Vitamin D and cognitive function: A Mendelian randomisation study
Pedersen NL; Kuzma E; Singh-Manoux A; Brenner H; Karhunen V; Cavadino A; Hutri-Kahonen N; Zhan YQ; Kilander L; Power C; Kjaergaard M; Raitakari OT; Lehtimaki T; Sen A; Herzig KH; Byberg L; Hypponen E; Zhou A; Lind L; Kivimaki M; Schmidt H; Eriksson JG; Jarvelin MR; Maddock J; Hagg S; Ingelsson E; Perna L; Guessous I; Melhus H; Michaelsson K; Schottker B; Engmann J; Schirmer H; Jorde R; Vollenweider P; Marques-Vidal P; Kumari M; Lahti J; Smart MC; Petrovic KE; Kahonen M; Saum KU; Rovio SP; Auvinen J; Llewellyn DJ; Raikkonen K; Bao YC; Schmidt R; Veijola J
Vitamin D and cognitive function: A Mendelian randomisation study
Pedersen NL
Kuzma E
Singh-Manoux A
Brenner H
Karhunen V
Cavadino A
Hutri-Kahonen N
Zhan YQ
Kilander L
Power C
Kjaergaard M
Raitakari OT
Lehtimaki T
Sen A
Herzig KH
Byberg L
Hypponen E
Zhou A
Lind L
Kivimaki M
Schmidt H
Eriksson JG
Jarvelin MR
Maddock J
Hagg S
Ingelsson E
Perna L
Guessous I
Melhus H
Michaelsson K
Schottker B
Engmann J
Schirmer H
Jorde R
Vollenweider P
Marques-Vidal P
Kumari M
Lahti J
Smart MC
Petrovic KE
Kahonen M
Saum KU
Rovio SP
Auvinen J
Llewellyn DJ
Raikkonen K
Bao YC
Schmidt R
Veijola J
NATURE PUBLISHING GROUP
Julkaisun pysyvä osoite on:
https://urn.fi/URN:NBN:fi-fe2021042717479
https://urn.fi/URN:NBN:fi-fe2021042717479
Tiivistelmä
The causal nature of the association between hypovitaminosis D and poor cognitive function in mid-to later-life is uncertain. Using a Mendelian randomisation(MR) approach, we examined the causal relationship between 25(OH)D and cognitive function. Data came from 172,349 participants from 17 cohorts. DHCR7(rs12785878), CYP2R1 rs12794714) and their combined synthesis score were chosen to proxy 25(OH)D. Cognitive tests were standardised into global and memory scores. Analyses were stratified by 25(OH)D tertiles, sex and age. Random effects meta-analyses assessed associations between 25(OH)D and cognitive function. Associations of serum 25(OH)D with global and memoryrelated cognitive function were non-linear (lower cognitive scores for both low and high 25(OH)D, p(curvature) <= 0.006), with much of the curvature attributed to a single study. DHCR7, CYP2R1, and the synthesis score were associated with small reductions in 25(OH)D per vitamin D-decreasing allele. However, coefficients for associations with global or memory-related cognitive function were nonsignificant and in opposing directions for DHCR7 and CYP2R1, with no overall association observed for the synthesis score. Coefficients for the synthesis score and global and memory cognition were similar when stratified by 25(OH)D tertiles, sex and age. We found no evidence for serum 25(OH)D concentration as a causal factor for cognitive performance in mid-to later life.
Kokoelmat
- Rinnakkaistallenteet [19207]