Evidence map›Paper›PMID 32296102›Full record

ArticleScientific reports2020

Telomere Maintenance Genes are associated with Type 2 Diabetes Susceptibility in Northwest Indian Population Group.

Itty Sethi, Varun Sharma, Indu Sharma, Gurvinder Singh, Gh Rasool Bhat, A J S Bhanwer, Swarkar Sharma, Ekta Rai

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.8field-weighted citation impact, top 15% 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

12 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
  2. Frontiers in endocrinology · 2026
    Article
  3. Review
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  6. Parental telomeres implications on immune senescence of newborns.American journal of clinical and experimental immunology · 2023
    Article
  7. Article
  8. Article
  9. Article
  10. Cells · 2021
    Article
  11. Article
  12. 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

8 authors at 2 institutions in 1 country.

Itty SethiHuman Genetics Research Group, School of Biotechnology, Shri Mata Vaishno Devi University, Katra, J&K, 182320, India.
Varun SharmaHuman Genetics Research Group, School of Biotechnology, Shri Mata Vaishno Devi University, Katra, J&K, 182320, India.
Indu SharmaHuman Genetics Research Group, School of Biotechnology, Shri Mata Vaishno Devi University, Katra, J&K, 182320, India.
Gurvinder SinghDepartment of Human Genetics, Guru Nanak Dev University, Amritsar, 143005, Punjab, India.
Gh Rasool BhatHuman Genetics Research Group, School of Biotechnology, Shri Mata Vaishno Devi University, Katra, J&K, 182320, India.
A J S BhanwerDepartment of Human Genetics, Guru Nanak Dev University, Amritsar, 143005, Punjab, India.
Swarkar SharmaHuman Genetics Research Group, School of Biotechnology, Shri Mata Vaishno Devi University, Katra, J&K, 182320, India. swarkar.sharma@smvdu.ac.in.ORCID http://orcid.org/0000-0001-8857-5906
Ekta RaiHuman Genetics Research Group, School of Biotechnology, Shri Mata Vaishno Devi University, Katra, J&K, 182320, India. ekta.rai@smvdu.ac.in.
Shri Mata Vaishno Devi University · INGuru Nanak Dev University · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Telomere length attrition has been implicated in various complex disorders including Type 2 Diabetes (T2D). However, very few candidate gene association studies have been carried out worldwide targeting telomere maintenance genes. In the present study, variants in various critical telomere maintenance pathway genes for T2D susceptibility in Northwest Indian population were explored. With case-control candidate gene association study design, twelve variants from seven telomere maintenance genes were evaluated. Amongst these five variants, rs9419958 (OBFC1), rs4783704 (TERF2), rs16847897 (TERC/LRRC31), rs10936599 (TERC/MYNN), and rs74019828 (CSNK2A2) showed significant association with T2D (at p-value ≤ 0.003, threshold set after Bonferroni correction) in the studied population. In silico analyses of these variants indicated interesting functional roles that warrant experimental validations. Findings showed that variants in telomere maintenance genes are associated with pathogenesis of T2D in Northwest Indian population. We anticipate further, such candidate gene association studies in other Indian populations and worldwide would contribute in understanding the missing heritability of T2D.

Indexed as

Genetic Predisposition to DiseaseTelomere HomeostasisAgedCase-Control StudiesComputational BiologyDiabetes Mellitus, Type 2FemaleGenome-Wide Association StudyHumansIndiaMaleMiddle AgedPolymorphism, Single NucleotideTelomereTelomere-Binding ProteinsTelomere-Binding Proteins

Identifiers

PMID32296102
PMCPMC7160122
OpenAlexW3017282421

What OpenQuestion holds

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LicenceCC BY
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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.