Monoamine oxidase a gene polymorphism and the pathogenesis of sudden infant death syndrome

Journal of Pediatrics

Volumn 163, Issue 1, 2013, Pages 89-93

  Courts, Cornelius ^a   Grabmüller, Melanie ^a   Madea, Burkhard ^a  

^a UNIVERSITY OF BONN   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

AMINE OXIDASE (FLAVIN CONTAINING) ISOENZYME A;

ALLELE; ARTICLE; CONTROLLED STUDY; FEMALE; GENE LOCUS; GENETIC POLYMORPHISM; GENETIC VARIABILITY; GENOTYPE; HUMAN; HUMAN TISSUE; INFANT; MAJOR CLINICAL STUDY; MALE; PATHOGENESIS; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; SUDDEN INFANT DEATH SYNDROME;

CASE-CONTROL STUDIES; FEMALE; HUMANS; INFANT; MALE; MONOAMINE OXIDASE; POLYMORPHISM, GENETIC; RETROSPECTIVE STUDIES; SUDDEN INFANT DEATH;

EID: 84879415144     PISSN: 00223476     EISSN: 10976833     Source Type: Journal    
DOI: 10.1016/j.jpeds.2012.12.072     Document Type: Article

References (41)

1. H.F. Krous, J.B. Beckwith, R.W. Byard, T.O. Rognum, T. Bajanowski, and T. Corey Sudden infant death syndrome and unclassified sudden infant deaths: a definitional and diagnostic approach Pediatrics 114 2004 234 238
2. E.A. Mitchell The changing epidemiology of SIDS following the national risk reduction campaigns Pediatr Pulmonol Suppl 16 1997 117 119
3. J.P. Nicholl, and A. O'Cathain Epidemiology of babies dying at different ages from the sudden infant death syndrome J Epidemiol Community Health 43 1989 133 139
4. F.R. Hauck, and K.O. Tanabe International trends in sudden infant death syndrome: stabilization of rates requires further action Pediatrics 122 2008 660 666
5. R.W. Byard, and H.F. Krous Sudden infant death syndrome: overview and update Pediatr Dev Pathol 6 2003 112 127
6. J.J. Filiano, and H.C. Kinney A perspective on neuropathologic findings in victims of the sudden infant death syndrome: the triple-risk model Biol Neonate 65 1994 194 197
7. M. Klintschar, B. Reichenpfader, and K.S. Saternus A functional polymorphism in the tyrosine hydroxylase gene indicates a role of noradrenalinergic signaling in sudden infant death syndrome J Pediatr 153 2008 190 193
8. H.C. Kinney, G.B. Richerson, S.M. Dymecki, R.A. Darnall, and E.E. Nattie The brainstem and serotonin in the sudden infant death syndrome Annu Rev Pathol 4 2009 517 550
9. H.C. Kinney, J.J. Filiano, and W.F. White Medullary serotonergic network deficiency in the sudden infant death syndrome: review of a 15-year study of a single dataset J Neuropathol Exp Neurol 60 2001 228 247
10. D.T. Mage, and E.M. Donner The fifty percent male excess of infant respiratory mortality Acta Paediatr 93 2004 1210 1215
11. D.L. Sparks, and J.C. Hunsaker III Sudden infant death syndrome: altered aminergic-cholinergic synaptic markers in hypothalamus J Child Neurol 6 1991 335 339
12. K.B. Sims, C.A. de la, R. Norio, E.M. Sankila, Y.P. Hsu, and W.B. Rinehart Monoamine oxidase deficiency in males with an X chromosome deletion Neuron 2 1989 1069 1076
13. O. Cases, I. Seif, J. Grimsby, P. Gaspar, K. Chen, and S. Pournin Aggressive behavior and altered amounts of brain serotonin and norepinephrine in mice lacking MAOA Science 268 1995 1763 1766
14. A.L. Scott, M. Bortolato, K. Chen, and J.C. Shih Novel monoamine oxidase A knock out mice with human-like spontaneous mutation Neuroreport 19 2008 739 743
15. H.G. Brunner, M. Nelen, X.O. Breakefield, H.H. Ropers, and B.A. van Oost Abnormal behavior associated with a point mutation in the structural gene for monoamine oxidase A Science 262 1993 578 580
16. S.Z. Sabol, S. Hu, and D. Hamer A functional polymorphism in the monoamine oxidase A gene promoter Hum Genet 103 1998 273 279
17. R.M. Denney, H. Koch, and I.W. Craig Association between monoamine oxidase A activity in human male skin fibroblasts and genotype of the MAOA promoter-associated variable number tandem repeat Hum Genet 105 1999 542 551
18. B. Blanchi, and M.H. Sieweke Mutations of brainstem transcription factors and central respiratory disorders Trends Mol Med 11 2005 23 30
19. E. Audero, E. Coppi, B. Mlinar, T. Rossetti, A. Caprioli, and M.A. Banchaabouchi Sporadic autonomic dysregulation and death associated with excessive serotonin autoinhibition Science 321 2008 130 133
20. L.M. Pavone, A. Spina, S. Rea, D. Santoro, V. Mastellone, and P. Lombardi Serotonin transporter gene deficiency is associated with sudden death of newborn mice through activation of TGF-beta1 signaling J Mol Cell Cardiol 47 2009 691 697
