PMID- 14615042 OWN - NLM STAT- MEDLINE DCOM- 20040120 LR - 20190701 IS - 0304-3940 (Print) IS - 0304-3940 (Linking) VI - 352 IP - 1 DP - 2003 Nov 27 TI - The role of -850 tumor necrosis factor-alpha and apolipoprotein E genetic polymorphism in patients with Down's syndrome-related dementia. PG - 29-32 AB - Down's syndrome (DS) is a disease with a complex etiology. It is likely that other factors besides genes located on chromosome 21 may play a role in clinical features of affected patients. Tumor necrosis factor-alpha (TNF-alpha) (6p21.3) and apolipoprotein E (APOE) (19q13.2) are candidate genes as they interact with the brain deposition of Abeta, one of the neuropathological hallmarks in DS. We examined 136 DS patients and 113 controls for -850 TNF-alpha and APOE polymorphisms. The -850T frequency in DS was significantly higher than in controls (P<0.005, OR 2.05, 95% CI 1.22-3.49) while the APOE E4 allele was negatively selected in patients compared to normal subjects (P<0.005, OR 0.38, 95% CI 0.20-0.71). Our findings suggest that the -850T allele, which is more common among patients at high risk of dementia such as those with DS, might eventually play a role in the development of dementia; no inference on the role of the allele APOE E4 in DS-related dementia may be derived from our results. FAU - Lucarelli, Paola AU - Lucarelli P AD - Institute of Molecular Biology and Pathology, National Research Council, Rome, 00185 Rome, Italy. FAU - Piciullo, Antonella AU - Piciullo A FAU - Verdecchia, Magda AU - Verdecchia M FAU - Palmarino, Mariella AU - Palmarino M FAU - Arpino, Carla AU - Arpino C FAU - Curatolo, Paolo AU - Curatolo P LA - eng PT - Comparative Study PT - Journal Article PL - Ireland TA - Neurosci Lett JT - Neuroscience letters JID - 7600130 RN - 0 (Apolipoproteins E) RN - 0 (Tumor Necrosis Factor-alpha) SB - IM MH - Adolescent MH - Adult MH - Apolipoproteins E/*genetics MH - Chi-Square Distribution MH - Child MH - Child, Preschool MH - Confidence Intervals MH - Dementia/complications/*genetics MH - Down Syndrome/complications/*genetics MH - Female MH - Gene Frequency/genetics MH - Genotype MH - Humans MH - Infant MH - Male MH - Odds Ratio MH - Polymorphism, Genetic/*genetics MH - Tumor Necrosis Factor-alpha/*genetics EDAT- 2003/11/15 05:00 MHDA- 2004/01/21 05:00 CRDT- 2003/11/15 05:00 PHST- 2003/11/15 05:00 [pubmed] PHST- 2004/01/21 05:00 [medline] PHST- 2003/11/15 05:00 [entrez] AID - S0304394003010061 [pii] AID - 10.1016/j.neulet.2003.08.021 [doi] PST - ppublish SO - Neurosci Lett. 2003 Nov 27;352(1):29-32. doi: 10.1016/j.neulet.2003.08.021.