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The effects of glucocorticoid treatment on cardiovascular system in patients with systemic lupus erythematosus. 糖皮质激素治疗对系统性红斑狼疮患者心血管系统的影响。
IF 1.1 4区 医学 Q4 Medicine Pub Date : 2022-12-01 DOI: 10.46497/ArchRheumatol.2022.9255
Dominika Blachut, Brygida Przywara-Chowaniec, Jan Harpula, Andrzej Tomasik, Ewa Nowalany-Kozielska, Beata Morawiec

Objectives: This study aims to assess variables concerning arterial stiffness including carotid-femoral pulse wave velocity, carotid-radial pulse wave velocity, ankle-brachial index, and the advancement of atherosclerosis development.

Patients and methods: Between October 2016 and December 2020, a total of 43 consecutive patients with systemic lupus erythematosus (SLE) (4 males, 39 females; mean age: 57±8 years; range, 42 to 65 years) were prospectively included in the study. All data were compared between the group treated with glucocorticoids and that not treated with these agents.

Results: The study group consisted of 43 patients with SLE, while 22 (51%) patients were treated with glucocorticoids. The mean duration of SLE was 12.3±5.3 years. Patients treated with glucocorticoids had lower values of ankle-brachial index compared to those who were not treated with glucocorticoids (p=0.041), although the values were within the range. A similar situation was reported for the carotid-femoral artery pulse wave velocity (p=0.032). However, carotid-radial artery pulse wave velocity was not significantly different between both groups (p=0.12).

Conclusion: Properly selected therapy is important in the prevention of CVD.

目的:本研究旨在评估动脉硬度的变量,包括颈动脉-股动脉脉波速度、颈动脉-桡动脉脉波速度、踝-肱指数和动脉粥样硬化发展的进展。患者和方法:2016年10月至2020年12月,共连续43例系统性红斑狼疮(SLE)患者(男4例,女39例;平均年龄:57±8岁;年龄范围42 - 65岁)被纳入前瞻性研究。所有数据在接受糖皮质激素治疗组和未接受糖皮质激素治疗组之间进行比较。结果:研究组有43例SLE患者,其中22例(51%)患者接受糖皮质激素治疗。SLE平均病程12.3±5.3年。与未接受糖皮质激素治疗的患者相比,接受糖皮质激素治疗的患者踝臂指数较低(p=0.041),尽管其值在范围内。颈动脉-股动脉脉波速度也有类似的情况(p=0.032)。两组间颈桡动脉脉波速度差异无统计学意义(p=0.12)。结论:合理选择治疗方法是预防心血管疾病的重要手段。
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引用次数: 0
The reliability of Juvenile Arthritis Magnetic Resonance Imaging Scoring system in the evaluation of the shoulder joint in juvenile idiopathic arthritis. 青少年关节炎磁共振成像评分系统在青少年特发性关节炎肩关节评估中的可靠性。
IF 1.1 4区 医学 Q4 Medicine Pub Date : 2022-12-01 DOI: 10.46497/ArchRheumatol.2022.9304
Murugan Sudhakar, Shivani Deswal, Namrita Sachdev, Somdipa Pal, Tribhuvan Pal Yadav

Objectives: We aimed to evaluate shoulder joint by magnetic resonance imaging (MRI) using the Juvenile Arthritis Magnetic Resonance Imaging Scoring (JAMRIS) system in children with juvenile idiopathic arthritis (JIA) and to compare clinical, laboratory parameters and disease activity scores with MRI parameters.

Patients and methods: A total of 32 shoulder joints of 20 patients (16 males, 4 females; mean age: 8.9±3.5 years; range, 2.5 to 14 years) with a known diagnosis of JIA and a clinical suspicion of shoulder joint involvement and underwent MRI were included. Reliability was determined by inter- and intra-observer correlation coefficients. Correlation of the clinical and laboratory parameters with JAMRIS scores was done using the non-parametric tests. Sensitivity of clinical examination to detect shoulder joint arthritis was also determined.

Results: Of the 32 joints, 27 joints in 17 patients showed MRI changes. Seven joints in five patients fulfilled the definition of clinical arthritis, all revealed MRI changes. In 25 joints without clinical arthritis, early and late MRI changes were seen in 19 (67%) and 12 (48%) joints, respectively. The inter- and intra-observer correlation coefficients for JAMRIS system were excellent. No correlation was found between MRI parameters, clinical, laboratory, and disease activity scores. The sensitivity of clinical examination to detect shoulder joint arthritis was 25.9%.

Conclusion: The JAMRIS system is reliable and reproducible to determine shoulder joint inflammation in JIA. Detection of shoulder joint arthritis by clinical examination has a poor sensitivity.

目的:采用少年关节炎磁共振成像评分(JAMRIS)系统对幼年特发性关节炎(JIA)儿童的肩关节进行磁共振成像(MRI)评估,并将临床、实验室参数和疾病活动性评分与MRI参数进行比较。患者与方法:20例患者共32个肩关节(男16例,女4例;平均年龄8.9±3.5岁;年龄在2.5至14岁之间),诊断为JIA,临床怀疑肩关节受累,并接受MRI检查。信度由观察者之间和观察者内部的相关系数决定。临床和实验室参数与JAMRIS评分的相关性采用非参数测试。临床检查对肩关节关节炎的敏感性也被确定。结果:32个关节中,17例患者27个关节出现MRI改变。5例患者的7个关节符合临床关节炎的定义,均显示MRI改变。在25个无临床关节炎的关节中,分别有19个(67%)和12个(48%)关节出现早期和晚期MRI改变。JAMRIS系统的观测器间和观测器内的相关系数都很好。MRI参数、临床、实验室和疾病活动度评分之间没有相关性。临床检查对肩关节关节炎的诊断敏感性为25.9%。结论:JAMRIS系统用于JIA患者肩关节炎症的检测可靠,重复性好。临床检查对肩关节关节炎的检测灵敏度较差。
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引用次数: 0
Validity and reliability of the Turkish version of Psoriasis Epidemiology Screening Tool for the detection of psoriatic arthritis in patients with psoriasis. 土耳其版牛皮癣流行病学筛查工具检测牛皮癣患者银屑病关节炎的效度和信度
IF 1.1 4区 医学 Q4 Medicine Pub Date : 2022-12-01 DOI: 10.46497/ArchRheumatol.2022.8221
Serdar Kaymaz, Uğur Karasu, Nida Kaçar, Hakan Alkan

Objectives: The Psoriasis Epidemiology Screening Tool (PEST) is a simple and useful questionnaire designed to screen arthritis in patients with psoriasis. This study aims to evaluate the validity and reliability of the PEST questionnaire in Turkish patients with psoriasis.

