psychiatric disorder

精神障碍
  • 文章类型: Journal Article
    预测急性精神病医院住院时间的可用证据包括人口统计学,诊断,和治疗变量。这项研究旨在评估急性精神病医院的中性粒细胞与淋巴细胞比率(NLR)与住院时间之间的关系。
    共有116名患者被送往浦和神经精神疗养院的急性精神病病房(Sa玉,日本)从2022年8月到2022年12月有资格参加这项研究。在入院第一天评估淋巴细胞和中性粒细胞的实验室数据,并根据数据计算NLR。参与者被分为两组,高NLR和低NLR,它们被设置为预测变量,以及使用NLR作为连续变量。进行多元线性回归以确定NLR与住院时间之间的关联。调整混杂因素。
    本研究共纳入90名参与者。NLR作为连续变量与住院时间的相关性不显著。当我们将参与者分为高NLR组和低NLR组时,即使通过协变量调整后,这种关联也是显著的(p<0.05).
    分类NLR与急性精神病医院住院时间呈正相关。分类的NLR可以预测急性精神病医院的患者的住院时间。
    UNASSIGNED: The available evidence for predicting length of stay in acute psychiatric hospitals includes demographics, diagnosis, and treatment variables. This study aimed to evaluate the association between neutrophil-to-lymphocyte ratio (NLR) and length of hospital stay in an acute psychiatric hospital.
    UNASSIGNED: A total of 116 patients who were admitted to an acute psychiatric ward at Urawa Neuropsychiatric Sanatorium (Saitama, Japan) from August 2022 to December 2022 were eligible for this study. Laboratory data of lymphocytes and neutrophils were assessed on the first day of admission and NLR was calculated based on the data. Participants were categorized into two groups, high NLR and low NLR, which were set as predictor variables, as well as using NLR as a continuous variable. Multiple linear regression was performed to determine the association between NLR and length of hospital stay, adjusting for confounding factors.
    UNASSIGNED: A total of 90 participants were included in this study. The association of NLR as a continuous variable and length of hospital stay was not significant. When we categorized participants into high- and low-NLR groups, the association was significant even after adjusting by covariates (p < 0.05).
    UNASSIGNED: Categorized NLR was positively associated with the length of hospital stay in patients admitted to an acute psychiatric hospital. Categorized NLR may predict the length of hospital stay for patients who are admitted to an acute psychiatric hospital.
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  • 文章类型: Journal Article
    腺苷酸环化酶(Adcys)催化cAMP的形成,中枢神经系统中细胞存活和神经传递途径所必需的第二信使。Adcy2,十个Adcy亚型之一,在CNS中高度表达。已经在啮齿动物和人类的各种神经障碍中报道了异常的Adcy2表达和突变。然而,由于缺乏遗传工具,Adcy2的功能丧失研究很少。在这次审查中,我们总结了Adcy2在神经系统疾病中的表达和功能的最新发现。具体来说,我们首先介绍生物化学,结构,简要介绍了Adcy2的功能。接下来,Adcy2在神经退行性疾病(阿尔茨海默病和帕金森病)的人类患者和啮齿动物模型中的表达和关联,精神疾病(Tourette综合征,精神分裂症,和双相情感障碍),和其他神经系统疾病(压力相关疾病,中风,癫痫,和Lesch-Nyhan综合征)进行了阐述。此外,我们讨论了当前研究的利弊以及未来需要回答的关键问题。我们希望对Adcy2进行重点审查,以促进该领域的未来研究。
    Adenylyl cyclases (Adcys) catalyze the formation of cAMP, a secondary messenger essential for cell survival and neurotransmission pathways in the CNS. Adcy2, one of ten Adcy isoforms, is highly expressed in the CNS. Abnormal Adcy2 expression and mutations have been reported in various neurological disorders in both rodents and humans. However, due to the lack of genetic tools, loss-of-function studies of Adcy2 are scarce. In this review, we summarize recent findings on Adcy2 expression and function in neurological diseases. Specifically, we first introduce the biochemistry, structure, and function of Adcy2 briefly. Next, the expression and association of Adcy2 in human patients and rodent models of neurodegenerative diseases (Alzheimer\'s disease and Parkinson\'s disease), psychiatric disorders (Tourette syndrome, schizophrenia, and bipolar disorder), and other neurological conditions (stress-associated disorders, stroke, epilepsy, and Lesch-Nyhan Syndrome) are elaborated. Furthermore, we discuss the pros and cons of current studies as well as key questions that need to be answered in the future. We hope to provide a focused review on Adcy2 that promotes future research in the field.
