Please use this identifier to cite or link to this item: http://hdl.handle.net/1942/36336
Title: Hypothalamic-pituitary hormones will be affected by the interaction between 5q13-14-rs2239670 (CARTPT) gene variants and diet in different obesity phenotypes
Authors: Mahmoudinezhad, Mahsa
Abbasalizad-Farhangi, Mahdieh
KAHROBA, Houman 
Issue Date: 2021
Publisher: SPRINGERNATURE
Source: BMC RESEARCH NOTES, 14 (1) (Art N° 443)
Abstract: Objective Evidence show that cocaine and amphetamine regulated transcript-prepropeptide (CART-PT) gene variants may affect obesity related traits, but little is known about its end points. In the current study, we aimed to evaluate the interaction of CARTPT gene polymorphism with diet quality indices including dietary approaches to stop hypertension (DASH) and Mediterranean diet score (MDS) on cardio-metabolic risk factors. This cross sectional study recruited 288 apparently healthy obese individuals. Diet quality indices including DASH and MDS were evaluated using semi quantitative food frequency questionnaire (FFQ). Polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) was used for CARTPT genotypes. Results No significant differences was reported for general characteristics and biochemical parameters across genotypes except for QUICKI among females (P = 0.01) and it was higher in heterozygous genotype. There was significant CARTPT-DASH interactions affecting serum fasting glucose level (P = 0.049). However, in relation to CERTPT-MDS interactions, the highest level of insulin (P = 0.003) and HOMA-IR (P = 0.003) values were shown among AA carriers in high adherence to MDS, while AA carriers in high compliance to MDS experienced decreased level of QUICKI (P = 0.001).
Notes: Abbasalizad-Farhangi, M (corresponding author), Tabriz Univ Med Sci, Drug Appl Res Ctr, Attar Neishabouri Ave,Golgasht St, Tabriz 5165665931, Iran.
abbasalizad_m@yahoo.com
Keywords: CARTPT; Diet quality indices; Cardio-metabolic risk factors; Obesity
Document URI: http://hdl.handle.net/1942/36336
e-ISSN: 1756-0500
DOI: 10.1186/s13104-021-05857-5
ISI #: WOS:000727846900002
Rights: © The Author(s) 2021. Open Access This article is licensed under a Creative Commons Attribution 4.0 International License
Category: A1
Type: Journal Contribution
Validations: vabb 2023
Appears in Collections:Research publications

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