Patients and methods: Between August 2019 and September 2019, a total of 158 adult patients with psoriasis (61 males, 68 females; mean age: 43.1±13.3 years; range, 29.8 to 56.4 years) who were not previously diagnosed with PsA were included. The testing procedure for translation and cultural adaptation was carried out according to the following steps: preparation, forward translation, reconciliation, back-translation/back-translation review, harmonization, finalization, and proofreading. Patients' demographic parameters, comorbidities, PEST, and Toronto Psoriatic Arthritis Screen (ToPAS 2) results were recorded. The patients were, then, assessed by a rheumatologist who was blinded to their PEST scores. The diagnosis of PsA was made according to the Classification criteria for Psoriatic Arthritis (CASPAR). The receiver operating characteristic (ROC) was assessed to obtain the sensitivity and specificity of the PEST questionnaire.

Results: Of the patients, 42 had PsA, while 87 did not. Each parameter of PEST showed a low-high internal consistency ranging from 0.366 to 0.781. When the Question 3 was excluded, Cronbach alpha value increased to 0.866. The Cronbach alpha value of the whole scale was 0.829. The test-retest reliability of the Turkish version of PEST was determined as 0.86 for the total score (ICC=0.866 95% CI: 0.601-0.955; p<0.0001). There was a strong positive correlation between PEST and ToPAS 2 (r=0.763; p<0.001) and a moderate positive correlation between PEST and CASPAR (r=0.455; p<0.001). A cut-off value of ≥3 yielded a sensitivity of 93% and a specificity of 89% for the diagnosis of PsA with the highest Youden's index. The PEST scale was found to have a higher sensitivity, but lower specificity in the head-to-head comparison with ToPAS 2.

Conclusion: The Turkish version of PEST is a reliable and valid tool for screening PsA in Turkish patients with psoriasis.

目的:银屑病流行病学筛查工具(PEST)是一种简单实用的调查问卷,旨在筛查银屑病患者的关节炎。本研究旨在评估PEST问卷在土耳其银屑病患者中的效度和信度。患者与方法:2019年8月至2019年9月,共158例成年牛皮癣患者(男性61例,女性68例;平均年龄:43.1±13.3岁;年龄范围29.8 - 56.4岁),既往未诊断为PsA的患者也包括在内。翻译和文化适应性测试程序按照以下步骤进行:准备、正译、核对、反译/反译审查、协调、定稿和校对。记录患者的人口统计学参数、合并症、PEST和多伦多银屑病关节炎筛查(topas2)结果。然后,由一名风湿病学家对患者进行评估,该专家对他们的PEST评分不知情。根据银屑病关节炎分类标准(CASPAR)诊断PsA。评估受试者工作特征(ROC)以获得PEST问卷的敏感性和特异性。结果:42例患者有PsA, 87例患者无PsA。PEST各参数的内部一致性为低-高,范围为0.366 ~ 0.781。排除问题3后,Cronbach alpha值增加到0.866。整个量表的Cronbach alpha值为0.829。土耳其版PEST总分的重测信度为0.86 (ICC=0.866 95% CI: 0.601-0.955;结论:土耳其版PEST是筛查土耳其银屑病患者PsA的可靠有效工具。
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引用次数: 0
An investigation of coronaphobia and physical activity among patients with rheumatoid arthritis. 类风湿关节炎患者冠状病毒恐惧症与身体活动的调查。
IF 1.1 4区 医学 Q4 Medicine Pub Date : 2022-12-01 DOI: 10.46497/ArchRheumatol.2022.9586
Gonca Sağlam, Emine Esra Ergül

Objectives: This study aims to investigate coronaphobia and physical activity levels in patients with rheumatoid arthritis (RA).

Patients and methods: Between December 2021 and February 2022, a total of 68 RA patients (11 males, 57 females; mean age: 48.3±10.1 years; range, 29 to 78 years) and 64 age- and sex-matched healthy individuals (4 males, 60 females; mean age: 47.9±10.2 years; range, 23 to 70 years) were included in this cross-sectional study. Demographic, physical, lifestyle, and medical characteristics of all participants were recorded. The COVID-19 Phobia Scale (C19PS) and the International Physical Activity Questionnaire-Short Form (IPAQ-SF) were administered to all participants. The RA patients were divided into two groups as: patients treated with biological and non-biological agents. The Disease Activity Score-28 (DAS28) and Clinical Disease Activity Index (CDAI) were used to measure disease activity.

Results: The total and subgroup scores of the C19P-S were found to be statistically significantly higher in both the biological and non-biological RA groups than in the control group (p=0.001). However, there was no statistically significant difference between the RA groups in terms of total and subgroup C19P-S scores. The mean IPAQ score was significantly lower in the RA group using biological drugs than in the control group (p=0.002). A significant correlation was found between DAS28 and total C19P-S scores (r:0.63, p<0.05), and CDAI and total C19P-S scores (r:0.79, p<0.05).

Conclusion: Patients with RA have an increased risk of coronaphobia and disease activity is correlated with coronaphobia. Patients treated with biological agents seem to have lower activity levels compared to other RA patients and healthy controls. These results should be considered in the management of RA during COVID-19 pandemic and preventive intervention strategies should be formulated to cope with coronaphobia.

