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Update in diagnosis and management of irritable bowel syndrome 肠易激综合征诊断和治疗的最新进展
Q2 MEDICINE, GENERAL & INTERNAL Pub Date : 2023-01-01 DOI: 10.4103/tcmj.tcmj_104_23
Tsung-Hsing Hung, Chih-Ying Wang, Hsing-Feng Lee
A BSTRACT Irritable bowel syndrome (IBS) is a functional gastrointestinal disorder characterized by a lack of structural or biochemical abnormalities. The current diagnosis of IBS is based on the Rome IV criteria, and it is recommended to approach IBS patients using a multidimensional clinical profile (MDCP). The pathophysiology of IBS is multifactorial and involves motility disorders, genetic factors, immune responses, visceral hypersensitivity, brain–gut dysregulation, and altered intestinal microbiota. The management of IBS includes both nonpharmacologic and pharmacologic therapies. Nonpharmacologic therapy options include physical activity, low fermentable oligosaccharides, disaccharides, monosaccharides, and polyol diet, as well as cognitive behavioral therapy. Pharmacologic therapy options include probiotics, antidepressants, antispasmodics, and new agents. In clinical practice, a multidisciplinary strategy, including nonpharmacologic or/and pharmacologic treatment for IBS, is emphasized. Therefore, clinicians should carefully consider the underlying pathophysiology before selecting an appropriate therapeutic option for the treatment of IBS. In other words, individualized treatment plans are necessary for managing IBS.
肠易激综合征(IBS)是一种以缺乏结构或生化异常为特征的功能性胃肠道疾病。目前肠易激综合征的诊断是基于Rome IV标准,建议使用多维临床概况(MDCP)来诊断肠易激综合征患者。肠易激综合征的病理生理是多因素的,涉及运动障碍、遗传因素、免疫反应、内脏过敏、脑-肠失调和肠道微生物群改变。肠易激综合征的治疗包括非药物治疗和药物治疗。非药物治疗方案包括体力活动、低发酵低聚糖、双糖、单糖和多元醇饮食,以及认知行为治疗。药物治疗选择包括益生菌、抗抑郁药、抗痉挛药和新药。在临床实践中,强调多学科策略,包括肠易激综合征的非药物或/和药物治疗。因此,临床医生在选择适当的治疗方案之前,应仔细考虑潜在的病理生理学。换句话说,个体化的治疗方案对于控制肠易激综合征是必要的。
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引用次数: 0
Comparative study of different combinations of mirabegron and antimuscarinics in treatment for overactive bladder syndrome in elderly patients. mirabegron与抗毒蕈素不同联合治疗老年膀胱过动症的比较研究。
IF 1.5 Q2 MEDICINE, GENERAL & INTERNAL Pub Date : 2023-01-01 DOI: 10.4103/tcmj.tcmj_209_21
Yuh-Chen Kuo, Hann-Chorng Kuo

Objectives: To compare the therapeutic efficacy, adverse events (AEs), and patient preference in elderly patients with overactive bladder (OAB) receiving different combinations of mirabegron and solifenacin.

Materials and methods: Elderly OAB patients received mirabegron 25 mg (M25) daily for 1 month (1M) followed by randomization to receive M25 (Group 1), mirabegron 50 mg (M50, Group 2), solifenacin 5 mg (S5, group 3); or M25 plus S5 (Group 4) for further 2 months. Efficacy and AEs were evaluated. At the end of 3M, patients' preferred option for future treatment was investigated.

Results: A total of 168 patients were enrolled, and 100 completed 3-month treatment. At 1M, all parameters improved significantly except postvoid residual (PVR), 23 (13.7%) patients had no symptom, 16 (9.5%) had no improvement, and 10 (6.0%) withdrew from the trial. Compared parameters at 3M with 1M revealed that quality of life, Patient's Perception of Bladder Condition scores, and voided volume improved significantly in group 1; the OAB Symptom Score (OABSS) increased in group 2; mean PVR and Global Response Assessment (GRA) deteriorated in group 3; and the OABSS and GRA improved in group 4. At 3M, the AEs prevalence increased significantly in group 3. Only 38.1% in group 4 preferred long-term usage of combination therapy.

Conclusion: M25 daily is effective and safe in treating elderly OAB patients. Dose escalation to 50 mg or shifting to S5 does not increase the therapeutic efficacy. Combining M25 with S5 provides better treatment efficacy but is associated with lower patient compliance than M25 alone.

