Bibliografia

  1. Lietz, G., Oxley, A., Leung, W. & Hesketh, J. Single Nucleotide Polymorphisms Upstream from the β-Carotene 15,15’-Monoxygenase Gene Influence Provitamin A Conversion Efficiency in Female Volunteers. J. Nutr. 142,161S–165S (2012).
  2. Hazra, A. et al. Common variants of FUT2 are associated with plasma vitamin B12 levels. Nat. Genet. 40,1160–1162 (2008).
  3. Horska, A. et al. Vitamin C levels in blood are influenced by polymorphisms in glutathione S-transferases. Eur. J. Nutr. 50,437–446 (2011).
  4. Cahill, L. E., Fontaine-Bisson, B. & El-Sohemy, A. Functional genetic variants of glutathione S-transferase protect against serum ascorbic acid deficiency. Am. J. Clin. Nutr. 90,1411–1417 (2009).
  5. Slater, N. A., Rager, M. L., Havrda, D. E. & Harralson, A. F. Genetic Variation in CYP2R1 and GC Genes Associated With Vitamin D Deficiency Status. J. Pharm. Pract. 30,31–36 (2017).
  6. Wang, T. J. et al. Common genetic determinants of vitamin D insufficiency: a genome-wide association study. Lancet 376,180–188 (2010).
  7. Glynn, R. J., Ridker, P. M., Goldhaber, S. Z., Zee, R. Y. L. & Buring, J. E. Effects of Random Allocation to Vitamin E Supplementation on the Occurrence of Venous Thromboembolism. Circulation 116,1497–1503 (2007).
  8. Solis, C. et al. Folate Intake at RDA Levels Is Inadequate for Mexican American Men with the Methylenetetrahydrofolate Reductase 677TT Genotype. J. Nutr. 138,67–72 (2008).
  9. Guinotte, C. L. et al. Methylenetetrahydrofolate Reductase 677C→T Variant Modulates Folate Status Response to Controlled Folate Intakes in Young Women. J. Nutr. 133,1272–1280 (2003).
  10. Allen, K. J. et al. Iron-Overload–Related Disease in HFEHereditary Hemochromatosis. N. Engl. J. Med. 358,221–230 (2008).
  11. Pichler, I. et al. Identification of a common variant in the TFR2 gene implicated in the physiological regulation of serum iron levels. Hum. Mol. Genet. 20,1232–1240 (2011).
  12. Benyamin, B. et al. Variants in TF and HFE Explain ∼40% of Genetic Variation in Serum-Transferrin Levels. Am. J. Hum. Genet. 84,60–65 (2009).
  13. Fang, Y. et al. Vitamin D Binding Protein Genotype and Osteoporosis. Calcif. Tissue Int. 85,85–93 (2009).
  14. Cornelis, M. C., El-Sohemy, A., Kabagambe, E. K. & Campos, H. Coffee, CYP1A2 Genotype, and Risk of Myocardial Infarction. JAMA 295,1135 (2006).
  15. Palatini, P. et al. CYP1A2 genotype modifies the association between coffee intake and the risk of hypertension. J. Hypertens. 27,1594–1601 (2009).
  16. Cornelis, M. C., Qi, L., Kraft, P. & Hu, F. B. TCF7L2, dietary carbohydrate, and risk of type 2 diabetes in US women. Am. J. Clin. Nutr. 89,1256–1262 (2009).
  17. Poch, E. et al. Molecular basis of salt sensitivity in human hypertension. Evaluation of renin-angiotensin-aldosterone system gene polymorphisms. Hypertens. (Dallas, Tex. 1979) 38,1204–9 (2001).
  18. Ferguson, J. F. et al. NOS3 gene polymorphisms are associated with risk markers of cardiovascular disease, and interact with omega-3 polyunsaturated fatty acids. Atherosclerosis 211,539–544 (2010).
  19. Corella, D. et al. APOA2, dietary fat, and body mass index: replication of a gene-diet interaction in 3 independent populations. Arch. Intern. Med. 169,1897–906 (2009).
  20. Nagai, N., Sakane, N., Tsuzaki, K. & Moritani, T. UCP1 genetic polymorphism (–3826 A/G) diminishes resting energy expenditure and thermoregulatory sympathetic nervous system activity in young females. Int. J. Obes. 35,1050–1055 (2011).
  21. Andreasen, C. H. et al. Low Physical Activity Accentuates the Effect of the FTO rs9939609 Polymorphism on Body Fat Accumulation. Diabetes 57,95–101 (2008).
  22. Reddon, H. et al. Physical activity and genetic predisposition to obesity in a multiethnic longitudinal study. Sci. Rep. 6,18672 (2016).
  23. Rodrigues, G. K. et al. A single FTO gene variant rs9939609 is associated with body weight evolution in a multiethnic extremely obese population that underwent bariatric surgery. Nutrition31,1344–1350 (2015).
  24. Grau, K. et al. TCF7L2 rs7903146–macronutrient interaction in obese individuals’ responses to a 10-wk randomized hypoenergetic diet. Am. J. Clin. Nutr. 91,472–479 (2010).
