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Exploring the Psychiatric Manifestations of Primary Sjögren’s Syndrome: A Narrative Review 探索原发性斯约格伦综合征的精神表现:叙述性综述
IF 2.3 Q3 Medicine Pub Date : 2024-05-14 DOI: 10.1155/2024/5520927
Mona Salehi, A. Zamiri, Jeffrey Kim, Chenique Texeira, Ketki Shah, S. Gunturu
Background. Primary Sjögren’s syndrome (pSS) is recognized for its autoimmune origin. Its hallmark symptoms, dry eyes and mouth, result from glandular inflammation. Prior literature indicates that pSS not only affects the peripheral system but also involves the central nervous system (CNS), giving rise to various neuropsychiatric symptoms. However, there is limited published research on the psychiatric comorbidities in individuals with pSS. Methods. A comprehensive search was conducted on PubMed and Google Scholar for this narrative review. The search spanned from inception until August 2023. Its aim was to locate studies focusing on the psychiatric manifestations of pSS and the potential underlying mechanisms. Results. The most commonly reported psychiatric complications among these individuals are depression and cognitive dysfunction. Other psychiatric manifestations that have been reported in pSS individuals include anxiety, sleep disorders, psychosis, catatonia, bipolar disorder, and obsessive-compulsive disorder. Conclusion. In conclusion, patients with pSS often display multiple psychiatric symptoms. These symptoms can significantly impair functioning and reduce quality of life. Hence, prompt diagnosis and management are crucial.
背景。原发性斯约格伦综合征(pSS)是公认的自身免疫性疾病。其标志性症状--眼干和口干,是由腺体炎症引起的。先前的文献表明,pSS 不仅会影响外周系统,还会累及中枢神经系统(CNS),引起各种神经精神症状。然而,有关 pSS 患者精神并发症的公开研究却很有限。研究方法我们在 PubMed 和 Google Scholar 上进行了全面搜索,以撰写这篇叙述性综述。搜索时间从开始到 2023 年 8 月。其目的是查找有关 pSS 精神病表现和潜在内在机制的研究。结果。在这些患者中,最常见的精神并发症是抑郁和认知功能障碍。已报道的 pSS 患者的其他精神表现包括焦虑、睡眠障碍、精神病、紧张症、躁郁症和强迫症。结论总之,pSS 患者通常表现出多种精神症状。这些症状会严重损害患者的功能,降低生活质量。因此,及时诊断和治疗至关重要。
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引用次数: 0
Association of Baseline Serum Soluble Tumour Necrosis Factor Receptor Levels with the Response of Rheumatoid Arthritis to Janus Kinase Inhibitor Therapy. 血清可溶性肿瘤坏死因子受体基线水平与类风湿性关节炎对 Janus 激酶抑制剂疗法反应的关系
IF 2.3 Q3 Medicine Pub Date : 2024-04-27 eCollection Date: 2024-01-01 DOI: 10.1155/2024/2898586
Takahiro Yoshikawa, Tetsuya Furukawa, Teppei Hashimoto, Naoto Azuma, Kiyoshi Matsui

Aim: The aim of this study was to investigate whether cytokines associated with tumour necrosis factor- (TNF-) α and interleukin- (IL-) 6 signalling could predict rheumatoid arthritis (RA) clinical remission (CR) with Janus kinase inhibitor (JAKinib) treatment using the Simplified Disease Activity Index (SDAI).

Methods: Eighty-nine patients with RA treated with JAKinibs were enrolled, and their clinical data were collected retrospectively. CR was defined as an SDAI ≤ 3.3 after 6 months of treatment with JAKinib. The serum samples of 89 patients were analysed for IL-6, soluble IL-6 receptor (sIL-6R), soluble gp130 (spg130), and soluble TNF receptor- (sTNFR-) I and sTNFR-II titres.

Results: There were no significant differences in the baseline clinical parameters between the CR and non-CR groups. Serum levels of IL-6, sIL-6R, and sgp130 were not significantly different; whereas, the serum sTNFR-I and sTNFR-II levels were significantly lower in the CR group. Univariate and multivariate logistic regression analysis showed that the baseline log sTNFR II values (OR: 0.002; p = 0.034) were predictors of CR.

Conclusions: Patients with RA can be stratified prior to JAKinib administration using serum sTNFR-I and sTNFR-II levels but not serum IL-6 axis cytokine levels (IL-6, sIL-6R, and sgp130).

