cognitive disorder

认知障碍
  • 文章类型: Case Reports
    在这个系列中,据报道,在2021年5月至2023年5月期间接受垂直袖状胃切除术(VSG)的3例患者同时发生Wernicke脑病(WE)和干脚气病.所有患者均为肥胖女性,接受垂直袖状胃切除术(VSG),无术后立即并发症。但两周后,在接下来的三十天内观察到呕吐和随后的脑病,并伴有眼球运动异常和无力。病人被转诊到神经科,由于对我们的高度怀疑,开始硫胺素替代疗法;同时,进行了诊断性神经影像学检查和血液检查.进行了神经和精神病学评估以及神经传导研究,以评估临床演变和后遗症。确诊一年后,所有患者都表现出情感和行为后遗症,顺行记忆障碍,和执行功能缺陷。两名患者符合Korsakoff综合征的标准。此外,观察到周围神经系统后遗症,所有患者均表现为感觉运动性多发性神经病。总之,韦尼克脑病需要高度的诊断怀疑,以便及时干预和预防不可逆的后遗症,这可能是毁灭性的。因此,提高医疗专业人员对这种疾病重要性的认识至关重要。
    In this case series, the simultaneous occurrence of Wernicke\'s encephalopathy (WE) and dry beriberi was reported in three patients who underwent vertical sleeve gastrectomy (VSG) between May 2021 and May 2023. All patients were obese women who underwent vertical sleeve gastrectomy (VSG) without immediate postoperative complications, but two weeks later, hyperemesis and subsequent encephalopathy with ocular movement abnormalities and weakness were observed over the following thirty days. Patients were referred to neurology, where due to the high suspicion of WE, thiamine replacement therapy was initiated; meanwhile, diagnostic neuroimaging and blood tests were conducted. Neurological and psychiatric evaluations and neuroconduction studies were performed to assess the clinical evolution and present sequelae. One year after diagnosis, all patients exhibited affective and behavioral sequelae, anterograde memory impairment, and executive functioning deficits. Two patients met the criteria for Korsakoff syndrome. Additionally, peripheral nervous system sequelae were observed, with all patients presenting with sensorimotor polyneuropathy. In conclusion, Wernicke\'s encephalopathy requires a high diagnostic suspicion for timely intervention and prevention of irreversible sequelae, which can be devastating. Therefore, raising awareness among medical professionals regarding the significance of this disease is essential.
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  • 文章类型: Journal Article
    背景:中风患者预先存在的认知障碍的起源仍然存在争议,血管或退化假设。
    目的:为了确定内皮功能障碍是否与先前存在的认知问题有关,中风患者的病变负荷和生物学异常。
    方法:患者起源于前瞻性STROKDEM研究。基线认知状态,使用智商代码评估,纳入时记录卒中的危险因素.排除IQ-CODE评分>64的患者。通过非侵入性数字测量内皮依赖性血流介导的扩张并计算反应性充血指数(RHI),在中风症状发作后72小时确定内皮功能。RHI≤1.67提示内皮功能障碍。在血液或血浆中分析内皮功能障碍的不同生物标志物。所有患者在卒中症状发作72h后行MRI检查。
    结果:共纳入86例患者(男性52例;平均年龄63.5±11.5岁)。RHI异常的患者更经常患有高血压或抗高血压治疗。33例(38.4%)患者的基线IQ-CODE异常,表明预先存在的认知问题。在15例RHI正常的患者(28.3%)和18例RHI异常的患者(54.6%)中观察到基线IQ-CODE>48(p=0.016)。IQ-CODE异常患者的RHI中位数明显较低。异常RHI与中位数较高的FAZEKAS评分相关(2.5vs.2;p=0.008),脑室周围病变的频率明显更高(p=0.015),更多的白质病变(p=0.007)和显着更高的脑萎缩评分(p<0.001)在MRI。与异常RHI显著相关的血管生物标志物是MCP-1(p=0.009),MIP_1a(p=0.042),和同型半胱氨酸血症(p<0.05)。
    结论:血管机制可能是先前存在的卒中认知问题的原因。卒中后内皮功能障碍的测量可能成为随访的重要因素。提供中风患者的功能和认知预后的指示。
    BACKGROUND: The origin of pre-existing cognitive impairment in stroke patients remains controversial, with a vascular or a degenerative hypothesis.
