Association of dopamine transporter and monoamine oxidase molecular polymorphisms with sudden infant death syndrome and stillbirth: New insights into the serotonin hypothesis

Neurogenetics

Volumn 10, Issue 1, 2009, Pages 65-72

  Filonzi, Laura ^a   Magnani, Cinzia ^a   Lavezzi, Anna Maria ^b   Rindi, Guido ^a   Parmigiani, Stefano ^a   Bevilacqua, Giulio ^a   Matturri, Luigi ^b   Nonnis Marzano, Francesco ^a  

^a UNIVERSITY OF PARMA   (Italy)

^b UNIVERSITY OF MILAN   (Italy)

Author keywords

5 HTT; DAT; MAOA; Neurotransmission; SIDS

Indexed keywords

AMINE OXIDASE (FLAVIN CONTAINING) ISOENZYME A; DOPAMINE TRANSPORTER; SEROTONIN TRANSPORTER;

ARTICLE; CLINICAL ARTICLE; CONTROLLED STUDY; DISEASE ASSOCIATION; DNA POLYMORPHISM; FEMALE; GENE EXPRESSION; GENE FREQUENCY; GENETIC ASSOCIATION; GENOTYPE; HAPLOTYPE; HUMAN; INFANT; MALE; NEUROTRANSMISSION; NEWBORN; PATHOGENESIS; PRIORITY JOURNAL; STILLBIRTH; SUDDEN INFANT DEATH SYNDROME;

DOPAMINE PLASMA MEMBRANE TRANSPORT PROTEINS; FEMALE; GENE FREQUENCY; GENOTYPE; HUMANS; INFANT; INFANT, NEWBORN; MALE; MONOAMINE OXIDASE; POLYMORPHISM, GENETIC; SEROTONIN; STILLBIRTH; SUDDEN INFANT DEATH;

EID: 58649118001     PISSN: 13646745     EISSN: None     Source Type: Journal    
DOI: 10.1007/s10048-008-0149-x     Document Type: Article

References (33)