目的:本研究旨在探讨与肿瘤坏死因子(TNF-)α和白细胞介素(IL-)6信号相关的细胞因子是否能利用简化疾病活动指数(SDAI)预测类风湿性关节炎(RA)在接受Janus激酶抑制剂(JAKinib)治疗后的临床缓解(CR):招募了89名接受JAKinibs治疗的RA患者,并回顾性地收集了他们的临床数据。使用JAKinib治疗6个月后,SDAI≤3.3即为CR。对89名患者的血清样本进行了IL-6、可溶性IL-6受体(sIL-6R)、可溶性gp130(spg130)、可溶性TNF受体(sTNFR-)I和sTNFR-II滴度分析:CR 组和非 CR 组的基线临床参数无明显差异。血清中 IL-6、sIL-6R 和 sgp130 的水平无明显差异;而 CR 组血清中 sTNFR-I 和 sTNFR-II 的水平明显较低。单变量和多变量逻辑回归分析显示,sTNFR II 的基线对数值(OR:0.002;P = 0.034)是预测 CR 的因素:结论:使用血清sTNFR-I和sTNFR-II水平,而非血清IL-6轴细胞因子水平(IL-6、sIL-6R和sgp130),可在服用JAKinib前对RA患者进行分层。
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引用次数: 0
Primary Immune Thrombocytopenic Purpura (ITP) and ITP Associated with Systemic Lupus Erythematosus: A Review of Clinical Characteristics and Treatment Modalities 原发性免疫性血小板减少性紫癜(ITP)和与系统性红斑狼疮相关的 ITP:临床特征和治疗方法综述
IF 2.3 Q3 Medicine Pub Date : 2024-03-01 DOI: 10.1155/2024/6650921
Krishna Bashyal, Sangam Shah, Calvin Ghimire, Shravya Balmuri, Pradip Chaudhary, Sandip Karki, Anuj Krishna Poudel, A. Pokharel, Vishal Devarkonda, Samina Hayat
Immune thrombocytopenic purpura (ITP) is an immune-mediated disorder characterized by the destruction of platelets and megakaryocytes due to autoantibodies against the platelet surface proteins. ITP without any apparent cause of thrombocytopenia is defined as primary ITP, and ITP in the setting of SLE is secondary ITP, which can be diagnosed after excluding other causes of thrombocytopenia by history, physical examination, and laboratory testing. Patients with ITP associated with SLE have higher median platelet count and less bleeding manifestations compared to the patients with primary ITP. It can be very challenging to diagnose primary ITP in SLE patients as other causes of thrombocytopenia including drug-induced thrombocytopenia, antiphospholipid syndrome, and thrombotic microangiopathic process should be ruled out. Corticosteroids are the main modality of treatment. IVIG can be used in severe cases. Splenectomy was found to be less effective in ITP associated with SLE compared to primary ITP. Control of disease activity with immunosuppressive therapy can be helpful in some cases associated with active disease flares in SLE patients.
免疫性血小板减少性紫癜(ITP)是一种免疫介导的疾病,其特点是血小板和巨核细胞因针对血小板表面蛋白的自身抗体而遭到破坏。通过病史、体格检查和实验室检查排除了导致血小板减少的其他原因后,可诊断为继发性血小板减少症。与原发性ITP患者相比,伴有系统性红斑狼疮的ITP患者的血小板计数中位数更高,出血表现更少。在系统性红斑狼疮患者中诊断原发性ITP非常具有挑战性,因为需要排除导致血小板减少的其他原因,包括药物诱发的血小板减少、抗磷脂综合征和血栓性微血管病变过程。皮质类固醇是主要的治疗方法。严重病例可使用 IVIG。与原发性ITP相比,脾切除术对伴有系统性红斑狼疮的ITP效果较差。对于某些伴有系统性红斑狼疮疾病活动性发作的病例,使用免疫抑制疗法控制疾病活动可能会有所帮助。
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引用次数: 0
Association of Cytokine IL-17, IL-4, IL-6, and IL-12 Gene Polymorphisms in Rheumatoid Arthritis Patients in a Tertiary Care Hospital in Bangladesh. 孟加拉国一家三甲医院类风湿关节炎患者细胞因子 IL-17、IL-4、IL-6 和 IL-12 基因多态性的相关性。
IF 2.3 Q3 Medicine Pub Date : 2024-02-02 eCollection Date: 2024-01-01 DOI: 10.1155/2024/3728179
Taskin Jahan, Ahmed Abu Saleh, Shaheda Anwar

Rheumatoid arthritis (RA) is a chronic autoimmune inflammatory disease that involves cytokines in its pathogenesis. This study is aimed at investigating if gene polymorphisms in cytokines like IL-17, IL-4, IL-6, and IL-12 affect RA susceptibility and severity in the Bangladeshi population. This was a cross-sectional comparative study that included 40 diagnosed RA patients according to the American College of Rheumatology (ACR) criteria 2010, who were free from other rheumatological diseases, and 40 healthy subjects for comparison. The study used PCR-RFLP to determine the IL-17, IL-4, IL-6, and IL-12 cytokine gene polymorphisms. Patients had a mean age of 37.22 ± 6.70 years. Among the patients, 31 were female and 9 were male. The mean disease duration was 18.11 ± 7.39 months. The study found that rheumatoid arthritis patients with the IL-17F (7488 A/G) polymorphism with GG genotype (P = 0.006, OR = 8.56, 95% CI = 1.77 - 41.33) and IL-12B (1188 A/C) polymorphism with AC (P = 0.012, OR = 3.69, 95% CI = 1.43 - 9.53) and CC (P = 0.013, OR = 7.58, 95% CI = 1.56 - 36.88) genotypes were significantly associated with disease risk. Furthermore, patients with the IL-17F (7488) GG genotype and IL-12B (1188) AC and CC genotypes had higher rheumatoid arthritis disease severity and activity parameters. The study found no significant association between polymorphisms involving IL-4 (590 C/T) and IL-6 (174 G/C) genes and rheumatoid arthritis disease risk in the Bangladeshi population. Gene polymorphisms in cytokines IL-17F (7488 A/G) and IL-12B (1188 A/C) can predict disease susceptibility and severity in Bangladeshi rheumatoid arthritis patients.