目的:本研究旨在探讨类风湿性关节炎(RA)患者的冠状病毒恐惧症和身体活动水平。患者和方法:2021年12月至2022年2月,共68例RA患者(男性11例,女性57例;平均年龄:48.3±10.1岁;年龄29至78岁)和64名年龄和性别匹配的健康个体(4名男性,60名女性;平均年龄:47.9±10.2岁;年龄在23岁到70岁之间)的患者被纳入了这项横断面研究。记录所有参与者的人口统计学、体格、生活方式和医学特征。对所有参与者进行COVID-19恐惧症量表(C19PS)和国际体育活动问卷-简表(IPAQ-SF)。RA患者分为两组:生物制剂组和非生物制剂组。采用疾病活动性评分-28 (DAS28)和临床疾病活动性指数(CDAI)来衡量疾病活动性。结果:生物组和非生物组的C19P-S总分和亚组评分均高于对照组,差异有统计学意义(p=0.001)。然而,RA组间C19P-S总分和亚组评分差异无统计学意义。RA生物药物治疗组IPAQ平均评分明显低于对照组(p=0.002)。DAS28与C19P-S总分存在显著相关性(r:0.63, p)。结论:RA患者发生冠状恐惧的风险增加,疾病活动度与冠状恐惧相关。与其他类风湿性关节炎患者和健康对照相比,接受生物制剂治疗的患者似乎有较低的活动水平。这些结果应在新冠肺炎大流行期间RA的管理中加以考虑,并制定预防干预策略以应对冠状病毒恐惧症。
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引用次数: 0
Does remission in rheumatoid arthritis bring kinesiophobia, quality of life, fatigue, and physical activity closer to normal? 类风湿关节炎的缓解是否会使运动恐惧症、生活质量、疲劳和身体活动更接近正常?
IF 1.1 4区 医学 Q4 Medicine Pub Date : 2022-12-01 DOI: 10.46497/ArchRheumatol.2022.9552
Aysun Özlü, Merve Akdeniz Leblebicier

Objectives: This study aimed to compare kinesiophobia, fatigue, physical activity, and quality of life (QoL) between the patients with rheumatoid arthritis (RA) in remission and a healthy population.

Patients and methods: The prospective controlled study included 45 female patients (mean age: 54.22±8.2 year; range, 37 to 67 year) with a diagnosis of RA determined to be in remission according to the Disease Activity Score in 28 Joints (DAS28) being ≤2.6 between January 2022 and February 2022. As a control group, 45 female healthy volunteers (mean age: 52.2±8.2 year; range, 34 to 70 year) of similar age were evaluated. The QoL, disease activity, pain, kinesiophobia, fatigue severity, and physical activity were assessed using the Health Assessment Questionnaire, DAS28, Visual Analog Scale, Tampa Scale of Kinesiophobia, Fatigue Severity Scale, and International Physical Activity Questionnaire, respectively.

Results: There was no significant difference between the groups in demographic data. A statistically significant difference was found between the groups in terms of pain, C-reactive protein level, fatigue, kinesiophobia, QoL, and total, high, and moderate physical activity scores (p<0.001). Among the RA patients in remission, there was a significant correlation between kinesiophobia and moderate physical activity and QoL, as well as between fatigue and high physical activity (p<0.05).

Conclusion: Patient education and multidisciplinary approach strategies should be developed to increase the QoL and physical activity and reduce kinesiophobia in RA patients in remission since there may be a decrease in physical activity due to kinesiophobia, fatigue, and fear of movement in this patient group compared to the healthy population, impairing their QoL.

目的:本研究旨在比较类风湿关节炎(RA)缓解期患者和健康人群的运动恐惧症、疲劳、体力活动和生活质量(QoL)。患者与方法:前瞻性对照研究纳入女性患者45例,平均年龄54.22±8.2岁;范围,37至67岁),根据28个关节的疾病活动评分(DAS28),在2022年1月至2022年2月期间≤2.6,诊断为RA缓解。作为对照组,45名女性健康志愿者(平均年龄:52.2±8.2岁;范围为34至70岁),年龄相近。分别采用健康评估问卷、DAS28、视觉模拟量表、坦帕运动恐惧症量表、疲劳严重程度量表和国际体育活动问卷对生活质量、疾病活动度、疼痛、运动恐惧症、疲劳严重程度和体育活动进行评估。结果:两组间人口学资料差异无统计学意义。两组患者在疼痛、c反应蛋白水平、疲劳、运动恐惧症、生活质量、总、高、中体力活动评分方面差异有统计学意义(p)。与健康人群相比,RA缓解期患者可能由于运动恐惧症、疲劳和运动恐惧而减少身体活动,从而损害其生活质量,因此应制定患者教育和多学科方法策略,以增加患者的生活质量和身体活动,减少患者的运动恐惧。
{"title":"Does remission in rheumatoid arthritis bring kinesiophobia, quality of life, fatigue, and physical activity closer to normal?","authors":"Aysun Özlü,&nbsp;Merve Akdeniz Leblebicier","doi":"10.46497/ArchRheumatol.2022.9552","DOIUrl":"https://doi.org/10.46497/ArchRheumatol.2022.9552","url":null,"abstract":"<p><strong>Objectives: </strong>This study aimed to compare kinesiophobia, fatigue, physical activity, and quality of life (QoL) between the patients with rheumatoid arthritis (RA) in remission and a healthy population.</p><p><strong>Patients and methods: </strong>The prospective controlled study included 45 female patients (mean age: 54.22±8.2 year; range, 37 to 67 year) with a diagnosis of RA determined to be in remission according to the Disease Activity Score in 28 Joints (DAS28) being ≤2.6 between January 2022 and February 2022. As a control group, 45 female healthy volunteers (mean age: 52.2±8.2 year; range, 34 to 70 year) of similar age were evaluated. The QoL, disease activity, pain, kinesiophobia, fatigue severity, and physical activity were assessed using the Health Assessment Questionnaire, DAS28, Visual Analog Scale, Tampa Scale of Kinesiophobia, Fatigue Severity Scale, and International Physical Activity Questionnaire, respectively.</p><p><strong>Results: </strong>There was no significant difference between the groups in demographic data. A statistically significant difference was found between the groups in terms of pain, C-reactive protein level, fatigue, kinesiophobia, QoL, and total, high, and moderate physical activity scores (p<0.001). Among the RA patients in remission, there was a significant correlation between kinesiophobia and moderate physical activity and QoL, as well as between fatigue and high physical activity (p<0.05).</p><p><strong>Conclusion: </strong>Patient education and multidisciplinary approach strategies should be developed to increase the QoL and physical activity and reduce kinesiophobia in RA patients in remission since there may be a decrease in physical activity due to kinesiophobia, fatigue, and fear of movement in this patient group compared to the healthy population, impairing their QoL.</p>","PeriodicalId":8328,"journal":{"name":"Archives of rheumatology","volume":"37 4","pages":"603-612"},"PeriodicalIF":1.1,"publicationDate":"2022-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/fb/20/ArchRheumatol-2022-37-603.PMC9985370.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10860672","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Identification of a novel mutation in complement receptor 2 in Chinese familial systemic lupus erythematosus. 中国家族性系统性红斑狼疮补体受体2新突变的鉴定。
IF 1.1 4区 医学 Q4 Medicine Pub Date : 2022-12-01 DOI: 10.46497/ArchRheumatol.2022.9167
Yuewu Tang, Yi Luo

Objectives: This study aims to analyze the relationship between complement receptor 2 (CR2) gene mutation and the clinical phenotype in Chinese familial systemic lupus erythematosus (SLE).

