Genetic association of rs373001 polymorphism in mir-130b gene with susceptibility to dyslipidaemia and correlation with lipid profile.
N, F., A, M., A, R., & U, N. (2026). Genetic association of rs373001 polymorphism in mir-130b gene with susceptibility to dyslipidaemia and correlation with lipid profile.. JPMA. The Journal of the Pakistan Medical Association. https://doi.org/10.47391/JPMA.30321
N F, A M, A R, U N. Genetic association of rs373001 polymorphism in mir-130b gene with susceptibility to dyslipidaemia and correlation with lipid profile.. JPMA. The Journal of the Pakistan Medical Association. 2026; doi: 10.47391/JPMA.30321
N F, A M, A R, et al. Genetic association of rs373001 polymorphism in mir-130b gene with susceptibility to dyslipidaemia and correlation with lipid profile.[J]. JPMA. The Journal of the Pakistan Medical Association. 2026. DOI: 10.47391/JPMA.30321.
@article{n2026,
author = {Fakhar N and Majeed A and Rashid A and Naeem U},
title = {Genetic association of rs373001 polymorphism in mir-130b gene with susceptibility to dyslipidaemia and correlation with lipid profile.},
journal = {JPMA. The Journal of the Pakistan Medical Association},
year = {2026},
doi = {10.47391/JPMA.30321},
note = {PMID: 42444221},
}
TY - JOUR AU - Fakhar N AU - Majeed A AU - Rashid A AU - Naeem U TI - Genetic association of rs373001 polymorphism in mir-130b gene with susceptibility to dyslipidaemia and correlation with lipid profile. T2 - JPMA. The Journal of the Pakistan Medical Association PY - 2026 DO - 10.47391/JPMA.30321 AN - PMID:42444221 ER -
OBJECTIVE: To find the association and correlation of rs373001 polymorphism in micro-ribonucleic acid-130b gene with the risk of dyslipidaemia. METHODS: The case-control study was conducted from April 2 to December 13, 2024, at the Department of Biochemistry and Molecular Biology, National University of Medical Sciences, Rawalpindi, Pakistan, in collaboration with the Chemical Pathology Laboratory, Army Medical College, Rawalpindi, and comprised dyslipidaemia cases and healthy controls. Genomic deoxyribonucleic acid extraction was done from blood samples using an organic method, and tetra-primer amplification refractory mutation system-polymerase chain reaction, followed by agarose gel electrophoresis. Data regarding lipid profile and fasting blood glucose was noted for all the participants. Data was analysed using SPSS 26. RESULTS: Of the 300 subjects, 150(50%) were in each of the two groups. There were 86(57%) males and 64(43%) females among the cases with mean age was 49.1±11.6 years, and 76(52%) females and 72(48%) males with 43.3±15.6 years among the controls. The rs373001 polymorphism of micro-ribonucleic acid-130b gene showed a C>T transition. The C allele (reference allele) frequency was n=123 (41%) in cases and n=144 (48%) in controls, while T allele (risk allele) frequency was n=177 (59%) in cases and n=156 (52%) in controls. The cases had 120(80%) CT, 1(0.7%) CC and 29(19.3%) TT genotypes, while the controls had 142(94.7%) CT, 1(0.7%) CC and 7(4.7%) TT genotypes. The TT genotype was a risk (adjusted odds ratio: 4.8, p<0.001) in recessive genetic model, while CT was protective (adjusted odds ratio: 0.2, p<0.001) in over-dominant model. A correlation was noted between genotypes and triglycerides levels (p=0.039) without confounders age and gender, but when adjusted with these confounders, no correlation was found (p>0.05). CONCLUSION: There was a positive association of the TT genotype of rs373001 polymorphism in micro-ribonucleic acid-130b gene with the risk of dyslipidaemia development in recessive genetic model and log-additive pattern of inheritance.