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Correlation of simple hematological parameters with disease activity and damage indices among Egyptian patients with systemic lupus erythematosus 埃及系统性红斑狼疮患者单纯性血液学参数与疾病活动性及损伤指标的相关性研究
Pub Date : 2025-04-01 DOI: 10.1016/j.rcreue.2025.04.003
Hanan H. Ahmed , Hebatallah S. Farag , Nesreen Sobhy

Objective

To evaluate the correlation of different hematological parameters in lupus patients with SLE disease activity index (SLEDAI), the Systemic Lupus International Collaboration Clinics/American College of Rheumatology Damage Index (SLICC/ACR DI), and some laboratory data related to kidney functions in active patients with nephritis.

Material and methods

80 inactive SLE patients (SLEDAI score < 10 points), and 80 active patients (SLEDAI  10 points) were enrolled in this study. All patients underwent full medical history taking, clinical evaluation including calculation of SLEDAI and SLICC/ACR DI scores, and laboratory investigations including complete blood count. The two groups were compared regarding different disease parameters. Correlations of some hematological parameters with SLEDAI, SLICC/ACR DI scores and some laboratory data related to kidney function in patients with nephritis were made.

Results

The active group showed statistically significantly higher mean NLR (P = 0.000), NC3R (P = 0.000), MLR (P = 0.000), PLR (P = 0.000), and RDW (P = 0.001), and statistically significantly lower mean MPV (P = 0.002). The mean MLR (P = 0.018) and PLR (P = 0.005) were statistically significantly higher in the active patients with nephritis. For both groups, there were no significant correlations between studied parameters and SLEDAI or SLICC/ACR DI, except with NC3R values in the active group which were associated with SLEDAI (r = .221, P = 0.049).

Conclusion

The hematological parameters in SLE have promising potential clinical application as a novel activity marker, especially in patients with nephritis.
目的评价狼疮患者SLE疾病活动性指数(SLEDAI)、系统性狼疮国际合作诊所/美国风湿病学会损伤指数(SLICC/ACR DI)与狼疮活动性肾炎患者肾功能相关的一些实验室数据的相关性。材料与方法80例SLE患者(SLEDAI评分<;10分),80例活动期患者(SLEDAI≥10分)入组。所有患者均接受了完整的病史记录、临床评估(包括SLEDAI和SLICC/ACR DI评分计算)和实验室检查(包括全血细胞计数)。比较两组患者不同的疾病参数。将部分血液学参数与肾炎患者SLEDAI、SLICC/ACR DI评分及一些与肾功能相关的实验室数据进行相关性分析。结果治疗组NLR (P = 0.000)、NC3R (P = 0.000)、MLR (P = 0.000)、PLR (P = 0.000)、RDW (P = 0.001)均显著高于治疗组,MPV (P = 0.002)均显著低于治疗组。活动期肾炎患者的平均MLR (P = 0.018)和PLR (P = 0.005)均高于活动期肾炎患者。两组研究参数与SLEDAI或SLICC/ACR DI之间均无显著相关性,但活性组NC3R值与SLEDAI相关(r = 0.221, P = 0.049)。结论血液学指标作为一种新的活动性指标在SLE患者尤其是肾炎患者中具有潜在的临床应用价值。
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引用次数: 0
ABC of lupus nephritis 狼疮性肾炎的ABC
Pub Date : 2025-04-01 DOI: 10.1016/j.rcreue.2025.03.003
José A. Gómez-Puerta
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引用次数: 0
Sociodemographic, clinical, and biochemical characteristics of patients who presented with and without lupus nephritis in a cohort of Mexican patients with systemic lupus erythematosus in a referral centre 在转诊中心的墨西哥系统性红斑狼疮患者队列中,出现和不出现狼疮肾炎的患者的社会人口学、临床和生化特征
Pub Date : 2025-04-01 DOI: 10.1016/j.rcreue.2025.02.005
Fabiola Pazos-Pérez , Aida Martínez-Badajoz , Francisco M. Bravo-Rojas , Estafanía Garduño-Hernández , María I. Gil-Arredondo , Rocío Catana-Hernández , Mario C. Ocampo-Torres , Juan C. Hernández-Rivera

Introduction

Systemic lupus erythematosus (SLE) is an autoimmune inflammatory disease that presents great clinical heterogeneity, so that up to 60% of patients may develop lupus nephropathy (LN).

