remission

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  • 文章类型: Journal Article
    本研究的目的是评估与暂时性抽动障碍(PTD)儿童预后相关的因素。我们进行了一项前瞻性队列研究,纳入了PTD患儿,随后在入组后1年内间隔三个月进行随访。共有259名PTD患者被纳入最终分析。在随访期结束时,77(30%)的患者已实现临床缓解。LASSOlogistic回归分析结果显示病程>3个月(OR=4.20,95%CI1.20-14.73),中度/重度抽动严重程度(OR=5.57,95%CI2.26-13.76),和合并症行为问题(OR=2.78,95%CI1.15-6.69)是与PTD患者缓解相关的重要因素。路径分析模型显示,共病行为问题和复发部分介导了抽搐严重程度和缓解之间的关联,具有37%的中介效应。结论:我们已经确定了与PTD儿童预后相关的几个重要因素,包括合并症行为问题和复发,被发现是重要的调解人。这些发现为PTD患者的临床管理提供了新的见解。
    The purpose of the present study was to estimate the factors linked to the prognosis of children with provisional tic disorder (PTD). We conducted a prospective cohort study enrolled children with PTD who were subsequently followed-up at three-month intervals for 1 year post-enrolment. A total of 259 PTD patients were included in the final analysis. At the end of the follow-up period, 77 (30%) of the patients had achieved clinical remission. Result of the LASSO logistic regression analysis revealed that a disease duration >3 months (OR=4.20, 95% CI 1.20-14.73), moderate/severe tic severity (OR=5.57, 95% CI 2.26-13.76), and comorbid behavioral problems (OR=2.78, 95% CI 1.15-6.69) were significant factors linked to remission in the PTD patients. The path analysis model showed that comorbid behavioral problems and recurrence partially mediated the association between tic severity and remission, with a mediating effect of 37%. Conclusions: We have identified several significant factors linked to prognosis in children with PTD, including comorbid behavioral problems and recurrence, which were found to be important mediators. These findings provide new insights for the clinical management of patients with PTD.
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  • 文章类型: Journal Article
    通过将健康教练整合到海上医疗诊所,我们可以为有患糖尿病风险的个人提供量身定制的支持,并使他们能够控制自己的健康。
    By integrating health coaching into maritime medical clinics, we can provide tailored support to individuals at risk of developing diabetes and empower them to take control of their health.
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  • 文章类型: Journal Article
    2型糖尿病(T2D)大流行的主要原因是慢性正能量平衡导致的肥胖过度和/或异常积累。任何形式的减肥都会极大地影响T2D的自然史,有利于预防,治疗,甚至在体重减轻的情况下缓解。然而,体重恢复,常伴有肥胖并发症如T2D的复发或恶化,是一种不可避免的生物学现象,是肥胖病理生理学的一个组成部分。这不仅可以在体重减轻之后发生,但在肥胖治疗期间,如果它不足以有效抵消旨在将肥胖恢复到体重减轻前的平衡状态的生理反应。在过去的几年里,许多对照和随机研究表明,减肥手术在减肥方面优于常规治疗,血糖控制,和T2D缓解率。最近,糖尿病学领域的治疗设备已经丰富了新的抗高血糖药物,在减轻体重方面具有相当大的功效,这可能在T2D的缓解中起致病作用,不是通过经典的肠促胰岛素效应,而是通过改善脂肪组织功能。所有这些概念都在这个立场声明中讨论,旨在加深肥胖和T2D之间的致病联系,从胰岛素抵抗和胰岛素缺乏之间的“简单”相互作用转变范式,并评估不同治疗干预措施的有效性,以改善T2D管理并在可能的情况下诱导糖尿病缓解。
    The primary cause of the pandemic scale of type 2 diabetes (T2D) is the excessive and/or abnormal accumulation of adiposity resulting from a chronic positive energy balance. Any form of weight loss dramatically affects the natural history of T2D, favoring prevention, treatment, and even remission in the case of significant weight loss. However, weight regain, which is often accompanied by the recurrence or worsening of obesity complications such as T2D, is an inevitable biological phenomenon that is an integral part of the pathophysiology of obesity. This can occur not only after weight loss, but also during obesity treatment if it is not effective enough to counteract the physiological responses aimed at restoring adiposity to its pre-weight-loss equilibrium state. Over the past few years, many controlled and randomized studies have suggested a superior efficacy of bariatric surgery compared to conventional therapy in terms of weight loss, glycemic control, and rates of T2D remission. Recently, the therapeutic armamentarium in the field of diabetology has been enriched with new antihyperglycemic drugs with considerable efficacy in reducing body weight, which could play a pathogenetic role in the remission of T2D, not through the classical incretin effect, but by improving adipose tissue functions. All these concepts are discussed in this position statement, which aims to deepen the pathogenetic links between obesity and T2D, shift the paradigm from a \"simple\" interaction between insulin resistance and insulin deficiency, and evaluate the efficacy of different therapeutic interventions to improve T2D management and induce diabetes remission whenever still possible.
