Key result
There was no significant association between ACE indel polymorphism and cardiorespiratory fitness variables, such as VO2 peak, in either physically active or sedentary young healthy women.
Why the study?
Is ACE indel polymorphism associated with cardiorespiratory fitness in physically active and sedentary young women?
Cross-Sectional (n=117)
No
Is ACE indel polymorphism associated with cardiorespiratory fitness in physically active and sedentary young women?
Genetic variation at the ACE locus does not appear to contribute to peak cardiorespiratory responses in healthy young women, regardless of their physical activity level.
Findings in young Brazilian women add limited data; leaves open ACE polymorphism effects on cardiorespiratory fitness.
BACKGROUND: Polymorphisms at the angiotensin-converting enzyme gene (ACE), such as the indel [rs1799752] variant in intron 16, have been shown to be associated with aerobic performance of athletes and non-athletes. However, the relationship between ACE indel polymorphism and cardiorespiratory fitness has not been always demonstrated. OBJECTIVES: The relationship between ACE indel polymorphism and cardiorespiratory fitness was investigated in a sample of young Caucasian Brazilian women. PATIENTS AND METHODS: This study investigated 117 healthy women (aged 18 to 30 years) who were grouped as physically active (n = 59) or sedentary (n = 58). All subjects performed an incremental exercise test (ramp protocol) on a cycle-ergometer with 20-25 W/min increments. Blood samples were obtained for DNA extraction and to analyze metabolic and hormonal profiles. ACE indel polymorphism was determined by polymerase chain reaction (PCR) and fragment size analysis. RESULTS: The physically active group had higher values of peak oxygen uptake (VO2 peak), carbon dioxide output (VCO2), ventilation (VE) and power output than the sedentary group (P < 0.05) at the peak of the exercise test. However, heart rate (HR), systolic blood pressure (SBP) and diastolic blood pressure (DBP) did not differ between groups. There was no relationship between ACE indel polymorphism and cardiorespiratory variables during the test in both the physically active and sedentary groups, even when the dominant (DD vs. D1 + 2) and recessive (2 vs. DI + DD) models of inheritance were tested. CONCLUSIONS: These results do not support the concept that the genetic variation at the ACE locus contributes to the cardiorespiratory responses at the peak of exercise test in physically active or sedentary healthy women. This indicates that other factors might mediate these responses, including the physical training level of the women.
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Verlengia et al. (2014) conducted a cross-sectional in Healthy (n=117). ACE indel polymorphism vs. Different ACE genotypes (DD, DI, II) was evaluated on Cardiorespiratory fitness variables (VO2 peak, VCO2, VE, power output) during maximal cardiopulmonary exercise test (p=>0.05). There was no significant association between ACE indel polymorphism and cardiorespiratory fitness variables, such as VO2 peak, in either physically active or sedentary young healthy women.
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