TY - JOUR
T1 - Genetics of co-developing conduct and emotional problems during childhood and adolescence
AU - Hannigan, Laurie J.
AU - Pingault, Jean-Baptiste
AU - Krapohl, Eva
AU - McAdams, Tom A.
AU - Rijsdijk, Fruhling V.
AU - Eley, Thalia C.
PY - 2018/7/2
Y1 - 2018/7/2
N2 - Common genetic influences offer a partial explanation for comorbidity between different psychiatric disorders1–3. However, the genetics underlying co-development – the cross-domain co-occurrence of patterns of change over time – of psychiatric symptoms during childhood and adolescence has not been well explored. Here, we show genetic influence on joint symptom trajectories of parent-reported conduct and emotional problems (overall N = 15,082) across development (4-16 years) using both twin- and genome-wide polygenic score analyses (genotyped N = 2,610). Specifically, we found 7 joint symptom trajectories, including two characterised, respectively, by jointly stable and jointly increasing symptoms of conduct and emotional problems (7.3% of the sample, collectively). Twin modelling analyses revealed substantial genetic influence on trajectories (h2 estimates range: .41-.78). Furthermore, individuals’ risk of being classified in the most symptomatic trajectory classes was significantly predicted by polygenic scores for years-of-education-associated alleles and depressive symptoms-associated alleles. Complementary analyses of child self-reported symptoms across late childhood and early adolescence yielded broadly similar results. Taken together, our results indicate that genetic factors are involved in the co-development of conduct and emotional problems across childhood and adolescence, and that individuals with co-developing symptoms across multiple domains may represent a clinical sub-group characterised by increased levels of genetic risk.
AB - Common genetic influences offer a partial explanation for comorbidity between different psychiatric disorders1–3. However, the genetics underlying co-development – the cross-domain co-occurrence of patterns of change over time – of psychiatric symptoms during childhood and adolescence has not been well explored. Here, we show genetic influence on joint symptom trajectories of parent-reported conduct and emotional problems (overall N = 15,082) across development (4-16 years) using both twin- and genome-wide polygenic score analyses (genotyped N = 2,610). Specifically, we found 7 joint symptom trajectories, including two characterised, respectively, by jointly stable and jointly increasing symptoms of conduct and emotional problems (7.3% of the sample, collectively). Twin modelling analyses revealed substantial genetic influence on trajectories (h2 estimates range: .41-.78). Furthermore, individuals’ risk of being classified in the most symptomatic trajectory classes was significantly predicted by polygenic scores for years-of-education-associated alleles and depressive symptoms-associated alleles. Complementary analyses of child self-reported symptoms across late childhood and early adolescence yielded broadly similar results. Taken together, our results indicate that genetic factors are involved in the co-development of conduct and emotional problems across childhood and adolescence, and that individuals with co-developing symptoms across multiple domains may represent a clinical sub-group characterised by increased levels of genetic risk.
KW - Comorbidity
KW - Behaviour genetics
KW - Conduct problems
KW - Emotional and behaviour problems
KW - Child Development
U2 - 10.1038/s41562-018-0373-9
DO - 10.1038/s41562-018-0373-9
M3 - Letter
JO - Nature Human Behaviour
JF - Nature Human Behaviour
ER -