Patients and methods: A total of one Chinese familial SLE patients (median age: 30.25 years; range, 22 to 49 years) were included between January 2017 and December 2018. The clinical features and diagnoses of familial SLE patients were analyzed using whole-exome sequencing (WES) of genomic deoxyribonucleic acid (DNA) samples. Sanger sequencing was used to verify candidate mutations detected in the examined family.

Results: The mother and her three daughters were diagnosed with SLE. The clinical characteristics showed that the patient and her mother were diagnosed with lupus nephritis. The eldest daughter had decreased renal function and lower serum albumin levels. Immunological index analysis showed that all four patients were positive for anti-SSA and antinuclear antibody (ANA), but that only the second daughter was positive for anti-double-stranded DNA (dsDNA). Complement 3 (C3) was significantly decreased in all patients, while evaluation of the Systemic Lupus Erythematosus Disease Activity Index (SLEDAI) showed that the second and third daughters had mild active SLE. The mother and eldest daughter were treated with prednisolone combined with cyclophosphamide, while the other two daughters were treated with prednisolone alone. The WES and Sanger sequencing analyses revealed an unreported missense T>C mutation c.2804 in the 15th exon of the CR gene in all four patients.

Conclusion: We identified a novel c.2804 (exon 15) T>C mutation in the CR gene of Chinese familial SLE. This mutation was previously reported, suggesting that the CR gene c.2804 (exon 15) T>C mutation is the probable cause of SLE in this family.

