major depressive disorder

重度抑郁症
  • 文章类型: Journal Article
    重度抑郁症(MDD)是一种多形性疾病,具有大量的症状和严重程度,在几个相关领域具有可测量的缺陷。在诊断患有抑郁症的患者中观察到的广泛表型是非常复杂的疾病的反映,其中生物和外部因素聚集在一起(例如,生活事件的响应/处理,脑内因素)收敛并介导发病机理,临床表现/表型和轨迹。患者来源的诱导多能干细胞(iPSC)使其能够分化成中枢神经系统中的特化细胞类型,以探索MDD的病理生理底物。这些模型可以补充动物模型,以促进药物发现和确定治疗方法。比如细胞疗法,药物再利用,和药物代谢的阐明,毒性,以及分子/细胞水平的作用机制,为精准精神病学铺平道路.尽管在过去的几十年里取得了显著的科学和临床进展,这种疾病仍然知之甚少,发病率和患病率继续增加,需要更多的研究来满足临床需求。这篇综述旨在总结并提供迄今为止使用患者来源的iPSCs进行精神疾病建模的研究的重要概述。特别强调MDD。
    Major Depressive Disorder (MDD) is a pleomorphic disease with substantial patterns of symptoms and severity with mensurable deficits in several associated domains. The broad spectrum of phenotypes observed in patients diagnosed with depressive disorders is the reflection of a very complex disease where clusters of biological and external factors (e.g., response/processing of life events, intrapsychic factors) converge and mediate pathogenesis, clinical presentation/phenotypes and trajectory. Patient-derived induced pluripotent stem cells (iPSCs) enable their differentiation into specialised cell types in the central nervous system to explore the pathophysiological substrates of MDD. These models may complement animal models to advance drug discovery and identify therapeutic approaches, such as cell therapy, drug repurposing, and elucidation of drug metabolism, toxicity, and mechanisms of action at the molecular/cellular level, to pave the way for precision psychiatry. Despite the remarkable scientific and clinical progress made over the last few decades, the disease is still poorly understood, the incidence and prevalence continue to increase, and more research is needed to meet clinical demands. This review aims to summarise and provide a critical overview of the research conducted thus far using patient-derived iPSCs for the modelling of psychiatric disorders, with a particular emphasis on MDD.
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  • 文章类型: Journal Article
    背景:虽然先前的研究已经探索了巴林达寡糖(MOs)作为治疗重度抑郁症(MDD)患者的疗效,MOs对脑功能或默认模式网络(DMN)影响的机制基础尚未表征。目的是检查MOs治疗对DMN不同区域功能连接的影响。
    方法:总共,27名MDD患者和29名健康对照受试者(HCs)接受了静息状态功能磁共振成像。然后患者接受MOs治疗8周,在基线和8周治疗期结束时进行扫描.使用成像数据的网络同质性(NH)分析评估与MOs治疗相关的DMN同质性变化。和模式分类方法用于确定异常基线NH缺陷是否可以区分MDD患者和对照组。还评估了NH异常预测患者对MO治疗反应的能力。
    结果:相对于HC,患者右前肌(PCu)的NH值基线下降.在8周治疗期结束时,MDD患者右侧PCu和左侧额内侧回(SMFG)的NH值降低和升高,分别。与基线时的这些患者相比,8周的MOs治疗与右角回的NH值降低以及左颞中回和右PCu的NH值增加相关。支持向量机(SVM)分析显示,右PCu和左SMFG中的NH异常最准确(87.50%)用于区分MDD患者和HC。
    结论:这些结果表明MOs治疗可以改变MDD患者的默认模式NH。该结果为阐明MOs对脑功能的影响提供了基础,并表明在本研究中观察到的独特的NH模式可能作为成像生物标志物用于区分MDD患者和健康受试者。
    BACKGROUND: While prior studies have explored the efficacy of Morinda officinalis oligosaccharides (MOs) as a treatment for patients with major depressive disorder (MDD), the mechanistic basis for the effects of MOs on brain function or the default-mode network (DMN) has yet to be characterized. The objective of this was to examine the effects of MOs treatment on functional connectivity in different regions of the DMN.