类风湿性关节炎(RA)是一种慢性自身免疫性炎症疾病,其发病机制与细胞因子有关。本研究旨在调查 IL-17、IL-4、IL-6 和 IL-12 等细胞因子的基因多态性是否会影响孟加拉国人群的 RA 易感性和严重程度。这是一项横断面比较研究,包括 40 名根据 2010 年美国风湿病学会(ACR)标准确诊的 RA 患者(无其他风湿病)和 40 名健康受试者作为对比。研究采用 PCR-RFLP 方法测定了 IL-17、IL-4、IL-6 和 IL-12 细胞因子基因的多态性。患者的平均年龄为(37.22 ± 6.70)岁。其中女性 31 人,男性 9 人。平均病程为(18.11 ± 7.39)个月。研究发现,类风湿性关节炎患者的 IL-17F (7488 A/G) 多态性基因型为 GG(P = 0.006,OR = 8.56,95% CI = 1.77 - 41.33)和 IL-12B(1188/A/C)多态性的 AC(P = 0.012,OR = 3.69,95% CI = 1.43 - 9.53)和 CC(P = 0.013,OR = 7.58,95% CI = 1.56 - 36.88)基因型与疾病风险显著相关。此外,IL-17F(7488)GG 基因型和 IL-12B(1188)AC 和 CC 基因型患者的类风湿性关节炎疾病严重程度和活动参数较高。研究发现,在孟加拉国人群中,IL-4(590 C/T)和IL-6(174 G/C)基因多态性与类风湿关节炎疾病风险之间没有明显关联。细胞因子IL-17F(7488 A/G)和IL-12B(1188 A/C)的基因多态性可预测孟加拉国类风湿性关节炎患者的疾病易感性和严重程度。
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引用次数: 0
Impact of Transcranial Direct Current Stimulation in Pain, Fatigue, and Health Quality of Life of Patients with Idiopathic Inflammatory Myopathies: A Randomized, Double-Blind, Sham-Controlled Crossover Clinical Trial. 经颅直流电刺激对特发性炎症性肌病患者疼痛、疲劳和生活质量的影响:随机、双盲、假对照交叉临床试验。
IF 2.3 Q3 Medicine Pub Date : 2024-02-01 eCollection Date: 2024-01-01 DOI: 10.1155/2024/1583506
Rafael Giovani Missé, Alexandre Moura Dos Santos, Isabela Bruna Pires Borges, Marcus Vinicius Grecco, Marlise Sítima Mendes Simões Faria, Lorenza Rosa Silvério da Silva, Bruna Lindoso Correia, Ana Woo Sook Kim, Clarice Tanaka, Júlia Maria D'Andrea Greve, Abrahão Fontes Baptista, Samuel Katsuyuki Shinjo

Objectives: To assess the effectiveness of transcranial direct current stimulation (tDCS) for pain, fatigue, physical function, and health-related quality of life in patients with idiopathic inflammatory myopathy (IIM).

Methods: This randomized, double-blind, sham-controlled, crossover clinical trial enrolled IIM patients with fatigue and pain who received tDCS (20 min, 2 mA) or sham stimulation for 10 daily sessions. Electrodes were placed according to the 10/20 EEG system. Both the groups underwent aerobic exercise training during the intervention period. The patients were evaluated for disease perception, pain, and fatigue using uni-multidimensional questionnaires and physical tests in the periods before and after the first and second interventions and after 12 weeks of follow-up.

Results: After the tDCS intervention, a reduction in the general score of multidimensional pain of 32.0 (1.5-38.0) vs. 0.0 (0.0-13.4) with effect size (ES) of -0.78 was noted, and after sham intervention, a reduction of 26.0 (0.0-37.0) vs. 5.0 (0.0-19.2) with ES of -0.54 (P = 0.047) was also noted. Similar results were evidenced with fatigue (22.5 (15.4-33.2) vs. 5.5 (0.0-14.6) with ES of -0.82) and sham intervention (21.0 (15.8-29.5) vs. 4.0 (4.0-17.5) with ES of -0.80 (P = 0.012)). There were no differences in the domains of the fatigue and pain questionnaires. Adherence was observed in 88.8% of the patients without adverse events.

Conclusion: The association of tDCS with aerobic training promoted additional effects in relation to the group subjected to placebo stimulation on general pain and fatigue scores, as well as on pain intensity, without changes in the subdomains of the pain and fatigue questionnaire. This trial is registered with NCT04678635.