目的:分析家族性系统性红斑狼疮(SLE)患者补体受体2 (CR2)基因突变与临床表型的关系。患者和方法:中国家族性SLE患者1例(中位年龄:30.25岁;范围为22至49岁),包括2017年1月至2018年12月。采用基因组脱氧核糖核酸(DNA)全外显子组测序(WES)分析家族性SLE患者的临床特征和诊断。Sanger测序用于验证在所检查的家族中检测到的候选突变。结果:母亲及其三个女儿均被诊断为SLE。临床表现表明患者及其母亲被诊断为狼疮性肾炎。大女儿肾功能下降,血清白蛋白水平降低。免疫指标分析显示,4例患者抗ssa和抗核抗体(ANA)均阳性,但只有二女儿抗双链DNA (dsDNA)阳性。所有患者的补体3 (C3)均显著降低,而系统性红斑狼疮疾病活动指数(SLEDAI)的评估显示,二女儿和三女儿患有轻度活动性SLE。母亲和大女儿使用强的松龙联合环磷酰胺治疗,另外两个女儿单独使用强的松龙治疗。WES和Sanger测序分析显示,在所有4例患者中,CR基因第15外显子存在未报道的T>C错义突变C .2804。结论:鉴定出一株新的c.2804(外显子15)中国家族性SLE CR基因T>C突变。这一突变先前有报道,表明CR基因c.2804(外显子15)T>C突变是本家族SLE的可能病因。
{"title":"Identification of a novel mutation in complement receptor 2 in Chinese familial systemic lupus erythematosus.","authors":"Yuewu Tang,&nbsp;Yi Luo","doi":"10.46497/ArchRheumatol.2022.9167","DOIUrl":"https://doi.org/10.46497/ArchRheumatol.2022.9167","url":null,"abstract":"<p><strong>Objectives: </strong>This study aims to analyze the relationship between complement receptor 2 (CR2) gene mutation and the clinical phenotype in Chinese familial systemic lupus erythematosus (SLE).</p><p><strong>Patients and methods: </strong>A total of one Chinese familial SLE patients (median age: 30.25 years; range, 22 to 49 years) were included between January 2017 and December 2018. The clinical features and diagnoses of familial SLE patients were analyzed using whole-exome sequencing (WES) of genomic deoxyribonucleic acid (DNA) samples. Sanger sequencing was used to verify candidate mutations detected in the examined family.</p><p><strong>Results: </strong>The mother and her three daughters were diagnosed with SLE. The clinical characteristics showed that the patient and her mother were diagnosed with lupus nephritis. The eldest daughter had decreased renal function and lower serum albumin levels. Immunological index analysis showed that all four patients were positive for anti-SSA and antinuclear antibody (ANA), but that only the second daughter was positive for anti-double-stranded DNA (dsDNA). Complement 3 (C3) was significantly decreased in all patients, while evaluation of the Systemic Lupus Erythematosus Disease Activity Index (SLEDAI) showed that the second and third daughters had mild active SLE. The mother and eldest daughter were treated with prednisolone combined with cyclophosphamide, while the other two daughters were treated with prednisolone alone. The WES and Sanger sequencing analyses revealed an unreported missense T>C mutation c.2804 in the 15<sup>th</sup> exon of the CR gene in all four patients.</p><p><strong>Conclusion: </strong>We identified a novel c.2804 (exon 15) T>C mutation in the CR gene of Chinese familial SLE. This mutation was previously reported, suggesting that the CR gene c.2804 (exon 15) T>C mutation is the probable cause of SLE in this family.</p>","PeriodicalId":8328,"journal":{"name":"Archives of rheumatology","volume":"37 4","pages":"566-573"},"PeriodicalIF":1.1,"publicationDate":"2022-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/63/da/ArchRheumatol-2022-37-566.PMC9985375.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10849502","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Association of tumor necrosis factor-alpha promoter region gene polymorphism at positions -308G/A, -857C/T, and -863C/A with etanercept response in Iraqi rheumatoid arthritis patients. 伊拉克类风湿关节炎患者肿瘤坏死因子- α启动子区基因-308G/A、-857C/T和-863C/A位点多态性与依那西普反应的关系
IF 1.1 4区 医学 Q4 Medicine Pub Date : 2022-12-01 DOI: 10.46497/ArchRheumatol.2022.9272
Samer Mohammed, Munaf Zalzala, Faiq Gorial
Objectives This study aims to evaluate the association between polymorphisms in the promoter region of the tumor necrosis factor-alpha (TNF-α) gene at locations -308G/A, -857C/T, and -863C/A with the tendency of being non-responder to etanercept. Patients and methods Between October 2020 and August 2021, a total of 80 patients (10 males, 70 females; mean age: 50 years; range, 30 to 72 years) with rheumatoid arthritis (RA) receiving etanercept for at least six months were included. The patients were divided into two groups responders and non-responders, based on their response after six months of continuous treatment. Following polymerase chain reaction amplification of the extracted deoxyribonucleic acid, sequencing by Sanger method was performed to identify the polymorphism at the TNF-α promoter region. Results In the responder group, the GG genotype of (-308G/A) and the AA genotype of (-863C/A) were both significantly present. The CC genotype of (-863C/A) was significantly present in the non-responders group. The CC of (-863C/A) SNP was the only genotype that appeared to increase the likelihood of being resistant to etanercept. The GG genotype of (-308G/A) was negatively correlated with the likelihood of being a non-responder. The (-857CC) and (-863CC) genotypes were significantly more prevalent in the non-responders group. Conclusion The presence of the (-863CC) genotype, alone or in combination with (-857CC), is linked to an increased likelihood of becoming a non-responder to etanercept. The GG genotype of -308G/A and the AA genotype of -863C/A significantly increase the likelihood of becoming responder to etanercept.
目的:本研究旨在评价肿瘤坏死因子-α (TNF-α)基因启动子区-308G/A、-857C/T和-863C/A位点多态性与依那西普无应答倾向之间的关系。患者与方法:2020年10月~ 2021年8月,共80例患者(男10例,女70例;平均年龄:50岁;范围:30 - 72岁)类风湿性关节炎(RA)患者接受依那西普治疗至少6个月。根据患者连续治疗6个月后的反应,将患者分为有反应组和无反应组。对提取的脱氧核糖核酸进行聚合酶链反应扩增后,采用Sanger法进行测序,鉴定TNF-α启动子区域的多态性。结果:应答组GG基因型(-308G/A)和AA基因型(-863C/A)均显著存在。CC基因型(-863C/A)在无反应组中显著存在。(-863C/A) SNP的CC是唯一增加依那西普耐药可能性的基因型。GG基因型(-308G/A)与无应答的可能性呈负相关。(-857CC)和(-863CC)基因型在无反应组中更为普遍。结论:(-863CC)基因型的存在,单独或联合(-857CC),与依那西普无应答的可能性增加有关。GG基因型-308G/A和AA基因型-863C/A显著增加依那西普的应答可能性。
{"title":"Association of tumor necrosis factor-alpha promoter region gene polymorphism at positions -308G/A, -857C/T, and -863C/A with etanercept response in Iraqi rheumatoid arthritis patients.","authors":"Samer Mohammed,&nbsp;Munaf Zalzala,&nbsp;Faiq Gorial","doi":"10.46497/ArchRheumatol.2022.9272","DOIUrl":"https://doi.org/10.46497/ArchRheumatol.2022.9272","url":null,"abstract":"Objectives This study aims to evaluate the association between polymorphisms in the promoter region of the tumor necrosis factor-alpha (TNF-α) gene at locations -308G/A, -857C/T, and -863C/A with the tendency of being non-responder to etanercept. Patients and methods Between October 2020 and August 2021, a total of 80 patients (10 males, 70 females; mean age: 50 years; range, 30 to 72 years) with rheumatoid arthritis (RA) receiving etanercept for at least six months were included. The patients were divided into two groups responders and non-responders, based on their response after six months of continuous treatment. Following polymerase chain reaction amplification of the extracted deoxyribonucleic acid, sequencing by Sanger method was performed to identify the polymorphism at the TNF-α promoter region. Results In the responder group, the GG genotype of (-308G/A) and the AA genotype of (-863C/A) were both significantly present. The CC genotype of (-863C/A) was significantly present in the non-responders group. The CC of (-863C/A) SNP was the only genotype that appeared to increase the likelihood of being resistant to etanercept. The GG genotype of (-308G/A) was negatively correlated with the likelihood of being a non-responder. The (-857CC) and (-863CC) genotypes were significantly more prevalent in the non-responders group. Conclusion The presence of the (-863CC) genotype, alone or in combination with (-857CC), is linked to an increased likelihood of becoming a non-responder to etanercept. The GG genotype of -308G/A and the AA genotype of -863C/A significantly increase the likelihood of becoming responder to etanercept.","PeriodicalId":8328,"journal":{"name":"Archives of rheumatology","volume":"37 4","pages":"613-625"},"PeriodicalIF":1.1,"publicationDate":"2022-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/c3/ed/ArchRheumatol-2022-37-613.PMC9985381.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10857194","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 4
Association of pain and clinical factors on disability and quality of life in systemic sclerosis: A cross-sectional study from Turkish League Against Rheumatism Network. 系统性硬化症患者的疼痛和临床因素对残疾和生活质量的影响:来自土耳其抗风湿联盟网络的横断面研究。
IF 1.1 4区 医学 Q4 Medicine Pub Date : 2022-11-11 eCollection Date: 2023-03-01 DOI: 10.46497/ArchRheumatol.2023.9243
Remzi Çevik, Serda Em, Kemal Nas, Murat Toprak, Gizem Cengiz, Mustafa Çalış, İlhan Sezer, Ayşe Ünal Enginar, Pınar Bora Karslı, Sinem Sağ, Betül Sargın, Meltem Alkan Melikoğlu, Yıldıray Aydın, Mehmet Tuncay Duruöz, Halise Hande Gezer, Hilal Ecesoy

Objectives: In this study, we aimed to evaluate the factors associated with disability and quality of life (QoL) in Turkish patients with systemic sclerosis (SSc).

Patients and methods: Between January 2018 and January 2019, a total of 256 SSc patients (20 males, 236 females; mean age: 50.9±12.4 years; range, 19 to 87 years) who were diagnosed with SSc were included in the study. Disability and health-related QoL (HRQoL) were evaluated by the Health Assessment Questionnaire (HAQ), scleroderma HAQ (SHAQ), Duruöz Hand Index (DHI), and Short Form-36 (SF-36). Linear regression analysis methods were used to describe factors associated with disability and QoL of the patients.