    METHODS: In total, 27 MDD patients and 29 healthy control subjects (HCs) underwent resting-state functional magnetic resonance imaging. The patients were then treated with MOs for 8 weeks, and scanning was performed at baseline and the end of the 8-week treatment period. Changes in DMN homogeneity associated with MOs treatment were assessed using network homogeneity (NH) analyses of the imaging data, and pattern classification approaches were employed to determine whether abnormal baseline NH deficits could differentiate between MDD patients and controls. The ability of NH abnormalities to predict patient responses to MOs treatment was also evaluated.
    RESULTS: Relative to HCs, patients exhibited a baseline reduction in NH values in the right precuneus (PCu). At the end of the 8-week treatment period, the MDD patients showed reduced and increased NH values in the right PCu and left superior medial frontal gyrus (SMFG), respectively. Compared to these patients at baseline, the 8-week MOs treatment was associated with reduced NH values in the right angular gyrus and increased NH values in the left middle temporal gyrus and the right PCu. Support vector machine (SVM) analyses revealed that NH abnormalities in the right PCu and left SMFG were the most accurate (87.50%) for differentiating between MDD patients and HCs.
    CONCLUSIONS: These results indicated that MOs treatment could alter default-mode NH in patients with MDD. The results provide a foundation for elucidation of the effects of MOs on brain function and suggest that the distinctive NH patterns observed in this study may be useful as imaging biomarkers for distinguishing between patients with MDD and healthy subjects.
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  • 文章类型: Journal Article
    重度抑郁症(MDDs)给个人和社会带来了沉重负担;然而,其长期趋势仍需要进一步详细分析。
    本研究旨在分析过去三十年中国居民MDD发病率的性别时间趋势和队列变化。
    利用年龄-时期-队列-相互作用模型并利用2019年全球疾病负担研究的数据,这项研究确定并分析了1990年至2019年中国5-94岁男性和女性MDD的发病率趋势。包括年龄,时期和出生队列。
    分析揭示了与年龄有关的影响,表明青少年和老年人MDD风险增加。具体来说,在65~69岁时进入老年的个体,MDD的风险显著增加64.9%.90-94岁人群的MDD风险增加了105.4%。这个年龄段的女性和男性分别增长了75.1%和103.4%,分别。就时期效应而言,MDD的风险从1990年到1994年呈现下降趋势,随后在2008年出现反弹.队列效应表现出不同的世代模式,第一代和第三代表现出相反的“年龄水平”趋势。第二代和第四代表现出“累积劣势”和“累积优势”模式,分别。年龄效应表明女性MDD发病率总体较高,而队列效应显示女性MDD发病率差异较大。
    这项研究强调了年龄的重大影响,中国不同性别MDD的时期和队列研究。针对弱势群体的优先干预措施,包括孩子,青少年,老年人,女性和千年后出生队列,对于减轻MDD的影响至关重要。
    UNASSIGNED: Major depressive disorders (MDDs) impose substantial burdens on individuals and society; however, further detailed analysis is still needed for its long-term trends.
    UNASSIGNED: This study aimed to analyse the gender-specific temporal trends and cohort variations of MDD incidence among Chinese residents over the past three decades.
    UNASSIGNED: Employing the age-period-cohort-interaction model and leveraging data from the Global Burden of Disease Study 2019, this research identified and analysed incidence trends of MDD among Chinese males and females aged 5-94 years from 1990 to 2019 across three dimensions, encompassing age, period and birth cohort.
    UNASSIGNED: The analysis reveals age-related effects, indicating heightened MDD risk among adolescents and older adults. Specifically, individuals entering the older adulthood at the age of 65-69 significantly increased the risk of MDD by 64.9%. People aged 90-94 years witnessed a 105.4% increase in MDD risk for the overall population, with females and males in this age group experiencing a 75.1% and 103.4% increase, respectively. In terms of period effects, the risk of MDD displayed a decline from 1990 to 1994, followed by a rebound in 2008. Cohort effects demonstrated diverse generational patterns, with generation I and generation III manifesting opposing \'age-as-level\' trends. Generation II and generation IV exhibited \'cumulative disadvantage\' and \'cumulative advantage\' patterns, respectively. Age effects indicated an overall higher risk of MDD incidence in females, while cohort effects showed greater variations of MDD incidence among females.
    UNASSIGNED: The study underscores the substantial effects of age, period and cohort on MDD across genders in China. Priority interventions targeting vulnerable populations, including children, adolescents, older adults, females and the post-millennium birth cohort, are crucial to mitigate the impact of MDD.
