Tripti Agarwal, Moti Lal, Himanshu Negandhi, Dorairaj Prabhakaran, Rajesh Khadgawat, Mohinder Pal Sachdeva, Vipin Gupta

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.6field-weighted citation impact, top 23% 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

2 citing papers in PubMed, 2 citations in OpenAlex.

  1. Integrating Polygenic Risk Scores (PRS) for Personalized Diabetes Care: Advancing Clinical Practice with Tailored Pharmacological Approaches.Diabetes therapy : research, treatment and education of diabetes and related disorders · 2025
    Review
  2. 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

9 authors at 5 institutions in 1 country.

Gagandeep Kaur WaliaPublic Health Foundation of India, Gurugram, India.ORCID 0000-0001-8081-2284
Pratiksha SharmaIndian Institute of Public Health-Delhi, Public Health Foundation of India, Gurugram, India.
Tripti AgarwalIndian Institute of Public Health-Delhi, Public Health Foundation of India, Gurugram, India.
Moti LalDepartment of Anthropology, University of Delhi, Delhi, India.
Himanshu NegandhiPublic Health Foundation of India, Gurugram, India.
Dorairaj PrabhakaranPublic Health Foundation of India, Gurugram, India.
Rajesh KhadgawatDepartment of Endocrinology, All India Institute of Medical Sciences, Ansari Nagar, New Delhi, India.
Mohinder Pal SachdevaDepartment of Anthropology, University of Delhi, Delhi, India.
Vipin GuptaDepartment of Anthropology, University of Delhi, Delhi, India.
University of Delhi · INCentre for Chronic Disease Control · INInstitute of Public Health Bengaluru · INAll India Institute of Medical Sciences · INPublic Health Foundation of India · IN

Funding

Wellcome Trust
6 · The paper itself

Abstract

backgroundMore than 250 loci have been identified by genome-wide scans for type 2 diabetes in different populations. South Asians have a very different manifestation of the diseases and hence role of these loci need to be investigated among Indians with huge burden of cardio-metabolic disorders. Thus the present study aims to validate the recently identified GWAS loci in an endogamous caste population in North India.

methods219 T2D cases and 184 controls were recruited from hospitals and genotyped for 15 GWAS loci of T2D. Regression models adjusted for covariates were run to examine the association for T2D and fasting glucose levels.

resultsWe validated three variants for T2D namely, rs11634397 at ZFAND6 (OR = 3.05, 95%CI = 1.02-9.19, p = 0.047) and rs8042680 at PRC1 (OR = 3.67, 95%CI = 1.13-11.93, p = 0.031) showing higher risk and rs6813195 at TMEM154 (OR = 0.28, 95%CI = 0.09-0.90, p = 0.033) showing protective effect. The combined risk of 9 directionally consistent variants was also found to be significantly associated with T2D (OR = 1.91, 95%CI = 1.18-3.08, p = 0.008). One variant rs10842994 at KLHDC5 was validated for 9.15mg/dl decreased fasting glucose levels (SE = -17.25-1.05, p = 0.027).

conclusionWe confirm the role of ZFAND6, PRC1 and TMEM154 in the pathophysiology of type 2 diabetes among Indians. More efforts are needed with larger sample sizes to validate the diabetes GWAS loci in South Asian populations for wider applicability.

Indexed as

Adaptor Proteins, Signal TransducingCell Cycle ProteinsDiabetes Mellitus, Type 2Membrane ProteinsAsian PeopleCommerceGlucoseHumansIndiaAdaptor Proteins, Signal TransducingCell Cycle ProteinsGlucoseMembrane ProteinsPRC1 protein, humanTMEM154 protein, humanZFAND6 protein, human

Identifiers

PMID37738238
PMCPMC10516421
OpenAlexW4386953754

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LicenceCC BY
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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.