目的:比较不同联合mirabegron与索利那新治疗老年膀胱过动症(OAB)的疗效、不良事件(ae)及患者偏好。材料与方法:老年OAB患者每日接受米拉米格隆25mg (M25)治疗1个月(1M),随后随机分组接受M25(1组)、米拉米格隆50mg (M50, 2组)、索利那新5mg (S5, 3组);或M25加S5(第4组)再申请2个月。对疗效和不良反应进行评价。在3M结束时,研究患者对未来治疗的首选方案。结果:共纳入168例患者,其中100例完成了3个月的治疗。在1M时,除空隙后残留(PVR)外,所有参数均有显著改善,23例(13.7%)患者无症状,16例(9.5%)患者无改善,10例(6.0%)患者退出试验。比较3M组与1M组的生活质量、患者膀胱状况感知评分、排尿量均有显著改善;2组OAB症状评分(OABSS)升高;平均PVR和总体反应评估(GRA)在第3组恶化;第4组OABSS和GRA均有改善。3M时,第3组ae发生率明显升高。第4组只有38.1%的患者选择长期使用联合治疗。结论:每日M25治疗老年OAB患者安全有效。剂量增加到50mg或转移到S5不会增加治疗效果。M25联合S5治疗效果更好,但患者依从性低于单独使用M25。
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引用次数: 1
Anxiety treatment of methamphetamine-dependent patients with buprenorphine: A randomized, double-blind, clinical trial. 丁丙诺啡治疗甲基苯丙胺依赖患者的焦虑:一项随机、双盲临床试验。
IF 1.5 Q2 MEDICINE, GENERAL & INTERNAL Pub Date : 2023-01-01 DOI: 10.4103/tcmj.tcmj_297_21
Jamshid Ahmadi, Amir Bazrafshan, Ali Sahraian, Sara Jalali, Maedeh Fakhermanesh, Zahra Hooshyari

Objectives: In this double-blind, randomized clinical trial, the effectiveness of buprenorphine (BUPRE) in the reduction of anxiety symptoms among the methamphetamine (MA) dependents was evaluated.

Materials and methods: The 60 MA-dependent patients were randomly assigned to three groups (0.1 mg, 1 mg, and 8 mg of BUPRE), The Hamilton Anxiety Rating Scale was administrated to assess the anxiety symptoms daily at baseline and second to the 5th day after intervention. The inclusion criteria were the MA dependence, age of over 18 years, and absence of any chronic physical illnesses; exclusion criteria were the presence of other drug dependence in combination with MA. The mixed-design analysis of variance was performed for data analysis.

Results: A significant main effect of time (F = 51.456, P < 0.001) and group (F = 4.572, P = 0.014) and group-by-time interaction (F = 8.475, P < 0.001) were detected.

Conclusions: This finding supports the efficacy of BUPRE to decrease anxiety. High doses of the drug (1 and 8 mg) were more effective than 0.1 mg. Here was not a significant difference between anxiety score when patients received 1 mg of BUPRE instead of 8 mg.