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  • 文章类型: Journal Article
    目的:电惊厥治疗(ECT)是治疗情绪障碍最有效的治疗方法之一,主要发生在单相(MDD)或躁郁症(BD)背景下的重度抑郁发作(MDE)。然而,ECT仍然是一种被忽视和未充分利用的治疗方法。老年人是发生药物不良反应的高危患者。在这种情况下,我们试图根据是否存在国际指南提供的使用ECT的一线适应症,确定65岁或以上患者在开始ECT前的MDE持续时间和治疗行数.
    方法:在这个多中心中,回顾性研究包括65岁或以上患有MDD或BD的MDE患者,这些患者已接受ECT治疗,收集有关MDE持续时间和ECT前接受治疗的行数的数据.使用ECT的原因,特别是一线适应症(自杀,紧迫性,存在紧张和精神病特征,以前的ECT反应,患者偏好)进行记录。组间的统计比较使用标准统计检验。
    结果:我们确定了335例患者。在ECT之前MDE的平均持续时间约为9个月。BD明显短于MDD-约7个月和10个月,分别。在MDD组中,慢性医学疾病的共同发生增加了ECT前的持续时间。使用ECT指南的一线适应症的存在并没有减少ECT前MDE的持续时间,除了以前对ECT有反应的地方。一线适应症减少了开始ECT之前的治疗线数量。
    结论:即使ECT由于其对MDE的有效性和安全性而似乎是老年人群的关键治疗方法,在这种治疗之前的延迟仍然太长了。
    OBJECTIVE: Electroconvulsive therapy (ECT) is one of the most effective treatments in mood disorders, mainly in major depressive episode (MDE) in the context of either unipolar (MDD) or bipolar disorder (BD). However, ECT remains a neglected and underused treatment. Older people are at high risk patients for the development of adverse drug reactions. In this context, we sought to determine the duration of MDEs and the number of lines of treatment before the initiation of ECT in patients aged 65 years or over according to the presence or absence of first-line indications for using ECT from international guidelines.
    METHODS: In this multicenter, retrospective study including patients aged 65 years or over with MDEs in MDD or BD who have been treated with ECT for MDEs, data on the duration of MDEs and the number of lines of treatment received before ECT were collected. The reasons for using ECT, specifically first-line indications (suicidality, urgency, presence of catatonic and psychotic features, previous ECT response, patient preference) were recorded. Statistical comparisons between groups used standard statistical tests.
    RESULTS: We identified 335 patients. The mean duration of MDEs before ECT was about 9 months. It was significantly shorter in BD than in MDD- about 7 and 10 months, respectively. The co-occurrence of chronic medical disease increased the duration before ECT in the MDD group. The presence of first-line indications for using ECT from guidelines did not reduce the duration of MDEs before ECT, except where there was a previous response to ECT. The first-line indications reduced the number of lines of treatment before starting ECT.
    CONCLUSIONS: Even if ECT seems to be a key treatment in the elderly population due to its efficacity and safety for MDEs, the delay before this treatment is still too long.
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  • 文章类型: Journal Article
    目的:焦虑性抑郁是在被诊断为重度抑郁障碍(MDD)的亚洲精神病患者中观察到的一个普遍特征。这项研究旨在调查诊断为MDD的台湾个体中焦虑抑郁症的患病率和临床表现。
    方法:我们招募了18岁以上通过临床访谈诊断为MDD的精神科门诊患者。这次招募是在台湾北部的五家医院进行的。我们收集了参与者的基线临床和人口统计信息。在21项汉密尔顿抑郁量表(HAM-D)上,使用焦虑/躯体化因子得分≥7的阈值来识别焦虑抑郁。
    结果:在我们对399名患者(84.21%为女性)的研究中,64.16%符合焦虑抑郁的标准。他们往往年纪大了,已婚,受教育程度较低,有了更多的孩子,发病年龄较大。焦虑抑郁症患者的HAM-D和临床总体印象-严重程度量表评分较高,更多的恐慌症(没有广场恐惧症),表现出躁动等症状,烦躁,集中困难,心理和躯体焦虑,躯体投诉,软骨病,减肥,和增加洞察力。令人惊讶的是,他们的自杀率与非焦虑抑郁症患者没有显著差异.这突出了认识和解决这些独特特征的重要性。
    结论:我们的研究结果揭示,与住院患者相比,台湾诊断为MDD的门诊患者中焦虑抑郁的患病率较低,但大大高于欧洲国家和美国报告的患病率。此外,焦虑抑郁症患者表现出更多的躯体症状。
    OBJECTIVE: Anxious depression is a prevalent characteristic observed in Asian psychiatric patients diagnosed with major depressive disorder (MDD). This study aims to investigate the prevalence and clinical presentation of anxious depression in Taiwanese individuals diagnosed with MDD.