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  • 文章类型: Journal Article
    免疫性血小板减少症(ITP)是由免疫介导的血小板破坏和血小板生成减少引起的自身免疫性出血性疾病。ITP的特征是孤立的血小板减少症(<100×109/L)和出血风险增加。该疾病具有复杂的病理生理学,其中免疫耐受性破坏导致血小板和巨核细胞破坏。治疗如皮质类固醇,静脉注射免疫球蛋白(IVIg),利妥昔单抗,和血小板生成素受体激动剂(TPO-RA)旨在增加血小板计数以防止出血并提高生活质量。TPO-RA通过刺激巨核细胞上的TPO受体来直接刺激血小板产生。Romiplostim是一种TPO-RA,已成为ITP治疗的中流砥柱。治疗显著增加巨核细胞成熟和生长,导致改善的血小板产生,并且最近已显示其在治疗的患者中具有额外的免疫调节作用。这篇综述将强调ITP的复杂病理生理学,并讨论Romiplostim在ITP中的用途及其潜在免疫调节自身免疫的能力。
    Immune thrombocytopenia (ITP) is an autoimmune bleeding disease caused by immune-mediated platelet destruction and decreased platelet production. ITP is characterized by an isolated thrombocytopenia (<100 × 109/L) and increased risk of bleeding. The disease has a complex pathophysiology wherein immune tolerance breakdown leads to platelet and megakaryocyte destruction. Therapeutics such as corticosteroids, intravenous immunoglobulins (IVIg), rituximab, and thrombopoietin receptor agonists (TPO-RAs) aim to increase platelet counts to prevent hemorrhage and increase quality of life. TPO-RAs act via stimulation of TPO receptors on megakaryocytes to directly stimulate platelet production. Romiplostim is a TPO-RA that has become a mainstay in the treatment of ITP. Treatment significantly increases megakaryocyte maturation and growth leading to improved platelet production and it has recently been shown to have additional immunomodulatory effects in treated patients. This review will highlight the complex pathophysiology of ITP and discuss the usage of Romiplostim in ITP and its ability to potentially immunomodulate autoimmunity.
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  • 文章类型: Journal Article
    先前的研究表明,克罗恩病(CD)患者的健康一级亲属(HFDRs)的肠道微生物与CD的发展之间没有相关性。这里,我们利用HFDRs作为对照来检查活跃(CD-A)和静止(CD-R)CD个体的微生物群和代谢组,从而最大限度地减少遗传和环境因素的影响。与非相对对照相比,使用HFDR对照可以识别出更少的差异分类单元。粪杆菌,Dorea,CD-R中镰刀菌减少,独立于炎症,并与粪便短链脂肪酸(SCFA)相关。使用大型多中心队列进行的验证证实了CD-R中粪杆菌和其他产生SCFA的属的减少。基于这些属的分类模型将CD与健康个体区分开,并显示出比使用无关对照鉴定的标记构建的模型更高的诊断能力。此外,这些标记对其他疾病的辨别能力有限.最后,我们的结果在多个队列中得到验证,强调它们的稳健性和诊断和治疗应用的潜力。
    Prior studies indicate no correlation between the gut microbes of healthy first-degree relatives (HFDRs) of patients with Crohn\'s disease (CD) and the development of CD. Here, we utilize HFDRs as controls to examine the microbiota and metabolome in individuals with active (CD-A) and quiescent (CD-R) CD, thereby minimizing the influence of genetic and environmental factors. When compared to non-relative controls, the use of HFDR controls identifies fewer differential taxa. Faecalibacterium, Dorea, and Fusicatenibacter are decreased in CD-R, independent of inflammation, and correlated with fecal short-chain fatty acids (SCFAs). Validation with a large multi-center cohort confirms decreased Faecalibacterium and other SCFA-producing genera in CD-R. Classification models based on these genera distinguish CD from healthy individuals and demonstrate superior diagnostic power than models constructed with markers identified using unrelated controls. Furthermore, these markers exhibited limited discriminatory capabilities for other diseases. Finally, our results are validated across multiple cohorts, underscoring their robustness and potential for diagnostic and therapeutic applications.
