Lack of association of the serotonin transporter polymorphism with the sudden infant death syndrome in the San Diego dataset

Pediatric Research

Volumn 68, Issue 5, 2010, Pages 409-413

  Paterson, David S ^a   Rivera, Keith D ^a   Broadbelt, Kevin G ^a   Trachtenberg, Felicia L ^b   Belliveau, Richard A ^a   Holm, Ingrid A ^a   Haas, Elisabeth A ^c   Stanley, Christina ^e   Krous, Henry F ^c,d   Kinney, Hannah C ^a   Markianos, Kyriacos ^a  

^a BOSTON CHILDREN S HOSPITAL   (United States)

^b NEW ENGLAND RESEARCH INSTITUTES   (United States)

^c RADY CHILDREN'S HOSPITAL   (United States)

^d UNIVERSITY OF CALIFORNIA   (United States)

^e San Diego County Medical Examiner's Office   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

GENOMIC DNA; SEROTONIN TRANSPORTER;

AFRICAN AMERICAN; ARTICLE; BRAIN STEM; CAUCASIAN; CONTROLLED STUDY; ETHNICITY; FEMALE; GENE FREQUENCY; GENETIC ASSOCIATION; GENETIC RISK; GENOTYPE; HISPANIC; HUMAN; HUMAN TISSUE; HYPOTHESIS; INFANT; MAJOR CLINICAL STUDY; MALE; PATHOGENESIS; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; PROTEIN POLYMORPHISM; SUDDEN INFANT DEATH SYNDROME;

CALIFORNIA; DATABASES, FACTUAL; FEMALE; GENE FREQUENCY; GENOTYPE; HUMANS; INFANT; MALE; POLYMORPHISM, GENETIC; SEROTONIN; SEROTONIN PLASMA MEMBRANE TRANSPORT PROTEINS; SUDDEN INFANT DEATH;

EID: 77958500046     PISSN: 00313998     EISSN: 15300447     Source Type: Journal    
DOI: 10.1203/PDR.0b013e3181f2edf0     Document Type: Article

References (34)

