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Brain Sci. 2017 Oct 28;7(11):143. doi: 10.3390/brainsci7110143.
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Assessment of a Person-Level Risk Calculator to Predict New-Onset Bipolar Spectrum Disorder in Youth at Familial Risk.评估一种个体水平风险计算器以预测有家族风险的青少年新发双相谱系障碍。
JAMA Psychiatry. 2017 Aug 1;74(8):841-847. doi: 10.1001/jamapsychiatry.2017.1763.
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Psychiatric Disorders and Quality of Life in the Offspring of Parents with Bipolar Disorder.双相情感障碍患者后代的精神疾病与生活质量
J Child Adolesc Psychopharmacol. 2017 Aug;27(6):483-493. doi: 10.1089/cap.2016.0056. Epub 2017 Jun 5.
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Baseline dimensional psychopathology and future mood disorder onset: findings from the Dutch Bipolar Offspring Study.基线维度精神病理学与未来情绪障碍的发病:荷兰双相情感障碍后代研究的结果
Acta Psychiatr Scand. 2017 Aug;136(2):201-209. doi: 10.1111/acps.12739. Epub 2017 May 20.
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A meta-analysis of neurocognition in youth with familial high risk for bipolar disorder.一项针对双相情感障碍家族高危青年神经认知的荟萃分析。
Eur Psychiatry. 2017 Jul;44:17-23. doi: 10.1016/j.eurpsy.2017.02.483. Epub 2017 Mar 3.
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Cognitive Impairment in Euthymic Pediatric Bipolar Disorder: A Systematic Review and Meta-Analysis.轻躁期儿科双相情感障碍的认知障碍:系统评价和荟萃分析。
J Am Acad Child Adolesc Psychiatry. 2017 Apr;56(4):286-296. doi: 10.1016/j.jaac.2017.01.008. Epub 2017 Feb 2.
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Functional Dysconnection of the Inferior Frontal Gyrus in Young People With Bipolar Disorder or at Genetic High Risk.功能连接异常的下额叶在年轻人与双相情感障碍或遗传高风险。
Biol Psychiatry. 2017 Apr 15;81(8):718-727. doi: 10.1016/j.biopsych.2016.08.018. Epub 2016 Aug 18.
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The search for neuroimaging and cognitive endophenotypes: A critical systematic review of studies involving unaffected first-degree relatives of individuals with bipolar disorder.寻找神经影像学和认知内表型:一项涉及双相情感障碍个体未受影响一级亲属的研究的关键性系统评价。
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Inhibited Temperament and Hippocampal Volume in Offspring of Parents with Bipolar Disorder.双相情感障碍患者后代的抑制性气质与海马体体积
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Altered Cortico-Striatal Connectivity in Offspring of Schizophrenia Patients Relative to Offspring of Bipolar Patients and Controls.精神分裂症患者后代相对于双相情感障碍患者后代及对照组的皮质-纹状体连接改变。
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捷克双相情感障碍家族风险儿童和青少年样本中的神经心理功能与气质特征

Neuropsychological Functioning and Temperament Traits in a Czech Sample of Children and Adolescents at Familial Risk of Bipolar Disorder.

作者信息

Goetz Michal, Novak Tomas, Viktorinova Michaela, Ptacek Radek, Mohaplova Marketa, Sebela Antonin

机构信息

Second Faculty of Medicine, Charles University Prague, Praha, Czechia.

Department of Child Psychiatry, Motol University Hospital, Praha, Czechia.

出版信息

Front Psychiatry. 2019 Apr 9;10:198. doi: 10.3389/fpsyt.2019.00198. eCollection 2019.

DOI:10.3389/fpsyt.2019.00198
PMID:31024359
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6466457/
Abstract

Although a positive family history is the strongest predictor for bipolar disorder (BD), most offspring of BD parents (BO) will not develop the disorder. Identification of vulnerability markers for BD is essential for specific individual risk estimation. Impairments in cognitive functioning and the presence of specific temperament traits are considered promising candidates. Sixty-three BO (48% female; 11.8 ± 3.3 years) and 54 control offspring (CO; 44% female; 12.3 ± 3.2 years) comparable in sex ( = 0.4) and age ( = 0.4) were enrolled. Detection of current sub/threshold mood symptoms by the Kiddie Schedule for Affective Disorders and Schizophrenia and General Behavior Inventory was applied to separate BO into ultrahigh-risk (UHR) and high-risk (HR) subgroups. Cognitive functions were tested by the Developmental Neuropsychological Assessment II test battery, d2 Test of Attention, and Amsterdam Neuropsychological Tasks. Temperament was assessed by the Temperament in Middle Childhood and Early Adolescent Temperament Questionnaires. The BO sample consisted of 5 BD, 17 UHR, and 41 HR participants. We did not observe any significant differences between the BO and CO groups or between the UHR, HR, and CO subgroups (Hedges' = 0.21-0.39) in cognitive functioning. The BO differed significantly in some temperament traits from the CO ( = 0.42-0.61), while the UHR subgroup exhibited lower effortful control and attention focusing than both HR and CO participants ( = 0.92-1.19). The cross-sectional design and wide age range of the sample limited our findings. Neuropsychological impairment does not seem to be a trait marker of BD in the premorbid stage. Temperament with low effortful control and low attention focusing might be associated with the development of mood disorders in BO.

摘要

尽管家族病史呈阳性是双相情感障碍(BD)最强的预测指标,但大多数双相情感障碍患者的后代(BO)不会患上这种疾病。识别双相情感障碍的易感性标志物对于特定个体风险评估至关重要。认知功能受损和特定气质特征的存在被认为是有希望的候选因素。招募了63名双相情感障碍患者的后代(48%为女性;11.8±3.3岁)和54名对照后代(CO;44%为女性;12.3±3.2岁),他们在性别(=0.4)和年龄(=0.4)上具有可比性。应用儿童情感障碍和精神分裂症的儿童版量表以及一般行为量表来检测当前的亚阈值/阈值情绪症状,以将双相情感障碍患者的后代分为超高风险(UHR)和高风险(HR)亚组。通过发育神经心理评估II测试电池、注意力的d2测试和阿姆斯特丹神经心理任务来测试认知功能。通过童年中期气质问卷和青少年早期气质问卷来评估气质。双相情感障碍患者的后代样本包括5名双相情感障碍患者、17名超高风险者和41名高风险参与者。我们没有观察到双相情感障碍患者的后代组与对照后代组之间或超高风险、高风险和对照后代亚组之间在认知功能上有任何显著差异(Hedges'=0.21 - 0.39)。双相情感障碍患者的后代在某些气质特征上与对照后代有显著差异(=0.42 - 0.61),而超高风险亚组在努力控制和注意力集中方面比高风险和对照后代参与者更低(=0.92 - 1.19)。样本的横断面设计和较宽的年龄范围限制了我们的研究结果。神经心理损伤似乎不是双相情感障碍病前阶段的特征标志物。努力控制低和注意力集中低的气质可能与双相情感障碍患者的后代情绪障碍的发展有关。