Evidence map›Paper›PMID 33543406›Full record

ArticleBiochemical genetics2021

Adiponectin Genetic Variant and Expression Coupled with Lipid Peroxidation Reveal New Signatures in Diabetic Dyslipidemia.

Kakali Ghoshal, Tanima Chatterjee, Subhankar Chowdhury, Sanghamitra Sengupta, Maitree Bhattacharyya

Abstract read
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In one paragraph

Article in Biochemical genetics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed, 1 pooled it
4.5field-weighted citation impact, top 5% 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

20 citing papers in PubMed, 1 synthesis or guideline pooled it, 33 citations in OpenAlex.

  1. Pooled it
  2. Biomolecular Basis of Life.Metabolites · 2025
    Review
  3. Review
  4. Article
  5. Article
  6. The Plasma Levels of Protein Adiponectin (Diabetes, metabolic syndrome and obesity : targets and therapy · 2024
    Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Nutrients · 2023
    Article
  15. Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. 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

5 authors at 2 institutions in 1 country.

Kakali GhoshalDepartment of Biochemistry, University of Calcutta, 35, Ballygunge Circular Road, Kolkata, 700019, India.
Tanima ChatterjeeDepartment of Biochemistry, University of Calcutta, 35, Ballygunge Circular Road, Kolkata, 700019, India.
Subhankar ChowdhuryInstitute of Postgraduate Medical Education and Research, Government of West Bengal, 224, Acharyya Jagadish Chandra Bose Road, Kolkata, 700020, India.
Sanghamitra SenguptaDepartment of Biochemistry, University of Calcutta, 35, Ballygunge Circular Road, Kolkata, 700019, India. sanghamitrasg@yahoo.com.
Maitree BhattacharyyaDepartment of Biochemistry, University of Calcutta, 35, Ballygunge Circular Road, Kolkata, 700019, India. bmaitree@gmail.com.ORCID http://orcid.org/0000-0001-6420-4342
University of Calcutta · INGovernment of West Bengal · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Increasing burden of non-communicable diseases like diabetes and cardiovascular disorders has made the global health scenario more challenging. Dyslipidemia in diabetes is a compounding risk factor for cardiovascular diseases, but there is dearth of identifying appropriate signatures to address this issue. The protein, adiponectin, is actively involved in regulating glucose levels as well as fatty acid breakdown playing crucial role in dyslipidemia and vascular complications. To identify the underlying genetic and molecular profile of adiponectin metabolic pathway in diabetic dyslipidemia and to correlate it with known biochemical and oxidative stress parameters of T2DM, we performed a case-control study in a total 264 individuals belonging to three categories such as diabetes with dyslipidemia (n = 88), diabetes without dyslipidemia (n = 86) and normal healthy controls (n = 90). Expression of adiponectin (ADIPOQ) and its receptors (ADIPOR1 and ADIPOR2) were measured in visceral and subcutaneous adipose tissues. A significant downregulated expression of ADIPOQ and its receptors in adipose tissues and PBMCs were linked with diabetic dyslipidemic condition. A multiple linear regression followed by MDR analysis implicated the elevated plasma malondialdehyde and decreased adiponectin level to be correlated with diabetic dyslipidemia. More interestingly, two single nucleotide polymorphisms of ADIPOQ (rs2241766 and rs1501299) were genetically associated with the risk of developing dyslipidemia. Other important biochemical factors found to be increased in diabetic dyslipidemic conditions included plasma C-reactive protein and 4-hydroxynonenal adducts. Our results explore, a complex interplay of genetic and biochemical parameters in diabetic dyslipidemia which is significant from the perspective of risk stratification and novel therapeutic strategy development.

Indexed as

Lipid PeroxidationPolymorphism, Single NucleotideAdiponectinAdultAllelesCase-Control StudiesDiabetes Mellitus, Type 2DyslipidemiasFemaleGenotypeHaplotypesHumansMaleMiddle AgedAdiponectinADIPOQ protein, humanAdiponectinDyslipidemiaGene-environment interactionPlasma malondialdehydePolymorphismT2DM

Identifiers

PMID33543406
OpenAlexW3127923389

What OpenQuestion holds

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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.