Longitudinal trajectories of mood symptoms and global functioning in youth at high risk for bipolar disorder.
Longitudinal trajectories of mood symptoms and global functioning in youth at high risk for bipolar disorder.
复制标题
DOI:
10.1016/j.jad.2020.08.018
复制
发表时间:
2020-12-01
影响因子:
6.6
通讯作者:
Miklowitz DJ
中科院分区:
文献类型:
--
作者:
Weintraub MJ;Schneck CD;Walshaw PD;Chang KD;Sullivan AE;Singh MK;Miklowitz DJ
Little is known about the longitudinal course of mood symptoms and functioning in youth who are at high risk for bipolar disorder (BD). Identifying distinct course trajectories and predictors of those trajectories may help refine treatment approaches. This study examined the longitudinal course of mood symptoms and functioning ratings in 126 youth at high risk for BD based on family history and early mood symptoms. Participants were enrolled in a randomized trial of family-focused therapy and followed longitudinally (mean 2.0 years, SD = 53.6 weeks). Using latent class growth analyses (LCGA), we observed three mood trajectories. All youth started the study with current, active mood symptoms. Following the index mood episode, there was a “significantly improving course” (n=41, 32.5% of sample), a “moderately symptomatic course” (n=21, 16.7%), and a “predominantly symptomatic course” (n=64, 50.8%) at follow-up. More severe depression, anxiety, and suicidality at the study’s baseline were associated with a poorer course of illness. LCGA also revealed three trajectories of global functioning that closely corresponded to symptom trajectories; however, fewer youth exhibited functional recovery than exhibited symptomatic recovery. Mood trajectories were assessed within the context of a treatment trial. Ratings of mood and functioning were based on retrospective recall. This study suggests considerable heterogeneity in the course trajectories of youth at high risk for BD, with a significant proportion showing long-term remission of symptoms. Treatments that enhance psychosocial functioning may be just as important as those that ameliorate symptoms in the early stages of BD.
登录
查看更多内容
影响因子:
2
作者:
Miklowitz DJ;Schneck CD;Walshaw PD;Garrett AS;Singh MK;Sugar CA;Chang KD
通讯作者:
Chang KD
DOI:
10.1111/j.1751-9004.2007.00054.x
发表时间:
2008-01-01
影响因子:
4.6
作者:
Jung, Tony;Wickrama, K. A. S.
通讯作者:
Wickrama, K. A. S.
影响因子:
6.6
作者:
Gitlin MJ;Miklowitz DJ
通讯作者:
Miklowitz DJ
DOI:
10.1111/j.1469-7610.2010.02210.x
发表时间:
2010-04-01
影响因子:
7.6
作者:
Luby, Joan L.;Navsaria, Neha
通讯作者:
Navsaria, Neha
影响因子:
5.4
作者:
Hafeman D;Axelson D;Demeter C;Findling RL;Fristad MA;Kowatch RA;Youngstrom EA;Horwitz SM;Arnold LE;Frazier TW;Ryan N;Gill MK;Hauser-Harrington JC;Depew J;Rowles BM;Birmaher B
通讯作者:
Birmaher B