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  • 文章类型: Case Reports
    抗精神病药恶性综合征(NMS)是一种罕见但可能致命的疾病,其特征是热疗,自主神经失调,精神状态改变,肌肉僵硬。它通常起因于抗精神病药物对多巴胺受体的阻断。我们介绍了一名70岁女性在不合规使用氯氮平后发展为NMS的情况。她出现了包括无关紧要的谈话在内的症状,呼吸困难,和全身肌肉无力。在检查中,她昏昏欲睡,格拉斯哥昏迷评分为11分,心动过速,呼吸急促,和所有四肢的高渗性。诊断评估显示尿素和肌酐水平升高,提高肌酸磷酸激酶,代谢性酸中毒,这与NMS一致。医疗管理包括停用氯氮平和开始使用溴隐亭。该报告强调了物理治疗对NMS恢复过程的重要性。物理治疗的目标是改善功能流动性,减轻肌肉僵硬,并避免长期不动的问题。动觉刺激,主动循环呼吸方法,柔和的摇摆运动,神经温暖,负重练习,和行动训练均纳入方案.观察到患者意识程度的显著进步,运动,和氧气依赖两个星期。患者最终在没有额外氧气的情况下管理室内空气,格拉斯哥昏迷量表评分提高,ICU流动性量表评分从1分增加到5分。这个例子强调了及时诊断和全方位NMS护理的必要性,物理治疗起着至关重要的作用。物理治疗可以显著增强整体愈合,改善呼吸功能,并通过量身定制的疗法促进神经肌肉再教育。结果表明,物理治疗必须被视为管理NMS的多学科战略的重要组成部分,目的是提高患者的治疗效果和生活质量。需要更多的研究来优化NMS患者的物理治疗干预措施。
    Neuroleptic malignant syndrome (NMS) is a rare but potentially fatal condition characterized by hyperthermia, autonomic dysregulation, altered mental status, and muscular rigidity. It typically results from the blockade of dopamine receptors by antipsychotic medications. We present the case of a 70-year-old female who developed NMS after non-compliant use of clozapine. She presented with symptoms including irrelevant talk, breathlessness, and generalized muscle weakness. On examination, she was drowsy with a Glasgow Coma Scale score of 11, tachycardia, tachypnea, and hypertonicity in all limbs. Diagnostic evaluations revealed increased urea and creatinine levels, raised creatine phosphokinase, and metabolic acidosis, which are consistent with NMS. Medical management included the discontinuation of clozapine and the initiation of bromocriptine. The report emphasizes how important physical therapy is to the NMS recovery process. The goals of physical therapy were to improve functional mobility, lessen muscle rigidity, and avoid problems from extended immobility. Kinesthetic stimulation, active cycle breathing methods, soft rocking motions, neural warmth, weight-bearing exercises, and mobility training were all incorporated into the protocol. Significant progress was observed in the patient\'s degree of consciousness, movement, and oxygen reliance over a two-week period. With the patient eventually managing room air without additional oxygen, the Glasgow Coma Scale score improved, and the ICU Mobility Scale score increased from 1 to 5. This instance emphasizes the need for prompt diagnosis and all-encompassing NMS care, with physiotherapy playing a critical role. Physiotherapy can significantly enhance overall healing, improve respiratory function, and facilitate neuromuscular re-education through tailored therapies. The results indicate that physiotherapy has to be regarded as a crucial component of the multidisciplinary strategy for managing NMS, with the goal of enhancing patient outcomes and quality of life. More studies are required to optimize physiotherapy interventions for NMS patients.