    METHODS: We recruited psychiatric outpatients aged over 18 who had been diagnosed with MDD through clinical interviews. This recruitment took place at five hospitals located in northern Taiwan. We gathered baseline clinical and demographic information from the participants. Anxious depression was identified using a threshold of an anxiety/somatization factor score ≥7 on the 21-item Hamilton Rating Scale for Depression (HAM-D).
    RESULTS: In our study of 399 patients (84.21% female), 64.16% met the criteria for anxious depression. They tended to be older, married, less educated, with more children, and an older age of onset. Anxious depression patients had higher HAM-D and Clinical Global Impression-Severity scale score, more panic disorder (without agoraphobia), and exhibited symptoms like agitation, irritability, concentration difficulties, psychological and somatic anxiety, somatic complaints, hypochondriasis, weight loss, and increased insight. Surprisingly, their suicide rates did not significantly differ from non-anxious depression patients. This highlights the importance of recognizing and addressing these unique characteristics.
    CONCLUSIONS: Our study findings unveiled that the prevalence of anxious depression among Taiwanese outpatients diagnosed with MDD was lower compared to inpatients but substantially higher than the reported rates in European countries and the United States. Furthermore, patients with anxious depression exhibited a greater occurrence of somatic symptoms.
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  • 文章类型: Journal Article
    背景:自杀未遂是重度抑郁症(MDD)患者最严重的合并症之一,与老年人相比,年轻人的自杀未遂患病率更高,有明显的性别差异。本研究旨在探讨自杀未遂之间的关系,临床症状,甲状腺激素,不同性别的年轻首发和未用药(FEND)MDD患者的代谢参数。
    方法:共招募1289例FENDMDD患者。抑郁症,焦虑,使用汉密尔顿抑郁量表(HAMD)评估精神病症状,汉密尔顿焦虑量表(HAMA),和阳性和阴性综合征量表(PANSS)阳性分量表,分别。还测试了甲状腺激素和糖脂代谢指标。采用网络分析来描绘甲状腺功能障碍之间的相互作用,临床症状,和代谢紊乱。
    结果:在年轻的FENDMDD患者中,男性自杀未遂率为17.4%,女性为19.8%,自杀未遂发生率无显著性别差异(χ2=1.06,p=0.303)。在网络模型中,PANSS阳性子量表(预期影响=0.578)和HAMD评分(预期影响=0.576)被确定为最影响男性患者的个体症状,而TSH(促甲状腺激素)(预期影响=0.972)和PANSS阳性子量表(预期影响=0.937)被确定为女性患者受影响最大的个体症状。此外,我们发现TSH(预期影响=0.438)是连接代谢紊乱和临床症状的关键节点.
    结论:我们的研究结果强调了精神病性症状在年轻的MDD自杀未遂患者中的重要作用。此外,我们的研究结果强调了血清TSH水平在年轻女性MDD自杀未遂患者的病理生理中的关键作用.
    BACKGROUND: Suicide attempts are one of the most serious comorbidities in patients with major depressive disorder (MDD), and the prevalence of suicide attempts is higher in younger people compared to older people, with significant gender differences. This study aimed to investigate the relationship between suicide attempts, clinical symptoms, thyroid hormones, and metabolic parameters in young first-episode and drug-naïve (FEND) MDD patients of different genders.
    METHODS: A total of 1289 FEND MDD patients were recruited. Depression, anxiety, and psychotic symptoms were assessed using the Hamilton Depression Rating Scale (HAMD), Hamilton Anxiety Rating Scale (HAMA), and the Positive and Negative Syndrome Scale (PANSS) positive subscale, respectively. Thyroid hormones and glucolipid metabolism indicators were also tested. Network analysis was employed to delineate the interplay between thyroid dysfunction, clinical symptoms, and metabolic disorders.
