Evidence map›Paper›PMID 28561418›Full record

ArticleHuman brain mapping2017

Heritability of hippocampal subfield volumes using a twin and non-twin siblings design.

Sejal Patel, Min Tae M Park, Gabriel A Devenyi, Raihaan Patel, Mario Masellis, Jo Knight, M Mallar Chakravarty

Abstract readTwin Study
In one paragraph

Article in Human brain mapping, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

16 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Sejal PatelCampbell Family Mental Health Research Institute, Neurogenetics, Centre for Addiction and Mental Health, Toronto, Ontario, Canada.ORCID 0000-0002-4676-9427
Min Tae M ParkCerebral Imaging Centre, Douglas Mental Health University Institute, McGill University, Verdun, Quebec, Canada.ORCID 0000-0002-4268-7432
Gabriel A DevenyiCerebral Imaging Centre, Douglas Mental Health University Institute, McGill University, Verdun, Quebec, Canada.
Raihaan PatelCerebral Imaging Centre, Douglas Mental Health University Institute, McGill University, Verdun, Quebec, Canada.
Mario MasellisDepartment of Neurology, Sunnybrook Health Sciences Centre, Toronto, Ontario, Canada.
Jo KnightCampbell Family Mental Health Research Institute, Neurogenetics, Centre for Addiction and Mental Health, Toronto, Ontario, Canada.
M Mallar ChakravartyCerebral Imaging Centre, Douglas Mental Health University Institute, McGill University, Verdun, Quebec, Canada.ORCID 0000-0002-0759-5508

Funding

Mapping the Human Connectome: Structure, Function, and HeritabilityU54MH091657 · NIMH · WASHINGTON UNIVERSITY · PI UGURBIL, KAMIL, VAN ESSEN, DAVID C · 2010 to 2014
$34.7M
CIHRNIMH NIH HHS U54 MH091657
6 · The paper itself

Abstract

The hippocampus is composed of distinct subfields linked to diverse functions and disorders. The subfields can be mapped using high-resolution magnetic resonance images, and their volumes can potentially be used as quantitative phenotypes for genetic investigation of hippocampal function. We estimated the heritability of hippocampus subfield volumes of 465 subjects from the Human Connectome Project (twins and non-twin siblings) using two methods. The first used a univariate model to estimate heritability with and without adjustment for total brain volume (TBV) and ipsilateral hippocampal volume to determine if heritability was uniquely attributable to subfield volume rather than confounds that attributed to global volumes. We observed the right: subiculum, cornu ammonis 2/3, and cornu ammonis 4/dentate gyrus subfields had the highest significant heritability estimates after adjusting for ipsilateral hippocampal volume. In the second analysis, we used a bivariate model to investigate the shared heritability and genetic correlation of the subfield volumes with TBV and ipsilateral hippocampal volume. Genetic correlation demonstrates shared genetic architecture between phenotypes and shared heritability is what proportion of the genetic architecture of one trait is shared by the other. Highest genetic correlations were between subfield volumes and ipsilateral hippocampal volume than with TBV. The pattern was opposite for shared heritability suggesting that subfields share greater proportion of the genetic architecture with TBV than with ipsilateral hippocampal volume. The relationship between the genetic architecture of TBV, hippocampal volume, and of individual subfields should be accounted for when using hippocampal subfield volumes as quantitative phenotypes for imaging genetics studies. Hum Brain Mapp 38:4337-4352, 2017. © 2017 Wiley Periodicals, Inc.

Indexed as

Quantitative Trait, HeritableSiblingsTwins, DizygoticTwins, MonozygoticAdultConnectomeFemaleFunctional LateralityHippocampusHumansMagnetic Resonance ImagingMaleModels, GeneticModels, NeurologicalOrgan SizeYoung Adultextended twin designgenetic correlationgenetic variationhippocampal subfield segmentationquantitative phenotypesunivariate and bivariate model

Identifiers

PMID28561418
PMCPMC6866954

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.