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  • 文章类型: Journal Article
    这项研究调查了莫努比拉韦治疗患有精神疾病的非住院COVID-19患者的临床疗效。
    这项回顾性队列研究使用TriNetX研究网络来确定在2022年1月1日至2023年5月1日期间经历非住院COVID-19的精神疾病患者。使用倾向评分匹配(PSM)方法将接受莫那普拉韦(治疗组)的患者与未接受莫那普拉韦(未治疗组)的患者进行匹配。结果包括短期结果-30天内全因住院或死亡的综合结果,以及COVID-19诊断后一年内发生COVID-19后疾病的风险。
    两组9421例患者,每个都具有平衡的基线特征,使用PSM方法鉴定。在30天的随访中,与未治疗组相比,治疗组住院或死亡风险降低(HR,0.760;95%CI,0.665-0.869)。与未治疗组相比,治疗组也表现出经历COVID-19后病症的风险降低,包括胸部/喉咙疼痛(HR,0.615;95%CI,0.543-0.696),异常呼吸(HR,0.761;95%CI,0.687-0.884),腹部症状(HR,0.748;95%CI,0.674-0.831),疲劳(HR,0.718;95%CI,0.638-0.808),头痛(HR,0.753;95%CI,0.665-0.852),认知症状(HR,0.769;95%CI,0.630-0.940),肌痛(HR,0.647;95%CI,0.530-0.789),咳嗽(HR,0.867;95%CI,0.770-0.978),和心悸(HR,0.641;95%CI,0.534-0.770),随访1年。
    Molnupiravir可能与较低的全因住院率或死亡率有关,并且在患有精神疾病的非住院COVID-19患者中,也降低了COVID-19后疾病的风险。
    UNASSIGNED: This study investigated the clinical effectiveness of molnupiravir for treating non-hospitalized COVID-19 patients with pre-existing psychiatric disorder.
    UNASSIGNED: This retrospective cohort study used the TriNetX research network to identify patients with psychiatric disorder who experienced non-hospitalized COVID-19 between 1 January 2022, and 1 May 2023. The propensity score matching (PSM) method was used to match patients receiving molnupiravir (treated group) with those who did not (untreated group). The outcome included short-term outcomes - the composite of all-cause hospitalization or death within 30 days and the risk of post-COVID-19 conditions up to a year after COVID-19 diagnosis.
    UNASSIGNED: Two groups of 9,421 patients, each with balanced baseline characteristics, were identified using the PSM method. During the 30-day follow-up, treated group was associated with a reduced risk of hospitalization or mortality compared to untreated group (HR, 0.760; 95% CI, 0.665-0.869). Compared to untreated group, treated group also exhibited a decreased risk of experiencing post-COVID-19 conditions, including chest/throat pain (HR, 0.615; 95% CI, 0.543-0.696), abnormal breathing (HR, 0.761; 95% CI, 0.687-0.884), abdominal symptoms (HR, 0.748; 95% CI, 0.674-0.831), fatigue (HR, 0.718; 95% CI, 0.638-0.808), headache (HR, 0.753; 95% CI, 0.665-0.852), cognitive symptoms (HR, 0.769; 95% CI, 0.630-0.940), myalgia (HR, 0.647; 95% CI, 0.530-0.789), cough (HR, 0.867; 95% CI, 0.770-0.978), and palpitation (HR, 0.641; 95% CI, 0.534-0.770) during the 1-year follow-up.
