PMID- 27574384 OWN - NLM STAT- PubMed-not-MEDLINE DCOM- 20160830 LR - 20200930 IS - 1061-1711 (Print) IS - 1615-5939 (Electronic) IS - 1061-1711 (Linking) VI - 25 IP - 3 DP - 2016 Sep TI - Genetic Polymorphisms Influence Cognition in Patients Undergoing Carotid Interventions. PG - 168-73 LID - 10.1055/s-0036-1580696 [doi] AB - While carotid interventions help decrease the risk of stroke, nearly 40% of patients experience cognitive deterioration. Genetic polymorphism in apolipoprotein E (ApoE) and brain-derived neurotrophic factor (BDNF) have been implicated in cognitive impairment; however, it is unclear whether they may influence cognitive changes in patients undergoing carotid intervention. In this study, we seek to assess the role of genetic polymorphisms in carotid intervention-related cognitive change. Polymorphisms related to cognitive function were chosen for this preliminary analysis. Over 2 years, patients undergoing carotid interventions were prospectively recruited. Patients underwent neuropsychological testing 2 weeks prior to and at 1 month following their procedure. Saliva samples were collected for genetic analysis. Logistic regressions were used to identify associations between polymorphisms and cognitive measures. A total of 91 patients were included; all were male with an average age of 70 years. The majority of patients exhibited hypertension (95%) and a history of smoking (81%). Presence of ApoE 4 allele was associated with depression (p= 0.047). After correcting for age and genetic polymorphisms in BDNF and serotonin transporter (5-HTT), ApoE 4 allele was associated with depression (p= 0.044) and showed a trend with baseline cognitive impairment (p= 0.10). Age >/= 70 years was associated with baseline cognitive impairment after adjusting for the three genetic polymorphisms (p= 0.03). Patients with ApoE 4 and BDNF A polymorphisms performed less well on the visual and verbal memory measures, respectively. Polymorphisms in ApoE and BDNF may provide insight on cognition in patients undergoing carotid interventions; however, the mechanism of this relationship remains unclear. FAU - Hitchner, Elizabeth AU - Hitchner E AD - Department of Vascular Surgery, VA Palo Alto Health Care System, Palo Alto, California. FAU - Morrison, Doug AU - Morrison D AD - Department of Vascular Surgery, Stanford University, Stanford, California. FAU - Liao, Phoebe AU - Liao P AD - Department of Psychiatry, Stanford University, Stanford, California. FAU - Rosen, Allyson AU - Rosen A AD - Department of Psychiatry, Stanford University, Stanford, California. FAU - Zhou, Wei AU - Zhou W AD - Department of Vascular Surgery, VA Palo Alto Health Care System, Palo Alto, California; Department of Surgery, Stanford University, Stanford, California. LA - eng GR - R01 NS070308/NS/NINDS NIH HHS/United States PT - Journal Article DEP - 20160408 PL - United States TA - Int J Angiol JT - The International journal of angiology : official publication of the International College of Angiology, Inc JID - 9504821 PMC - PMC5001867 OTO - NOTNLM OT - carotid endarterectomy OT - carotid stenosis OT - carotid stent OT - cognition OT - genetic OT - internal carotid artery OT - polymorphism EDAT- 2016/08/31 06:00 MHDA- 2016/08/31 06:01 PMCR- 2017/09/01 CRDT- 2016/08/31 06:00 PHST- 2016/08/31 06:00 [entrez] PHST- 2016/08/31 06:00 [pubmed] PHST- 2016/08/31 06:01 [medline] PHST- 2017/09/01 00:00 [pmc-release] AID - 150106 [pii] AID - 10.1055/s-0036-1580696 [doi] PST - ppublish SO - Int J Angiol. 2016 Sep;25(3):168-73. doi: 10.1055/s-0036-1580696. Epub 2016 Apr 8.