目的评估经颅直流电刺激(tDCS)对特发性炎症性肌病(IIM)患者的疼痛、疲劳、身体功能和健康相关生活质量的影响:这项随机、双盲、假对照、交叉临床试验招募了疲劳和疼痛的特发性炎症性肌病患者,他们每天接受 10 次 tDCS(20 分钟,2 毫安)或假刺激。电极根据 10/20 脑电图系统放置。两组患者在干预期间都接受了有氧运动训练。在第一次和第二次干预前后以及随访 12 周后,使用单多维问卷和体能测试对患者的疾病感知、疼痛和疲劳程度进行评估:tDCS干预后,多维疼痛总分降低了32.0(1.5-38.0)分 vs. 0.0(0.0-13.4)分,效应大小(ES)为-0.78;假干预后,多维疼痛总分降低了26.0(0.0-37.0)分 vs. 5.0(0.0-19.2)分,效应大小(ES)为-0.54(P = 0.047)。疲劳(22.5 (15.4-33.2) vs. 5.5 (0.0-14.6),ES 为-0.82)和假干预(21.0 (15.8-29.5) vs. 4.0 (4.0-17.5),ES 为-0.80 (P = 0.012))也有类似结果。在疲劳和疼痛问卷调查的领域中没有差异。88.8%的患者坚持治疗,无不良反应:结论:与安慰剂刺激组相比,tDCS与有氧训练的结合对一般疼痛和疲劳评分以及疼痛强度产生了额外的效果,但疼痛和疲劳问卷的子域没有发生变化。该试验已在 NCT04678635 上注册。
{"title":"Impact of Transcranial Direct Current Stimulation in Pain, Fatigue, and Health Quality of Life of Patients with Idiopathic Inflammatory Myopathies: A Randomized, Double-Blind, Sham-Controlled Crossover Clinical Trial.","authors":"Rafael Giovani Missé, Alexandre Moura Dos Santos, Isabela Bruna Pires Borges, Marcus Vinicius Grecco, Marlise Sítima Mendes Simões Faria, Lorenza Rosa Silvério da Silva, Bruna Lindoso Correia, Ana Woo Sook Kim, Clarice Tanaka, Júlia Maria D'Andrea Greve, Abrahão Fontes Baptista, Samuel Katsuyuki Shinjo","doi":"10.1155/2024/1583506","DOIUrl":"10.1155/2024/1583506","url":null,"abstract":"<p><strong>Objectives: </strong>To assess the effectiveness of transcranial direct current stimulation (tDCS) for pain, fatigue, physical function, and health-related quality of life in patients with idiopathic inflammatory myopathy (IIM).</p><p><strong>Methods: </strong>This randomized, double-blind, sham-controlled, crossover clinical trial enrolled IIM patients with fatigue and pain who received tDCS (20 min, 2 mA) or sham stimulation for 10 daily sessions. Electrodes were placed according to the 10/20 EEG system. Both the groups underwent aerobic exercise training during the intervention period. The patients were evaluated for disease perception, pain, and fatigue using uni-multidimensional questionnaires and physical tests in the periods before and after the first and second interventions and after 12 weeks of follow-up.</p><p><strong>Results: </strong>After the tDCS intervention, a reduction in the general score of multidimensional pain of 32.0 (1.5-38.0) <i>vs.</i> 0.0 (0.0-13.4) with effect size (ES) of -0.78 was noted, and after sham intervention, a reduction of 26.0 (0.0-37.0) <i>vs</i>. 5.0 (0.0-19.2) with ES of -0.54 (<i>P</i> = 0.047) was also noted. Similar results were evidenced with fatigue (22.5 (15.4-33.2) <i>vs.</i> 5.5 (0.0-14.6) with ES of -0.82) and sham intervention (21.0 (15.8-29.5) <i>vs.</i> 4.0 (4.0-17.5) with ES of -0.80 (<i>P</i> = 0.012)). There were no differences in the domains of the fatigue and pain questionnaires. Adherence was observed in 88.8% of the patients without adverse events.</p><p><strong>Conclusion: </strong>The association of tDCS with aerobic training promoted additional effects in relation to the group subjected to placebo stimulation on general pain and fatigue scores, as well as on pain intensity, without changes in the subdomains of the pain and fatigue questionnaire. This trial is registered with NCT04678635.</p>","PeriodicalId":51715,"journal":{"name":"International Journal of Rheumatology","volume":null,"pages":null},"PeriodicalIF":2.3,"publicationDate":"2024-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10853024/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139708482","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
Demographic, Clinical Profile of Rheumatoid Arthritis Patients and Their Association with Disease Severity in Ghana. 加纳类风湿性关节炎患者的人口、临床概况及其与疾病严重程度的关系。
IF 2.3 Q3 Medicine Pub Date : 2024-01-12 eCollection Date: 2024-01-01 DOI: 10.1155/2024/6639079
Tonnies Abeku Buckman, Samuel Asamoah Sakyi, Kwame Yeboah-Mensah, Maxwell Hubert Antwi, Isaac Darban, Lawrence Owusu-Brenya, Joseph Yorke, Andy Opoku Boateng, Ebenezer Senu, Albert Dompreh, Akwasi Minnah Addei, Richard Boateng, Ortis Yankey, Samuel Tandoh