Results: All disability scores were higher and HRQoL scores were lower in diffuse cutaneous SSc patients compared limited cutaneous SSc, and differentiations were significant (p=0.001 and p=0.007). In multiple regression, pain (VAS) was the strongest predictor for high disability and low QoL scores (p<0.001) as HAQ (β=0.397, 0.386, 0.452), SHAQ (β=0.397, 0.448, 0.372), DHI (β=0.446, 0.536, 0.389), PCS (β=-0.417,-0.499, -0.408) and MCS (β=-0.478, -0.441, -0.370) in combined, lcSSc and dcSSc patients respectively. The factors associated with high disability and low QoL scores were forced vital capacity for HAQ (β=-0.172, p=0.002) and SF-36 PCS (β=0.187, p=0.001); disease duration for HAQ (β=0.208, p<0.001), DHI (β=0.147, p=0.006), and SF-36 PCS (β=-0.134, p=0.014); 6-minute walk test for HAQ (β=-0.161, p=0.005) and SF-36 PCS (β=0.153, p=0.009); and modified Rodnan skin score for SHAQ (β=0.250, p<0.001) and DHI (β=0.233, p<0.001) in SSc patients. Diffusing capacity of the lungs for carbon monoxide for HAQ (β=-0.189, p=0.010) and SHAQ (β=-0.247, p=0.002); erythrocyte sedimentation rate for DHI (β=0.322, p<0.001); age for SF-36 PCS (β=-0.221, p=0.003) and body mass index for SF-36 PCS (β=-0.200, p=0.008) and MCS (β=-0.175, p=0.034) were the other variables associated with high disability or low QoL scores in SSc subsets.

Conclusion: Clinicians should consider the management of the pain and its sources as a key to improve better functional state and quality of daily life in SSc.

研究目的本研究旨在评估土耳其系统性硬化症(SSc)患者残疾和生活质量(QoL)的相关因素:在 2018 年 1 月至 2019 年 1 月期间,共有 256 名确诊为 SSc 的患者(男性 20 人,女性 236 人;平均年龄:50.9±12.4 岁;范围:19 至 87 岁)被纳入研究。通过健康评估问卷(HAQ)、硬皮病HAQ(SHAQ)、Duruöz手指数(DHI)和短表格-36(SF-36)对残疾和健康相关生活质量(HRQoL)进行评估。采用线性回归分析方法描述了与患者残疾和 QoL 相关的因素:结果:与局限性皮肤型 SSc 相比,弥漫性皮肤型 SSc 患者的所有残疾评分均较高,HRQoL 评分较低,且差异显著(P=0.001 和 P=0.007)。在多元回归中,疼痛(VAS)是预测高残疾和低 QoL 评分的最有力因素(p 结论:临床医生应考虑对弥漫性皮肤型 SSc 患者进行治疗:临床医生应将疼痛及其来源的管理视为改善 SSc 患者功能状态和日常生活质量的关键。
{"title":"Association of pain and clinical factors on disability and quality of life in systemic sclerosis: A cross-sectional study from Turkish League Against Rheumatism Network.","authors":"Remzi Çevik, Serda Em, Kemal Nas, Murat Toprak, Gizem Cengiz, Mustafa Çalış, İlhan Sezer, Ayşe Ünal Enginar, Pınar Bora Karslı, Sinem Sağ, Betül Sargın, Meltem Alkan Melikoğlu, Yıldıray Aydın, Mehmet Tuncay Duruöz, Halise Hande Gezer, Hilal Ecesoy","doi":"10.46497/ArchRheumatol.2023.9243","DOIUrl":"10.46497/ArchRheumatol.2023.9243","url":null,"abstract":"<p><strong>Objectives: </strong>In this study, we aimed to evaluate the factors associated with disability and quality of life (QoL) in Turkish patients with systemic sclerosis (SSc).</p><p><strong>Patients and methods: </strong>Between January 2018 and January 2019, a total of 256 SSc patients (20 males, 236 females; mean age: 50.9±12.4 years; range, 19 to 87 years) who were diagnosed with SSc were included in the study. Disability and health-related QoL (HRQoL) were evaluated by the Health Assessment Questionnaire (HAQ), scleroderma HAQ (SHAQ), Duruöz Hand Index (DHI), and Short Form-36 (SF-36). Linear regression analysis methods were used to describe factors associated with disability and QoL of the patients.</p><p><strong>Results: </strong>All disability scores were higher and HRQoL scores were lower in diffuse cutaneous SSc patients compared limited cutaneous SSc, and differentiations were significant (p=0.001 and p=0.007). In multiple regression, pain (VAS) was the strongest predictor for high disability and low QoL scores (p<0.001) as HAQ (β=0.397, 0.386, 0.452), SHAQ (β=0.397, 0.448, 0.372), DHI (β=0.446, 0.536, 0.389), PCS (β=-0.417,-0.499, -0.408) and MCS (β=-0.478, -0.441, -0.370) in combined, lcSSc and dcSSc patients respectively. The factors associated with high disability and low QoL scores were forced vital capacity for HAQ (β=-0.172, p=0.002) and SF-36 PCS (β=0.187, p=0.001); disease duration for HAQ (β=0.208, p<0.001), DHI (β=0.147, p=0.006), and SF-36 PCS (β=-0.134, p=0.014); 6-minute walk test for HAQ (β=-0.161, p=0.005) and SF-36 PCS (β=0.153, p=0.009); and modified Rodnan skin score for SHAQ (β=0.250, p<0.001) and DHI (β=0.233, p<0.001) in SSc patients. Diffusing capacity of the lungs for carbon monoxide for HAQ (β=-0.189, p=0.010) and SHAQ (β=-0.247, p=0.002); erythrocyte sedimentation rate for DHI (β=0.322, p<0.001); age for SF-36 PCS (β=-0.221, p=0.003) and body mass index for SF-36 PCS (β=-0.200, p=0.008) and MCS (β=-0.175, p=0.034) were the other variables associated with high disability or low QoL scores in SSc subsets.</p><p><strong>Conclusion: </strong>Clinicians should consider the management of the pain and its sources as a key to improve better functional state and quality of daily life in SSc.</p>","PeriodicalId":8328,"journal":{"name":"Archives of rheumatology","volume":"38 1","pages":"9-21"},"PeriodicalIF":1.1,"publicationDate":"2022-11-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/29/a4/ArchRheumatol-2023-38-009.PMC10208607.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9529297","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Patients with inflammatory myopathies overlapping with systemic sclerosis: A Brazilian-Japanese bicentric study. 炎症性肌病与系统性硬化重叠的患者:一项巴西-日本双中心研究。
IF 1.1 4区 医学 Q4 Medicine Pub Date : 2022-09-20 eCollection Date: 2023-03-01 DOI: 10.46497/ArchRheumatol.2023.9597
Jucier Gonçalves Júnior, Naoki Mugii, Pleiades Tiharu Inaoka, Renata Miossi, Fernando Henrique Carlos De Souza, João Calvino Soares De Oliveira, Fujiko Someya, Yasuhito Hamaguchi, Takashi Matsushita, Percival Degrava Sampaio-Barros, Samuel Katsuyuki Shinjo

