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Spectrum of renal histopathologic lesions in patients with nonlupus rheumatologic diseases 非风湿病患者肾脏组织病理学病变谱
IF 0.7 Q4 RHEUMATOLOGY Pub Date : 2023-04-01 DOI: 10.4103/injr.injr_93_22
P. Prasad, M. Bhargav, Alka Singh, V. Agrawal, Manoj Jain
Background: Nonlupus rheumatic diseases regularly involve solid organs, including the kidney. Renal lesions can be either a manifestation of the same systemic disease, a side effect of drug therapy, or an unrelated renal disease. Our aim was to evaluate the spectrum of renal histopathological lesions found in this group of patients. Methods: Native renal biopsies of patients with systemic rheumatic disorders received between January 2014 and August 2019 were reviewed, along with their immunofluorescence findings. The clinical data were recorded from the Hospital Information System. Patients with systemic lupus erythematosus were excluded. Results: Eighty-one clinically diagnosed cases of nonlupus rheumatic diseases were studied (age range 8–70 years, mean 42.8 years, male: female ratio 1:1.3). The most common systemic autoimmune disease was anti-neutrophil cytoplasmic antibodies -associated vasculitis (n = 21) followed by immunoglobulin-A (IgA) vasculitis (Henoch-schonlein purpura) (n = 12) and rheumatoid arthritis (n = 10). The most common histopathological lesion was pauci-immune crescentic glomerulonephritis (n = 26), followed by IgA nephropathy (n = 12) and amyloidosis (n = 8). All patients were treated as per the standard therapeutic regimens. Conclusion: A diverse group of renal lesions can be found in patients with rheumatic disorders. The diagnosis of such lesions aids the clinician in the decision-making for either intensifying or reducing the drug therapy and in predicting the prognosis.
背景:非狼疮性风湿性疾病经常累及实体器官,包括肾脏。肾脏病变可以是同一系统性疾病的表现,药物治疗的副作用,也可以是无关的肾脏疾病。我们的目的是评估在这组患者中发现的肾脏组织病理学病变的频谱。方法:回顾2014年1月至2019年8月期间接受的系统性风湿性疾病患者的自体肾活检及其免疫荧光结果。临床数据来自医院信息系统。系统性红斑狼疮患者被排除在外。结果:研究了81例临床诊断为非狼疮性风湿性疾病的病例(年龄8–70岁,平均42.8岁,男女比例1:1.3)。最常见的全身性自身免疫性疾病是抗中性粒细胞胞浆抗体相关血管炎(n=21),其次是免疫球蛋白A(IgA)血管炎(过敏性紫癜)(n=12)和类风湿性关节炎(n=10)。最常见的组织病理学病变是缺乏免疫新月体肾小球肾炎(n=26),其次是IgA肾病(n=12)和淀粉样变性(n=8)。所有患者均按照标准治疗方案进行治疗。结论:风湿性疾病患者可发现不同类型的肾脏病变。这种病变的诊断有助于临床医生决定加强或减少药物治疗以及预测预后。
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引用次数: 0
Impact of COVID-19 on rheumatic diseases in india: Determinants of mortality and adverse outcome: A retrospective, cross-sectional cohort study COVID-19对印度风湿病的影响:死亡率和不良后果的决定因素:一项回顾性横断面队列研究
IF 0.7 Q4 RHEUMATOLOGY Pub Date : 2023-04-01 DOI: 10.4103/injr.injr_278_21
Avinash Jain, V. Shobha, S. Chandrashekara, P. Shenoy, S. Pandya, Prakash Chotalia, Sharath Kumar, S. Malviya, Y. Singh, A. Patil, Vikas Gupta, P. Srivastava, Vijayaraju Parimi, C. Kodishala, R. Janardana, B. Pinto, S. Bhandari, G. Rankawat, P. Jadhav, Damodaram Potugari, Vishnu Sharma, A. Parmar, Sunitha Kayidhi, P. Antony, Ashish Badika, Amit Sharma