    OBJECTIVE: To determine whether endothelial dysfunction is associated with pre-existing cognitive problems, lesion load and biological anomalies in stroke patients.
    METHODS: Patients originated from the prospective STROKDEM study. The baseline cognitive state, assessed using the IQ-CODE, and risk factors for stroke were recorded at inclusion. Patients with an IQ-CODE score >64 were excluded. Endothelial function was determined 72 h after stroke symptom onset by non-invasive digital measurement of endothelium-dependent flow-mediated dilation and calculation of the reactive hyperemia index (RHI). RHI ≤ 1.67 indicated endothelial dysfunction. Different biomarkers of endothelial dysfunction were analysed in blood or plasma. All patients underwent MRI 72 h after stroke symptom onset.
    RESULTS: A total of 86 patients were included (52 males; mean age 63.5 ± 11.5 years). Patients with abnormal RHI have hypertension or antihypertensive treatment more often. The baseline IQ-CODE was abnormal in 33 (38.4%) patients, indicating a pre-existing cognitive problem. Baseline IQ-CODE > 48 was observed in 15 patients (28.3%) with normal RHI and in 18 patients (54.6%) with abnormal RHI (p = 0.016). The RHI median was significantly lower in patients with abnormal IQ-CODE. Abnormal RHI was associated with a significantly higher median FAZEKAS score (2.5 vs. 2; p = 0.008), a significantly higher frequency of periventricular lesions (p = 0.015), more white matter lesions (p = 0.007) and a significantly higher cerebral atrophy score (p < 0.001) on MRI. Vascular biomarkers significantly associated with abnormal RHI were MCP-1 (p = 0.009), MIP_1a (p = 0.042), and homocysteinemia (p < 0.05).
    CONCLUSIONS: A vascular mechanism may be responsible for cognitive problems pre-existing stroke. The measurement of endothelial dysfunction after stroke could become an important element of follow-up, providing an indication of the functional and cognitive prognosis of stroke patients.
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  • 文章类型: Journal Article
    背景:甲基苯丙胺(METH)是一种高度成瘾的药物,直接影响中枢神经系统。使用METH不仅危害用户的健康,而且给社会带来风险和成本。长时间的METH依赖已被证明会损害认知,这可能是冲动求药行为和高复发率的主要因素。然而,METH成瘾和METH诱导的认知功能下降的分子机制仍然知之甚少。
    方法:为了阐明支持METH成瘾的潜在分子机制,我们使用无标记定量蛋白质组学方法比较了12名长期METH使用者和12名健康对照者的血清蛋白表达水平.进行生物信息学分析以确定功能网络和蛋白质-蛋白质相互作用。
    结果:总计,在两组之间鉴定了23种差异表达的蛋白质。差异表达蛋白与认知功能障碍有关,神经炎症,免疫损伤,代谢紊乱,和钙的结合和调节。
    结论:这23种蛋白可能支持慢性METH暴露引起的多系统损伤。我们的发现为METH成瘾的分子基础提供了新的见解,并为METH依赖的个体提供了潜在的预防和治疗策略。
    BACKGROUND: Methamphetamine (METH) is a highly addictive drug that directly affects the central nervous system. METH use not only harms the user\'s health but also poses risks and costs to society. Prolonged METH dependence has been shown to impair cognition, which may be the primary factor in impulsive drug-seeking behaviors and high relapse rates. However, the molecular mechanisms underlying METH addiction and METH-induced cognitive decline remain poorly understood.
    METHODS: To illuminate the potential molecular mechanisms underpinning METH addiction, we compared serum protein expression levels between 12 long-term METH users and 12 healthy controls using label-free quantitative proteomics. Bioinformatic analyses were conducted to determine functional networks and protein-protein interactions.
    RESULTS: In total, 23 differentially expressed proteins were identified between the two groups. The differentially expressed proteins were related to cognitive dysfunction, neuroinflammation, immune impairment, metabolic disturbances, and calcium binding and regulation.
    CONCLUSIONS: These 23 proteins may underpin the multi-system damage induced by chronic METH exposure. Our findings provide novel insights into the molecular basis of METH addiction and inform potential prevention and treatment strategies for individuals with METH dependence.
