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Sökning: id:"swepub:oai:DiVA.org:su-176732" > Toward Robust Funct...

Toward Robust Functional Neuroimaging Genetics of Cognition

Uddén, Julia (författare)
Stockholms universitet,Institutionen för lingvistik,Biologisk psykologi,Max Planck Institute for Psycholinguistics, the Netherlands; Radboud University, the Netherlands
Hultén, Annika (författare)
Bendtz, Katarina (författare)
Stockholms universitet,Biologisk psykologi
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Mineroff, Zachary (författare)
Kucera, Katerina S. (författare)
Vino, Arianna (författare)
Fedorenko, Evelina (författare)
Hagoort, Peter (författare)
Fisher, Simon E. (författare)
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 (creator_code:org_t)
2019
2019
Engelska.
Ingår i: Journal of Neuroscience. - 0270-6474 .- 1529-2401. ; 39:44, s. 8778-8787
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
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  • A commonly held assumption in cognitive neuroscience is that, because measures of human brain function are closer to underlying biology than distal indices of behavior/cognition, they hold more promise for uncovering genetic pathways. Supporting this view is an influential fMRI-based study of sentence reading/listening by Pinel et al. (2012), who reported that common DNA variants in specific candidate genes were associated with altered neural activation in language-related regions of healthy individuals that carried them. In particular, different single-nucleotide polymorphisms (SNPs) of FOXP2 correlated with variation in task-based activation in left inferior frontal and precentral gyri, whereas a SNP at the KIAA0319/TTRAP/THEM2 locus was associated with variable functional asymmetry of the superior temporal sulcus. Here, we directly test each claim using a closely matched neuroimaging genetics approach in independent cohorts comprising 427 participants, four times larger than the original study of 94 participants. Despite demonstrating power to detect associations with substantially smaller effect sizes than those of the original report, we do not replicate any of the reported associations. Moreover, formal Bayesian analyses reveal substantial to strong evidence in support of the null hypothesis (no effect). We highlight key aspects of the original investigation, common to functional neuroimaging genetics studies, which could have yielded elevated false-positive rates. Genetic accounts of individual differences in cognitive functional neuroimaging are likely to be as complex as behavioral/ cognitive tests, involving many common genetic variants, each of tiny effect. Reliable identification of true biological signals requires large sample sizes, power calculations, and validation in independent cohorts with equivalent paradigms.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Neurovetenskaper (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Neurosciences (hsv//eng)
MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Medicinsk genetik (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Medical Genetics (hsv//eng)

Nyckelord

fMRI
FOXP2
individual differences
KIAA0319/TTRAP/THEM2
language
neuroimaging genetics
psykologi
Psychology

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