P-selectin 1087G/A polymorphism is associated with neuropsychological test performance in older adults with cardiovascular disease.

John Gunstad, Andreana Benitez, Karin F Hoth, Mary Beth Spitznagel, Jeanne McCaffery, John McGeary, Lynn S Kakos, Athena Poppas, Robert H Paul, Angela L Jefferson, Lawrence H Sweet, Ronald A Cohen
Author Information
  1. John Gunstad: Department of Psychology, Kent State University, Kent, OH 44242, USA. jgunstad@kent.edu

Abstract

BACKGROUND AND PURPOSE: There is growing evidence that the cell adhesion molecule P-selectin (SELP) contributes to the adverse vascular processes that promote cognitive impairment in individuals with cardiovascular disease. Previous research has shown that SELP genotypes moderate circulating levels of P-selectin and that patients undergoing coronary artery bypass graft with the SELP 1087A allele were less likely to show postoperative cognitive decline and more likely to exhibit lower levels of C-reactive protein than noncarriers. Thus, we expected that carriers of the 1087A allele (n=43) would exhibit better cognitive functioning than persons with 2 1087G alleles (n=77) and that C-reactive protein levels would be important for this relationship.
METHODS: One hundred twenty older adults with diagnosed cardiovascular disease were recruited from outpatient cardiology clinics. Each participant underwent a comprehensive neuropsychological test battery and a blood draw.
RESULTS: Participants with the SELP 1087A allele performed more poorly on tests of attention (Trail Making Test A: t[116]=3.20, P=0.002), executive function (Trail Making Test B: t[116]=2.89, P=0.005), psychomotor speed (Digit-Symbol Coding: t[117]=2.54, P=0.012), and memory (California Verbal Learning Test Discrimination: t[116]=2.05, P=0.04). There were no significant differences between the SELP genotype groups on demographic/medical variables or C-reactive protein levels.
CONCLUSIONS: Contrary to expectations, the present analyses showed that older patients with cardiovascular disease with the SELP 1087A allele performed more poorly on neuropsychological testing. Findings from the present study were counter to previous research with coronary artery bypass graft candidates. Further work using neuroimaging and alternative measures of cardiovascular function is needed to clarify the mechanisms of this association.

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Grants

  1. R03 AG027480-02/NIA NIH HHS
  2. P30 AG013846-08/NIA NIH HHS
  3. K23 AG030962-01/NIA NIH HHS
  4. F32 AG022773-02/NIA NIH HHS
  5. P30 AG013846/NIA NIH HHS
  6. F32 AG022773-01/NIA NIH HHS
  7. K23 AG030962-02/NIA NIH HHS
  8. R01 HL089311-02/NHLBI NIH HHS
  9. R01 DK075119-01/NIDDK NIH HHS
  10. R03 AG027480-01A1/NIA NIH HHS
  11. R01 HL089311/NHLBI NIH HHS
  12. R01 NS052470-02/NINDS NIH HHS
  13. R03 AG027480/NIA NIH HHS
  14. R01 NS052470/NINDS NIH HHS
  15. K23 AG030962-03/NIA NIH HHS
  16. K23 AG030962/NIA NIH HHS
  17. F32 AG022773/NIA NIH HHS
  18. R01 DK075119/NIDDK NIH HHS

MeSH Term

Adult
Aged
Aged, 80 and over
Alleles
C-Reactive Protein
Cardiovascular Diseases
Coronary Artery Bypass
Female
Humans
Male
Middle Aged
Neuropsychological Tests
P-Selectin
Polymorphism, Single Nucleotide

Chemicals

P-Selectin
C-Reactive Protein

Word Cloud

Created with Highcharts 10.0.0SELPcardiovasculardiseaselevels1087AalleleP=0P-selectincognitiveC-reactiveproteinolderneuropsychologicalTestresearchpatientscoronaryarterybypassgraftlikelyexhibitadultstestperformedpoorlyTrailMakingfunctiont[116]=2presentBACKGROUNDANDPURPOSE:growingevidencecelladhesionmoleculecontributesadversevascularprocessespromoteimpairmentindividualsPreviousshowngenotypesmoderatecirculatingundergoinglessshowpostoperativedeclinelowernoncarriersThusexpectedcarriersn=43betterfunctioningpersons21087Gallelesn=77importantrelationshipMETHODS:OnehundredtwentydiagnosedrecruitedoutpatientcardiologyclinicsparticipantunderwentcomprehensivebatteryblooddrawRESULTS:ParticipantstestsattentionA:t[116]=320002executiveB:89005psychomotorspeedDigit-SymbolCoding:t[117]=254012memoryCaliforniaVerbalLearningDiscrimination:0504significantdifferencesgenotypegroupsdemographic/medicalvariablesCONCLUSIONS:ContraryexpectationsanalysesshowedtestingFindingsstudycounterpreviouscandidatesworkusingneuroimagingalternativemeasuresneededclarifymechanismsassociation1087G/Apolymorphismassociatedperformance

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