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Genetic Variation in Acid Ceramidase Predicts Non-completion of an Exercise Intervention.
Lewis, Lauren S; Huffman, Kim M; Smith, Ira J; Donahue, Mark P; Slentz, Cris A; Houmard, Joseph A; Hubal, Monica J; Hoffman, Eric P; Hauser, Elizabeth R; Siegler, Ilene C; Kraus, William E.
Affiliation
  • Lewis LS; Department of Obstetrics and Gynecology, Duke University School of Medicine, Durham, NC, United States.
  • Huffman KM; Duke Molecular Physiology Institute, Duke University School of Medicine, Durham, NC, United States.
  • Smith IJ; Division of Rheumatology and Immunology, Department of Medicine, Duke University School of Medicine, Durham, NC, United States.
  • Donahue MP; Division of Cardiology, Department of Medicine, Duke University School of Medicine, Durham, NC, United States.
  • Slentz CA; Division of Cardiology, Department of Medicine, Duke University School of Medicine, Durham, NC, United States.
  • Houmard JA; Duke Molecular Physiology Institute, Duke University School of Medicine, Durham, NC, United States.
  • Hubal MJ; Human Performance Laboratory, East Carolina University, Greenville, NC, United States.
  • Hoffman EP; Children's Genetic Medical Research Center, Children's National Medical Center, Washington, DC, United States.
  • Hauser ER; Children's Genetic Medical Research Center, Children's National Medical Center, Washington, DC, United States.
  • Siegler IC; Duke Molecular Physiology Institute, Duke University School of Medicine, Durham, NC, United States.
  • Kraus WE; Cooperative Studies Program-Epidemiology Center Durham, Veterans Administration Medical Center, Durham, NC, United States.
Front Physiol ; 9: 781, 2018.
Article in En | MEDLINE | ID: mdl-30008672
ABSTRACT
Genetic variation is associated with a number of lifestyle behaviours; it may be associated with adherence and individual responses to exercise training. We tested single nucleotide polymorphisms (SNPs) in the acid ceramidase gene (ASAH1) for association with subject adherence and physiologic benefit with exercise training in two well-characterised randomised, controlled 8-month exercise

interventions:

STRRIDE I (n = 239) and STRRIDE II (n = 246). Three ASAH1 non-coding SNPs in a linkage disequilibrium block were associated with non-completion rs2898458(G/T), rs7508(A/G), and rs3810(A/G) were associated with non-completion in both additive (OR = 1.8, 1.8, 2.0; P < 0.05 all) and dominant (OR = 2.5, 2.6, 3.5; P < 0.05 all) models; with less skeletal muscle ASAH expression (p < 0.01) in a subset (N = 60); and poorer training response in cardiorespiratory fitness (peak VO2 change rs3810 r2 = 0.29, P = 0.04; rs2898458 r2 = 0.29, P = 0.08; rs7508 r2 = 0.28, p = 0.09); and similar in direction and magnitude in both independent exploratory and replication studies. Adherence to exercise may be partly biologically and genetically moderated through metabolic regulatory pathways participating in skeletal muscle adaptation to exercise training.
Key words

Full text: 1 Database: MEDLINE Type of study: Clinical_trials / Prognostic_studies / Risk_factors_studies Language: En Journal: Front Physiol Year: 2018 Type: Article Affiliation country: United States

Full text: 1 Database: MEDLINE Type of study: Clinical_trials / Prognostic_studies / Risk_factors_studies Language: En Journal: Front Physiol Year: 2018 Type: Article Affiliation country: United States