Mitochondrial deoxyribonucleic acid may play a role in a subset of sudden infant death syndrome cases

Acta Paediatrica, International Journal of Paediatrics

Volumn 103, Issue 7, 2014, Pages 775-779

  Laer K ^a   Vennemann, M ^a   Rothamel T ^a   Klintschar, M ^a  

^a HANNOVER MEDICAL SCHOOL   (Germany)

Author keywords

ATP depletion; Haplogroups; Mitochondrial DNA; Sudden infant death syndrome

Indexed keywords

MITOCHONDRIAL DNA;

ARTICLE; CAUCASIAN; CONTROLLED STUDY; DNA POLYMORPHISM; ESSENTIAL GENE; FEMALE; HAPLOTYPE; HUMAN; INFANT; MAJOR CLINICAL STUDY; MALE; OXIDATIVE PHOSPHORYLATION; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; SEQUENCE ANALYSIS; SINGLE NUCLEOTIDE POLYMORPHISM; SNAPSHOT ASSAY; SUDDEN INFANT DEATH SYNDROME;

EID: 84902088448     PISSN: 08035253     EISSN: 16512227     Source Type: Journal    
DOI: 10.1111/apa.12609     Document Type: Article

References (27)

1. Guntheroth WG, Spiers PS,. The triple risk hypotheses in sudden infant death syndrome. Pediatrics 2002; 110: e64.
2. Opdal SH, Opstad A, Vege A, Rognum TO,. IL-10 gene polymorphisms are associated with infectious cause of sudden infant death. Hum Immunol 2003; 64: 1183-9.
3. Wang DW, Desai RR, Crotti L, Arnestad M, Insolia R, Pedrazzini M, et al. Cardiac sodium channel dysfunction in sudden infant death syndrome. Circulation 2007; 115: 368-76.
4. Kinney HC, Richerson GB, Dymecki SM, Darnall RA, Nattie EE,. The brainstem and serotonin in the sudden infant death syndrome. Annu Rev Pathol 2009; 4: 517-50.
5. Weese-Mayer DE, Berry-Kravis EM, Zhou L, Maher BS, Curran ME, Silvestri JM, et al. Sudden infant death syndrome: case-control frequency differences at genes pertinent to early autonomic nervous system embryologic development. Pediatr Res 2004; 56: 391-5.
6. Klintschar M, Reichenpfader B, Saternus KS,. A functional polymorphism in the tyrosine hydroxylase gene indicates a role of noradrenalinergic signaling in sudden infant death syndrome. J Pediatr 2008; 153: 190-3.
7. Läer K, Vennemann M, Rothämel T, Klintschar M,. Association between polymorphisms in the P2RY1 and SSTR2 genes and sudden infant death syndrome. Int J Legal Med 2013; 127: 1087-91.
8. Klintschar M, Heimbold C,. No association of SIDS with two polymorphisms in genes relevant for the noradrenergic system: COMT and DBH. Acta Paediatr 2012; 101: 1079-82.
9. Klintschar M, Heimbold C,. Association between a functional polymorphism in the MAOA gene and sudden infant death syndrome. Pediatrics 2012; 129: e756-61.
10. Opdal SH, Rognum TO, Vege A, Stave AK, Dupuy BM, Egeland T,. Increased number of substitutions in the D-loop of mitochondrial DNA in the sudden infant death syndrome. Acta Paediatr 1998; 87: 1039-44.
11. Kelmanson IA,. An assessment of behavioural characteristics in infants who died of sudden infant death syndrome using the Early Infancy Temperament Questionnaire. Acta Paediatr 1996; 85: 977-80.
12. Oyen N, Skjaerven R, Irgens LM,. Population-based recurrence risk of sudden infant death syndrome compared with other infant and fetal deaths. Am J Epidemiol 1996; 144: 300-5.
13. Beal SM, Blundell HK,. Recurrence incidence of sudden infant death syndrome. Arch Dis Child 1988; 63: 924-30.
14. Vege A, Chen Y, Opdal SH, Saugstad OD, Rognum TO,. Vitreous humor hypoxanthine levels in SIDS and infectious death. Acta Paediatr 1994; 83: 634-9.
15. Deixler E,. Sudden infant death syndrome (SIDS) caused by ATP-depletion following hyperventilation, tissue-hypoxia and hypermetabolism-a hypothesis. Z Geburtshilfe Neonatol 2009; 213: 122-34.
16. Opdal SH, Vege A, Egeland T, Musse MA, Rognum TO,. Possible role of mtDNA mutations in sudden infant death. Pediatr Neurol 2002; 27: 23-9.
17. Opdal SH, Rognum TO, Torgersen H, Vege A,. Mitochondrial DNA point mutations detected in four cases of sudden infant death syndrome. Acta Paediatr 1999; 88: 957-60.
18. Opdal SH, Vege A, Arnestad M, Musse MA, Rognum TO,. Mitochondrial tRNA genes and flanking regions in sudden infant death syndrome. Acta Paediatr 2007; 96: 211-4.
19. Divne AM, Råsten-Almqvist P, Rajs J, Gyllensten U, Allen M,. Analysis of the mitochondrial genome in sudden infant death syndrome. Acta Paediatr 2003; 92: 386-8.
20. Köhnemann S, Sibbing U, Pfeiffer H, Hohoff C,. A rapid mtDNA assay of 22 SNPs in one multiplex reaction increases the power of forensic testing in European Caucasians. Int J Legal Med 2008; 122: 517-23.
21. Krous HF, Beckwith JB, Byard RW, Rognum TO, Bajanowski T, Corey T, et al. Sudden infant death syndrome and unclassified sudden infant deaths: a definitional and diagnostic approach. Pediatrics 2004; 114: 234-8.
22. Köhnemann S, Pfeiffer H,. Application of mtDNA SNP analysis in forensic casework. Forensic Sci Int Genet 2011; 5: 216-21.
23. Ghezzi D, Marelli C, Achilli A, Goldwurm S, Pezzoli G, Barone P,. Mitochondrial DNA haplogroup K is associated with a lower risk of Parkinson's disease in Italians. Eur J Hum Genet 2005; 13: 748-52.
24. Hofmann S, Jaksch M, Bezold R, Mertens S, Aholt S, Paprotta A, et al. Population genetics and disease susceptibility: characterization of central European haplogroups by mtDNA gene mutations, correlation with D loop variants and association with disease. Hum Mol Genet 1997; 6: 1835-46.
25. Ottoni C, Ricaut FX, Vanderheyden N, Brucato N, Waelkens M, Decorte R,. Mitochondrial analysis of a Byzantine population reveals the differential impact of multiple historical events in South Anatolia. Eur J Hum Genet 2011; 19: 571-6.
26. Wallace DC,. Diseases of the mitochondrial DNA. Annu Rev Biochem 1992; 61: 1175-212.
27. Fernández-Moreno MA, Bornstein B, Petit N, Garesse R,. The pathophysiology of mitochondrial biogenesis: towards four decades of mitochondrial DNA research. Mol Genet Metab 2000; 71: 481-95.