Background: Rheumatoid arthritis (RA) is one of the frequent chronic, systemic, inflammatory autoimmune disorders with an estimated global prevalence of 1%. RA leads to joint destruction and disability if left untreated. Ghana has seen very few studies on RA, and little is known about the disease's severity and related variables. This study sought to characterize the clinical presentation and determine disease severity and associated risk factors with disease severity among RA patients in a tertiary hospital in Ghana.

Methods: This cross-sectional study was conducted between September 2020 and August 2021. This study included 56 consecutively consenting RA patients from the Komfo Anokye Teaching Hospital orthopaedic unit. Diagnosis of RA was based on the updated American College of Rheumatology/European League Against Rheumatism (ACR/EULAR) 2022 rheumatoid arthritis classification criteria by a rheumatologist. A study questionnaire was used to gather participant demographics and clinical features, and results from the laboratory were taken from the patients' charts and medical records. The patients' disease severity was evaluated based on the rheumatoid arthritis disease activity score, which is based on a 28-joint count (DAS28), and their functioning was evaluated using the modified health assessment questionnaire.

Results: The participants' mean age was 51.25 ± 13.22 years. Out of the total participants, 46 were females, and 10 were males (female-to-male ratio 4.6 : 1). Moreover, 37.50% had arthritis of the hand; 5.30% had severe disease, and 94.60% were not severe. A majority (76.80%) were on methotrexate medication. The most frequently involved joints were the knee (42.90%), wrist (32.10%), and elbow (12.50%). There was no statistically significant association with disease severity and a functional status score of >0.5 (cOR: 10.60, 95% CI (0.52-217.30); p = 0.124). In addition, marital status (p = 0.04), disease duration (p = 0.04), family complaints (p = 0.02), and ESR (p = 0.03) were significantly associated with disease severity.

Conclusion: RA is predominant among elder populations and females. Disease duration, family complaints, and ESR are associated with disease severity. The findings of this study call for interventions towards ensuring early diagnosis of RA among high-risk populations to enhance good management practices.

