Rumination is an important cognitive vulnerability for adolescent and adult depression. However, little is known about the aetiological origins of rumination, as well as its association with depression. Adolescent rumination (self-report) and depressive symptoms (self- and parent-report) were assessed in 674 pairs of same-gender Chinese adolescent twins (11-17 years of age). Females accounted for 53.7 % of the sample. There were significant correlations between self-reported rumination and self-reported depression (r = 0.41), as well as parent-reported adolescent depression (r = 0.22). Genetic influences were significant and modest on all three measures, ranging from 24 % to 42 %. The three measures were also significantly influenced by shared environment, ranging from 20 % to 28 %, and non-shared environmental factors, ranging from 30 % to 56 %. Moreover, the genetic correlations between rumination and depression were significant (within-rater: r (g) = 0.99; cross-rater: r (g) = 0.59) and largely accounted for the phenotypic correlations (within-rater: 68 %; cross-rater: 77 %), while non-shared environmental correlations were also significant (within-rater: r (e) = 0.26; cross-rater: r (e) = 0.12) and accounted for the remainder of the phenotypic correlations (within-rater: 32 %; cross-rater: 23 %). The shared environmental correlations were non-significant. No significant gender and age differences were found in aetiological models. These findings suggest that rumination may be an endophenotype reflecting genetic risk for depression.
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Kovacs M., 2003, Children's depression inventory: Technical manual update
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Kings Coll London, Inst Psychiat, Social Genet & Dev Psychiat Ctr, London WC2R 2LS, EnglandKings Coll London, Inst Psychiat, Social Genet & Dev Psychiat Ctr, London WC2R 2LS, England
Lau, Jennifer Y. F.
Eley, Thalia C.
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Kings Coll London, Social Genet & Dev Psychiat Res Ctr, Inst Psychiat, MRC, London SE5 8AF, EnglandKings Coll London, Social Genet & Dev Psychiat Res Ctr, Inst Psychiat, MRC, London SE5 8AF, England
Lau, Jennifer Y. F.
Rijsdijk, Fruehling
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Kings Coll London, Social Genet & Dev Psychiat Res Ctr, Inst Psychiat, MRC, London SE5 8AF, EnglandKings Coll London, Social Genet & Dev Psychiat Res Ctr, Inst Psychiat, MRC, London SE5 8AF, England
Rijsdijk, Fruehling
Eley, Thalia C.
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Kings Coll London, Social Genet & Dev Psychiat Res Ctr, Inst Psychiat, MRC, London SE5 8AF, EnglandKings Coll London, Social Genet & Dev Psychiat Res Ctr, Inst Psychiat, MRC, London SE5 8AF, England
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Kings Coll London, Inst Psychiat, Social Genet & Dev Psychiat Ctr, London WC2R 2LS, EnglandKings Coll London, Inst Psychiat, Social Genet & Dev Psychiat Ctr, London WC2R 2LS, England
Lau, Jennifer Y. F.
Eley, Thalia C.
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Kings Coll London, Inst Psychiat, Social Genet & Dev Psychiat Ctr, London WC2R 2LS, EnglandKings Coll London, Inst Psychiat, Social Genet & Dev Psychiat Ctr, London WC2R 2LS, England
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Kings Coll London, Social Genet & Dev Psychiat Res Ctr, Inst Psychiat, MRC, London SE5 8AF, EnglandKings Coll London, Social Genet & Dev Psychiat Res Ctr, Inst Psychiat, MRC, London SE5 8AF, England
Lau, Jennifer Y. F.
Rijsdijk, Fruehling
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Kings Coll London, Social Genet & Dev Psychiat Res Ctr, Inst Psychiat, MRC, London SE5 8AF, EnglandKings Coll London, Social Genet & Dev Psychiat Res Ctr, Inst Psychiat, MRC, London SE5 8AF, England
Rijsdijk, Fruehling
Eley, Thalia C.
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Kings Coll London, Social Genet & Dev Psychiat Res Ctr, Inst Psychiat, MRC, London SE5 8AF, EnglandKings Coll London, Social Genet & Dev Psychiat Res Ctr, Inst Psychiat, MRC, London SE5 8AF, England