  25. Mattei, J., Qi, Q., Hu, F. B., Sacks, F. M. & Qi, L. TCF7L2 genetic variants modulate the effect of dietary fat intake on changes in body composition during a weight-loss intervention. Am. J. Clin. Nutr. 96,1129–1136 (2012).
  26. Garaulet, M., Smith, C. E., Hernández-González, T., Lee, Y.-C. & Ordovás, J. M. PPARγ Pro12Ala interacts with fat intake for obesity and weight loss in a behavioural treatment based on the Mediterranean diet. Mol. Nutr. Food Res. 55,1771–1779 (2011).
  27. Enattah, N. S. et al. Identification of a variant associated with adult-type hypolactasia. Nat. Genet.30,233–237 (2002).
  28. Koek, W. N. H. et al. The T-13910C polymorphism in the lactase phlorizin hydrolase gene is associated with differences in serum calcium levels and calcium intake. J. Bone Miner. Res.25,1980–1987 (2010).
  29. Dzialanski, Z. et al. Lactase persistence versus lactose intolerance: Is there an intermediate phenotype? Clin. Biochem. 49,248–252 (2016).
  30. Wolters, V. M. & Wijmenga, C. Genetic Background of Celiac Disease and Its Clinical Implications. Am. J. Gastroenterol. 103,190–195 (2008).
  31. Sapone, A. et al. Divergence of gut permeability and mucosal immune gene expression in two gluten-associated conditions: celiac disease and gluten sensitivity. BMC Med.9,23 (2011).
  32. Monsuur, A. J. et al. Effective Detection of Human Leukocyte Antigen Risk Alleles in Celiac Disease Using Tag Single Nucleotide Polymorphisms. PLoS One 3,e2270 (2008).
  33. Melis, M., Sollai, G., Muroni, P., Crnjar, R. & Tomassini Barbarossa, I. Associations between Orosensory Perception of Oleic Acid, the Common Single Nucleotide Polymorphisms (rs1761667 and rs1527483) in the CD36 Gene, and 6-n-Propylthiouracil (PROP) Tasting. Nutrients 7,2068–2084 (2015).
  34. Eny, K. M., Wolever, T. M. S., Fontaine-Bisson, B. & El-Sohemy, A. Genetic variant in the glucose transporter type 2 is associated with higher intakes of sugars in two distinct populations. Physiol. Genomics 33,355–360 (2008).
  35. Mandel, A. L. & Breslin, P. A. S. High Endogenous Salivary Amylase Activity Is Associated with Improved Glycemic Homeostasis following Starch Ingestion in Adults. J. Nutr. 142,853–858 (2012).
  36. Stutzmann, F. et al. Common genetic variation near MC4R is associated with eating behaviour patterns in European populations. Int. J. Obes. 33,373–378 (2009).
  37. Bryan, A., Hutchison, K. E., Seals, D. R. & Allen, D. L. A transdisciplinary model integrating genetic, physiological, and psychological correlates of voluntary exercise. Health Psychol. 26,30–9 (2007).
  38. Caldwell Hooper, A. E., Bryan, A. D. & Hagger, M. S. What keeps a body moving? The brain-derived neurotrophic factor val66met polymorphism and intrinsic motivation to exercise in humans. J. Behav. Med. 37,1180–1192 (2014).
  39. Ahmetov, I. et al. GENOME-WIDE ASSOCIATION STUDY IDENTIFIES THREE NOVEL GENETIC MARKERS ASSOCIATED WITH ELITE ENDURANCE PERFORMANCE </strong> Biol. Sport 32,3–9 (2014).
  40. Zarebska, A. et al. THE GSTP1 c.313A>G POLYMORPHISM MODULATES THE CARDIORESPIRATORY RESPONSE TO AEROBIC TRAINING. Biol. Sport 31,261–266 (2014).
  41. He, Z. et al. NRF2 Genotype Improves Endurance Capacity in Response to Training. Int. J. Sports Med. 28,717–721 (2007).
  42. Santiago, C. et al. Trp64Arg polymorphism in ADRB3 gene is associated with elite endurance performance. Br. J. Sports Med. 45,147–149 (2011).
  43. GARTON, F. C. & NORTH, K. N. The Effect of Heterozygosity for the ACTN3 Null Allele on Human Muscle Performance. Med. Sci. Sport. Exerc. 48,509–520 (2016).
  44. Ma, F. et al. The association of sport performance with ACE and ACTN3 genetic polymorphisms: a systematic review and meta-analysis. PLoS One 8,e54685 (2013).
  45. DE MOOR, M. H. M. et al. Genome-Wide Association Study of Exercise Behavior in Dutch and American Adults. Med. Sci. Sport. Exerc. 41,1887–1895 (2009).
  46. Zubieta, J.-K. et al. COMT val158met Genotype Affects micro-Opioid Neurotransmitter Responses to a Pain Stressor. Science (80-. ). 299,1240–1243 (2003).
  47. Tammimäki, A. & Männistö, P. T. Catechol-O-methyltransferase gene polymorphism and chronic human pain. Pharmacogenet. Genomics 22,673–691 (2012).
  48. September, A. V et al. Variants within the COL5A1 gene are associated with Achilles tendinopathy in two populations. Br. J. Sports Med. 43,357–365 (2009).