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  • 文章类型: Journal Article
    COVID-19大流行严重影响了人类生活,构成严重的身体和心理威胁,尤其是老年人。虽然所有年龄段的人都容易感染COVID-19,但由于与年龄相关的免疫生理变化和先前存在的健康状况,老年人患各种疾病的风险更高。免疫健康和身体活动之间的相互作用被认为在大流行期间具有更大的意义。我们研究的最新发现表明,方步运动(SSE)的干预,其特征是有节奏和受控的步进模式,导致老年人脑源性神经营养因子(BDNF)水平升高。BDNF,已知不仅影响神经细胞,还影响免疫细胞,表明SSE和免疫系统调节之间存在潜在的联系。因此,这种锻炼方案有望抵消与年龄相关的免疫生理变化,微调免疫反应,减轻潜在新病毒结果的严重程度,例如“疾病X”。这篇综述旨在强调将SSE整合为基于家庭的计划的重要性,作为增强免疫韧性的有力工具,为未来潜在的流行病做好准备,并在充满挑战的时期赋予老年人权力。通过上交所的实践,老年人可能会加强他们应对大流行带来的挑战的能力,并保持对自己福祉的控制感。
    The COVID-19 pandemic has significantly impacted human life, posing serious physical and psychological threats, particularly to the elderly. While individuals of all ages are susceptible to contracting COVID-19, older people face a heightened risk of developing various diseases due to age-related immunophysiological changes and preexisting health conditions. The interplay between immune health and physical activity is believed to hold even greater significance during a pandemic. Recent findings from our research indicate that the intervention of square stepping exercise (SSE), characterized by a rhythmic and controlled stepping pattern, resulted in increased levels of Brain-Derived Neurotrophic Factor (BDNF) in the elderly. BDNF, known to influence not only nerve cells but also immune cells, suggests a potential link between SSE and immune system modulation. Consequently, this exercise regimen holds promise in counteracting age-related immunophysiological changes, fine-tuning immune responses, and mitigating the severity of potential new virus outcomes, such as \'Disease X.\' This review aims to underscore the significance of integrating SSE as a home-based program, serving as a potent tool to enhance immune resilience, prepare for future potential pandemics, and empower older individuals during challenging times. Through the practice of SSE, older adults may strengthen their ability to navigate the challenges posed by pandemics and maintain a sense of control over their well-being.
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  • 文章类型: Journal Article
    在目前的工作中,从霍山石斛中鉴定出一种具有减轻认知障碍的中性多糖(DHP-2W),并阐明了其结构。通过柱色谱法成功地从霍山D中纯化了多糖,并对其活性进行了评估。分子量为508.934kDa,该多糖由甘露糖和葡萄糖以75.81:24.19的摩尔比组成。结构表征揭示DHP-2W具有由4)-β-D-Manp-(1和4)-β-D-Glcp-(1。体内实验表明,DHP-2W改善了D-半乳糖治疗小鼠的认知障碍,缓解了氧化应激和炎症。DHP-2W通过抑制Bcl2/Bax/Caspase3通路和激活AMPK/SIRT通路减轻D-半乳糖诱导的认知障碍,从而抑制细胞凋亡。此外,DHP-2W对血清中黄嘌呤腺嘌呤二核苷酸水平有明显的调节作用,莽草酸,老年小鼠的犬尿烯酸。这些,反过来,对AMPK/SIRT1和Bcl2/Bax/Caspase3产生积极影响,从而对认知障碍产生保护作用。
    In the present work, a neutral polysaccharide (DHP-2W) with attenuating cognitive disorder was identified from Dendrobium huoshanense and its structure was clarified. The polysaccharide was successfully purified from D. huoshanense by column chromatography and its activity was evaluated. With a molecular weight of 508.934kDa, this polysaccharide is composed of mannose and glucose at a molar ratio of 75.81: 24.19. Structural characterization revealed that DHP-2W has a backbone consisting of 4)-β-D-Manp-(1 and 4)-β-D-Glcp-(1. In vivo experiments revealed that DHP-2W improved cognitive disorder in D-galactose treated mice and relieved oxidative stress and inflammation. DHP-2W attenuates D-galactose-induced cognitive disorder by inhibiting the BCL2/BAX/CASP3 pathway and activating the AMPK/SIRT pathway, thereby inhibiting apoptosis. Furthermore, DHP-2W had a significant effect on regulating the serum levels of Flavin adenine dinucleotide, Shikimic acid, and Kynurenic acid in aged mice. These, in turn, had a positive impact on AMPK/SIRT1 and BCL2/BAX/CASP3, resulting in protective effects against cognitive disorder.