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  • 文章类型: Journal Article
    目的:探讨垂体手术对肢端肥大症患者糖代谢的影响及垂体手术后糖尿病缓解的预测因素。
    方法:对西班牙33家三级医院首次接受经蝶手术的肢端肥大症患者进行了一项国家多中心回顾性研究(ACRO-SPAIN研究)。根据2000年和2010年标准评估肢端肥大症的手术缓解。
    结果:共604例肢端肥大症患者纳入研究,总的中位随访时间为91个月(四分位距[IQR]45-163)。在肢端肥大症诊断时,23.8%的患者患有糖尿病(DM),糖化血红蛋白(HbA1c)中位数为6.9%(IQR6.4-7.9)[51.9mmol/mol(IQR46.4-62.8)]。在多变量分析中,年龄较大(比值比[OR]1.02,95%CI1.00-1.05),血脂异常(OR5.25,95%CI2.81至9.79),关节病(OR1.39,95%CI2.82至9.79),和较高的IGF-I水平(OR1.30,95%CI1.05至1.60)与更高的DM患病率相关。在手术后的最后一次随访中,21.1%的DM患者(其中56.7%的肢端肥大症手术缓解)经历了糖尿病缓解。糖尿病的治愈率在老年患者中更为常见(风险比[HR]1.77,95%CI1.31~2.43),当达到手术治愈时(HR2.10,95%CI1.01~4.37),当手术后垂体前叶功能未受影响时(HR3.38,95%CI1.17~9.75).
    结论:肢端肥大症患者术后血糖代谢得到改善,21%的糖尿病患者糖尿病缓解;年龄较大的患者更常见,以及那些经历了手术治愈的人和那些在手术后保留了垂体前叶功能的人。
    OBJECTIVE: To investigate the impact of pituitary surgery on glucose metabolism and to identify predictors of remission of diabetes after pituitary surgery in patients with acromegaly.
    METHODS: A national multicenter retrospective study of patients with acromegaly undergoing transsphenoidal surgery for the first time at 33 tertiary Spanish hospitals (ACRO-SPAIN study) was performed. Surgical remission of acromegaly was evaluated according to the 2000 and 2010 criteria.
    RESULTS: A total of 604 acromegaly patients were included in the study with a total median follow up of 91 months (interquartile range [IQR] 45-163). At the acromegaly diagnosis, 23.8% of the patients had diabetes mellitus (DM) with a median glycated hemoglobin (HbA1c) of 6.9% (IQR 6.4-7.9) [51.9 mmol/mol (IQR 46.4-62.8)]. In the multivariate analysis, older age (odds ratio [OR] 1.02, 95% CI 1.00-1.05), dyslipidemia (OR 5.25, 95% CI 2.81 to 9.79), arthropathy (OR 1.39, 95% CI 2.82 to 9.79), and higher IGF-I levels (OR 1.30, 95% CI 1.05 to 1.60) were associated with a greater prevalence of DM. At the last follow-up visit after surgery, 21.1% of the DM patients (56.7% of them with surgical remission of acromegaly) experienced diabetes remission. The cure rate of DM was more common in older patients (hazard ratio [HR] 1.77, 95% CI 1.31 to 2.43), when surgical cure was achieved (HR 2.10, 95% CI 1.01 to 4.37) and when anterior pituitary function was not affected after surgery (HR 3.38, 95% CI 1.17 to 9.75).
    CONCLUSIONS: Glucose metabolism improved in patients with acromegaly after surgery and 21% of the diabetic patients experienced diabetes remission; being more frequent in patients of older age, and those who experienced surgical cure and those with preserved anterior pituitary function after surgery.