Objective

To identify demographic, clinical, and biochemical characteristics of patients presenting with and without lupus nephritis at the time of SLE diagnosis in a cohort of Mexican patients

Materials and methods

This is a cross-sectional, analytical, and single-centre study. Frequencies and percentages were used for categorical variables and the comparison was made with Pearson's Chi2 statistical test or Fisher's exact test. For the quantitative variables, their distribution was calculated and according to this, Student's t was used in case of normal distribution and Mann-Whitney U for those with free distribution.

Results

Of 160 patients, 79 (49.37%) had LN. These individuals had a higher prevalence of serositis (14.3 vs. 8.1%, p = 0.048) and arterial hypertension (40.50% vs. 24.6%, p = 0.033), while those without LN had a higher prevalence of rheumatoid arthritis and joint disease (6 vs. 1%, p = 0.052), allergies (43.2 vs. 20.25%, p = 0.002), infections (23.45 vs. 10%, p = 0.020), and lower levels of C3 (52.25±28.7 vs. 74.6±32.2 mg/dl, p < 0.001).

Conclusions

The characteristics described in our cohort are like those presented in other Latino and Asian series. However, the presence of concomitant infections at the time of SLE diagnosis has not been described and should be considered for future research.
系统性红斑狼疮(SLE)是一种自身免疫性炎症性疾病,具有很大的临床异质性,因此高达60%的患者可发展为狼疮肾病(LN)。目的:在一组墨西哥患者中,确定SLE诊断时伴有和不伴有狼疮性肾炎患者的人口学、临床和生化特征。材料和方法:这是一项横断面、分析性、单中心研究。分类变量采用频率和百分比,采用Pearson's Chi2统计检验或Fisher's精确检验进行比较。对于定量变量,计算其分布,在正态分布情况下使用Student’st,在自由分布情况下使用Mann-Whitney U。结果160例患者中有79例(49.37%)发生LN。这些个体浆膜炎患病率较高(14.3和8.1%,p = 0.048)和高血压(40.50%比24.6%,p = 0.033),而那些没有LN风湿性关节炎和关节疾病患病率较高(6和1%,p = 0.052),过敏( 43.2和20.25%,p = 0.002 )、感染(23.45和10%,p = 0.020),和低水平的C3(52.25±28.7和74.6±32.2 mg / dl, p & lt; 0.001)。结论:在我们的队列中描述的特征与其他拉丁美洲和亚洲系列的特征相似。然而,在SLE诊断时是否存在合并感染尚未被描述,应在未来的研究中予以考虑。
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引用次数: 0
Effect of induction therapy with mycophenolate or cyclophosphamide on serum BAFF levels in patients with systemic lupus erythematosus 霉酚酸盐或环磷酰胺诱导治疗对系统性红斑狼疮患者血清BAFF水平的影响
Pub Date : 2025-04-01 DOI: 10.1016/j.rcreue.2024.12.002
Alejandra Betancur Herrera , Juan José Mariño Restrepo , Tulio Lopera Restrepo , Laura Robledo Montoya , Juan Felipe Soto Restrepo , Adriana Lucía Vanegas García , Carlos Horacio Muñoz Vahos , Juan Camilo Díaz Coronado , Ricardo Antonio Pineda Tamayo , Gloria Vásquez

Introduction

Systemic lupus erythematosus (SLE) is a complex autoimmune disease in which B cell hyperactivity plays a key role in its pathophysiology. In this disease, the B cell activating factor (BAFF) is implicated in the loss of immunological tolerance, and high concentrations of this factor have been linked to disease progression. It is unknown how induction therapies with cyclophosphamide (CFM) or mycophenolate (MMF) modulate BAFF levels.

Objective

To determine how induction therapies modulate BAFF concentrations.

Materials and methods

An analytical observational study was performed with 20 patients with SLE from two institutions between 2020–2022, clinical and laboratory information was obtained from medical records. Measurement of serum BAFF levels was performed using an ELISA kit and statistical analyses with GraphPad Prism version 9.