    UNASSIGNED: Molnupiravir could be associated with lower rates of all-cause hospitalization or death and also lower risk of post-COVID-19 condition among non-hospitalized COVID-19 patients with pre-existing psychiatric disorder.
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  • 文章类型: Journal Article
    背景:在过去的十年中,细胞周期蛋白依赖性激酶4/6抑制剂(CDK4/6i)的出现代表了乳腺癌治疗的重大突破。在临床试验和现实环境中,观察到使用CDK4/6i的患者可能会出现精神不良事件(PAEs).在这里,我们进行了一项药物警戒研究,以全面评估CDK4/6i与PAEs之间的相关性.
    方法:我们获得了2015年1月至2023年12月期间提交给FDA不良事件报告系统(FAERS)的个别病例安全性报告。在不相称性分析中,计算每种不良事件-药物组合的报告比值比(ROR)和信息成分(IC)值.应用单因素logistic回归分析探讨CDK4/6i治疗后PAEs的相关因素。
    结果:共确认了95,591份与CDK4/6i相关的报告,6.72%报告PAEs,这一比例呈逐年上升趋势。根据ROR和IC值,17类PAEs定义为CDK4/6i相关PAEs。在这些PAEs中,失眠,压力,饮食失调,情绪低落,睡眠障碍非常常见,每个占CDK4/6i报告的10%以上。Ribociclib显示CDK4/6i相关PAEs的最高风险信号(ROR=1.89[1.75-2.04],IC025=0.79),其次是palbociclib(ROR=1.47[1.41-1.53],IC025=0.49),而abemaciclib没有表现出显著的信号(ROR=0.52[0.44-0.62],IC025=-1.13)。女性性别,年龄小和体重超过80kg是CDK4/6i相关PAEs发生的显著危险因素.
    结论:使用来自现实世界的数据,药物不良反应的大规模自发报告系统,我们的研究描绘了PAEs到CDK4/6i的光谱。这可能为医疗保健专业人员提供有价值的见解,以管理接受CDK4/6i治疗的患者的PAEs风险。特别是那些患有精神疾病的人。
    BACKGROUND: The emergence of cyclin-dependent kinases 4/6 inhibitors (CDK4/6i) represented a major breakthrough in the treatment of breast cancer over the past decade. In both clinical trials and real-world settings, it was observed that patients using CDK4/6i might experience psychiatric adverse events (PAEs). Herein, we conducted a pharmacovigilance study to comprehensively assess the correlation between CDK4/6i and PAEs.
    METHODS: We obtained individual case safety reports submitted to the FDA Adverse Events Reporting System (FAERS) during the period from January 2015 to December 2023. In disproportionality analysis, the reporting odds ratio (ROR) and information component (IC) values were calculated for each adverse event-drug combination. Univariate logistic regression analysis was utilized to explore factors associated with PAEs following CDK4/6i treatment.
    RESULTS: A total of 95,591 reports related to CDK4/6i were identified, with 6.72% reporting PAEs, and this proportion exhibited an annual upward trend. Based on the ROR and IC values, 17 categories of PAEs were defined as CDK4/6i-related PAEs. Among these PAEs, insomnia, stress, eating disorder, depressed mood, and sleep disorder were very common, each accounting for over 10% of CDK4/6i reports. Ribociclib showed the highest risk signal of CDK4/6i-related PAEs (ROR = 1.89[1.75-2.04], IC025 = 0.79), followed by palbociclib (ROR = 1.47[1.41-1.53], IC025 = 0.49), while abemaciclib did not exhibit a significant signal (ROR = 0.52[0.44-0.62], IC025 = -1.13). Female sex, younger age and weight exceeding 80 kg were significant risk factors for the incidence of CDK4/6i-related PAEs.
    CONCLUSIONS: Using data from a real-world, large-scale spontaneous reporting system for adverse drug reactions, our study delineated the spectrum of PAEs to CDK4/6i. This potentially offered valuable insights for healthcare professionals to manage the risk of PAEs in patients receiving CDK4/6i treatment, particularly those with psychiatric disorders.
