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Genetic Scores of eNOS, ACE and VEGFA Genes Are Predictive of Endothelial Dysfunction Associated Osteoporosis in Postmenopausal Women.
Singh, Puneetpal; Singh, Monica; Khinda, Rubanpal; Valecha, Srishti; Kumar, Nitin; Singh, Surinderpal; Juneja, Pawan K; Kaur, Taranpal; Mastana, Sarabjit.
Afiliação
  • Singh P; Division of Molecular Genetics, Department of Human Genetics, Punjabi University, Patiala 147002, India.
  • Singh M; Division of Molecular Genetics, Department of Human Genetics, Punjabi University, Patiala 147002, India.
  • Khinda R; Division of Molecular Genetics, Department of Human Genetics, Punjabi University, Patiala 147002, India.
  • Valecha S; Division of Molecular Genetics, Department of Human Genetics, Punjabi University, Patiala 147002, India.
  • Kumar N; Division of Molecular Genetics, Department of Human Genetics, Punjabi University, Patiala 147002, India.
  • Singh S; Aggarwal Orthopedic Hospital, Ludhiana 141001, India.
  • Juneja PK; Aggarwal Orthopedic Hospital, Ludhiana 141001, India.
  • Kaur T; Amrit Sagar Hospital, Ferozepur 152001, India.
  • Mastana S; Human Genomics Lab., School of Sport, Exercise and Health Sciences, Loughborough University, Loughborough LE11 3TU, UK.
Article em En | MEDLINE | ID: mdl-33499313
The present study aimed to examine the participation and contribution of endothelial nitric oxide synthase (eNOS), angiotensin converting enzyme (ACE) and vascular endothelial growth factor (VEGFA) genes for the risk of endothelial dysfunction (ED)-associated osteoporosis risk in postmenopausal women of Punjab, India. Women with ED were categorized into women with osteoporosis (n = 346) and women without osteoporosis (n = 330). They were examined for selected SNPs within eNOS, ACE and VEGFA genes. Linear regression analysis revealed a positive association of ED with bone mineral densities (BMDs) at femoral neck (r2 = 0.78, p < 0.001) and lumbar spine (r2 = 0.24, p = 0.001) after Bonferroni correction. Three susceptibility haplotypes were exposed within eNOS (CTAAAT), ACE (ACDG) and VEGFA (GATA) genes. Bearers of CTAAAT (OR 2.43, p = 0.007), ACDG (OR 2.50, p = 0.002) and GATA (OR 2.10, p = 0.009) had substantial impact for osteoporosis after correcting the effects with traditional risk factors (TRD).With uncertainty measure (R2h) and Akaike information criterion (AIC), best fit models showed that CTAAAT manifested in multiplicative mode (ß ± SE: 2.19 ± 0.86, p < 0.001), whereas ACDG (ß ± SE: 1.73 ± 0.54, p = 0.001) and GATA (ß ± SE: 3.07 ± 0.81, p < 0.001) expressed in dominant modes. Area under receiver operating characteristic curve using weighted risk scores (effect estimates) showed substantial strength for model comprising TRD + GATA (AUC = 0.8, p < 0.001) whereas, model comprising TRD + GATA + CTAAAT exhibited excellent ability to predict osteoporosis (AUC = 0.824, p < 0.001).
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Osteoporose / Osteoporose Pós-Menopausa Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Osteoporose / Osteoporose Pós-Menopausa Idioma: En Ano de publicação: 2021 Tipo de documento: Article