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Association of BCHE gene SNP rs1803274 (K-variant) and rs3495 with obesity in Pakistani population group

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00179906%3A_____%2F25%3A10498793" target="_blank" >RIV/00179906:_____/25:10498793 - isvavai.cz</a>

  • Alternative codes found

    RIV/62690094:18450/25:50022223 RIV/62690094:18470/25:50022223 RIV/61989100:27360/25:10257805

  • Result on the web

    <a href="https://verso.is.cuni.cz/pub/verso.fpl?fname=obd_publikace_handle&handle=mSwOM3G-4v" target="_blank" >https://verso.is.cuni.cz/pub/verso.fpl?fname=obd_publikace_handle&handle=mSwOM3G-4v</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1038/s41366-025-01715-7" target="_blank" >10.1038/s41366-025-01715-7</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Association of BCHE gene SNP rs1803274 (K-variant) and rs3495 with obesity in Pakistani population group

  • Original language description

    BackgroundObesity plays a crucial role in the development of metabolic disorders including diabetes, coronary and renal diseases. There are several factors involved in the pathology of obesity, including chronic inflammation and exposure to environmental contaminants. Recently, the cholinergic co-hydrolyzing enzyme BChE has been associated with clinical conditions such as diabetes and obesity. This study aims to investigate the levels of BChE and inflammatory markers in the serum, as well as the association between two specific BCHE gene variants (rs1803274 and rs3495) and the risk of obesity in the Pakistani population.MethodsThe study recruited 350 people with obesity and 200 volunteers with no obesity. Proinflammatory cytokines (TNF-alpha, IL-6, and IL-1 beta) levels were quantified using ELISA kits, while the analysis of BCHE gene SNPs rs1803274 (K-variant) and rs3495 was conducted using the tetra-primer amplification refractory mutation-PCR (tetra-ARM-PCR) and PCR-restriction fragment length polymorphism (RFLP) methods, respectively. Additionally, clinico-pathological parameters HDL, LDL, BMI, Homa-IR, insulin, glucose, blood pressure was also assessed in subjects of current study.ResultsResults showed significantly higher levels of BChE, TNF-alpha, IL-1 beta, and IL-6 in the obesity group compared to the group without obesity. Furthermore, the obesity group exhibited higher blood pressure and LDL levels, as well as lower HDL levels when compared to group without obesity. Logistic regression analysis revealed a relationship between obesity and higher BChE activity, blood pressure, LDL, and lower HDL levels. The study also found a statistically significant association between the BCHE gene SNPs rs1803274 (K-variant) and rs3495 and the risk of obesity (OR = 2.01; CI = 1.21-3.33; p = 0.0063; OR = 1.80; CI = 1.09-2.96, respectively).ConclusionsIn conclusion, the study suggests that BChE and inflammatory cytokines play a significant role in the development and pathogenesis of obesity and can also act as good diagnostic biomarkers for obesity and its related metabolic disorders.

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database

  • CEP classification

  • OECD FORD branch

    30104 - Pharmacology and pharmacy

Result continuities

  • Project

  • Continuities

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2025

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    International Journal of Obesity

  • ISSN

    0307-0565

  • e-ISSN

    1476-5497

  • Volume of the periodical

    49

  • Issue of the periodical within the volume

    5

  • Country of publishing house

    GB - UNITED KINGDOM

  • Number of pages

    7

  • Pages from-to

    881-887

  • UT code for WoS article

    001407508800001

  • EID of the result in the Scopus database

    2-s2.0-85217236277