    RESULTS: Among young FEND MDD patients, the rate of suicide attempts was 17.4% in males and 19.8% in females, showing no significant gender difference in the incidence of suicide attempts (χ2 = 1.06, p = 0.303). In the network model, PANSS positive subscale (Expected Influence = 0.578) and HAMD scores (Expected Influence = 0.576) were identified as the individual symptoms that most affected male patients, whereas TSH (Thyroid-Stimulating Hormone) (Expected Influence = 0.972) and PANSS positive subscale (Expected Influence = 0.937) were identified as the individual symptoms that most affected female patients. In addition, we found that TSH (Expected Influence = 0.438) was a pivotal node connecting metabolic disturbances and clinical symptoms.
    CONCLUSIONS: Our findings emphasize the important role of psychotic symptoms in young MDD patients with suicide attempts. Moreover, our results highlight the pivotal role of serum TSH levels in the pathophysiology of young female MDD patients with suicide attempts.
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  • 文章类型: Journal Article
    目的:本研究的目的是确定SLE患者中不安腿综合征(RLS)的患病率,描述他们的临床特征,检查其对健康相关生活质量(HRQoL)的影响,并评估其与抑郁症的关系。
    方法:共招募124例SLE患者,有了人口统计数据,并收集临床特征。RLS诊断基于国际RLS研究组标准,而抑郁症是通过患者健康问卷评估的。HRQoL通过疾病特异性验证问卷进行评估,LupusQoL,通过疼痛视觉模拟量表检查疼痛强度,并通过患者整体评估评估疾病活动性.使用t检验或Wilcoxon以及分类变量独立性的卡方检验,比较了有RLS和无RLS的SLE患者之间的这些变量。P值≤0.05被认为具有统计学意义。
    结果:在SLE患者中(平均年龄48岁,87.1%为女性),32%有RLS。发现患有RLS的SLE患者的诊断延迟更长(1vs0.5年;p=0.019),并且不太可能被雇用(65%vs45%,p=0.040)与非RLS患者相比。此外,RLS患者更有可能同时存在重度抑郁症(MDD)(p=0.019),更高水平的疼痛(p=0.006)和基于患者总体评估的疾病活动(p=0.014).Further,RLS患者组的大多数LupusQoL域显著较低,提示HRQoL较差.
    结论:RLS存在于三分之一的SLE队列中,显著损害HRQoL并与抑郁症相关,更高的疼痛,增加疾病活动。这些发现强调了SLE患者早期RLS检测和管理的重要性。
    OBJECTIVE: The aim of this study was to determine the prevalence of restless leg syndrome (RLS) among patients with SLE, describe their clinical characteristics, examine its impact on health-related quality of life (HRQoL), and evaluate its association with depression.
    METHODS: A total of 124 SLE patients were recruited, with data on demographics, and clinical features collected. RLS diagnosis was based on the international RLS study group criteria, while depression was assessed by the patient health questionnaire. HRQoL was assessed by a disease-specific validated questionnaire, the LupusQoL, pain intensity was examined through the pain visual analogue scale, and disease activity was evaluated via the patient global assessment. These variables were compared between SLE patients with RLS and without RLS using t-tests or Wilcoxon and the chi-square test of independence for categorical variables. A p-value ≤0.05 was considered statistically significant.
    RESULTS: Among the SLE patients (mean age 48, 87.1 % women), 32 % had RLS. The SLE patients with RLS were found to have a longer delay in diagnosis (1 vs 0.5 years; p = 0.019) and were less likely to be employed (65 % vs 45 %, p = 0.040) compared to non-RLS patients. In addition, RLS patients were more likely to have coexisting Major Depressive Disorder (MDD) (p = 0.019), higher levels of pain (p = 0.006) and disease activity based on patient global assessment (p = 0.014). Further, most of the domains of LupusQoL were significantly lower in the RLS patients group suggesting a worse HRQoL.
    CONCLUSIONS: RLS was present in one-third of the SLE cohort, significantly impairing HRQoL and correlating with depression, higher pain, and increased disease activity. These findings underscore the importance of early RLS detection and management in SLE patients.