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  • 文章类型: Journal Article
    背景:以前的研究已经研究了认知功能和生活方式之间的关系;然而,这种关系的性质预计在不同的文化和低收入环境中会有所不同,因为生活方式不同于高收入国家。
    目的:本研究旨在调查2021年60岁及以上人群的生活方式因素与认知功能之间的相关性。
    方法:这个横截面,基于社区的研究涉及来自霍拉马巴德综合城市卫生中心的300名老年人,伊朗,通过分层整群抽样选择。使用人口统计信息问卷收集数据,迷你精神状态检查,和生活方式问卷。数据管理和分析采用SPSS(22版)和独立t检验,皮尔逊相关系数,方差分析,采用多元线性回归分析。P值<0.05被认为是显著的。
    结果:该研究包括156名男性(52%)和144名女性(48%)。研究发现认知功能与生活方式之间存在显著相关性(P<0.001)。多元线性回归分析表明,身体健康,环境卫生,锻炼,事故预防,避免用药对认知功能的积极作用最为显著。相反,社会健康对认知功能有显著的负面影响。(P<0.001)。
    结论:结果表明,生活方式的特定方面,比如身体健康,事故预防,避免用药与老年人的认知功能有关。因此,生活方式促进计划可以增强老年人的认知功能并改善其生活质量.
    BACKGROUND: Previous studies have examined relationship between cognitive function and lifestyle; however, the nature of this relationship is expected to vary in diverse cultural and low-income setting where lifestyle practices differ from those in high-income countries.
    OBJECTIVE: This study aims to investigate the correlation between lifestyle factors and cognitive function among individuals aged 60 years and older in 2021.
    METHODS: This cross-sectional, Community-based study involved 300 older adults from comprehensive urban health centers in Khorramabad, Iran, selected through stratified cluster sampling. Data were collected using the demographic information questionnaire, Mini-Mental State Examination, and Lifestyle Questionnaire. Data management and analysis were performed using SPSS (version 22) and independent t-tests, Pearson\'s correlation coefficient, ANOVA, and multiple linear regression analysis were used. A p value < 0.05 was considered significant.
    RESULTS: The study included 156 males (52%) and 144 females (48%). Findings revealed a significant correlation between cognitive function and lifestyle (P < 0.001). Multiple linear regression analysis indicated that physical health, environmental health, exercise, accident prevention, and avoidance of medication exerted the most significant positive effect on cognitive function. Conversely, social health exhibited a notable negative influence on cognitive function. (P < 0.001).
    CONCLUSIONS: The results suggest that specific aspects of lifestyle, such as physical health, accident prevention, and avoidance of medication are associated with cognitive function in older adults. Consequently, lifestyle promotion programs may enhance cognitive function and improve the quality of life among older adults.
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  • 文章类型: Journal Article
    这项研究的目的是评估早期认知训练对增强中风患者认知功能的功效。本研究采用准实验设计,45例患者分为两组,并采用序贯抽样。实验组(n=22)每周接受6次为期两周的早期认知训练,而对照组(n=23)接受常规医院护理。蒙特利尔认知评估的印尼版本用于评估认知功能(MoCA-Ina)。在治疗的第二天,取得了测试前的数据,并在干预后收集试验后数据.统计检验结果MoCA-Ina评分在干预组和对照组之间有相当大的变化(分别为p=0.000和p=0.003)。几项测试确定得分为p=0.017;干预后的得分在两组之间有很大差异。这意味着在急性期运动后认知功能得到改善。
    The purpose of this study was to assess the efficacy of early cognitive training in enhancement of cognitive function in stroke patients. This research used a quasi-experimental design, 45 patients were divided into two groups, and sequential sampling was employed. The experimental group (n = 22) received two weeks of early cognitive training six times per week, whereas the control group (n = 23) received regular hospital care. The Indonesian version of the Montreal Cognitive Assessment was used to evaluate cognitive function (MoCA-Ina). On the second day of therapy, pre-test data were taken, and post-test data were gathered after the intervention. Statistical test outcomes The MoCA-Ina score changed considerably between the intervention and control groups (p = 0.000 and p = 0.003, respectively). Several tests determined that the score was p = 0.017; the score after the intervention was substantially different between the two groups. It means cognitive function improves after exercise in the acute phase.