目的:在这项双盲、随机临床试验中,评估丁丙诺啡(BUPRE)减轻甲基苯丙胺(MA)依赖者焦虑症状的有效性。材料与方法:将60例ma依赖患者随机分为三组(0.1 mg、1 mg、8 mg BUPRE),每日基线及干预后第2 ~ 5天使用汉密尔顿焦虑评定量表评估焦虑症状。纳入标准为MA依赖、年龄在18岁以上、无慢性躯体疾病;排除标准为合并MA存在其他药物依赖。数据分析采用混合设计方差分析。结果:时间(F = 51.456, P < 0.001)、分组(F = 4.572, P = 0.014)和分组时间交互作用(F = 8.475, P < 0.001)的主效应显著。结论:本研究结果支持BUPRE降低焦虑的有效性。高剂量的药物(1和8毫克)比0.1毫克更有效。当患者接受1毫克BUPRE而不是8毫克BUPRE时,焦虑评分没有显著差异。
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引用次数: 0
Association between inhaled corticosteroid use and risk of hyperglycemia in patients with chronic obstructive pulmonary disease: A systematic review and meta-analysis 慢性阻塞性肺疾病患者吸入皮质类固醇使用与高血糖风险之间的关系:一项系统综述和荟萃分析
Q2 MEDICINE, GENERAL & INTERNAL Pub Date : 2023-01-01 DOI: 10.4103/tcmj.tcmj_131_23
Fathur Nur Kholis, Kevin Gracia Pratama, Jessica Novia Hadiyanto
A BSTRACT Objectives: Chronic obstructive pulmonary disease (COPD) patients have a higher risk of developing diabetes, and studies suggest that inhaled corticosteroids (ICSs) use may be associated with a higher risk of diabetes, particularly at higher doses. This study aims to investigate the effects of ICS use on the risk of diabetes and blood glucose levels in COPD patients. Materials and Methods: A systematic search was carried out on the PubMed, EBSCOhost, and ProQuest databases using the terms “Inhaled Corticosteroids,” “Diabetes,” and “Chronic Obstructive Pulmonary Disease” for the period between 2013 and 2023. The systematic review adhered to the PRISMA 2020 guideline. A meta-analysis was conducted using a random-effects model using the RevMan 5 software. Results: A total of 14 studies were included in the final analysis, with 10 randomized controlled trials (RCTs) and 4 observational studies. Two observational studies investigated the relationship between ICS dose and diabetes risk. A meta-analysis of the RCTs studies showed a nonstatistically significant tendency toward increased blood glucose (odds ratio [OR] 1.07 and 95% confidence interval [CI] 0.88–1.30) after a 52-week follow-up. Whereas the observational studies showed a tendency toward an increased risk of diabetes (OR 1.40 and 95% CI 0.96–2.03). Furthermore, a subgroup meta-analysis of high-dose ICS (>900 mg/day) showed a significant increase in the risk of diabetes (OR 1.20 and 95% CI 1.09–1.32). Conclusion: Short-term use of ICS does not have a significant effect on blood glucose. However, long-term use, especially at higher doses, can increase the risk of developing diabetes.
【摘要】目的:慢性阻塞性肺疾病(COPD)患者发生糖尿病的风险较高,研究表明,吸入性皮质类固醇(ICSs)的使用可能与糖尿病的高风险相关,特别是在高剂量时。本研究旨在探讨ICS使用对慢性阻塞性肺病患者糖尿病风险和血糖水平的影响。材料和方法:在PubMed、EBSCOhost和ProQuest数据库中系统检索2013年至2023年期间的“吸入皮质类固醇”、“糖尿病”和“慢性阻塞性肺疾病”。系统评价遵循PRISMA 2020指南。采用RevMan 5软件采用随机效应模型进行meta分析。结果:最终纳入14项研究,其中随机对照试验(rct) 10项,观察性研究4项。两项观察性研究调查了ICS剂量与糖尿病风险之间的关系。随机对照试验研究的荟萃分析显示,52周随访后血糖升高的趋势无统计学意义(优势比[OR] 1.07, 95%可信区间[CI] 0.88-1.30)。然而,观察性研究显示有增加糖尿病风险的趋势(OR 1.40, 95% CI 0.96-2.03)。此外,高剂量ICS (>900 mg/天)的亚组荟萃分析显示糖尿病风险显著增加(OR 1.20, 95% CI 1.09-1.32)。结论:短期使用ICS对血糖无明显影响。然而,长期使用,尤其是高剂量使用,会增加患糖尿病的风险。
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引用次数: 0
The relationship between child development and small for gestational age among preschool children. 学龄前儿童发育与胎龄小的关系。
IF 1.5 Q2 MEDICINE, GENERAL & INTERNAL Pub Date : 2023-01-01 DOI: 10.4103/tcmj.tcmj_227_21
Sheng-Hsun Chou, Shu-Hui Wen, Hsin-Chi Wu

Objectives: This study aimed to assess the impact of small for gestational age (SGA) on the development of Taiwanese preschool children using the Chinese Child Developmental Inventory (CCDI).

Materials and methods: A total of 982 children were enrolled in this study between June 2011 and December 2015. The samples were divided into two groups: SGA (n = 116, mean age = 2.98) and non-SGA (n = 866, mean age = 3.33) groups. The development scores were based on the CCDI, which consist of eight dimensions of development between the two groups. The linear regression analysis was adopted to examine the relationship of SGA with child development.

Results: On average, the children in the SGA group scored less in all eight subitems of the CCDI than those in the non-SGA group. However, regression analysis revealed that there was no significant difference in both performance and delay frequency in the CCDI between the two groups.