Objectives: This study aims to describe and compare the demographic, clinical, and laboratory characteristics and follow-up of representative samples of patients with myopathies and systemic sclerosis overlap syndromes (Myo-SSc) from two tertiary centers.

Patients and methods: This is a cross-sectional and retrospective study conducted between January 2000 and December 2020. Fourty-five patients were analyzed with Myo-SSc (6 males, 39 females; mean age: 50.2±15.4 years; range, 45 to 65 years) from two tertiary centers (n=30 from Brazil and n=15 from Japan).

Results: The median follow-up was 98 (range, 37 to 168) months. Muscle impairment started simultaneously with the diagnosis of systemic sclerosis in 57.8% (26/45) of cases. Muscle involvement occurred before the onset of systemic sclerosis in 35.5% (16/45) of cases, and after in 6.7% (3/45). Polymyositis was observed in 55.6% (25/45) of cases, followed by dermatomyositis in 24.4% (11/45) and antisynthetase syndrome in 20.0% (9/45). Concerning systemic sclerosis, the diffuse and limited forms occurred in 64.4% (29/45) and 35.6% (16/45) of the cases, respectively. Comparing the subgroups, Myo or SSc onset was earlier in Brazilian patients, and they had a higher frequency of dysphagia (20/45, [66.7%]) and digital ulcers (27/45, [90%]), whereas Japanese patients had higher modified Rodnan skin scores (15 [9 to 23]) and prevalence of positive anti-centromere antibodies (4/15 [23.7%]). The current disease status and mortality were similar in both groups.

Conclusion: In the present study, Myo-SSc affected middle-aged women, and its manifestation spectrum varied according to geographic distribution.

目的:本研究旨在描述和比较来自两个三级中心的肌病和系统性硬化重叠综合征(Myo-SSc)患者的人口统计学、临床和实验室特征以及随访。患者和方法:这是一项在2000年1月至2020年12月期间进行的横断面和回顾性研究。对来自两个三级中心(巴西n=30,日本n=15)的45名Myo-SSc患者(6名男性,39名女性;平均年龄:50.2±15.4岁;范围:45-65岁)进行分析。结果:中位随访时间为98个月(范围:37-168)。57.8%(26/45)的病例在诊断为系统性硬化的同时出现肌肉损伤。35.5%(16/45)的病例在系统性硬化症发作前发生肌肉受累,6.7%(3/45)的患者在发作后发生肌肉受累。55.6%(25/45)的病例观察到多发性肌炎,其次是皮肌炎24.4%(11/45)和抗合成酶综合征20.0%(9/45)。关于系统性硬化症,弥漫型和局限型分别发生在64.4%(29/45)和35.6%(16/45)的病例中。比较这些亚组,巴西患者的Myo或SSc发病较早,吞咽困难(20/45,[66.7%])和手指溃疡(27/45,[90%])的发生率较高,而日本患者的改良Rodnan皮肤评分(15[9-23])和抗着丝粒抗体阳性率(4/15[23.7%])较高。两组目前的疾病状况和死亡率相似。结论:在本研究中,Myo-SSc影响中年妇女,其表现谱因地理分布而异。
{"title":"Patients with inflammatory myopathies overlapping with systemic sclerosis: A Brazilian-Japanese bicentric study.","authors":"Jucier Gonçalves Júnior,&nbsp;Naoki Mugii,&nbsp;Pleiades Tiharu Inaoka,&nbsp;Renata Miossi,&nbsp;Fernando Henrique Carlos De Souza,&nbsp;João Calvino Soares De Oliveira,&nbsp;Fujiko Someya,&nbsp;Yasuhito Hamaguchi,&nbsp;Takashi Matsushita,&nbsp;Percival Degrava Sampaio-Barros,&nbsp;Samuel Katsuyuki Shinjo","doi":"10.46497/ArchRheumatol.2023.9597","DOIUrl":"10.46497/ArchRheumatol.2023.9597","url":null,"abstract":"<p><strong>Objectives: </strong>This study aims to describe and compare the demographic, clinical, and laboratory characteristics and follow-up of representative samples of patients with myopathies and systemic sclerosis overlap syndromes (Myo-SSc) from two tertiary centers.</p><p><strong>Patients and methods: </strong>This is a cross-sectional and retrospective study conducted between January 2000 and December 2020. Fourty-five patients were analyzed with Myo-SSc (6 males, 39 females; mean age: 50.2±15.4 years; range, 45 to 65 years) from two tertiary centers (n=30 from Brazil and n=15 from Japan).</p><p><strong>Results: </strong>The median follow-up was 98 (range, 37 to 168) months. Muscle impairment started simultaneously with the diagnosis of systemic sclerosis in 57.8% (26/45) of cases. Muscle involvement occurred before the onset of systemic sclerosis in 35.5% (16/45) of cases, and after in 6.7% (3/45). Polymyositis was observed in 55.6% (25/45) of cases, followed by dermatomyositis in 24.4% (11/45) and antisynthetase syndrome in 20.0% (9/45). Concerning systemic sclerosis, the diffuse and limited forms occurred in 64.4% (29/45) and 35.6% (16/45) of the cases, respectively. Comparing the subgroups, Myo or SSc onset was earlier in Brazilian patients, and they had a higher frequency of dysphagia (20/45, [66.7%]) and digital ulcers (27/45, [90%]), whereas Japanese patients had higher modified Rodnan skin scores (15 [9 to 23]) and prevalence of positive anti-centromere antibodies (4/15 [23.7%]). The current disease status and mortality were similar in both groups.</p><p><strong>Conclusion: </strong>In the present study, Myo-SSc affected middle-aged women, and its manifestation spectrum varied according to geographic distribution.</p>","PeriodicalId":8328,"journal":{"name":"Archives of rheumatology","volume":"38 1","pages":"138-147"},"PeriodicalIF":1.1,"publicationDate":"2022-09-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/24/19/ArchRheumatol-2023-38-138.PMC10208608.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9526650","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
High prevalence of latent tuberculosis using the QuantiFERON-TB Gold Plus test in Takayasu arteritis. 使用QuantiFERON-TB Gold Plus检测高松动脉炎中潜伏性结核病的高流行率
IF 1.1 4区 医学 Q4 Medicine Pub Date : 2022-09-01 DOI: 10.46497/ArchRheumatol.2022.9077
Ana Luisa Souza Pedreira, Rodrigo Pinheiro Leal Costa, Josenor Filipe Pitanga Silva, Mittermayer Barreto Santiago