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  • 文章类型: Journal Article
    背景:建议将omega-3多不饱和脂肪酸补充剂作为诊断为重度抑郁症的成人的辅助治疗。在过去的十年中,与omega-3联合治疗的重复数据的评估已在成人中广泛进行。然而,这些发现在儿科人群中的普适性仍不确定.该评估的目标是双重的:(1)评估omega-3和相关联合疗法在降低抑郁症状严重程度方面的有效性,和(2)包括缓解率(即,抑郁症状减少50%以上)作为治疗功效的量度。方法:我们从成立之初到2023年10月对PubMed/EMBASE进行了文献检索。使用Stata(17.0版)进行数据分析。结果:我们共确定了3168篇文章。在对已确定的研究进行资格筛选后,9项研究(n=561名参与者)被纳入我们的分析.配对比较显示,与安慰剂相比,任何干预措施的抑郁症状都没有显着改善。然而,聚类排序图确定omega-3加肌醇是小儿抑郁症最有效的治疗方法(77.3%的疗效).与安慰剂相比,Omega-3与心理教育心理治疗配对显着降低了缓解率(标准化平均差=0.44,95%置信区间:0.00-0.87,p=0.048),导致91.5%的缓解率,使其成为研究中最有效的治疗方法。结论:综合来看,这项网络荟萃分析提供了令人信服的证据支持omega-3在患有抑郁症的儿科组中的抗抑郁作用.未来的研究应该旨在研究omega-3作为年轻人抑郁症患者的单一疗法,以及调查与心理社会干预措施相比,omega-3对受影响个体的疗效。
    Background: The administration of omega-3 polyunsaturated fatty acid supplements is recommended as an adjuvant therapy for adults diagnosed with major depressive disorder. The evaluation of replicated data in combination treatment with omega-3 has been extensively conducted in adults over the past decade. However, the generalizability of these findings to pediatric groups is still uncertain. The objectives of this evaluation were twofold: (1) to evaluate the effectiveness of omega-3 and associated combination therapies in reducing the severity of depressive symptoms, and (2) to include remission rates (i.e., reduction of more than 50% in depression symptoms) as a measure of therapeutic efficacy. Methods: We conducted a literature search on PubMed/EMBASE from inception to October 2023. Data analyses were conducted using Stata (version 17.0). Results: We identified a total of 3168 articles. After eligibility screening of identified studies, nine studies (n = 561 participants) were included in our analysis herein. Pairwise comparisons revealed no significant improvement in depression symptoms for any intervention versus placebo. However, a clustered ranking plot identified omega-3 plus inositol as the most effective treatment for pediatric depression (77.3% efficacy). Omega-3 paired with psychoeducational psychotherapy significantly lowered the remission rate compared to placebo (standardized mean difference = 0.44, 95% confidence interval: 0.00-0.87, p = 0.048), resulting in a 91.5% remission rate, making it the most effective treatment in the study. Conclusions: Taken together, this network meta-analysis presents compelling evidence supporting the antidepressant effects of omega-3 in pediatric groups with depression. Future research should aim to investigate omega-3 as monotherapy for young individuals with depression, as well as investigate the efficacy of omega-3 in comparison to psychosocial interventions for affected individuals.
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  • 文章类型: Journal Article
    目的:重度抑郁症(MDD)的特征是持续的症状,例如疲劳,对活动失去兴趣,悲伤和毫无价值的感觉。MDD通常与心血管疾病(CVD)共存,然而,这些条件之间的确切联系仍不清楚。这篇综述探讨了MDD和CVD发展的潜在因素,包括遗传,表观遗传,血小板活化,炎症,下丘脑-垂体-肾上腺(HPA)轴激活,内皮细胞(EC)功能障碍,和血脑屏障(BBB)破坏。
    结果:膜相关鸟苷酸激酶WW和含PDZ结构域的蛋白1(MAGI-1)中的单核苷酸多态性(SNP)与神经质和包括MDD的精神疾病相关。MAGI-1中的SNP也与慢性炎症性疾病有关,如自发性肾小球硬化,乳糜泻,溃疡性结肠炎,和克罗恩病。在克罗恩病和溃疡性结肠炎患者的结肠上皮样本中观察到MAGI-1表达增加。MAGI-1还在调节小鼠的EC激活和动脉粥样硬化中起作用,并且对于流感病毒A(IAV)感染至关重要。内质网应激诱导的EC凋亡,和凝血酶诱导的EC通透性。尽管在人类疾病中研究不足,但证据表明MAGI-1可能在连接CVD和MDD中发挥作用。因此,可能需要对MAG-1进行进一步研究,以阐明其在这些疾病中的潜在参与.