Conclusion: SGA children had similar developmental scores in CCDI as non-SGA children for preschool age in Taiwan.

摘要目的:本研究旨在利用中国儿童发展量表(CCDI)评估小胎龄(SGA)对台湾学龄前儿童发展的影响。材料与方法:2011年6月至2015年12月共纳入982名儿童。将样本分为SGA组(n = 116,平均年龄2.98)和非SGA组(n = 866,平均年龄3.33)。发展得分是基于CCDI,它由两组之间的八个发展维度组成。采用线性回归分析检验SGA与儿童发育的关系。结果:平均而言,SGA组儿童CCDI的8个分项得分均低于非SGA组。然而,回归分析显示,两组CCDI的性能和延迟频率均无显著差异。结论:台湾学龄前SGA儿童与非SGA儿童的CCDI发展得分相近。
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引用次数: 0
Continuous positive airway pressure improved daytime sleepiness and memory function in patients with obstructive sleep apnea. 持续气道正压改善阻塞性睡眠呼吸暂停患者白天嗜睡和记忆功能。
IF 1.5 Q2 MEDICINE, GENERAL & INTERNAL Pub Date : 2023-01-01 DOI: 10.4103/tcmj.tcmj_4_22
Ya-Ling Hong, Yu-Chih Shen, En-Ting Chang, Shu-Chin Kung

Objectives: Obstructive sleep apnea (OSA) is a sleep disorder which results in daytime sleepiness and impaired memory function. The aim of this study was to investigate the effect of continuous positive airway pressure (CPAP) on daytime sleepiness and memory function in OSA patients. We also investigated whether CPAP compliance impacted the effect of this treatment.

Materials and methods: The nonrandomized, nonblinded clinical trial enrolled 66 patients with moderate-to-severe OSA subjects. All subjects completed a polysomnographic study, daytime sleepiness questionnaires (the Epworth Sleepiness Scale and the Pittsburgh Sleep Quality Index), and four memory function tests (working memory; processing speed [PS]; logical memory [LM]; face memory [FM]).

Results: Before CPAP treatment, no significant differences (P < 0.05) were noted in the demographic data, daytime sleepiness, or memory function between two groups (with/without CPAP). However, OSA patients treated with CPAP for 2 months showed significant improvements in daytime sleepiness, PS, mostly of LM, and FM comparing to 2 months ago. As compared to those who did not receive CPAP treatment, CPAP can improve only parts of LM (delayed LM [DLM] and LM percentage [LMP]). In addition, compared to control group, a significant improvement of daytime sleepiness and LM (LM learning, DLM, and LMP) in good compliance with CPAP treatment group and of DLM and LMP in the low compliance with CPAP treatment group was found.

Conclusion: CPAP treatment for 2 months could improve some of LM in OSA patients, especially in patients exhibiting good CPAP compliance.