背景:类风湿性关节炎(RA)是一种常见的慢性、全身性、炎症性自身免疫性疾病,全球发病率约为 1%。如果不及时治疗,类风湿性关节炎会导致关节破坏和残疾。加纳对 RA 的研究很少,对该病的严重程度和相关变量知之甚少。本研究旨在分析加纳一家三甲医院RA患者的临床表现特征,确定疾病严重程度以及与疾病严重程度相关的风险因素:这项横断面研究在 2020 年 9 月至 2021 年 8 月期间进行。研究对象包括来自Komfo Anokye教学医院骨科的56名连续同意的RA患者。风湿病学家根据最新的美国风湿病学会/欧洲抗风湿联盟(ACR/EULAR)2022年类风湿性关节炎分类标准对RA进行诊断。研究问卷用于收集参与者的人口统计学特征和临床特征,实验室结果来自患者的病历和医疗记录。患者的疾病严重程度根据类风湿关节炎疾病活动度评分进行评估,该评分基于 28 个关节计数(DAS28),患者的功能使用改良健康评估问卷进行评估:参与者的平均年龄为 51.25±13.22 岁。在所有参与者中,女性 46 人,男性 10 人(男女比例为 4.6:1)。此外,37.50%的人患有手关节炎,5.30%的人病情严重,94.60%的人病情不严重。大多数患者(76.80%)正在服用甲氨蝶呤。最常受累的关节是膝关节(42.90%)、腕关节(32.10%)和肘关节(12.50%)。疾病严重程度与功能状态评分大于 0.5(cOR:10.60,95% CI (0.52-217.30);P = 0.124)无统计学意义。此外,婚姻状况(p = 0.04)、病程(p = 0.04)、家庭主诉(p = 0.02)和血沉(p = 0.03)与疾病严重程度也有显著相关性:结论:RA主要发生在老年人群和女性中。结论:RA主要发生在老年人群和女性中,病程、家庭投诉和血沉与疾病严重程度相关。这项研究结果呼吁采取干预措施,确保高危人群中的 RA 患者得到早期诊断,以加强良好的管理方法。
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引用次数: 0
Clinically Recognized Depression and Mental Health Treatment in a Single Center Cohort of Patients with Systemic Sclerosis 单中心系统性硬化症患者队列中临床公认的抑郁和心理健康治疗
IF 2.3 Q3 Medicine Pub Date : 2023-12-19 DOI: 10.1155/2023/6141790
Marissa B. Savoie, Alexandra Poeschla, Na Lu, Yuqing Zhang, M. Bolster, Sara Schoenfeld, F. Castelino
Introduction. In this study, we investigated the prevalence of depression, depression treatment, and symptom burden in patients with systemic sclerosis (SSc) and examined their associations with the center for epidemiologic studies depression scale revised (CESD-R) scores. Methods. The Prospective Registry in Scleroderma at Massachusetts General Hospital (PRISM) is a longitudinal registry of patients with SSc. Among participants with CESD-R score ≥ 16 , indicating possible depression, a chart review was performed for mental health diagnoses and treatments. We examined the relation of demographic and clinical factors to the presence of mental health diagnoses or treatment using logistic regression. We evaluated the association of SSc symptoms and the COVID-19 pandemic with a CESD-R score using quantile regression. Results. Of 214 patients enrolled in PRISM, 129 participants (38% diffuse and 59% limited) completed at least one CESD-R questionnaire. In the first survey, 29% had possible depression ( CESD − R ≥ 16 ) and 16% had probable depression ( CESD − R ≥ 23 ). Of 20 participants with probable depression, 90% received treatment for a mood disorder. In a multivariable logistic regression model among participants with CESD − R ≥ 16 , none of the evaluated variables (CESD-R score, age, gender, employment status, race, and ethnicity) was associated with mental health diagnosis or treatment. Higher baseline dyspnea index, modified Rodnan skin score, and the University of California Los Angeles Scleroderma Clinical Trials Consortium Gastrointestinal total score and subscores were associated with higher CESD-R score. Conclusion. In this single-center cross-sectional study, 16% of participants had significant depressive symptoms. Dyspnea, extent of skin involvement, and gastrointestinal symptoms were associated with depression symptoms.
简介在这项研究中,我们调查了系统性硬化症(SSc)患者的抑郁患病率、抑郁治疗情况和症状负担,并研究了它们与流行病学研究中心抑郁量表修订版(CESD-R)评分之间的关系。研究方法麻省总医院硬皮病前瞻性登记(PRISM)是一项系统性硬化症患者的纵向登记。在 CESD-R 评分≥16,表明可能患有抑郁症的参与者中,我们对他们的精神健康诊断和治疗进行了病历审查。我们使用逻辑回归法研究了人口统计学和临床因素与精神健康诊断或治疗的关系。我们使用量化回归法评估了 SSc 症状和 COVID-19 大流行与 CESD-R 评分之间的关系。结果。在参与 PRISM 的 214 名患者中,129 名参与者(38% 弥漫性和 59% 局限性)至少完成了一份 CESD-R 问卷。在第一次调查中,29% 的人可能患有抑郁症(CESD - R ≥ 16),16% 的人可能患有抑郁症(CESD - R ≥ 23)。在 20 名可能患有抑郁症的参与者中,90% 接受了情绪障碍治疗。在 CESD - R ≥ 16 患者的多变量逻辑回归模型中,所有评估变量(CESD-R 评分、年龄、性别、就业状况、种族和民族)均与精神健康诊断或治疗无关。较高的基线呼吸困难指数、改良罗德南皮肤评分以及加州大学洛杉矶分校硬皮病临床试验联盟胃肠道总分和亚分与较高的 CESD-R 评分相关。结论在这项单中心横断面研究中,16%的参与者有明显的抑郁症状。呼吸困难、皮肤受累程度和胃肠道症状与抑郁症状有关。
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引用次数: 0
Glucocorticoid Withdrawal Symptoms and Quality of Life in Patients with Systemic Lupus Erythematosus 系统性红斑狼疮患者的糖皮质激素戒断症状和生活质量
Q3 Medicine Pub Date : 2023-11-10 DOI: 10.1155/2023/5750791
Matee Karoonkatima, Pongthorn Narongroeknawin, Sumapa Chaiamnuay, Paijit Asavatanabodee, Rattapol Pakchotanon
Background/Objective. Chronic glucocorticoid (GCS) therapy is associated with increased risk of organ damage in systemic lupus erythematosus (SLE). However, discontinuation of low-dose GCS might cause withdrawal symptoms. This study is aimed at identifying GCS withdrawal symptoms and health-related quality of life (HRQoL) among SLE patients. Methods. SLE patients whose prednisolone had been previously withdrawn or taken <5 mg/day were enrolled. Serum morning cortisol levels were collected after 72-hour GCS discontinuation, and low-dose ACTH stimulation test (LDST) was performed. Patient report outcomes (PROs) included SLE-specific quality of life questionnaire (SLEQoL), functional assessment of chronic illness therapy (FACIT), patient health questionnaire (PHQ-9), and Pittsburgh’s sleep quality index (PSQI). Results. Serum morning cortisol of 100 SLE patients was tested. Most patients were female (88%). Seventy-four patients showed remission. The mean ± SD of prednisolone was 0.73 ± 1.08 mg/day. Total SLEQoL and FACIT ( mean ± SD ) of all patients were 67.05 ± 26.15 and 13.7 ± 8.87 , respectively. Eighteen percent of patients had moderate-severe depressive symptoms, and 49% were poor sleepers. Adrenal function was determined by LDST in only 39 patients; 5 patients (12.8%) were adrenal insufficiency (AI), and 34 patients were normal adrenal function. Compared to normal adrenal function patients, SLE patients with AI had higher proportion of moderate-severe depressive symptom ( PHQ 9 > 9 ), but not statistically significant (40% vs. 20.6%, p = 0.34 ). PROs were comparable between groups. Independent factors associated with SLEQoL were FACIT (adjusted β 1.31, 95% CI 0.76, 1.86, p < 0.001 ), PHQ-9 (adjusted β 5.21, 95% CI 4.32, 6.09, p < 0.001 ), and PSQI (adjusted β 4.23, 95% CI 3.01, 5.45, p
背景/目标。慢性糖皮质激素(GCS)治疗与系统性红斑狼疮(SLE)器官损伤的风险增加有关。然而,停用低剂量GCS可能会引起戒断症状。本研究旨在确定SLE患者的GCS戒断症状和健康相关生活质量(HRQoL)。方法。先前停用或服用过5mg /天强的松龙的SLE患者被纳入研究。停用GCS 72小时后采集血清皮质醇水平,并进行低剂量ACTH刺激试验(LDST)。患者报告结果(PROs)包括sle特异性生活质量问卷(SLEQoL)、慢性疾病治疗功能评估(FACIT)、患者健康问卷(PHQ-9)和匹兹堡睡眠质量指数(PSQI)。结果。对100例SLE患者进行了晨间血清皮质醇检测。大多数患者为女性(88%)。74名患者出现缓解。泼尼松龙的平均±SD为0.73±1.08 mg/d。所有患者的SLEQoL和FACIT(平均±SD)分别为67.05±26.15和13.7±8.87。18%的患者有中度至重度抑郁症状,49%的患者睡眠质量差。仅39例患者采用LDST检测肾上腺功能;肾上腺功能不全5例(12.8%),肾上腺功能正常34例。与肾上腺功能正常的患者相比,SLE合并AI患者出现中重度抑郁症状的比例更高(PHQ−9 >9),但无统计学意义(40% vs. 20.6%, p = 0.34)。各组间的PROs具有可比性。与SLEQoL相关的独立因素有:FACIT(校正β 1.31, 95% CI 0.76, 1.86, p <0.001), PHQ-9(调整后的β 5.21, 95% CI 4.32, 6.09, p <0.001)和PSQI(调整后的β 4.23, 95% CI 3.01, 5.45, p <0.001),但与AI无关(调整后的β -5.2, 95% CI -33.26, 22.93, 0.71, p = 0.71)。结论。先前接触过GCS的SLE患者在停用低剂量GCS期间可能出现AI和戒断症状,如睡眠障碍和抑郁。疲劳、抑郁和睡眠不良与低SLEQoL显著相关。
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引用次数: 0
The Use of Bone Density Scan in Monitoring Treatment Response in Patients Diagnosed with Osteoporosis: A Retrospective Cohort Study. 骨密度扫描在监测骨质疏松症患者治疗反应中的应用:一项回顾性队列研究。
IF 2.3 Q3 Medicine Pub Date : 2023-10-23 eCollection Date: 2023-01-01 DOI: 10.1155/2023/2160346
Mohammed O Ibrahim, Ahmad Kolleri, Amel Ginawi

