Journal
PHYSIOLOGICAL GENOMICS
Volume 50, Issue 9, Pages 688-690Publisher
AMER PHYSIOLOGICAL SOC
DOI: 10.1152/physiolgenomics.00140.2017
Keywords
exercise; mitochondria; near-infrared spectroscopy; physical activity; single nucleotide polymorphism
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Funding
- National Heart, Lung, and Blood Institute (NHLBI) [HL-089856, HL-089897]
- National Center for Advancing Translational Sciences UCLA CTSI Grant [UL1TR000124]
- Swiss National Science Foundation [P300P3_ 151705, P300PB_167767]
- American Thoracic Society Foundation/Breathe LA Project Grant [ATS-2014-03]
- NHLBI [K08 HL-136928, R00HL-121087]
- Parker B. Francis Research Opportunity Award
- Parker B. Francis Foundation Fellowship
- NATIONAL HEART, LUNG, AND BLOOD INSTITUTE [R00HL121087, U01HL089897, R01HL089856, U01HL089856, K08HL136928, R01HL089897, K12HL120004] Funding Source: NIH RePORTER
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Muscle oxidative capacity is a major determinant of maximum oxygen uptake ((V)over dot O-2max). (V)over dot O-2max predicts survival in humans. Muscle oxidative capacity is low in chronic obstructive pulmonary disease (COPD) and can be assessed from the muscle oxygen consumption recovery rate constant (k) by near-infrared spectroscopy. We hypothesized that 11 SNPs, previously associated with the increase in (V)over dot O-2max following exercise training, would correlate with k in 152 non-Hispanic White and African American smokers with and without COPD. Associations were adjusted for age, weight, FEV1% predicted, steps/day, and principal components of genetic ancestry. No SNPs were significantly associated with k. rs2792022 within BTAF1 (beta = 0.130, P = 0.053) and rs24575771 within SLC22A3 (beta = 0.106, P = 0.058) approached nominal significance. Case-control stratification identified three SNPs nominally associated with k in moderate-to-severe COPD (rs6481619 within SVIL beta = 0.152, P = 0.013; BTAF1 beta = 0.196, P = 0.046; rs7386139 within DEPTOR beta = 0.159, P = 0.047). These data support further study of the genomic contributions to skeletal muscle dysfunction in COPD.
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