目的:阻塞性睡眠呼吸暂停(OSA)是一种导致白天嗜睡和记忆功能受损的睡眠障碍。本研究旨在探讨持续气道正压通气(CPAP)对OSA患者日间嗜睡和记忆功能的影响。我们还调查了CPAP依从性是否会影响这种治疗的效果。材料与方法:非随机、非盲法临床试验纳入66例中重度OSA患者。所有受试者都完成了一项多导睡眠图研究,白天嗜睡问卷(Epworth嗜睡量表和匹兹堡睡眠质量指数),以及四项记忆功能测试(工作记忆;处理速度[PS];逻辑存储器;面部记忆[FM])。结果:CPAP治疗前,两组患者(加/不加CPAP治疗)在人口学数据、日间嗜睡、记忆功能方面均无显著差异(P < 0.05)。然而,与2个月前相比,接受CPAP治疗2个月的OSA患者在白天嗜睡、PS(主要是LM)和FM方面有显著改善。与未接受CPAP治疗的患者相比,CPAP仅能改善部分LM(延迟LM [DLM]和LM百分比[LMP])。此外,与对照组相比,良好依从性CPAP治疗组白天嗜睡和LM (LM学习、DLM和LMP)显著改善,低依从性CPAP治疗组DLM和LMP显著改善。结论:CPAP治疗2个月可以改善OSA患者的部分LM,特别是对CPAP依从性好的患者。
{"title":"Continuous positive airway pressure improved daytime sleepiness and memory function in patients with obstructive sleep apnea.","authors":"Ya-Ling Hong,&nbsp;Yu-Chih Shen,&nbsp;En-Ting Chang,&nbsp;Shu-Chin Kung","doi":"10.4103/tcmj.tcmj_4_22","DOIUrl":"https://doi.org/10.4103/tcmj.tcmj_4_22","url":null,"abstract":"<p><strong>Objectives: </strong>Obstructive sleep apnea (OSA) is a sleep disorder which results in daytime sleepiness and impaired memory function. The aim of this study was to investigate the effect of continuous positive airway pressure (CPAP) on daytime sleepiness and memory function in OSA patients. We also investigated whether CPAP compliance impacted the effect of this treatment.</p><p><strong>Materials and methods: </strong>The nonrandomized, nonblinded clinical trial enrolled 66 patients with moderate-to-severe OSA subjects. All subjects completed a polysomnographic study, daytime sleepiness questionnaires (the Epworth Sleepiness Scale and the Pittsburgh Sleep Quality Index), and four memory function tests (working memory; processing speed [PS]; logical memory [LM]; face memory [FM]).</p><p><strong>Results: </strong>Before CPAP treatment, no significant differences (<i>P</i> < 0.05) were noted in the demographic data, daytime sleepiness, or memory function between two groups (with/without CPAP). However, OSA patients treated with CPAP for 2 months showed significant improvements in daytime sleepiness, PS, mostly of LM, and FM comparing to 2 months ago. As compared to those who did not receive CPAP treatment, CPAP can improve only parts of LM (delayed LM [DLM] and LM percentage [LMP]). In addition, compared to control group, a significant improvement of daytime sleepiness and LM (LM learning, DLM, and LMP) in good compliance with CPAP treatment group and of DLM and LMP in the low compliance with CPAP treatment group was found.</p><p><strong>Conclusion: </strong>CPAP treatment for 2 months could improve some of LM in OSA patients, especially in patients exhibiting good CPAP compliance.</p>","PeriodicalId":45873,"journal":{"name":"Tzu Chi Medical Journal","volume":"35 1","pages":"84-88"},"PeriodicalIF":1.5,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/d7/81/TCMJ-35-84.PMC9972931.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9389134","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Experimental animal models and evaluation techniques in intracerebral hemorrhage. 脑出血实验动物模型及评价技术。
IF 1.5 Q2 MEDICINE, GENERAL & INTERNAL Pub Date : 2023-01-01 DOI: 10.4103/tcmj.tcmj_119_22
Shaik Ismail Mohammed Thangameeran, Cheng-Yoong Pang, Chien-Hui Lee, Sheng-Tzung Tsai, Wei-Fen Hu, Hock-Kean Liew

Intracerebral hemorrhage (ICH) is the most lethal type of cerebral stroke without effective therapy. Although clinical trials with various surgeries have been conducted, none have improved clinical outcomes compared to the current medical management for ICH. Several ICH animal models, including autologous blood injection, collagenase injection, thrombin injection, and microballoon inflation methods, have been developed to elucidate the underlying mechanisms of ICH-induced brain injury. These models could also be used for discovering new therapy for ICH preclinically. We summarize the existing ICH animal models and the evaluation parameters used to measure the disease outcomes. We conclude that these models, resembling the different aspects of ICH pathogenesis, have their advantages and disadvantages. None of the current models closely represent the severity of ICH seen in clinical settings. More appropriate models are needed to streamline ICH's clinical outcomes and be used for validating newly developed treatment protocols.