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  • 文章类型: Journal Article
    线粒体疾病是已知的影响能量代谢的先天性错误,与糖尿病等慢性疾病一样常见,影响了大约5000人中的1人。线粒体疾病/功能障碍的作用在神经发育障碍如ASD中得到了强调,多动症,智力残疾,和说话延迟,以及各种精神病。神经发育障碍越来越被认为具有行为和精神症状。我们的研究旨在调查线粒体疾病的报道,注意神经发育障碍和精神/行为状况。
    这是通过对PubMed/MEDLINE文献的系统回顾完成的,Scopus,和Cochrane图书馆至2022年11月。
    我们发现了277种出版物,其中139人符合纳入标准。我们主要发现综述文章提及与ASD相关的线粒体功能障碍/疾病,并简要提及精神病/行为合并症。
    这表明需要在ASD之外进行更广泛的研究,以了解线粒体疾病或功能障碍与各种神经发育和精神/行为合并症之间的关系。
    UNASSIGNED: Mitochondrial diseases are known inborn errors affecting energy metabolism and are as common as chronic diseases such as diabetes, affecting approximately 1 in 5,000 people. The role of mitochondrial diseases/dysfunction has been highlighted in neurodevelopmental disorders like ASD, ADHD, intellectual disability, and speech delay, as well as various psychiatric conditions. Neurodevelopmental disorders are increasingly recognized as having behavioral and psychiatric symptoms. Our study aimed to investigate reports of mitochondrial disorders, noting neurodevelopmental disorders and psychiatric/behavioral conditions.
    UNASSIGNED: This was done through a systematic review of literature from PubMed/MEDLINE, Scopus, and Cochrane Library up to November 2022.
    UNASSIGNED: We found 277 publications, of which 139 met the inclusion criteria. We mostly found review articles with mention of mitochondrial dysfunction/disorder in relation to ASD with brief mentions of psychiatric/behavioral comorbidities.
    UNASSIGNED: This suggests a need for broader research efforts beyond ASD to understand the relationship between mitochondrial disorder or dysfunction and various neurodevelopmental and psychiatric/behavioral comorbidities.
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  • 文章类型: Case Reports
    Munchausen代理综合征(MSBP)是一种罕见的虐待形式,其特征是近亲在儿童中制造或诱发疾病症状,通常是父母,导致多次咨询和不同程度的侵入性医疗干预。文献中描述了各种临床表现,从器质性表现到精神病学表现。这种综合征仍然是一个具有挑战性的诊断,需要提高医疗保健专业人员的认识。及时识别是防止潜在的长期合并症甚至死亡的关键。这里,我们报告了两例表现为出血的MSBP,肇事者是母亲。
    Munchausen\'s syndrome by proxy (MSBP) is a rare form of abuse characterized by the fabrication or induction of symptoms of illness in a child by a close relative, typically a parent, leading to multiple consultations and varying degrees of invasive medical interventions. Various clinical presentations are described in the literature, ranging from organic manifestations to psychiatric expressions. This syndrome remains a challenging diagnosis to make and requires increased awareness among healthcare professionals. Prompt recognition is key to preventing potential long-term comorbidities and even fatalities. Here, we are reporting two cases of MSBP manifested by bleeding, with the perpetrator being the mother.