Objectives: This study aims to investigate latent tuberculosis using the QuantiFERON-TB Gold Plus method in patients with Takayasu arteritis (TA).

Patients and methods: This case-control study included 22 patients with TA (3 males, 19 females; median age: 36.5 years; IQR, 32 to 50 years), 22 healthy individuals (3 males, 19 females; median age: 38.5 years; IQR, 32.5 to 50 years), and 66 patients with diffuse connective tissue diseases (DCTDs) (4 males, 62 females; median age: 41 years; IQR, 29.8 to 54 years). Two control groups were formed: (i) age- and sex-matched healthy individuals and (ii) patients with other DCTDs. Epidemiological data were collected, and the QFT-Plus test was performed. The QFT-plus positivity was compared among the groups.

Results: A higher prevalence of QFT-Plus positive cases was observed in the TA group (8/22) than in the healthy control group (1/22) (p=0.020) or in the group with other DCTDs (3/66) (p=0.001). There was a statistically significant difference in the past pulmonary tuberculosis prevalence between the TA and DCTD groups (p=0.013).

Conclusion: The prevalence of latent tuberculosis in TA patients (36.4%) was higher than that in both control groups and higher than the prevalence of latent tuberculosis among the general Brazilian population. Although a positive association was found, it is not possible to establish a direct cause-effect relationship. Given the increasing use of anti-cytokine therapies in TA, it is necessary to thoroughly screen patients with TA before initiating immunosuppressive therapy to avoid tuberculosis reactivation.

目的:本研究旨在利用QuantiFERON-TB Gold Plus方法研究高松动脉炎(TA)患者的潜伏性结核。患者和方法:本病例对照研究纳入22例TA患者(男性3例,女性19例;中位年龄:36.5岁;IQR, 32 ~ 50岁),健康个体22例(男性3例,女性19例;中位年龄:38.5岁;IQR, 32.5 ~ 50岁),弥漫性结缔组织病(DCTDs) 66例(男性4例,女性62例;中位年龄:41岁;IQR, 29.8至54岁)。形成两个对照组:(i)年龄和性别匹配的健康个体和(ii)患有其他DCTDs的患者。收集流行病学资料,并进行QFT-Plus检测。比较各组间QFT-plus阳性率。结果:TA组QFT-Plus阳性检出率(8/22)高于健康对照组(1/22)(p=0.020)和其他DCTDs组(3/66)(p=0.001)。TA组与DCTD组过去肺结核患病率差异有统计学意义(p=0.013)。结论:TA患者的潜伏性结核患病率(36.4%)高于两组对照组,也高于巴西普通人群的潜伏性结核患病率。虽然发现了正相关,但不可能建立直接的因果关系。鉴于抗细胞因子治疗在TA中的使用越来越多,有必要在开始免疫抑制治疗之前彻底筛查TA患者,以避免结核病再激活。
{"title":"High prevalence of latent tuberculosis using the QuantiFERON-TB Gold Plus test in Takayasu arteritis.","authors":"Ana Luisa Souza Pedreira,&nbsp;Rodrigo Pinheiro Leal Costa,&nbsp;Josenor Filipe Pitanga Silva,&nbsp;Mittermayer Barreto Santiago","doi":"10.46497/ArchRheumatol.2022.9077","DOIUrl":"https://doi.org/10.46497/ArchRheumatol.2022.9077","url":null,"abstract":"<p><strong>Objectives: </strong>This study aims to investigate latent tuberculosis using the QuantiFERON-TB Gold Plus method in patients with Takayasu arteritis (TA).</p><p><strong>Patients and methods: </strong>This case-control study included 22 patients with TA (3 males, 19 females; median age: 36.5 years; IQR, 32 to 50 years), 22 healthy individuals (3 males, 19 females; median age: 38.5 years; IQR, 32.5 to 50 years), and 66 patients with diffuse connective tissue diseases (DCTDs) (4 males, 62 females; median age: 41 years; IQR, 29.8 to 54 years). Two control groups were formed: <i>(i)</i> age- and sex-matched healthy individuals and <i>(ii)</i> patients with other DCTDs. Epidemiological data were collected, and the QFT-Plus test was performed. The QFT-plus positivity was compared among the groups.</p><p><strong>Results: </strong>A higher prevalence of QFT-Plus positive cases was observed in the TA group (8/22) than in the healthy control group (1/22) (p=0.020) or in the group with other DCTDs (3/66) (p=0.001). There was a statistically significant difference in the past pulmonary tuberculosis prevalence between the TA and DCTD groups (p=0.013).</p><p><strong>Conclusion: </strong>The prevalence of latent tuberculosis in TA patients (36.4%) was higher than that in both control groups and higher than the prevalence of latent tuberculosis among the general Brazilian population. Although a positive association was found, it is not possible to establish a direct cause-effect relationship. Given the increasing use of anti-cytokine therapies in TA, it is necessary to thoroughly screen patients with TA before initiating immunosuppressive therapy to avoid tuberculosis reactivation.</p>","PeriodicalId":8328,"journal":{"name":"Archives of rheumatology","volume":"37 3","pages":"344-350"},"PeriodicalIF":1.1,"publicationDate":"2022-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/a6/0c/ArchRheumatol-2022-37-344.PMC9791558.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10458326","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
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Archives of rheumatology
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