Heritability of cerebellar subregion volumes in adolescent and young adult twins

Author:

Strike Lachlan T.123ORCID,Kerestes Rebecca4ORCID,McMahon Katie L.5ORCID,de Zubicaray Greig I.2ORCID,Harding Ian H.46ORCID,Medland Sarah E.127ORCID

Affiliation:

1. Psychiatric Genetics, QIMR Berghofer Medical Research Institute Brisbane Australia

2. School of Psychology and Counselling, Faculty of Health Queensland University of Technology Kelvin Grove Queensland Australia

3. School of Biomedical Sciences, Faculty of Medicine University of Queensland Brisbane Australia

4. Department of Neuroscience, Central Clinical School Monash University Melbourne Australia

5. School of Clinical Sciences, Centre for Biomedical Technologies Queensland University of Technology Brisbane Queensland Australia

6. Cerebellum and Neurodegeneration, QIMR Berghofer Medical Research Institute Brisbane Australia

7. School of Psychology University of Queensland Brisbane Australia

Abstract

AbstractTwin studies have found gross cerebellar volume to be highly heritable. However, whether fine‐grained regional volumes within the cerebellum are similarly heritable is still being determined. Anatomical MRI scans from two independent datasets (QTIM: Queensland Twin IMaging, N = 798, mean age 22.1 years; QTAB: Queensland Twin Adolescent Brain, N = 396, mean age 11.3 years) were combined with an optimised and automated cerebellum parcellation algorithm to segment and measure 28 cerebellar regions. We show that the heritability of regional volumetric measures varies widely across the cerebellum ( 47%–91%). Additionally, the good to excellent test–retest reliability for a subsample of QTIM participants suggests that non‐genetic variance in cerebellar volumes is due primarily to unique environmental influences rather than measurement error. We also show a consistent pattern of strong associations between the volumes of homologous left and right hemisphere regions. Associations were predominantly driven by genetic effects shared between lobules, with only sparse contributions from environmental effects. These findings are consistent with similar studies of the cerebrum and provide a first approximation of the upper bound of heritability detectable by genome‐wide association studies.

Funder

National Health and Medical Research Council

Eunice Kennedy Shriver National Institute of Child Health and Human Development

Publisher

Wiley

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