Introduction: There is varying impact of COVID19 on world population depending on ethnicity, age and underlying co-morbidities. However, the lack of data regarding the effect of COVID on patients with rheumatological disorders (RDs) from different nations adds to uncertainty on disease outcome. Across the world, many rheumatology associations have joined hands to collate-related information. A national database under Indian Rheumatology Associations (IRAs) was developed to understand the impact of underlying RD and immunosuppressants during the COVID pandemic on its severity and outcome in our country. Methods: All registered members of IRA were invited to participate in this registry and provide information of reverse transcription–polymerase chain reaction confirmed severe acute respiratory syndrome coronavirus 2 (SARS-CoV2)-infected RD patients using an online platform https://iradatabaseard.in/iracovid/index.php. The results of the data were analyzed using the appropriate statistics. Multivariate logistic regression was used to analyze the impact of different variables on mortality. Odds ratio and 95% confidence interval were used to define risk of death. Results: In this retrospective cross-sectional study, data for 447 RD patients who were infected with SARS-CoV2 data were available as of December 1, 2020. The mean age was 47.9 ± 14.4 years, including two children and 93 (20.8%) geriatric age group patients, male: female ratio was 0.4:1 and mean disease duration was 79.3 ± 77.1 months. Rheumatoid arthritis was the most common RD. Underlying disease was quiescent in 54.7% and active in 18.4% patients. Most common medications at the time of COVID diagnosis were steroids (57.76%) and hydroxychloroquine (67.34%). Fever and cough were the most common symptoms. More than half of the patients (54.4%) needed hospitalization. Oxygen requirement was noted in 18.8%, intensive care unit admission, and invasive ventilation was needed in 6.0%, and 2.9% patients, respectively. Complete recovery was seen in 95.5% of patients and 4.47% (n = 20) expired due to COVID. The presence of comorbidity, dyspnea, and a higher neutrophil count was statistically significantly associated with death (P < 0.05). None of the other factors affected COVID-19 outcome. Conclusion: This is the largest cohort from a single nation looking at the interface between RD and COVID. The results indicate that patients with RD do not show increased mortality despite current use of disease-modifying anti-rheumatic drugs/immunosuppressants.
引言:新冠肺炎19对世界人口的影响因种族、年龄和潜在的合并症而异。然而,缺乏关于新冠肺炎对来自不同国家的风湿病患者影响的数据,增加了疾病结果的不确定性。在世界各地,许多风湿病协会联合起来整理相关信息。印度风湿病协会(IRAs)开发了一个国家数据库,以了解新冠肺炎疫情期间潜在的RD和免疫抑制剂对我国严重程度和结果的影响。方法:所有注册的IRA成员都被邀请参加该注册,并使用在线平台提供逆转录聚合酶链式反应确诊的严重急性呼吸综合征冠状病毒2型(SARS-CoV2)感染的RD患者的信息https://iradatabaseard.in/iracovid/index.php.使用适当的统计数据对数据的结果进行了分析。采用多变量逻辑回归分析不同变量对死亡率的影响。使用比值比和95%置信区间来定义死亡风险。结果:在这项回顾性横断面研究中,截至2020年12月1日,已有447名感染严重急性呼吸系统综合征冠状病毒2型的RD患者的数据。平均年龄为47.9±14.4岁,包括2名儿童和93名(20.8%)老年年龄组患者,男女比例为0.4:1,平均病程为79.3±77.1个月。类风湿性关节炎是最常见的RD。54.7%的患者处于静止状态,18.4%的患者处于活动状态。在确诊新冠肺炎时,最常见的药物是类固醇(57.76%)和羟氯喹(67.34%)。发烧和咳嗽是最常见的症状。超过一半的患者(54.4%)需要住院治疗。18.8%的患者需要吸氧,6.0%和2.9%的患者需要有创通气。95.5%的患者完全康复,4.47%(n=20)因新冠肺炎死亡。合并症、呼吸困难和中性粒细胞计数升高与死亡具有统计学意义(P<0.05)。其他因素均不影响新冠肺炎的结局。结论:这是一个国家研究RD和新冠肺炎之间关系的最大队列。结果表明,尽管目前使用了治疗疾病的抗风湿药物/免疫抑制剂,但RD患者的死亡率并未增加。
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引用次数: 0
Park-Harris growth arrest lines associated with majeed syndrome – A case report Park-Harris生长停滞线与马吉德综合征相关——一例报告
IF 0.7 Q4 RHEUMATOLOGY Pub Date : 2023-04-01 DOI: 10.4103/injr.injr_160_22
S. Acharya, A. Hegde, G. Subramaniam, Krishna Adhikari
