Frequency of PPAR-γ, FTO and ABCC8 genetic variation in Pakistani cardiovascular smokers.


Journal

Environmental science and pollution research international
ISSN: 1614-7499
Titre abrégé: Environ Sci Pollut Res Int
Pays: Germany
ID NLM: 9441769

Informations de publication

Date de publication:
Dec 2020
Historique:
received: 08 06 2020
accepted: 20 07 2020
pubmed: 28 7 2020
medline: 5 11 2020
entrez: 27 7 2020
Statut: ppublish

Résumé

Smoking is considered as one of the major reasons behind genetic variations in cardiometabolic disorders. However, effect of nicotine via smoking on Pakistani population still needs to be elucidated. This study was aimed to investigate genetic variation among PPAR-γ, FTO, and ABCC8 genes in cardiometabolic patients along with their biochemical parameters. A total of 472 CVD patients were enrolled in this study and divided into three groups; n = 144 for PPAR-γ (C/G) variation and n = 164 in each group to investigate FTO (T/A) and ABCC8 (G/T) variation, respectively. Polymorphisms within groups were identified by using Tetra and/or Tri ARM-PCR. This study showed positive association among genetic polymorphisms in PPAR-γ, FTO, and ABCC8 groups with altered metabolic parameters in CVD patients. Findings showed that smoking is major contributory factor for genetic polymorphism that was strongly associated with elevated blood glucose and serum TGs accompanying PPAR-γ, FTO, and ABCC8 genetic polymorphism in 25%, 24%, and 20% in smokers and 11%, 10%, and 5% in non-smoker CVD patients, respectively. However, highest polymorphism occurred in PPAR-γ both in smokers and non-smoker CVD patients that show that smoking-mediated gene polymorphism might be a contributory factor in provoking CVD risk approximately twice in smokers as compared to that in non-smoker CVD patients.

Identifiants

pubmed: 32712935
doi: 10.1007/s11356-020-10226-z
pii: 10.1007/s11356-020-10226-z
doi:

Substances chimiques

ABCC8 protein, human 0
PPAR gamma 0
PPARG protein, human 0
Sulfonylurea Receptors 0
Alpha-Ketoglutarate-Dependent Dioxygenase FTO EC 1.14.11.33
FTO protein, human EC 1.14.11.33

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

42611-42620

Subventions

Organisme : Higher Education Commision, Pakistan
ID : 6429/Punjab/NRPU/R&D/HEC/2016
Organisme : Higher Education Commision, Pakistan
ID : 8365/Punjab/NRPU/R&D/HEC/2017

Auteurs

Kanwal Rehman (K)

Department of Pharmacy, University of Agriculture, Faisalabad, Pakistan.
Institute of Physiology and Pharmacology, University of Agriculture, Faisalabad, Pakistan.

Ayesha Tahir (A)

Institute of Physiology and Pharmacology, University of Agriculture, Faisalabad, Pakistan.

Sania Niaz (S)

Institute of Physiology and Pharmacology, University of Agriculture, Faisalabad, Pakistan.

Sara Shabbir (S)

Department of Pharmacy, University of Agriculture, Faisalabad, Pakistan.

Komal Jabeen (K)

Department of Pharmacy, University of Agriculture, Faisalabad, Pakistan.
Institute of Physiology and Pharmacology, University of Agriculture, Faisalabad, Pakistan.

Amna Faheem (A)

Institute of Physiology and Pharmacology, University of Agriculture, Faisalabad, Pakistan.

Muhammad Sajid Hamid Akash (MSH)

Department of Pharmaceutical Chemistry, Government College University Faisalabad, Faisalabad, Pakistan. sajidakash@gmail.com.

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Classifications MeSH