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  • 文章类型: Journal Article
    在啮齿动物模型中,D-半乳糖(D-gal)给药被证明可诱导认知障碍和衰老。香叶醇(GNL)属于无环类异戊二烯单萜。GNL通过改变重要的信号通路和细胞因子来减少炎症,因此,它似乎可以用作治疗与炎症相关的疾病的药物。在这里,我们研究了GNL对D-gal诱导的小鼠氧化应激和神经炎症介导的记忆丧失的治疗作用.使用六组小鼠(每组6只小鼠)进行研究。第一组接受生理盐水,然后将D-gal(150mg/wt)溶解在生理盐水溶液中(0.9%,w/v)给予第二组口服9周。在第三组中,从第二周到第十周,小鼠口服(无麻醉)D-gal(150mg/kg体重)治疗,4小时后,GNL每周治疗两次(40mg/kg体重)。从第二周起直到实验结束,用GNL处理组IV中的小鼠。为了比较年轻和老年小鼠,使用4月龄(组V)和16月龄(组VI)对照小鼠。我们评估了抗氧化剂水平的变化,PI3K/Akt水平,和Nrf2级别。我们还检查了D-gal和GNL如何治疗病理性衰老变化。GNL的管理诱导了空间学习和记忆的显着增加,并自发地改变了行为。增强抗氧化和抗炎作用以及激活PI3K/Akt是介导这种作用的机制。Further,GNL处理上调Nrf2和HO-1以减少氧化应激和细胞凋亡。使用99mTc-HMPAO脑流量γ生物测定法证实了这一点。因此,我们的数据表明GNL是治疗神经炎症诱导的认知障碍的有前景的药物.
    D-galactose (D-gal) administration was proven to induce cognitive impairment and aging in rodents\' models. Geraniol (GNL) belongs to the acyclic isoprenoid monoterpenes. GNL reduces inflammation by changing important signaling pathways and cytokines, and thus it is plausible to be used as a medicine for treating disorders linked to inflammation. Herein, we examined the therapeutic effects of GNL on D-gal-induced oxidative stress and neuroinflammation-mediated memory loss in mice. The study was conducted using six groups of mice (6 mice per group). The first group received normal saline, then D-gal (150 mg/wt) dissolved in normal saline solution (0.9%, w/v) was given orally for 9 weeks to the second group. In the III group, from the second week until the 10th week, mice were treated orally (without anesthesia) with D-gal (150 mg/kg body wt) and GNL weekly twice (40 mg/kg body wt) four hours later. Mice in Group IV were treated with GNL from the second week up until the end of the experiment. For comparison of young versus elderly mice, 4 month old (Group V) and 16-month-old (Group VI) control mice were used. We evaluated the changes in antioxidant levels, PI3K/Akt levels, and Nrf2 levels. We also examined how D-gal and GNL treated pathological aging changes. Administration of GNL induced a significant increase in spatial learning and memory with spontaneously altered behavior. Enhancing anti-oxidant and anti-inflammatory effects and activating PI3K/Akt were the mechanisms that mediated this effect. Further, GNL treatment upregulated Nrf2 and HO-1 to reduce oxidative stress and apoptosis. This was confirmed using 99mTc-HMPAO brain flow gamma bioassays. Thus, our data suggested GNL as a promising agent for treating neuroinflammation-induced cognitive impairment.