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引用次数: 0
Immune-mediated necrotizing myositis with hydroxy-3-methyl-glutaryl-coenzyme A reductase antibody positivity in MSA-negative and statin-naive profile 免疫介导的坏死性肌炎伴羟基-3-甲基-戊二酰辅酶A还原酶抗体阳性的msa阴性和他汀类药物初始谱
IF 0.7 Q4 RHEUMATOLOGY Pub Date : 2023-04-01 DOI: 10.4103/injr.injr_82_22
K. Nagamounika, Josna Joseph, R. Kumar, J. Mathew
Statin-naïve immune-mediated necrotizing myopathy (IMNM) is a rare disease entity, the diagnosis of which is complicated in the absence of a reliable biomarker. In this context, this case, which is the first one reported from a tertiary care center in South India, is unique. The presence of hydroxy-3-methyl-glutaryl-coenzyme A reductase (HMGCR) antibody supplements the clinical diagnosis, specifically in the serological absence of myositis-specific antibodies. A comprehensive diagnostic approach including HMGCR antibody positivity is advisable in IMNM.
Statin-naïve免疫介导的坏死性肌病(IMNM)是一种罕见的疾病,由于缺乏可靠的生物标志物,其诊断很复杂。在这种情况下,该病例是印度南部三级保健中心报告的首例病例,具有独特性。羟-3-甲基戊二酰辅酶A还原酶(HMGCR)抗体的存在补充了临床诊断,特别是在血清学缺乏肌炎特异性抗体的情况下。IMNM建议采用包括HMGCR抗体阳性在内的综合诊断方法。
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引用次数: 0
Successful use of tofacitinib in reactive arthritis following COVID-19 infection 托法替尼在新冠肺炎感染后反应性关节炎中的成功应用
IF 0.7 Q4 RHEUMATOLOGY Pub Date : 2023-01-01 DOI: 10.4103/injr.injr_231_21
P. Padhan, D. Maikap
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引用次数: 0
Primary sjögren's presenting with glomerulonephritis, pure motor neuropathy, pancreatitis, and hypogammaglobulinemia 原发性干燥综合征表现为肾小球肾炎、单纯运动神经病变、胰腺炎和低丙种球蛋白血症
IF 0.7 Q4 RHEUMATOLOGY Pub Date : 2023-01-01 DOI: 10.4103/injr.injr_280_21
K. Chandwar, P. Dogga, J. Dixit, K. Kishor, R. Sahoo, A. Wakhlu
{"title":"Primary sjögren's presenting with glomerulonephritis, pure motor neuropathy, pancreatitis, and hypogammaglobulinemia","authors":"K. Chandwar, P. Dogga, J. Dixit, K. Kishor, R. Sahoo, A. Wakhlu","doi":"10.4103/injr.injr_280_21","DOIUrl":"https://doi.org/10.4103/injr.injr_280_21","url":null,"abstract":"","PeriodicalId":54167,"journal":{"name":"Indian Journal of Rheumatology","volume":"18 1","pages":"103 - 105"},"PeriodicalIF":0.7,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"48725309","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Clinical and serological profile of systemic sclerosis patients in a tertiary care center in Kashmir, North India 印度北部克什米尔三级保健中心系统性硬化症患者的临床和血清学分析
IF 0.7 Q4 RHEUMATOLOGY Pub Date : 2023-01-01 DOI: 10.4103/injr.injr_173_22
F. Sofi, M. Sheikh, Shaariq Naqati, Mushtaq Ahmad, MohammadYonus Soharwardy, BilalAhmad Rather, S. Qayoom
{"title":"Clinical and serological profile of systemic sclerosis patients in a tertiary care center in Kashmir, North India","authors":"F. Sofi, M. Sheikh, Shaariq Naqati, Mushtaq Ahmad, MohammadYonus Soharwardy, BilalAhmad Rather, S. Qayoom","doi":"10.4103/injr.injr_173_22","DOIUrl":"https://doi.org/10.4103/injr.injr_173_22","url":null,"abstract":"","PeriodicalId":54167,"journal":{"name":"Indian Journal of Rheumatology","volume":"6 1","pages":""},"PeriodicalIF":0.7,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"70775700","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Ultrasonography in rheumatology: Beyond the joints and the vessels! 风湿病超声检查:超越关节和血管!
