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Sökning: (WFRF:(Nordin Adolfsson Annelie)) > (2020-2023) > Effects of polygeni...

Effects of polygenic risk for Alzheimer's disease on rate of cognitive decline in normal aging

Kauppi, Karolina (författare)
Karolinska Institutet,Umeå universitet,Institutionen för integrativ medicinsk biologi (IMB),Department of Medical Epidemiology and Biostatistics, Karolinska Institutet,Stockholm, Sweden
Rönnlund, Michael, 1967- (författare)
Umeå universitet,Institutionen för psykologi
Nordin Adolfsson, Annelie (författare)
Umeå universitet,Psykiatri
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Pudas, Sara, Fil. Dr. 1983- (författare)
Umeå universitet,Institutionen för integrativ medicinsk biologi (IMB)
Adolfsson, Rolf (författare)
Umeå universitet,Psykiatri
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 (creator_code:org_t)
2020-07-24
2020
Engelska.
Ingår i: Translational Psychiatry. - : Nature Publishing Group. - 2158-3188. ; 10:1
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
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  • Most people's cognitive abilities decline with age, with significant and partly genetically driven, individual differences in rate of change. Although APOE 4 and genetic scores for late-onset Alzheimer's disease (LOAD) have been related to cognitive decline during preclinical stages of dementia, there is limited knowledge concerning genetic factors implied in normal cognitive aging. In the present study, we examined three potential genetic predictors of age-related cognitive decline as follows: (1) the APOE 4 allele, (2) a polygenic score for general cognitive ability (PGS-cog), and (3) a polygenic risk score for late-onset AD (PRS-LOAD). We examined up to six time points of cognitive measurements in the longitudinal population-based Betula study, covering a 25-year follow-up period. Only participants that remained alive and non-demented until the most recent dementia screening (1-3 years after the last test occasion) were included (n=1087). Individual differences in rate of cognitive change (composite score) were predicted by the PRS-LOAD and APOE 4, but not by PGS-cog. To control for the possibility that the results reflected a preclinical state of Alzheimer's disease in some participants, we re-ran the analyses excluding cognitive data from the last test occasion to model cognitive change up-until a minimum of 6 years before potential onset of clinical Alzheimers. Strikingly, the association of PRS-LOAD, but not APOE 4, with cognitive change remained. The results indicate that PRS-LOAD predicts individual difference in rate of cognitive decline in normal aging, but it remains to be determined to what extent this reflects preclinical Alzheimer's disease brain pathophysiology and subsequent risk to develop the disease.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Psykiatri (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Psychiatry (hsv//eng)
MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Neurovetenskaper (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Neurosciences (hsv//eng)

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