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  • 文章类型: Systematic Review
    脆弱是全球范围内的重大医疗保健挑战,对开发更多针对脆弱的评估工具的兴趣日益增加。最近,人们越来越意识到社会变量与老年人的虚弱之间存在相关性。然而,对虚弱的社会领域和相关的不良后果缺乏了解,特别是在亚太地区。这项研究旨在通过概述亚太地区老年人的脆弱筛查工具来表征社会脆弱领域及其健康结果。
    系统评价,使用PRISMA指南,是在2002年至2023年之间发表的来自三个电子数据库的文章上进行的:PubMed,Scopus,和科学直接。使用GoogleScholar对所包含文章的参考文献进行了手动搜索。收录的文章必须是英文的,并且基于在同行评审期刊上发表的经验证据,并着重于评估亚太地区60岁或以上老年人的社会脆弱领域(东亚,东南亚,和大洋洲)。
    共有31项研究被纳入主题分析,其中回顾了16种测量6个社会领域的筛查工具。这六个领域是:社交网络,其次是社会活动,社会支持,财政困难,社会角色,社会经济,分为四类:社会资源,社会需要,社会行为(或社会活动),和一般资源。六个社会领域预测死亡率,身体上的困难,和残疾发生率。其他不良健康结果也与这些社会领域有关,包括认知障碍,精神疾病,和营养障碍(每个n=5个领域),痴呆(n=4域),和口腔脆弱,听力损失,肥胖,和慢性疼痛(每个n=3个结构域)。
    总的来说,社会脆弱是一个具有多个维度的复杂结构,包括社会和一般资源的脆弱,社会行为,和社会需求,导致几种健康障碍。这些发现有助于理解老年人社会脆弱的概念框架及其相关的健康结果。因此,它可以促进专业人员和研究人员监测和减少与社会脆弱的每个领域相关的不良健康结果的风险,有助于更好的衰老过程。
    UNASSIGNED: Frailty is a significant healthcare challenge worldwide, increasing interest in developing more assessment tools covering for frailty. Recently, there has been a growing awareness of a correlation between social variables and frailty in older people. However, there is a lack of understanding of the social domains of frailty and the related adverse outcomes, particularly in the Asia-Pacific settings. This study aimed to characterize the social frailty domains and their health outcomes by overviewing the frailty screening tools in older people living in the Asia-Pacific region.
    UNASSIGNED: A systematic review, using the PRISMA guideline, was conducted on articles published between 2002 and 2023 from three electronic databases: PubMed, Scopus, and ScienceDirect. A manual search was conducted for the references of the included articles using Google Scholar. Included articles must be in English and were based on empirical evidence published in peer-reviewed journals and focus on the assessment of domains of social frailty in older people aged 60 or over in the Asia-Pacific (East Asia, Southeast Asia, and Oceania).
    UNASSIGNED: A total of 31 studies were included in the thematic analysis, from which 16 screening tools measuring six social domains were reviewed. The six domains were: social networks, followed by social activities, social support, financial difficulties, social roles, and socioeconomic, arranged in four categories: social resources, social needs, social behaviors (or social activities), and general resources. The six social domains predicted mortality, physical difficulties, and disability incidence. Other adverse health outcomes were also associated with these social domains, including cognitive disorders, mental illness, and nutritional disorders (n = 5 domains each), dementia (n = 4 domains), and oral frailty, hearing loss, obesity, and chronic pain (n = 3 domains each).
    UNASSIGNED: Overall, social frailty is a complex construct with multiple dimensions, including the frailty of social and general resources, social behaviors, and social needs, leading to several health disorders. The findings contribute to understanding the conceptual framework of social frailty in older people and its related health outcomes. Therefore, it could facilitate professionals and researchers to monitor and reduce the risks of adverse health outcomes related to each domain of social frailty, contributing to a better aging process.