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  • 文章类型: Journal Article
    维生素D结合蛋白(VDBP)作为负责结合和递送维生素D及其代谢物至靶器官的关键转运蛋白。VDBP在组织损伤后的炎症反应中起着至关重要的作用,并参与肌动蛋白降解。最近的研究揭示了它在各种疾病中的潜在作用,导致人们对了解VDBP在精神和神经系统疾病中的意义越来越感兴趣。这篇综述的目的是提供有关VDBP参与神经和精神疾病的现有理解的摘要。通过检查VDBP和这些疾病之间复杂的相互作用,这篇综述有助于更深入地了解潜在的机制和潜在的治疗途径.从VDBP的研究中获得的见解可以为诊断的新策略铺平道路,预后,以及治疗精神和神经系统疾病。
    Vitamin D binding protein (VDBP) serves as a key transporter protein responsible for binding and delivering vitamin D and its metabolites to target organs. VDBP plays a crucial part in the inflammatory reaction following tissue damage and is engaged in actin degradation. Recent research has shed light on its potential role in various diseases, leading to a growing interest in understanding the implications of VDBP in psychiatric and neurological disorders. The purpose of this review was to provide a summary of the existing understanding regarding the involvement of VDBP in neurological and psychiatric disorders. By examining the intricate interplay between VDBP and these disorders, this review contributes to a deeper understanding of underlying mechanisms and potential therapeutic avenues. Insights gained from the study of VDBP could pave the way for novel strategies in the diagnosis, prognosis, and treatment of psychiatric and neurological disorders.
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  • 文章类型: Journal Article
    睡眠与精神疾病有关。然而,他们的因果关系仍然未知。
    该研究探索了七个睡眠参数之间的因果关系(睡眠持续时间,失眠,睡眠呼吸暂停,时间型,白天打瞌睡,白天打盹,和打鼾)和三种精神疾病,包括重度抑郁症(MDD),精神分裂症,和注意缺陷/多动障碍(ADHD)使用两个样本孟德尔随机(MR)。睡眠参数的全基因组关联研究(GWAS)汇总数据来自英国生物银行,FinnGen生物银行,和EBI数据库。MR-Egger,加权中位数,逆方差加权(IVW),简单模式,加权模式,最大似然,惩罚加权中位数,和IVW(固定效应)用于进行MR分析。异质性由Cochran的Q统计量检测。通过MREgger检测水平多效性。通过留一法分析研究了灵敏度。
    失眠(OR=2.02,95CI=1.34-3.03,p=0.001,错误发现率(FDR)校正的p值=0.011)和白天午睡(OR=1.81,95CI=1.34-2.44,FDR校正的p值<0.001)与MDD风险增加相关。较长的睡眠时间(OR=2.20,95CI=1.24-3.90,FDR校正的p值=0.049)与精神分裂症的风险增加有关,而白天打瞌睡(OR=4.44,95CI=1.20~16.41,校正p值=0.088)和白天打盹(OR=2.11,95CI=1.11~4.02,FDR校正p值=0.088)与精神分裂症风险增加有暗示性关联.睡眠时间延长与ADHD风险降低有暗示性关联(OR=0.66,95CI=0.42-0.93,FDR校正p值=0.088)。
    这项研究为睡眠和精神疾病之间的复杂关系提供了进一步的证据。我们的发现强调了解决睡眠问题在预防精神疾病方面的潜在益处。
    UNASSIGNED: Sleep is associated with psychiatric disorders. However, their causality remains unknown.
    UNASSIGNED: The study explored the causal relationship between seven sleep parameters (sleep duration, insomnia, sleep apnea, chronotype, daytime dozing, napping during the day, and snoring) and three psychiatric disorders including major depressive disorder (MDD), schizophrenia, and attention-deficit/hyperactivity disorder (ADHD) using two-sample Mendelian randomization (MR). Genome-wide association study (GWAS) summary data for sleep parameters were obtained from the United Kingdom biobank, FinnGen biobank, and EBI databases. MR-Egger, weighted median, inverse-variance weighted (IVW), simple mode, weighted mode, maximum likelihood, penalized weighted median, and IVW(fixed effects) were used to perform the MR analysis. The heterogeneity was detected by Cochran\'s Q statistic. The horizontal pleiotropy was detected by MR Egger. The sensitivity was investigated by the leave-one-out analysis.
