Investigation of the association between the TCF7L2 rs7903146 (C/T) gene polymorphism and obesity in a Cameroonian population: a pilot study

被引:3
|
作者
Nguimmo-Metsadjio, Aurelie [1 ,2 ]
Atogho-Tiedeu, Barbara [1 ,2 ]
Noubiap, Jean Jacques [3 ,4 ,5 ]
Evehe, Marie-Solange [1 ,2 ]
Djokam-Dadjeu, Rosine [1 ,2 ]
Donfack, Olivier Sontsa [1 ,2 ]
Nanfa, Dieudonne [1 ,2 ]
Mato, Edith Pascale M. [1 ,2 ]
Ngwa, Elvis Ndonwi [1 ,2 ]
Guewo-Fokeng, Magellan [1 ,2 ]
Pokam-Fosso, Priscille [1 ,2 ]
Mbacham, Wilfred F. [1 ,6 ]
Mbanya, Jean Claude [2 ,7 ,8 ]
Sobngwi, Eugene [2 ,7 ,8 ]
机构
[1] Univ Yaounde I, Dept Biochem, Fac Sci, Yaounde, Cameroon
[2] Univ Yaounde I, Biotechnol Ctr, Lab Mol Med & Metab, Yaounde, Cameroon
[3] Groote Schuur Hosp, Dept Med, Cape Town, South Africa
[4] Univ Cape Town, Cape Town, South Africa
[5] Med Diagnost Ctr, Yaounde, Cameroon
[6] Univ Yaounde I, Biotechnol Ctr, Lab Publ Hlth Res Biotechnol, Yaounde, Cameroon
[7] Univ Yaounde I, Fac Med & Biomed Sci, Dept Internal Med & Specialties, Yaounde, Cameroon
[8] Yaounde Cent Hosp, Natl Obes Ctr, Yaounde, Cameroon
关键词
Obesity; Genetic association; TCF7L2; rs7903146 (C/T) polymorphism; Sub-Saharan Africa; Cameroon; TYPE-2; DIABETES-MELLITUS; WAIST CIRCUMFERENCE; URBAN; SERUM; PREVALENCE; VARIANT;
D O I
10.1186/s41043-017-0087-z
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Objective: This study aimed at investigating the association between the rs7903146 (C/T) polymorphism of the TCF7L2 gene with obesity in a Cameroonian population. Method: This was a case-control pilot study including 61 obese and 61 non-obese Cameroonian adults. Anthropometric indices of obesity, blood pressure, fasting blood glucose, and blood lipids were measured. The rs7903146 (C/T) polymorphism of the TCF7L2 gene was genotyped using polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP), and genotypes were correlated with clinical and biological parameters. Results: The T allele was predominant in the study population with a frequency of 93%. No statistically significant difference was however observed between the genotypic (p = 0.50) and allelic frequencies (p = 0.58) of obese and non-obese subjects. Comparison of clinical and biochemical parameters of C allele carriers (CX = CC + CT) with those of TT genotype showed that there was no significant difference between the lipid profile of these two groups. Conclusion: The rs7903146 (C/T) polymorphism of the TCF7L2 gene might not be associated with obesity in the Cameroonian population.
引用
收藏
页数:6
相关论文
共 50 条
  • [42] Association of TCF7L2 rs7903146 Polymorphism with the Risk of Type 2 Diabetes Mellitus (T2DM) Among Kurdish Population in Erbil Province, Iraq
    Suhad Mustafa
    Delan Younus
    Indian Journal of Clinical Biochemistry, 2021, 36 : 312 - 318
  • [43] Polycystic Ovary Syndrome Is Not Associated with rs7903146 Polymorphism of TCF7L2 Gene: A Systematic Review and Meta-Analysis
    Ramos, Ramon Bossardi
    Fabris, Vitor Costa
    Brondani, Leticia de Almeida
    Spritzer, Poli Mara
    ENDOCRINE REVIEWS, 2014, 35 (03)
  • [44] Genetic variations in transcription factor 7-like 2 (TCF7L2) gene: association of TCF7L2 rs12255372(G/T) or rs7903146(C/T) with breast cancer risk and clinico-pathological parameters
    Naidu, R.
    Yip, C. H.
    Taib, N. A. M.
    MEDICAL ONCOLOGY, 2012, 29 (02) : 411 - 417
  • [45] Serotonin is elevated in risk-genotype carriers of TCF7L2 - rs7903146
    Andreas Leiherer
    Axel Muendlein
    Christoph H. Saely
    Peter Fraunberger
    Heinz Drexel
    Scientific Reports, 9
  • [46] Significant Influence of Type 2 Diabetes on the Association between the TCF7L2 rs7903146 Polymorphism and Angiographically documented coronary Artery disease.
    Muendlein, Axel
    Saely, Christoph
    Rhomberg, Simone
    Sonderegger, Gudrun
    Rein, Philipp
    Vonbank, Alexander
    Winder, Thomas
    Beer, Stefan
    Drexel, Heinz
    WIENER KLINISCHE WOCHENSCHRIFT, 2009, 121 : S20 - S21
  • [47] Genetic Associations of TCF7L2 (rs7903146) and PPARG (rs1801282) with Prediabetes in the Ethnic Kazakh Population
    Dyussupova, Azhar
    Svyatova, Gulnara
    Berezina, Galina
    Dyussupov, Altay
    Omarkulov, Bauyrzhan
    Dzharmukhametova, Anastassiya
    Yurkovskaya, Oxana
    Akhmetova, Venera
    Dyussupova, Asylzhan
    DIAGNOSTICS, 2024, 14 (24)
  • [48] Role of the single nucleotide polymorphism rs7903146 of TCF7L2 in inducing nonsense-mediated decay
    Nicod, Nathalie
    Pradas-Juni, Marta
    Gomis, Ramon
    SPRINGERPLUS, 2014, 3 : 1 - 5
  • [49] New insights on the involvement of the intronic SNP rs7903146 on alternative splicing of TCF7L2
    Pradas-Juni, M.
    Nicod, N.
    Fernandez-Rebollo, E.
    Valcarcel, J.
    Gomis, R.
    DIABETOLOGIA, 2012, 55 : S126 - S126
  • [50] Significant association of TCF7L2 variant rs7903146 with angiographically characterized coronary artery disease in women
    Muendlein, A.
    Saely, C. H.
    Rhomberg, S.
    Vonbank, A.
    Rein, P.
    Winder, T.
    Drexel, H.
    EUROPEAN HEART JOURNAL, 2010, 31 : 804 - 804