脑出血(ICH)是脑中风最致命的类型,没有有效的治疗。尽管已经进行了各种手术的临床试验,但与目前对脑出血的医疗管理相比,没有一种手术能改善临床结果。几种脑出血动物模型,包括自体血液注射、胶原酶注射、凝血酶注射和微球囊充气方法,已经被开发出来阐明脑出血诱导脑损伤的潜在机制。这些模型也可用于发现脑出血临床前治疗的新方法。我们总结了现有的ICH动物模型和用于衡量疾病结局的评价参数。我们的结论是,这些模型类似于脑出血发病的不同方面,有其优点和缺点。目前的模型都不能很好地代表临床环境中所见的脑出血的严重程度。需要更合适的模型来简化脑出血的临床结果,并用于验证新开发的治疗方案。
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引用次数: 0
Humoral immune response to an mRNA-1273 booster after chAdOx1-nCoV-19-priming among patients undergoing hemodialysis 血液透析患者在chadox1 - ncov -19启动后对mRNA-1273增强剂的体液免疫应答
Q2 MEDICINE, GENERAL & INTERNAL Pub Date : 2023-01-01 DOI: 10.4103/tcmj.tcmj_107_23
Bo-Yu Cheng, Ting-Yun Lin, Szu-Chun Hung
A BSTRACT Objectives: Patients who are undergoing dialysis due to end-stage kidney disease are susceptible to greater coronavirus disease 2019 (COVID-19) complications. While vaccination is seen as the most effective tactic against COVID-19, the dialysis population usually has impaired immune responses to vaccination. Owing to the global vaccine supply shortage in the early phase of the COVID-19 pandemic, hemodialysis patients in Taiwan were administered homologous ChAdOx1 nCoV-19/ChAdOx1 nCoV-19 at 12-week intervals, with a third booster shot of mRNA-1273 given 12 weeks after the second dose. We assessed the antibody responses of these patients to this extended-interval dosing protocol. Materials and Methods: A total of 168 hemodialysis patients (mean age: 67 ± 13 years) without prior COVID-19 infection were vaccinated between June 16, 2021, and January 5, 2022, and followed until February 10, 2022. The primary outcome was seroconversion with an antispike immunoglobulin G (IgG) antibody level ≥50 arbitrary units (AU)/mL at 4 weeks after the administration of an mRNA-1273 booster shot. The secondary outcome was the level of antispike IgG antibodies. Multivariable linear regression models were used to evaluate the associations between the baseline characteristics and the antispike IgG level. Results: A total of 163 (97.0%) patients reached the primary endpoint, with antibody levels after the third booster dose of mRNA-1273 being significantly higher than those after the second dose of ChAdOx1 nCoV-19 (median IgG titer 12,007 [4394–23,860] vs. 846 [interquartile range 295–2114] AU/mL; P < 0.001). Patients who were male, older, had a higher body mass index, had a lower total lymphocyte count, and used immunosuppressants had lower antibody levels. Conclusion: A third booster dose of mRNA-1273 after two consecutive priming doses of ChAdOx1 nCoV-19 with extended intervals resulted in adequate humoral immune responses among hemodialysis patients.
【摘要】目的:终末期肾病患者接受透析治疗时易发生冠状病毒病2019 (COVID-19)并发症。虽然疫苗接种被视为对抗COVID-19最有效的策略,但透析人群通常对疫苗接种的免疫反应受损。由于COVID-19大流行早期全球疫苗供应短缺,台湾血液透析患者每隔12周注射同源ChAdOx1 nCoV-19/ChAdOx1 nCoV-19,在第二次注射后12周注射第三次mRNA-1273加强针。我们评估了这些患者对延长间隔给药方案的抗体反应。材料与方法:于2021年6月16日至2022年1月5日期间,对168例既往无COVID-19感染的血液透析患者(平均年龄:67±13岁)接种疫苗,随访至2022年2月10日。主要终点是在注射mRNA-1273加强剂后4周抗刺突免疫球蛋白G (IgG)抗体水平≥50任意单位(AU)/mL的血清转化。次要指标为抗刺突IgG抗体水平。采用多变量线性回归模型评估基线特征与抗刺突IgG水平之间的关系。结果:共有163例(97.0%)患者达到主要终点,第三次mRNA-1273加强剂后的抗体水平显著高于第二次ChAdOx1 nCoV-19增强剂后的抗体水平(IgG滴度中位数12,007[4394-23,860]对846[四分位数范围295-2114]AU/mL;P & lt;0.001)。男性、年龄较大、身体质量指数较高、总淋巴细胞计数较低、使用免疫抑制剂的患者抗体水平较低。结论:在连续两次延长间隔的ChAdOx1 nCoV-19启动剂量后,第三次加强剂量mRNA-1273可在血液透析患者中产生足够的体液免疫反应。
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引用次数: 0
Rodent models of senile normal-pressure hydrocephalus. 老年常压脑积水啮齿动物模型。
IF 1.5 Q2 MEDICINE, GENERAL & INTERNAL Pub Date : 2023-01-01 DOI: 10.4103/tcmj.tcmj_120_22
Li-Jin Chen, Sheng-Tzung Tsai, Guo-Fang Tseng