    UNASSIGNED: Insomnia (OR = 2.02, 95%CI = 1.34-3.03, p = 0.001, False-discovery rate (FDR) corrected p-value = 0.011) and napping during the day (OR = 1.81, 95%CI = 1.34-2.44, FDR corrected p-value<0.001) were associated with an increased risk of MDD. Longer sleep duration (OR = 2.20, 95%CI = 1.24-3.90, FDR corrected p-value = 0.049) had an association with the increased risk of schizophrenia, while daytime dozing (OR = 4.44, 95%CI = 1.20-16.41, corrected p-value = 0.088)and napping during the day (OR = 2.11, 95%CI = 1.11-4.02, FDR corrected p-value = 0.088) had a suggestive association with an increased risk of schizophrenia. Longer sleep duration had a suggestive association with a decreased risk of ADHD (OR = 0.66, 95%CI = 0.42-0.93, FDR corrected p-value = 0.088).
    UNASSIGNED: This study provides further evidence for a complex relationship between sleep and psychiatric disorders. Our findings highlight the potential benefits of addressing sleep problems in the prevention of psychiatric disorders.
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  • 文章类型: Journal Article
    精神紊乱如躁郁症和精神分裂症是高度遗传性的。虽然基因对精神疾病的贡献是相当肯定的,导致特定条件的特定遗传因素长期以来一直是个谜。人类基因组计划的初步报告授权,对人类基因组的全面分析,叫做“基因组学,“成为可能。随后大规模基因组技术的发展使我们能够阐明各种疾病相关的遗传信息,加快我们对各种疾病的了解。关于精神疾病的基因组研究也不例外。在这篇评论中,我介绍了精神病学基因组学的重大进展,特别关注我们对躁郁症的研究。国际财团和倡导团体加速精神病学基因组学,增加样本量和统计能力,以获得稳健的发现。精神分裂症的遗传结构已在常见和罕见的变异研究中得到阐明。自闭症谱系障碍(ASD)的遗传结构主要通过罕见的变异分析得到阐明。至于双相情感障碍,常见变异分析先于罕见变异分析,但是我们正在努力阐明相关的罕见变体。虽然基因组方法已经解释了特定疾病的特定遗传因素,重叠的风险基因或多效性比预期的要多。当前精神疾病的疾病学边界或多或少受到了挑战。为了更深入地理解基因型与表型的关系,试图理解基于基因型的表型,称为“基因型优先”方法,已经开始。我将讨论这种新方法,以更好地理解和治疗精神疾病。
    Psychiatric disorders such as bipolar disorder and schizophrenia are highly heritable. While the genetic contribution to psychiatric disorders is quite sure, specific genetic factors contributing to particular conditions have long been a mystery. Empowered by the initial report of the Human Genome Project, the analysis of the comprehensive set of the human genome, called \"genomics,\" became possible. Subsequent development of large-scale genomic technologies enabled us to elucidate various disease-related genetic information, accelerating our understanding of various diseases. Genomic research on psychiatric disorders is not an exception. In this Review, I introduce significant advancements in psychiatric genomics with a special focus on our investigation of bipolar disorder. International consortiums and advocacy groups accelerate psychiatric genomics, increasing the sample size and statistical power for robust findings. The genetic architecture of schizophrenia has been elucidated in both common and rare variant studies. The genetic architecture of autism spectrum disorder (ASD) has been elucidated mainly by rare variant analysis. As to bipolar disorder, common variant analysis precedes rare variant analysis, but we are struggling to elucidate relevant rare variants. While the genomic approach has explained specific genetic factors for particular disorders, overlapping risk genes or pleiotropy has been observed more than expected. The boundary in the current nosology of psychiatric disorders is more or less challenged. To understand the genotype-phenotype relation more deeply, an attempt to understand phenotypes based on genotypes, called the \"genotype first\" approach, has started. I discuss this new approach for better understanding and treatment of psychiatric disorders.
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