Osteoporosis is characterized as a metabolic bone disease defined by low bone mineral density (BMD) and bone tissue degeneration, particularly a reduction in the number of trabeculae and a drop in cortical bone thickness, and a rise in porosity, which is mainly due to an imbalance between bone resorption and formation. As a result, it increases bone fragility, and the susceptibility to fracture increases, especially among the elderly. The objective is to assess the effectiveness of dual-energy X-ray absorptiometry (DXA) scan in monitoring the response to osteoporosis treatment and compare the scan's response to different osteoporosis treatments. This retrospective cohort study included 51 adults selected from 300 patients diagnosed with osteoporosis based on World Health Organization (WHO) diagnostic criteria of a T-score of -2.5. Data were acquired from the electronic medical records between 2016 and 2019 from a private hospital in Dubai, United Arab Emirates (UAE). The study included sociodemographic characteristics, biomedical parameters, comorbidities, history of fracture, medications, laboratory, and DXA scan results. Ninety-four percent of the patients were females; the mean (±SD) age was 58.1 ± 11.5 years. Most patients were expatriates (84.3%), of which Asian ethnicity was 66.7%. The mean (±SD) duration of osteoporosis was 2.82 ± 1.8 years. Eleven (21.6%) patients had a history of fragility fracture. Ninety-six percent of the patients had vitamin D deficiency. One-third (29.4%) of the patients had hyperparathyroidism. Alendronate/cholecalciferol, received by nine patients (17.6%), showed a significant improvement (p = 0.018) in the BMD of the femoral neck among the study group. In conclusion, the DXA scan as a monitoring tool has shown a significant improvement in the BMD of the femoral neck among patients taking alendronate/cholecalciferol treatment compared to other medications.

