Using molecular classification to predict gains in maximal aerobic capacity following endurance exercise training in humans

TY - JOUR

T1 - Using molecular classification to predict gains in maximal aerobic capacity following endurance exercise training in humans

AU - Timmons, James A

AU - Knudsen, Steen

AU - Rankinen, Tuomo

AU - Koch, Lauren G

AU - Sarzynski, Mark

AU - Jensen, Thomas

AU - Keller, Pernille

AU - Scheele, Camilla

AU - Vollaard, Niels B J

AU - Nielsen, Søren

AU - Åkerström, Thorbjörn

AU - MacDougald, Ormond A

AU - Jansson, Eva

AU - Greenhaff, Paul L

AU - Tarnopolsky, Mark A

AU - van Loon, Luc J C

AU - Pedersen, Bente Klarlund

AU - Sundberg, Carl Johan

AU - Wahlestedt, Claes

AU - Britton, Steven L

AU - Bouchard, Claude

N1 - CURIS 2010 5200 100

PY - 2010/6/1

Y1 - 2010/6/1

N2 - A low maximal oxygen consumption (Vo2max is a strong risk factor for premature mortality. Supervised endurance exercise training increases Vo2max with a very wide range of effectiveness in humans. Discovering the DNA variants that contribute to this heterogeneity typically requires substantial sample sizes. In the present study, we first use RNA expression, profiling to produce a molecular classifier that predicts Vo2max training response. We then, hypothesized that the classifier genes would harbor DNA variants that contributed to the heterogeneous Vo2max response. Two independent preintervention RNA expression data sets were generated (n = 41 gene chips) from subjects that underwent supervised endurance training: one identified and the second blindly validated an RNA. expression signature that predicted change in Vo2max ("predictor" genes). The HERITAGE Family Study (n = 473) was used for genotyping. We discovered a 29-RNA signature that predicted V̇o2max training response on a continuous scale; these genes contained ∼6 new single-nucleotide polymorphisms associated with gains in Vo2max in the HERITAGE Family Study. Three of four novel candidate genes from the HERITAGE Family Study were confirmed as RNA predictor genes (i.e., "reciprocal" RNA validation of a quantitative trait locus genotype), enhancing the performance of the 29-RNA-based predictor. Notably, RNA abundance for the predictor genes was unchanged by exercise training, supporting the idea that expression was preset by genetic variation. Regression analysis yielded a model where 11 single-nucleotide polymorphisms explained 23% of the variance in gains in Vo2max, corresponding to ∼50% of the estimated genetic variance for Vo2max. In conclusion, combining RNA profiling with single-gene DNA marker association analysis yields a strongly validated molecular predictor with meaningful explanatory power. Vo2max responses to endurance training can be predicted by measuring a ∼30-gene RNA expression signature in muscle prior to training. The general approach taken could accelerate the discovery of genetic biomarkers, sufficiently discrete for diagnostic purposes, for a range of physiological and pharmacological phenotypes in humans.

AB - A low maximal oxygen consumption (Vo2max is a strong risk factor for premature mortality. Supervised endurance exercise training increases Vo2max with a very wide range of effectiveness in humans. Discovering the DNA variants that contribute to this heterogeneity typically requires substantial sample sizes. In the present study, we first use RNA expression, profiling to produce a molecular classifier that predicts Vo2max training response. We then, hypothesized that the classifier genes would harbor DNA variants that contributed to the heterogeneous Vo2max response. Two independent preintervention RNA expression data sets were generated (n = 41 gene chips) from subjects that underwent supervised endurance training: one identified and the second blindly validated an RNA. expression signature that predicted change in Vo2max ("predictor" genes). The HERITAGE Family Study (n = 473) was used for genotyping. We discovered a 29-RNA signature that predicted V̇o2max training response on a continuous scale; these genes contained ∼6 new single-nucleotide polymorphisms associated with gains in Vo2max in the HERITAGE Family Study. Three of four novel candidate genes from the HERITAGE Family Study were confirmed as RNA predictor genes (i.e., "reciprocal" RNA validation of a quantitative trait locus genotype), enhancing the performance of the 29-RNA-based predictor. Notably, RNA abundance for the predictor genes was unchanged by exercise training, supporting the idea that expression was preset by genetic variation. Regression analysis yielded a model where 11 single-nucleotide polymorphisms explained 23% of the variance in gains in Vo2max, corresponding to ∼50% of the estimated genetic variance for Vo2max. In conclusion, combining RNA profiling with single-gene DNA marker association analysis yields a strongly validated molecular predictor with meaningful explanatory power. Vo2max responses to endurance training can be predicted by measuring a ∼30-gene RNA expression signature in muscle prior to training. The general approach taken could accelerate the discovery of genetic biomarkers, sufficiently discrete for diagnostic purposes, for a range of physiological and pharmacological phenotypes in humans.

U2 - 10.1152/japplphysiol.01295.2009

DO - 10.1152/japplphysiol.01295.2009

M3 - Journal article

C2 - 20133430

SN - 8750-7587

VL - 108

SP - 1487

EP - 1496

JO - Journal of Applied Physiology

JF - Journal of Applied Physiology

IS - 6

ER -