1. Blakely RD, Defelice LJ, Galli A 2005 Biogenic amine neurotransmitter transporters: just when you thought you knew them. Physiology (Bethesda) 20:225-231
2. Heils A, Mossner R, Lesch KP 1997 The human serotonin transporter gene polymorphism\-basic research and clinical implications. J Neural Transm 104:1005-1014
3. Hranilovic D, Stefulj J, Furac I, Kubat M, Balija M, Jernej B 2003 Serotonin transporter gene promoter (5-HTTLPR) and intron 2 (VNTR) polymorphisms in Croatian suicide victims. Biol Psychiatry 54:884-889
4. Lesch KP, Mossner R 1998 Genetically driven variation in serotonin uptake: is there a link to affective spectrum, neurodevelopmental, and neurodegenerative disorders? Biol Psychiatry 44:179-192
5. Greenberg BD, Tolliver TJ, Huang SJ, Li Q, Bengel D, Murphy DL 1999 Genetic variation in the serotonin transporter promoter region affects serotonin uptake in human blood platelets. Am J Med Genet 88:83-87
6. van Dyck CH, Malison RT, Staley JK, Jacobsen LK, Seibyl JP, Laruelle M, Baldwin RM, Innis RB, Gelernter J 2004 Central serotonin transporter availability measured with [123I]beta-CIT SPECT in relation to serotonin transporter genotype. Am J Psychiatry 161:525-531
7. Kinney HC, Belliveau RA, Trachtenberg FL, Rava LA, Paterson DS 2007 The development of the medullary serotonergic system in early human life. Auton Neurosci 132:81-102
8. Paterson DS, Trachtenberg FL, Thompson EG, Belliveau RA, Beggs AH, Darnall R, Chadwick AE, Krous HF, Kinney HC 2006 Multiple serotonergic brainstem abnormalities in sudden infant death syndrome. JAMA 296:2124-2132
9. Kinney HC, Randall LL, Sleeper LA, Willinger M, Belliveau RA, Zec N, Rava LA, Dominici L, Iyasu S, Randall B, Habbe D, Wilson H, Mandell F, McClain M, Welty TK 2003 Serotonergic brainstem abnormalities in Northern Plains Indians with the sudden infant death syndrome. J Neuropathol Exp Neurol 62:1178-1191
10. Panigrahy A, Filiano J, Sleeper LA, Mandell F, Valdes-Dapena M, Krous HF, Rava LA, Foley E, White WF, Kinney HC 2000 Decreased serotonergic receptor binding in rhombic lip-derived regions of the medulla oblongata in the sudden infant death syndrome. J Neuropathol Exp Neurol 59:377-384
11. Ozawa Y, Okado N 2002 Alteration of serotonergic receptors in the brain stems of human patients with respiratory disorders. Neuropediatrics 33:142-149
12. Ozawa Y, Takashima S 2002 Developmental neurotransmitter pathology in the brainstem of sudden infant death syndrome: a review and sleep position. Forensic Sci Int 130:S53-S59
13. Machaalani R, Say M, Waters KA 2009 Serotoninergic receptor 1A in the sudden infant death syndrome brainstem medulla and associations with clinical risk factors. Acta Neuropathol 117:257-265
14. Narita N, Narita M, Takashima S, Nakayama M, Nagai T, Okado N 2001 Serotonin transporter gene variation is a risk factor for sudden infant death syndrome in the Japanese population. Pediatrics 107:690-692
15. Nonnis Marzano F, Maldini M, Filonzi L, Lavezzi AM, Parmigiani S, Magnani C, Bevilacqua G, Matturri L 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
16. Opdal SH, Vege A, Rognum TO 2008 Serotonin transporter gene variation in sudden infant death syndrome. Acta Paediatr 97:861-865
17. Weese-Mayer DE, Berry-Kravis EM, Maher BS, Silvestri JM, Curran ME, Marazita ML 2003 Sudden infant death syndrome: association with a promoter polymorphism of the serotonin transporter gene. Am J Med Genet 117A:268-274
18. Weese-Mayer DE, Zhou L, Berry-Kravis EM, Maher BS, Silvestri JM, Marazita ML 2003 Association of the serotonin transporter gene with sudden infant death syndrome: a haplotype analysis. Am J Med Genet 122A:238-245
19. Haas C, Braun J, Bär W, Bartsch C 2009 No association of serotonin transporter gene variation with sudden infant death syndrome (SIDS) in Caucasians. Leg Med (Tokyo) 11:S210-S212
20. Willinger M, James LS, Catz C 1991 Defining the sudden infant death syndrome (SIDS): deliberations of an expert panel convened by the National Institute of Child Health and Human Development. Pediatr Pathol 11:677-684
21. Wigginton JE, Cutler DJ, Abecasis GR 2005 A note on exact tests of Hardy-Weinberg equilibrium. Am J Hum Genet 76:887-893
22. Klauck SM, Poustka F, Benner A, Lesch KP, Poustka A 1997 Serotonin transporter (5-HTT) gene variants associated with autism? Hum Mol Genet 6:2233-2238
23. Reneman L, Schilt T, de Win MM, Booij J, Schmand B, van den Brink W, Bakker O 2006 Memory function and serotonin transporter promoter gene polymorphism in ecstasy (MDMA) users. J Psychopharmacol 20:389-399
24. Jacob CP, Strobel A, Hohenberger K, Ringel T, Gutknecht L, Reif A, Brocke B, Lesch KP 2004 Association between allelic variation of serotonin transporter function and neuroticism in anxious cluster C personality disorders. Am J Psychiatry 161:569-572
25. Williams RB, Marchuk DA, Gadde KM, Barefoot JC, Grichnik K, Helms MJ, Kuhn CM, Lewis JG, Schanberg SM, Stafford-Smith M, Suarez EC, Clary GL, Svenson IK, Siegler IC 2003 Serotonin-related gene polymorphisms and central nervous system serotonin function. Neuropsychopharmacology 28:533-541
26. David SP, Murthy NV, Rabiner EA, Munafo MR, Johnstone EC, Jacob R, Walton RT, Grasby PM 2005 A functional genetic variation of the serotonin (5-HT) transporter affects 5-HT1A receptor binding in humans. J Neurosci 25:2586-2590
27. Guhathakurta S, Ghosh S, Sinha S, Chatterjee A, Ahmed S, Chowdhury SR, Gangopadhyay PK, Singh M, Usha R 2006 Serotonin transporter promoter variants: analysis in Indian autistic and control population. Brain Res 1092:28-35
28. Murakami F, Shimomura T, Kotani K, Ikawa S, Nanba E, Adachi K 1999 Anxiety traits associated with a polymorphism in the serotonin transporter gene regulatory region in the Japanese. J Hum Genet 44:15-17
29. Arbelle S, Benjamin J, Golin M, Kremer I, Belmaker RH, Ebstein RP 2003 Relation of shyness in grade school children to the genotype for the long form of the serotonin transporter promoter region polymorphism. Am J Psychiatry 160:671-676
30. Esau L, Kaur M, Adonis L, Arieff Z 2008 The 5-HTTLPR polymorphism in South African healthy populations: a global comparison. J Neural Transm 115:755-760
31. Hu X, Oroszi G, Chun J, Smith TL, Goldman D, Schuckit MA 2005 An expanded evaluation of the relationship of four alleles to the level of response to alcohol and the alcoholism risk. Alcohol Clin Exp Res 29:8-16
32. Wendland JR, Martin BJ, Kruse MR, Lesch KP, Murphy DL 2006 Simultaneous genotyping of four functional loci of human SLC6A4, with a reappraisal of 5-HTTLPR and rs25531. Mol Psychiatry 11:224-226
33. Weese-Mayer DE, Berry-Kravis EM, Zhou L, Maher BS, Curran ME, Silvestri JM, Marazita ML 2004 Sudden infant death syndrome: case-control frequency differences at genes pertinent to early autonomic nervous system embryologic development. Pediatr Res 56:391-395
34. Hunt CE 2004 Genes and sudden infant death syndrome. Pediatr Res 56:321-322