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  • 文章类型: Journal Article
    高血糖与更糟糕的卒中结局相关,但尚不确定急性卒中期间严格的血糖控制是否与更好的结局相关.我们进行了一项荟萃分析,以比较中风患者急性期严格血糖控制与宽松血糖控制的效果。
    进行了文献检索,以确定比较急性卒中(缺血性或出血性)患者在卒中发病后24小时内严格血糖控制与相对宽松血糖控制的安全性和有效性的随机对照试验。我们要求患者入组时的血糖水平不低于6.11mmol/L,对于强化血糖控制范围,我们定义的血糖水平低于对照组。主要疗效结局指标是90天时任何原因导致的死亡。次要疗效结果包括具有改良Rankin评分(mRS)的参与者人数。我们将mRS得分0-2定义为有利得分,复发性中风,和美国国立卫生研究院卒中量表或欧洲卒中量表评分。我们将低血糖参与者的数量定义为我们的主要安全结果。根据年龄进行亚组分析,各种各样的干预措施,维持葡萄糖水平,美国国立卫生研究院卒中量表(NIHSS)评分或欧洲卒中量表(ESS)评分的低血糖状态。
    确定了15项随机对照试验(RCT),其中2957名参与者符合纳入标准,并将其纳入本荟萃分析。尽管并非全部包括每个结局指标的数据。主要疗效终点数据,90天死亡率,在11个随机对照试验中可用,共2575人。干预组和对照组之间没有显着差异(比值比(OR):1.00;95%置信区间(CI):0.81-1.23;P=0.99)。对于次要端点,干预组和对照组的mRS从0到2没有差异(OR:0.96;95%CI:0.80-1.15;P=0.69;数据来自9个RCT),或复发性卒中(OR:1.34;95%CI:0.92-1.96;P=0.13;数据来自3个RCT)。对于NIHSS分数或ESS分数,强化对照的差异较小(标准化平均差:-0.29;95%CI:-0.54~-0.04;P=0.02).在严格控制的情况下,低血糖明显增加:(OR为9.46(95%CI:4.59-19.50;P<0.00001;数据来自9项RCT)。
    严格和宽松的血糖控制对死亡率没有差异,独立性,或急性中风的复发性中风结果,而是低血糖的增加.对神经尺度有轻微的改善,但这一相关性需要在未来足够有力的研究中得到证实.
    UNASSIGNED: Hyperglycemia is associated with worse stroke outcomes, but it is uncertain whether tight glycemic control during the acute stroke period is associated with a better outcome. We conducted a meta-analysis to compare the effect of tight glycemic control versus loose glycemic control in the acute phase of stroke patients.
    UNASSIGNED: A literature search was performed to identify randomized controlled trials comparing the safety and efficacy of tight glycemic control with a relatively loose control of blood glucose of acute stroke (ischemic or hemorrhagic) patients within 24 h after stroke onset. We required that the blood glucose level of the patients should not be lower than 6.11 mmol/L at the time of enrollment, and for the intensive blood glucose control range, we defined the blood glucose level as lower than that of the control group. The primary efficacy outcome measure was deaths from any cause at 90 days. Secondary efficacy outcomes comprised the number of participants with modified Rankin score (mRS). We define mRS scores 0-2 as favorable scores, recurrent stroke, and the National Institute of Health Stroke Scale or the European Stroke Scale scores. We defined the number of participants with hypoglycemia as our primary safety outcome. Subgroup analysis was performed according to age, the variety of interventions, maintained glucose level, and status of hypoglycemia on National Institute of Health Stroke Scale (NIHSS) scores or European Stroke Scale (ESS) scores.
    UNASSIGNED: Fifteen randomized controlled trials (RCTs) with 2957 participants meeting the including criteria were identified and included in this meta-analysis, although not all included data on every outcome measure. Data on the primary efficacy endpoint, mortality at 90 days, was available in 11 RCTs, a total of 2575 participants. There was no significant difference between the intervention and control groups (odds ratio (OR): 1.00; 95% confidence interval (CI): 0.81-1.23; P = 0.99). For secondary endpoints, there was no difference between intervention and control groups for a mRS from 0 to 2 (OR: 0.96; 95% CI: 0.80-1.15; P = 0.69; data from 9 RCTs available), or recurrent stroke (OR: 1.34; 95% CI: 0.92-1.96; P = 0.13; data from 3 RCTs available). For NIHSS scores or ESS scores, there was a small difference in favor of intensive controls (standardized mean difference: -0.29; 95% CI: -0.54 to -0.04; P = 0.02). There was a marked increase in hypoglycemia with tight control: (OR of 9.46 (95% CI: 4.59-19.50; P < 0.00001; data from 9 RCTs available).
    UNASSIGNED: There was no difference between tight and loose glycemic control on mortality, independence, or recurrent stroke outcome in acute stroke, but an increase in hypoglycemia. There was a small effect improvement on neurological scales, but the relevance of this needs to be confirmed in future adequately powered studies.
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