IF 0.7 Q4 RHEUMATOLOGY Pub Date : 2023-01-01 DOI: 10.4103/injr.injr_32_23
A. Chattopadhyay, D. Misra
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引用次数: 0
Tumor necrosis factor inhibitors versus janus kinase inhibitors in patients with incomplete response to methotrexate in rheumatoid arthritis 类风湿性关节炎患者对甲氨蝶呤不完全反应的肿瘤坏死因子抑制剂与janus激酶抑制剂
IF 0.7 Q4 RHEUMATOLOGY Pub Date : 2023-01-01 DOI: 10.4103/injr.injr_251_21
K. Chandwar, Chandani Shah, P. Srivastava
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引用次数: 0
M694V gene polymorphism may not contribute to the pathogenesis of reactive arthritis in the North Indian population M694V基因多态性可能与北印度人群反应性关节炎的发病机制无关
IF 0.7 Q4 RHEUMATOLOGY Pub Date : 2023-01-01 DOI: 10.4103/injr.injr_64_22
Latika Gupta, A. Anuja, K. Thomas, M. Singh, A. Mathew, V. Agarwal
Introduction: Reactive arthritis (ReA) is a postinfectious, nonseptic arthritis that is characterized by an acute lower limb predominant oligoarthritis. Inflammasome activation and its contribution to autoinflammatory loop are described in spondyloarthritis (SpA). ReA may present a forme fruste of diseases with autoinflammation as in familial Mediterranean fever. Therefore, we investigated the presence of gene polymorphisms of the Mediterranean fever (MEFV) gene in patients with ReA. Methods: Patients of ReA presenting to a Tertiary Hospital in North India were enrolled and evaluated for MEFV gene polymorphism by restriction fragment length polymorphism analysis. Results: Forty-nine patients (male:female – 37:12), including five juvenile ReA were included during the study. The median age was 25 (±11) years and disease duration was 0.76 (±1.33) months. Twenty-six cases were triggered by preceding enteritis and 23 by urethritis. Ten healthy controls of age 27 (male:female – 7:3, interquartile range ± 1.5) were included for comparison. All 49 patients of adult and juvenile ReA were negative for the M694V mutation. Conclusions: This is the first study assessing the prevalence of MEFV gene mutation in SpA in India. It is difficult to ascertain if the lack of association is limited to the Indian subcontinent.
简介:反应性关节炎(ReA)是一种感染后的非视性关节炎,其特征是以急性下肢为主的寡关节炎。炎症小体激活及其对自身炎症循环的作用在脊椎关节炎(SpA)中有描述。ReA可能表现为家族性地中海热等具有自身炎症的疾病。因此,我们研究了ReA患者地中海热(MEFV)基因多态性的存在。方法:对在北印度一家三级医院就诊的ReA患者进行登记,并通过限制性片段长度多态性分析评估MEFV基因多态性。结果:49名患者(男性:女性–37:12),包括5名青少年ReA。中位年龄25(±11)岁,病程0.76(±1.33)个月。26例由先前的肠炎引发,23例由尿道炎引发。纳入10名年龄为27岁的健康对照(男性:女性-7:3,四分位间距±1.5)进行比较。所有49名成人和青少年ReA患者的M694V突变均为阴性。结论:这是第一项评估印度SpA中MEFV基因突变患病率的研究。很难确定缺乏联系是否仅限于印度次大陆。
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Indian Journal of Rheumatology
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