Variegation of autism related traits across seven neurogenetic disorders.
Variegation of autism related traits across seven neurogenetic disorders.
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DOI:
10.1038/s41398-022-01895-0
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发表时间:
2022-04-07
影响因子:
6.8
通讯作者:
Raznahan A
中科院分区:
文献类型:
--
作者:
Lee NR;Niu X;Zhang F;Clasen LS;Kozel BA;Smith ACM;Wallace GL;Raznahan A
Gene dosage disorders (GDDs) constitute a major class of genetic risks for psychopathology, but there is considerable debate regarding the extent to which different GDDs induce different psychopathology profiles. The current research speaks to this debate by compiling and analyzing dimensional measures of several autism-related traits (ARTs) across seven diverse GDDs. The sample included 350 individuals with one of 7 GDDs, as well as reference idiopathic autism spectrum disorder (ASD; n = 74) and typically developing control (TD; n = 171) groups. The GDDs were: Down, Williams–Beuren, and Smith–Magenis (DS, WS, SMS) syndromes, and varying sex chromosome aneuploidies (“plusX”, “plusXX”, “plusY”, “plusXY”). The Social Responsiveness Scale (SRS-2) was used to measure ARTs at different levels of granularity—item, subscale, and total. General linear models were used to examine ART profiles in GDDs, and machine learning was used to predict genotype from SRS-2 subscales and items. These analyses were completed with and without covariation for cognitive impairment. Twelve of all possible 21 pairwise GDD group contrasts showed significantly different ART profiles (7/21 when co-varying for IQ, all Bonferroni-corrected). Prominent GDD–ART associations in post hoc analyses included relatively preserved social motivation in WS and relatively low levels of repetitive behaviors in plusX. Machine learning revealed that GDD group could be predicted with plausible accuracy (~60–80%) even after controlling for IQ. GDD effects on ARTs are influenced by GDD subtype and ART dimension. This observation has consequences for mechanistic, clinical, and translational aspects of psychiatric neurogenetics.
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DOI:
10.1093/brain/awab096
发表时间:
2021-08-17
期刊:
Brain : a journal of neurology
影响因子:
--
作者:
Moreau CA;Raznahan A;Bellec P;Chakravarty M;Thompson PM;Jacquemont S
通讯作者:
Jacquemont S
DOI:
10.1176/appi.ajp.2020.20010015
发表时间:
2021-01-01
期刊:
The American journal of psychiatry
影响因子:
--
作者:
Chawner SJRA;Doherty JL;Anney RJL;Antshel KM;Bearden CE;Bernier R;Chung WK;Clements CC;Curran SR;Cuturilo G;Fiksinski AM;Gallagher L;Goin-Kochel RP;Gur RE;Hanson E;Jacquemont S;Kates WR;Kushan L;Maillard AM;McDonald-McGinn DM;Mihaljevic M;Miller JS;Moss H;Pejovic-Milovancevic M;Schultz RT;Green-Snyder L;Vorstman JA;Wenger TL;IMAGINE-ID Consortium;Hall J;Owen MJ;van den Bree MBM
通讯作者:
van den Bree MBM
影响因子:
3.9
作者:
Boyd, Brian A.;McDonough, Stephen G.;Bodfish, James W.
通讯作者:
Bodfish, James W.
DOI:
10.1002/ajmg.c.31330
发表时间:
2012-05-15
影响因子:
3.1
作者:
Kou, Yan;Betancur, Catalina;Xu, Huilei;Buxbaum, Joseph D.;Ma'ayan, Avi
通讯作者:
Ma'ayan, Avi
DOI:
10.1111/j.1469-7610.2012.02573.x
发表时间:
2012-10
期刊:
Journal of child psychology and psychiatry, and allied disciplines
影响因子:
--
作者:
Lee NR;Wallace GL;Adeyemi EI;Lopez KC;Blumenthal JD;Clasen LS;Giedd JN
通讯作者:
Giedd JN