Cerebrospinal fluid (CSF) and its drainage are crucial in clearing metabolic waste and maintaining the microenvironment of the central nervous system for proper functioning. Normal-pressure hydrocephalus (NPH) is a serious neurological disorder of the elderly with obstruction of CSF flow outside the cerebral ventricles, causing ventriculomegaly. The stasis of CSF in NPH compromises brain functioning. Although treatable, often with shunt implantation for drainage, the outcome depends highly on early diagnosis, which, however, is challenging. The initial symptoms of NPH are hard to be aware of and the complete symptoms overlap with those of other neurological diseases. Ventriculomegaly is not specific to NPH as well. The lack of knowledge on the initial stages in its development and throughout its progression further deters early diagnosis. Thus, we are in dire need for an appropriate animal model for researches into a more thorough understanding of its development and pathophysiology so that we can enhance the diagnosis and therapeutic strategies to improve the prognosis of NPH following treatment. With this, we review the few currently available experimental rodent NPH models for these animals are smaller in sizes, easier in maintenance, and having a rapid life cycle. Among these, a parietal convexity subarachnoid space kaolin injection adult rat model appears promising as it shows a slow onset of ventriculomegaly in association with cognitive and motor disabilities resembling the elderly NPH in humans.

脑脊液(CSF)及其排泄对于清除代谢废物和维持中枢神经系统正常运作的微环境至关重要。常压脑积水(NPH)是一种严重的老年人神经系统疾病,脑室外脑脊液流动受阻,导致脑室肿大。脑脊液在NPH中的停滞会损害大脑功能。虽然可以治疗,通常通过分流管植入引流,但结果高度依赖于早期诊断,然而,这是具有挑战性的。NPH的初始症状难以察觉,其完整症状与其他神经系统疾病的症状重叠。脑室增大也不是NPH所特有的。缺乏对其发展的最初阶段和整个发展过程的了解进一步阻碍了早期诊断。因此,我们迫切需要一种合适的动物模型进行研究,以更深入地了解其发展和病理生理,从而提高诊断和治疗策略,改善NPH治疗后的预后。在此基础上,我们回顾了目前可用的几种实验性啮齿动物NPH模型,这些模型具有体积较小、易于维护和生命周期快的特点。其中,顶凸蛛网膜下腔高岭土注射成年大鼠模型看起来很有希望,因为它显示了与认知和运动障碍相关的脑室肿大的缓慢发作,类似于人类老年NPH。
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引用次数: 0
Role of cancer-associated mesenchymal stem cells in the tumor microenvironment: A review. 肿瘤相关间充质干细胞在肿瘤微环境中的作用综述
IF 1.5 Q2 MEDICINE, GENERAL & INTERNAL Pub Date : 2023-01-01 DOI: 10.4103/tcmj.tcmj_138_22
Kai-Hung Wang, Dah-Ching Ding

Mesenchymal stem cells (MSCs) were applied to the therapy for degenerative diseases, immune, and inflammation. In tumor microenvironments (TME), different sources of MSCs showed that tumor-promoting and -inhibiting effects were mediated by different signaling pathways. Cancer-associated MSCs (CaMSCs) could be recruited from bone marrow or local tissues and mainly showed tumor-promoting and immunosuppressive effects. The transformed CaMSCs preserve the characteristics of stem cells, but the properties of regulating TME are different. Hence, we specifically focus on CaMSCs and discuss the detailed mechanisms of regulating the development of cancer cells and immune cells. CaMSCs could be a potential therapeutic target in various types of cancer. However, the detailed mechanisms of CaMSCs in the TME are relatively less known and need further study.

间充质干细胞(MSCs)应用于退行性疾病、免疫和炎症的治疗。在肿瘤微环境(TME)中,不同来源的MSCs显示出不同的信号通路介导的促肿瘤和抑制作用。肿瘤相关间充质干细胞(CaMSCs)可以从骨髓或局部组织中募集,主要表现为促肿瘤和免疫抑制作用。转化后的CaMSCs保留了干细胞的特征,但调节TME的特性不同。因此,我们特别关注CaMSCs,并讨论了调节癌细胞和免疫细胞发育的详细机制。CaMSCs可能是多种类型癌症的潜在治疗靶点。然而,CaMSCs在TME中的具体机制尚不清楚,需要进一步研究。
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引用次数: 1
期刊
Tzu Chi Medical Journal
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