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  • 文章类型: Journal Article
    哮喘研究和管理需要满足最终用户-患者的优先事项,护理人员和临床医生。对哮喘的自然史和疾病进展的更好理解强调了早期识别哮喘患者的重要性以及早期干预的潜在作用。轻度哮喘的管理需要一致的方法,在管理严重疾病时使用相同的细节和考虑。围绕可治疗特征方法的证据继续发展,支持个性化医疗在哮喘中的作用。口服皮质类固醇(OCS)管理仍然是哮喘管理中的紧迫问题。减少OCS剂量的策略和实施生物疗法以节省类固醇的益处将是解决此问题的重要步骤。哮喘缓解的概念提供了一个雄心勃勃的目标和治疗结果。
    Asthma research and management needs to meet the priorities of the end user-patients, carers and clinicians. A better understanding of the natural history of asthma and the progression of disease has highlighted the importance of early identification of patients with asthma and the potential role of early intervention. Management of mild asthma requires a consistent approach with the same detail and consideration used when managing severe disease. Evidence around treatable traits approaches continues to evolve, supporting the role of a personalized medicine in asthma. Oral corticosteroid (OCS) stewardship continues to be an urgent issue in asthma management. Strategies to taper OCS doses and the implementation of biologic therapies for their steroid sparing benefits will be important steps to address this problem. The concept of remission in asthma provides an ambitious target and treatment outcome.
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  • 文章类型: Journal Article
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  • 文章类型: Editorial
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  • 文章类型: Journal Article
    背景:尽管抗逆转录病毒疗法(ART)有效地阻止了HIV感染的疾病进展,彻底根除这种病毒仍然遥不可及。此外,诸如长期ART毒性等挑战,耐药性,ART所需的每日和终身依从性的苛刻方案凸显了对替代治疗和预防方法的迫切需要。近年来,广泛中和抗体(bNAb)已经成为有希望的候选物,提供治疗潜力,预防性,以及可能针对艾滋病毒感染的治愈性干预措施。
    目的:本综述旨在全面概述HIV-1感染者中bNAb被动免疫的相关知识现状。
    结果:临床试验的最新发现强调了bNAb在治疗中的潜力,预防,寻求HIV-1的治疗方法.虽然单一bNAb的单一疗法不足以维持病毒抑制和防止病毒逃逸,最终导致病毒反弹,联合治疗与强效,通过有效限制逃逸突变的出现,非重叠表位靶向bNAb已证明延长的病毒抑制和延迟的反弹时间。尽管主要在具有bNAb敏感菌株的个体中。此外,BNAb的被动免疫为抗体介导的预防HIV-1感染提供了“概念证明”,虽然还没有完全预防。因此,在HIV-1治疗和预防中使用bNAb的进一步研究仍势在必行.
    BACKGROUND: Although antiretroviral therapy (ART) effectively halts disease progression in HIV infection, the complete eradication of the virus remains elusive. Additionally, challenges such as long-term ART toxicity, drug resistance, and the demanding regimen of daily and lifelong adherence required by ART highlight the imperative need for alternative therapeutic and preventative approaches. In recent years, broadly neutralizing antibodies (bNAbs) have emerged as promising candidates, offering potential for therapeutic, preventative, and possibly curative interventions against HIV infection.
    OBJECTIVE: This review aims to provide a comprehensive overview of the current state of knowledge regarding the passive immunization of bNAbs in HIV-1-infected individuals.
    RESULTS: Recent findings from clinical trials have highlighted the potential of bNAbs in the treatment, prevention, and quest for an HIV-1 cure. While monotherapy with a single bNAb is insufficient in maintaining viral suppression and preventing viral escape, ultimately leading to viral rebound, combination therapy with potent, non-overlapping epitope-targeting bNAbs have demonstrated prolonged viral suppression and delayed time to rebound by effectively restricting the emergence of escape mutations, albeit largely in individuals with bNAb-sensitive strains. Additionally, passive immunization with bNAb has provided a \"proof of concept\" for antibody-mediated prevention against HIV-1 acquisition, although complete prevention has not been obtained. Therefore, further research on the use of bNAbs in HIV-1 treatment and prevention remains imperative.
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