Cross-lagged Relationships Between Depressive Symptoms and Altered Default Mode Network Connectivity Over the Course of Adolescence

被引:3
|
作者
Afzali, Mohammad H. [1 ]
Dagher, Alain [4 ]
Bourque, Josiane [6 ]
Spinney, Sean [1 ,2 ,3 ]
Conrod, Patricia [1 ,5 ]
机构
[1] Univ Montreal, Dept Psychiat, Montreal, PQ, Canada
[2] Univ Montreal, Dept Comp Sci & Operat Res, Montreal, PQ, Canada
[3] Mila Quebec AI Inst, Quebec City, PQ, Canada
[4] McGill Univ, Montreal Neurol Inst, Montreal, PQ, Canada
[5] Ctr Hosp Univ St Justine, Res Ctr, Montreal, PQ, Canada
[6] Univ Penn, Dept Psychiat, Philadelphia, PA 19104 USA
基金
加拿大健康研究院;
关键词
STATE FUNCTIONAL CONNECTIVITY; CINGULATE CORTEX; MAJOR DEPRESSION; 1ST-EPISODE; RUMINATION; PRECUNEUS; DISORDER; AMYGDALA; ONSET; RISK;
D O I
10.1016/j.bpsc.2021.10.018
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
BACKGROUND: Although the peak onset of depressive symptoms occurs during adolescence, very few studies have directly examined depression-related changes in resting-state (RS) default mode network activity during adolescence, controlling for potential neural markers of risk. METHODS: This study used data from a longitudinal adolescent cohort to investigate age-specific, persistent (i.e., lagged), and dynamic associations between RS functional connectivity within the default mode network and depressive symptoms during adolescence using a random intercept cross-lagged panel framework. The Neuroventure sample consisted of 151 adolescents ages 12-14 at study entry without any neurological illness who were assessed three times during a 5-year follow-up with 97% follow-up across the three assessments. Depressive symptoms were measured using the depression subscale of the Brief Symptoms Inventory. RS functional magnetic resonance imaging data were collected using a 3T Siemens Magnetom Trio scanner in a single 6-minute sequence. RESULTS: After controlling for relationships between random intercepts, future depression risk was predicted by RS couplings in the perigenual anterior cingulate cortex and anterior dorsomedial prefrontal cortex (beta = -0.69, p =.014) and in the left inferior parietal lobule and anterior superior frontal gyrus (beta = -0.43, p =.035). Increases in depressive symptoms at previous time points significantly predicted changes in functional connectivity between the posterior cingulate cortex and the precuneus and posterior middle temporal gyrus (beta = 0.37, p =.039) and between the dorsal precuneus and posterior middle temporal gyrus (beta = 0.47, p =.036). CONCLUSIONS: This study was able to disassociate the RS brain markers of depression from those that appear to follow early-onset depression.
引用
收藏
页码:774 / 781
页数:8
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