Lack of association of estrogen receptor alpha gene polymorphisms with cardiorespiratory and metabolic variables in young women

Rebelo, A. C.; Verlengia R.; Kunz V.; Tamburus N.; Cerda A.; Hirata, R; Hirata, M; Silva, E.

Abstract

This study examined the association of estrogen receptor alpha gene (ESR1) polymorphisms with cardiorespiratory and metabolic parameters in young women. In total, 354 healthy women were selected for cardiopulmonary exercise testing and short-term heart rate (HR) variability (HRV) evaluation. The HRV analysis was determined by the temporal indices rMSSD (square root of the mean squared differences of successive R-R intervals (RRi) divided by the number of RRi minus one), SDNN (root mean square of differences from mean RRi, divided by the number of RRi) and power spectrum components by low frequency (LF), high frequency (HF) and LF/HF ratio. Blood samples were obtained for serum lipids, estradiol and DNA extraction. ESR1 rs2234693 and rs9340799 polymorphisms were analyzed by PCR and fragment restriction analysis. HR and oxygen uptake (VO2) values did not differ between the ESR1 polymorphisms with respect to autonomic modulation. We not find a relationship between ESR1 T-A, T-G, C-A and C-G haplotypes and cardiorespiratory and metabolic variables. Multiple linear regression analysis demonstrated that VO2, total cholesterol and triglycerides influence HRV (p < 0.05). The results suggest that ESR1 variants have no effect on cardiorespiratory and metabolic variables, while HRV indices are influenced by aerobic capacity and lipids in healthy women. © 2012 by the authors; licensee MDPI, Basel, Switzerland.

Más información

Título según SCOPUS: Lack of association of estrogen receptor alpha gene polymorphisms with cardiorespiratory and metabolic variables in young women
Título de la Revista: INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES
Volumen: 13
Número: 10
Editorial: MDPI
Fecha de publicación: 2012
Página de inicio: 13691
Página final: 13703
Idioma: English
DOI:

10.3390/ijms131013691

Notas: SCOPUS