1. Task Force on Sudden Infant Death Syndrome 2004 The changing concept of sudden infant death syndrome: diagnostic coding shifts, controversies regarding the sleeping environment, and new variables to consider in reducing risk Pediatrics 116 1245 1255
2. CE Hunt FR Hauck 2006 Sudden infant death syndrome Can Med Assoc J 174 1861 1869
3. F Nonnis Marzano M Maldini L Filonzi AM Lavezzi S Parmigiani C Magnani 2008 Genes regulating the serotonin metabolic pathway in the brain stem and their role in the etiopathogenesis of the sudden infant death syndrome Genomics 91 485 491
4. CA Wilson MS Chu 2005 Thermal insulation and SIDS-an investigation of selected Eastern and Western infant bedding combinations Early Hum Dev 81 695 709
5. DS Paterson FL Trachtenberg EG Thompson RA Belliveau AH Beggs R Darnall 2006 Multiple serotoninergic brainstem abnormalities in sudden infant death syndrome JAMA 296 2124 2132
6. T Sawaguchi M Namiki 2003 Recent trend of the incidence of sudden infant death syndrome in Japan Early Hum Dev 75 175 179
7. World Health Organization (WHO) (2006) Neonatal and perinatal mortality: country, regional and global estimates, pp 1-75
8. L Matturri G Ottaviani AM Lavezzi 2005 Techniques and criteria in pathologic and forensic medical diagnostics in sudden unexpected infant and perinatal death Am J Clin Pathol 124 259 268
9. AM Lavezzi G Ottaviani M Mauri L Matturri 2004 Hypoplasia of the arcuate nucleus and maternal smoking during pregnancy in sudden unexplained perinatal and infant death Neuropathology 24 284 289
10. N Okado M Narita N Narita 2002 A serotonin malfunction hypothesis by finding clear mutual relationships between several risk factors and symptoms associated with sudden infant death syndrome Med Hypotheses 58 232 236
11. DE Weese-Mayer MJ Ackerman ML Marazita EM Berry-Kravis 2007 Sudden infant death syndrome: review of implicated genetic factors Am J Med Genet 143 771 788
12. N Narita M Narita S Takashima M Nakayama T Nagai N Okado 2001 Serotonin transporter gene variation is a risk factor for sudden infant death syndrome in the Japanese population Pediatrics 107 690 692
13. DE Weese-Mayer L Zhou EM Berry-Kravis BS Maher JM Silvestri ML Marazita 2003 Association of the serotonin transporter gene with the sudden infant death syndrome: a haplotype analysis Am J Med Genet 122A 238 245
14. Z Lin BK Madras 2006 Human genetics and pharmacology of neurotransmitter transporters Handb Exp Pharmacol 175 327 371
15. DJ Vanderbergh AM Persico AL Hawkins CA Griffin X Li EW Jabs 1992 Human dopamine transporter gene (DAT1) maps to chromosome 5p 15.3 and displays a VNTR Genomics 14 1104 1106
16. J Gelernter H Kranzler JF Cubells H Ichinose T Nagatsu 1998 DRD allele frequencies and linkage disequilibria, including the -141CIns/Del promoter polymorphism, in European-American, African-American, and Japanese subjects Genomics 51 21 26
17. J Mill P Asherson C Browes U D'Souza I Craig 2002 Expression of the dopamine transporter gene is regulated by the 3-UTR VNTR: evidence from brain and lymphocytes using quantitative RT-PCR Am J Med Genet 114 975 979
18. A Heinz D Goldman DW Jones R Palmour D Hommer JG Gorey KS Lee M Linnoila DR Weinberger 2000 Genotype influences in vivo dopamine transporter availability in human striatum Neuropsychopharmacology 22 133 139
19. CH van Dyck RT Malison LK Jacobsen JP Seibyl JK Staley M Laruelle 2005 Increased dopamine transporter availability associated with the 9-repeat allele of the SLC6A3 gene J Nucl Med 46 745 751
20. SZ Sabol S Hu D Hamer 1998 A functional polymorphism in the monoamine oxidase A gene promoter Hum Genet 103 273 279
21. RM Denney H Koch IW Craig 1999 Association between monoamine oxidase A activity in human male skin fibroblasts and genotype of the MAOA promoter-associated variable number tandem repeat Hum Genet 105 542 551
22. YH Wu DF Fischer DF Swaab 2007 A promoter polymorphism in the monoamine oxidase A gene is associated with the pineal MAOA activity in Alzheimer's disease patients Brain Res 1167 13 19
23. SM Hemmings CJ Kinnear DJ Niehaus JC Moolman-Smook C Lochner JA Knowles 2003 Investigating the role of dopaminergic and serotonergic candidate genes in obsessive-compulsive disorder Eur Neuropsychopharmacol 13 93 98
24. G Gerra L Garofano C Pellegrini S Bosari A Zaimovic G Moi 2005 Allelic association of a dopamine transporter gene polymorphism with antisocial behaviour in heroin-dependent patients Addict Biol 10 275 281
25. SR Shi RJ Cote L Wu C Liu Y Shi D Liu 2002 DNA extraction from archival formalin-fixed, paraffin embedded tissue sections based on the antigen retrieval principle: heating under the influence of pH J Histochem Cytochem 50 1005 1011
26. Moore DD (1999) Manipulation of DNA. In: Ausubel FM, Brent R, Kingston RE, Moore DD, Seidman JG, Smith JA, Struhl K (eds) Current protocols in molecular biology. Wiley, New York, pp 2.2.1-2.2.3
27. IL Cohen X Liu C Schutz BN White EC Jenkins WT Brown 2003 Association of autism severity with monoamine oxidase A functional polymorphism Clin Genet 64 190 197
28. M Das AD Bhowmik S Sinha A Chattopadhyay K Chaudhuri M Singh 2006 MAOA promoter polymorphism and attention deficit hyperactivity disorder (ADHD) in Indian children Am J Med Genet B 141 637 642
29. K Malmberg HL Wargelius P Lichtenstein L Oreland JO Larsson 2008 ADHD and disruptive behaviour scores-associations with MAO-A and 5-HTT genes and with platelet MAO-B activity in adolescents BMC Psychiatry 8 28
30. A Caspi J McClay TE Moffitt J Mill J Martin IW Craig 2002 Role of genotype in the cycle of violence in maltreated children Science 297 851 854
31. SH Opdal A Vege TO Rognum 2008 Serotonin transporter gene variation in sudden infant death syndrome Acta Paediatr 97 861 865
32. AM Persico G Bird FH Gabbay GR Uhl 1996 D2 dopamine receptor gene TaqI A1 and B1 restriction fragment length polymorphisms: enhanced frequencies in psychostimulant-preferring polysubstance abusers Biol Psychiatry 40 776 784
33. J Deckert M Catalano YV Syagailo M Bosi O Okladnova D Di Bella 1999 Excess of high activity monoamine oxidase A gene promoter alleles in female patients with panic disorder Hum Mol Genet 8 621 624