Evidence map›Paper›PMID 40469136›Full record

ArticlePakistan journal of medical sciences2025

Patatin-like phospholipase domain-containing 3 (PNPLA3) variants rs 738408 and rs 738409 single nucleotide polymorphism as predictor of metabolic associated fatty liver disease and its progression.

Benash Altaf, Shireen Jawed, Wan Syaheedah Wan Ghazali, Ahmad Aizat Abdul Aziz, Rana Muhammad Tahir Salam, Abid Rasheed, Mahaneem Mohamed

Abstract read
In one paragraph

Article in Pakistan journal of medical sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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2citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Benash AltafBenash Altaf, (MBBS, MPhil) Aziz Fatimah Medical and Dental College, Faisalabad, Pakistan.
Shireen JawedShireen Jawed, (MBBS, MPhil) Frontier Medical and Dental College, Abbottabad, Pakistan.
Wan Syaheedah Wan GhazaliWan Syaheedah Wan Ghazali, (MD,PhD) Department of Physiology, School of Medical Sciences, Universiti Sains Malaysia.
Ahmad Aizat Abdul AzizAhmad Aizat Abdul Aziz, Human Genomic Center, School of Medical Sciences, Universiti Sains Malaysia.
Rana Muhammad Tahir SalamRana Muhammad Tahir Salam, (MBBS) Sonologist, Aziz Fatimah Hospital, Faisalabad, Pakistan.
Abid RasheedAbid Rasheed, Government College University, Faisalabad, Pakistan.
Mahaneem MohamedMahaneem Mohamed, (MD,PhD) Department of Physiology, School of Medical Sciences, Universiti Sains Malaysia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective: To identify the PNPLA3 genetic variants as the potential predictors for metabolic associated fatty liver disease (MAFLD) and its progression among Pakistani population. Method: A cross sectional study comprising of 158 participants. They were included in this study with non-probability purposive sampling technique from Radiology Department of Aziz Fatimah Teaching Hospital and Aziz Fatimah Medical and Dental College, Pakistan. The duration of study was December 5, 2021 to April 4, 2024. Blood samples (10mL) were drawn for liver enzymes, gene analysis and ultimately PCR products were sent for Sanger sequencing. Data was analyzed using SPSS version 26 with p-Values ≤0.05 considered significant. Results: From 158 studied participants, 43.7% were male, and 56.3% were female. Of total population 51.3% were MAFLD positive while 48.7% were control subjects. Present results showed that CT and TT genotypes of rs738408 were frequently found in MAFLD group (p=0.039 and 0.060, respectively) and significant predictor for developing MAFLD (OR=2.484, p=0.019 and OR=5.167, p<0.001, respectively). Concerning progression of the disease CT genotype showed that subject with this genotype progress to moderate grade of fatty liver disease (OR=2.832, p=0.013). Whereas Odd ratio for TT genotype was significant for severe grade fatty liver diseases (OR=15.50, p=0.007). GG genotype of rs738409 was frequently found in MAFLD group (p=0.032). Odds ratio for GG genotype of rs738409 was significant for developing MAFLD (OR=4.565, p=0.025) and responsible to progress to moderate grade of fatty liver disease (OR= 5.083, p=0.022). Conclusion: CT and TT genotypes of 738408 and GG genotype of 738409 are associated with MAFLD and are at more risk for disease progression.

Indexed as

AdiponutrinGenetic variantsMetabolic associated fatty liver diseasePNPLA3rs738408rs 738409

Identifiers

PMID40469136
PMCPMC12130962

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