    OBJECTIVE: Major Depressive Disorder (MDD) is characterized by persistent symptoms such as fatigue, loss of interest in activities, feelings of sadness and worthlessness. MDD often coexist with cardiovascular disease (CVD), yet the precise link between these conditions remains unclear. This review explores factors underlying the development of MDD and CVD, including genetic, epigenetic, platelet activation, inflammation, hypothalamic-pituitary-adrenal (HPA) axis activation, endothelial cell (EC) dysfunction, and blood-brain barrier (BBB) disruption.
    RESULTS: Single nucleotide polymorphisms (SNPs) in the membrane-associated guanylate kinase WW and PDZ domain-containing protein 1 (MAGI-1) are associated with neuroticism and psychiatric disorders including MDD. SNPs in MAGI-1 are also linked to chronic inflammatory disorders such as spontaneous glomerulosclerosis, celiac disease, ulcerative colitis, and Crohn\'s disease. Increased MAGI-1 expression has been observed in colonic epithelial samples from Crohn\'s disease and ulcerative colitis patients. MAGI-1 also plays a role in regulating EC activation and atherogenesis in mice and is essential for Influenza A virus (IAV) infection, endoplasmic reticulum stress-induced EC apoptosis, and thrombin-induced EC permeability. Despite being understudied in human disease; evidence suggests that MAGI-1 may play a role in linking CVD and MDD. Therefore, further investigation of MAG-1 could be warranted to elucidate its potential involvement in these conditions.
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  • 文章类型: Journal Article
    目的:重度抑郁症(MDD)是一种普遍的精神疾病,沃替西汀由于其独特的药理作用而具有很有希望的抗抑郁作用。然而,沃替西汀治疗MDD的剂量-反应关系尚不明确.我们旨在进行剂量反应荟萃分析以填补这一空白。
    方法:我们系统地检索了多个电子数据库,寻找沃替西汀治疗MDD的随机对照试验,最后一次搜索是在2月8日进行的,2024.使用限制三次样条模型的单阶段随机效应剂量反应荟萃分析评估剂量反应关系。主要结果是疗效(抑郁量表评分的平均变化),次要结果包括反应,因任何原因辍学(可接受性),不良事件(耐受性),和任何不良事件(安全性)。
    结果:剂量反应荟萃分析包括16项研究,将4,294名参与者分配到沃替西汀组,将2,299名参与者分配到安慰剂组.估计50%有效剂量为4.37毫克/天,接近最大有效剂量(95%有效剂量)为17.93mg/天。对剂量-效力曲线的视觉检查表明,在20mg/天可能尚未达到平台。可接受性,耐受性和安全性随着剂量的增加而下降。亚组分析表明,在可接受性方面没有观察到显著差异,各剂量组之间的耐受性和安全性。
    结论:当超过当前许可剂量时,沃替西汀可能会提供额外的治疗益处,而不会显著影响安全性。进行超过当前批准剂量的临床试验似乎有必要充分理解其功效和风险。
    OBJECTIVE: Major depressive disorder (MDD) is a prevalent psychiatric condition and vortioxetine offers promising antidepressant effects due to its unique pharmacological profile. However, the dose-response relationships of vortioxetine for MDD is not well established. We aimed to conduct dose-response meta-analyses to fill this gap.
    METHODS: We systematically searched multiple electronic databases for randomized controlled trials of vortioxetine for MDD, with the last search conducted on 08 February, 2024. The dose-response relationship was evaluated using a one-stage random-effects dose-response meta-analysis with restricted cubic spline model. The primary outcome was efficacy (mean change in depression scale score), with secondary outcomes including response, dropout for any reasons (acceptability), dropout for adverse events (tolerability), and any adverse events (safety).
    RESULTS: The dose-response meta-analysis comprised 16 studies, with 4,294 participants allocated to the vortioxetine group and 2,299 participants allocated to the placebo group. The estimated 50% effective dose was 4.37 mg/day, and the near-maximal effective dose (95% effective dose) was 17.93 mg/day. Visual inspection of the dose-efficacy curve suggests that a plateau possibly had not been reached yet at 20 mg/day. Acceptability, tolerability and safety decreased as the dose increased. Subgroup analysis indicated that no significant differences were observed in acceptability, tolerability and safety among the dosage groups.
    CONCLUSIONS: Vortioxetine may potentially provide additional therapeutic benefits when exceeding the current licensed dosage without significantly impacting safety. Conducting clinical trials exceeding the current approved dosage appears necessary to fully comprehend its efficacy and risk.
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