21. F. Nonnis-Marzano, M. Maldini, L. Filonzi, A.M. Lavezzi, S. Parmigiani, and C. Magnani Genes regulating the serotonin metabolic pathway in the brain stem and their role in the etiopathogenesis of the sudden infant death syndrome Genomics 91 2008 485 491
22. L. Filonzi, C. Magnani, A.M. Lavezzi, G. Rindi, S. Parmigiani, and G. Bevilacqua Association of dopamine transporter and monoamine oxidase molecular polymorphisms with sudden infant death syndrome and stillbirth: new insights into the serotonin hypothesis Neurogenetics 10 2009 65 72
23. M. Klintschar, and C. Heimbold Questionable association between a monoamine oxidase A promoter polymorphism and sudden infant death syndrome Neurogenetics 11 2010 367 368
24. L. Filonzi, C. Magnani, and F. Nonnis-Marzano Confirmed association between monoamine oxidase A molecular polymorphisms and Sudden Infant Death Syndrome Neurogenetics 12 2011 91 92
25. M. Klintschar, and C. Heimbold Association between a functional polymorphism in the MAOA gene and sudden infant death syndrome Pediatrics 129 2012 e756 e761
26. D.A. Roff, and P. Bentzen The statistical analysis of mitochondrial DNA polymorphisms: chi 2 and the problem of small samples Mol Biol Evol 6 1989 539 545
27. C.E. Hunt Gene-environment interactions: implications for sudden unexpected deaths in infancy Archives of Disease in Childhood 90 2005 48 53
28. D.E. Weese-Mayer, E.M. Berry-Kravis, B.S. Maher, J.M. Silvestri, M.E. Curran, and M.L. Marazita Sudden infant death syndrome: association with a promoter polymorphism of the serotonin transporter gene Am J Med Genet A 117A 2003 268 274
29. S.H. Opdal, A. Vege, and T.O. Rognum Serotonin transporter gene variation in sudden infant death syndrome Acta Paediatr 97 2008 861 865
30. A. Panigrahy, J. Filiano, L.A. Sleeper, F. Mandell, M. Valdes-Dapena, and H.F. Krous Decreased serotonergic receptor binding in rhombic lip-derived regions of the medulla oblongata in the sudden infant death syndrome J Neuropathol Exp Neurol 59 2000 377 384
31. H.C. Kinney, L.L. Randall, L.A. Sleeper, M. Willinger, R.A. Belliveau, and N. Zec Serotonergic brainstem abnormalities in Northern Plains Indians with the sudden infant death syndrome J Neuropathol Exp Neurol 62 2003 1178 1191
32. J.R. Duncan, D.S. Paterson, J.M. Hoffman, D.J. Mokler, N.S. Borenstein, and R.A. Belliveau Brainstem serotonergic deficiency in sudden infant death syndrome JAMA 303 2010 430 437
33. J. Deckert, M. Catalano, Y.V. Syagailo, M. Bosi, O. Okladnova, and B.D. Di Excess of high activity monoamine oxidase A gene promoter alleles in female patients with panic disorder Hum Mol Genet 8 1999 621 624
34. J. Samochowiec, K.P. Lesch, M. Rottmann, M. Smolka, Y.V. Syagailo, and O. Okladnova Association of a regulatory polymorphism in the promoter region of the monoamine oxidase A gene with antisocial alcoholism Psychiatry Res 86 1999 67 72
35. G. Koller, B. Bondy, U.W. Preuss, M. Bottlender, and M. Soyka No association between a polymorphism in the promoter region of the MAOA gene with antisocial personality traits in alcoholics Alcohol Alcohol 38 2003 31 34
36. L.C. Lim, J. Powell, P. Sham, D. Castle, N. Hunt, and R. Murray Evidence for a genetic association between alleles of monoamine oxidase A gene and bipolar affective disorder Am J Med Genet 60 1995 325 331
37. N. Craddock, J. Daniels, E. Roberts, M. Rees, P. McGuffin, and M.J. Owen No evidence for allelic association between bipolar disorder and monoamine oxidase A gene polymorphisms Am J Med Genet 60 1995 322 324
38. A. Desautels, G. Turecki, J. Montplaisir, K. Brisebois, A. Sequeira, and B. Adam Evidence for a genetic association between monoamine oxidase A and restless legs syndrome Neurology 59 2002 215 219
39. B.H. Brummett, A.D. Krystal, I.C. Siegler, C. Kuhn, R.S. Surwit, and S. Zuchner Associations of a regulatory polymorphism of monoamine oxidase-A gene promoter (MAOA-uVNTR) with symptoms of depression and sleep quality Psychosom Med 69 2007 396 401
40. S.B. Manuck, J.D. Flory, R.E. Ferrell, J.J. Mann, and M.F. Muldoon A regulatory polymorphism of the monoamine oxidase-A gene may be associated with variability in aggression, impulsivity, and central nervous system serotonergic responsivity Psychiatry Res 95 2000 9 23
41. E.G. Jonsson, N. Norton, K. Forslund, M. Mattila-Evenden, G. Rylander, and M. Asberg Association between a promoter variant in the monoamine oxidase A gene and schizophrenia Schizophr Res 61 2003 31 37