Evidence mapPaperPMID 34912452Full record

ArticleInternational journal of endocrinology2021

Clinical Manifestations of Hyperandrogenism and Ovulatory Dysfunction Are Not Associated with His1058 C/T SNP (rs1799817) Polymorphism of Insulin Receptor Gene Tyrosine Kinase Domain in Kashmiri Women with PCOS.

Shayaq Ul Abeer Rasool, Sairish Ashraf, Mudasar Nabi, Shariq R Masoodi, Khalid M Fazili, Shajrul Amin

Open access · goldAbstract read
In one paragraph

Article in International journal of endocrinology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.9field-weighted citation impact, top 22% 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

10 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
  2. Meta-analysis ofJournal of diabetes and metabolic disorders · 2025
    Review
  3. Review
  4. Article
  5. Association of candidate gene (Journal of the Turkish German Gynecological Association · 2024
    Article
  6. Article
  7. Article
  8. Review
  9. Acanthosis Nigricans: Pointer of Endocrine Entities.Diagnostics (Basel, Switzerland) · 2022
    Review
  10. 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

6 authors at 2 institutions in 1 country.

Shayaq Ul Abeer RasoolDepartment of Biotechnology, University of Kashmir, Srinagar, India.ORCID https://orcid.org/0000-0002-4357-0367
Sairish AshrafDepartment of Biochemistry, University of Kashmir, Srinagar, India.ORCID https://orcid.org/0000-0002-4612-4397
Mudasar NabiDepartment of Biochemistry, University of Kashmir, Srinagar, India.ORCID https://orcid.org/0000-0002-5635-2393
Shariq R MasoodiDepartment of Endocrinology, Sher-i-Kashmir Institute of Medical Sciences, Srinagar, India.ORCID https://orcid.org/0000-0002-8664-9614
Khalid M FaziliDepartment of Biotechnology, University of Kashmir, Srinagar, India.ORCID https://orcid.org/0000-0003-3375-4784
Shajrul AminDepartment of Biochemistry, University of Kashmir, Srinagar, India.ORCID https://orcid.org/0000-0002-1631-3429
University of Kashmir · INSher-i-Kashmir Institute of Medical Sciences · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPolycystic ovary syndrome (PCOS) is the most common endocrine metabolic disorder affecting premenopausal women. Besides primary features like anovulation, hyperandrogenism, and polycystic ovaries, women with PCOS present with multiple metabolic, cardiovascular, and psychological disorders. The etiology is multifactorial and the different genetic variants are suggested to play an important role in pathogenesis. Insulin resistance is a ubiquitous finding in PCOS and SNPs in genes involved in the insulin signaling pathway are possible candidates that can explain the development of clinical manifestations of PCOS.

aimWe aimed to investigate the association of INSR His1058 C/T (rs1799817) single nucleotide polymorphism with PCOS in Kashmiri women. The genotypic-phenotypic correlation of the tested SNP with hyperandrogenism, ovulatory dysfunction, and metabolic markers was evaluated.

resultsThe allele frequency (OR = 1.00, 95% CI = 0.67-1.48,

conclusionThe INSR C/T SNP (rs1799817) does not increase the risk of PCOS in Kashmiri women. This SNP is unlikely to play a significant role in the development and manifestation of clinical symptoms of polycystic ovary syndrome.

Identifiers

PMID34912452
PMCPMC8668320
OpenAlexW4200252920

What Socratic holds

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LicenceCC BY
Read underepoch 390

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 Socratic graph.