骨质疏松症是一种代谢性骨病,其特征是骨密度低和骨组织退化,特别是小梁数量减少和皮质骨厚度下降,以及孔隙率增加,这主要是由于骨吸收和形成之间的不平衡。结果,它增加了骨骼的脆性,增加了骨折的易感性,尤其是在老年人中。目的是评估双能X射线吸收仪(DXA)扫描在监测骨质疏松症治疗反应方面的有效性,并比较该扫描对不同骨质疏松症疗法的反应。这项回顾性队列研究包括从300名诊断为骨质疏松症的患者中选择的51名成年人,这些患者的T评分为-2.5,符合世界卫生组织(世界卫生组织)的诊断标准。数据是从2016年至2019年间阿拉伯联合酋长国迪拜一家私人医院的电子医疗记录中获取的。该研究包括社会人口学特征、生物医学参数、合并症、骨折史、药物、实验室和DXA扫描结果。94%的患者是女性;平均(±SD)年龄为58.1±11.5岁。大多数患者为外籍(84.3%),其中亚裔为66.7%。骨质疏松症的平均(±SD)持续时间为2.82±1.8年。11名(21.6%)患者有脆性骨折病史。96%的患者缺乏维生素D。三分之一(29.4%)的患者患有甲状旁腺功能亢进症。9名患者(17.6%)接受阿仑膦酸盐/胆钙化醇治疗,研究组股骨颈骨密度显著改善(p=0.018)。总之,与其他药物相比,DXA扫描作为监测工具显示,接受阿仑膦酸盐/胆钙化醇治疗的患者股骨颈BMD显著改善。
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引用次数: 0
Rheumatic Heart Disease in East Africa: A Systematic Review and Meta-Analysis. 东非风湿性心脏病:系统综述和荟萃分析。
IF 2.3 Q3 Medicine Pub Date : 2023-09-19 eCollection Date: 2023-01-01 DOI: 10.1155/2023/8834443
Guesh Mebrahtom, Abrha Hailay, Woldu Aberhe, Kidane Zereabruk, Teklehaimanot Haile

Background: Despite being a grave problem, there is little information on rheumatic heart disease's prevalence in East Africa. Therefore, the purpose of this systematic review and meta-analysis was to estimate the pooled prevalence of rheumatic heart disease in East Africa.

Materials and methods: A computerized systematic search of using multiple database searching engines was performed in search of relevant English articles from the inception of the databases to December 2019. It was done in accordance with the preferred reporting items for systematic review and meta-analysis (PRISMA) standard. The funnel plot was used to assess publication bias. R and RStudio for Windows were used for all statistical analysis. The random-effect model was used for calculating the pooled estimate of the prevalence of rheumatic heart disease.

Results: The database search retrieved 1073 papers, and 80 articles (78 cross-sectional and two cohort study designs) with a total of 184575 individuals were found to be appropriate for the review. In East Africa, the overall prevalence of rheumatic heart disease was 14.67% (95% CI: 13.99% to 15.35%). In Ethiopia, Uganda, Tanzania, and Sudan, respectively, the subgroup analysis of rheumatic heart disease pooled prevalence was 22% (95% CI: 13% to 36%), 11% (95%t CI: 5% to 20%), 9% (95%t CI: 5% to 16%), and 3% (95%t CI: 1% to 10%), while the pooled prevalence of rheumatic heart disease in adults was 20% (95% CI: 12% to 30%), and in children, it was 4% (95% CI: 2% to 8%).

Conclusions: From this report, the prevalence of rheumatic heart disease in East Africa is very high, affecting about one in seven people. Therefore, future strategies should emphasize preventive measures at appropriate times to minimize the burden of this type of preventable heart disease.

背景:尽管这是一个严重的问题,但关于风湿性心脏病在东非的流行情况的信息很少。因此,本系统综述和荟萃分析的目的是估计东非风湿性心脏病的合并患病率。材料和方法:从数据库建立到2019年12月,使用多个数据库搜索引擎进行计算机化系统搜索,搜索相关英文文章。这是根据系统综述和荟萃分析(PRISMA)标准的首选报告项目进行的。漏斗图用于评估发表偏倚。R和RStudio for Windows用于所有统计分析。随机效应模型用于计算风湿性心脏病患病率的汇总估计。结果:数据库搜索检索了1073篇论文,发现80篇文章(78篇横断面和两个队列研究设计)适合进行审查,共184575人。在东非,风湿性心脏病的总患病率为14.67%(95%CI:13.99%-15.35%)。在埃塞俄比亚、乌干达、坦桑尼亚和苏丹,风湿性心病合并患病率的亚组分析分别为22%(95%CI:13%-36%)、11%(95%CI:5%-20%)、9%(95%CI:5%至16%)和3%(95%CI:1%至10%),而成人风湿性心脏病的合并患病率为20%(95%CI:12%-30%),儿童为4%(95%CI:2%-8%)。因此,未来的战略应该强调在适当的时候采取预防措施,以最大限度地减少这种可预防的心脏病的负担。
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引用次数: 1
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International Journal of Rheumatology
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