Results

20 patients with a diagnosis of SLE, 18 with CFM and 2 with MMF, were included, nine patients at baseline and eleven at 3–6 months. The median BAFF in SLE patients was 902.2 pg/mL and 379.7 pg/mL in healthy controls, statistically significant differences (p = .0003). BAFF levels were also found to be different among patients treated with antimalarials (p = .0465) and an inverse correlation with creatinine values and prednisolone doses was also observed.

Conclusions

BAFF levels are affected during induction therapy, observing an initial reduction and subsequent recovery at 3–6 months, our results suggest that chloroquine and high doses of prednisolone maintain lower serum BAFF levels.
系统性红斑狼疮(SLE)是一种复杂的自身免疫性疾病,B细胞过度活跃在其病理生理中起着关键作用。在这种疾病中,B细胞活化因子(BAFF)与免疫耐受性的丧失有关,并且该因子的高浓度与疾病进展有关。目前尚不清楚环磷酰胺(CFM)或霉酚酸盐(MMF)诱导治疗如何调节BAFF水平。目的探讨诱导疗法对BAFF浓度的调节作用。材料与方法对2020-2022年间来自两家机构的20例SLE患者进行了一项分析性观察研究,临床和实验室信息来自医疗记录。使用ELISA试剂盒测定血清BAFF水平,并使用GraphPad Prism version 9进行统计分析。结果20例SLE患者,18例CFM, 2例MMF, 9例基线,11例3-6个月。SLE患者BAFF中位数为902.2 pg/mL,健康对照组为379.7 pg/mL,差异有统计学意义(p = .0003)。BAFF水平在接受抗疟药物治疗的患者中也存在差异(p = .0465),并且与肌酐值和强的松龙剂量呈负相关。结论BAFF水平在诱导治疗期间受到影响,在3-6个月观察到最初的降低和随后的恢复,我们的结果表明氯喹和大剂量强的松龙维持较低的血清BAFF水平。
{"title":"Effect of induction therapy with mycophenolate or cyclophosphamide on serum BAFF levels in patients with systemic lupus erythematosus","authors":"Alejandra Betancur Herrera ,&nbsp;Juan José Mariño Restrepo ,&nbsp;Tulio Lopera Restrepo ,&nbsp;Laura Robledo Montoya ,&nbsp;Juan Felipe Soto Restrepo ,&nbsp;Adriana Lucía Vanegas García ,&nbsp;Carlos Horacio Muñoz Vahos ,&nbsp;Juan Camilo Díaz Coronado ,&nbsp;Ricardo Antonio Pineda Tamayo ,&nbsp;Gloria Vásquez","doi":"10.1016/j.rcreue.2024.12.002","DOIUrl":"10.1016/j.rcreue.2024.12.002","url":null,"abstract":"<div><h3>Introduction</h3><div>Systemic lupus erythematosus (SLE) is a complex autoimmune disease in which B cell hyperactivity plays a key role in its pathophysiology. In this disease, the B cell activating factor (BAFF) is implicated in the loss of immunological tolerance, and high concentrations of this factor have been linked to disease progression. It is unknown how induction therapies with cyclophosphamide (CFM) or mycophenolate (MMF) modulate BAFF levels.</div></div><div><h3>Objective</h3><div>To determine how induction therapies modulate BAFF concentrations.</div></div><div><h3>Materials and methods</h3><div>An analytical observational study was performed with 20 patients with SLE from two institutions between 2020–2022, clinical and laboratory information was obtained from medical records. Measurement of serum BAFF levels was performed using an ELISA kit and statistical analyses with GraphPad Prism version 9.</div></div><div><h3>Results</h3><div>20 patients with a diagnosis of SLE, 18 with CFM and 2 with MMF, were included, nine patients at baseline and eleven at 3–6 months. The median BAFF in SLE patients was 902.2 pg/mL and 379.7 pg/mL in healthy controls, statistically significant differences (p = .0003). BAFF levels were also found to be different among patients treated with antimalarials (p = .0465) and an inverse correlation with creatinine values and prednisolone doses was also observed.</div></div><div><h3>Conclusions</h3><div>BAFF levels are affected during induction therapy, observing an initial reduction and subsequent recovery at 3–6 months, our results suggest that chloroquine and high doses of prednisolone maintain lower serum BAFF levels.</div></div>","PeriodicalId":101099,"journal":{"name":"Revista Colombiana de Reumatología (English Edition)","volume":"32 2","pages":"Pages 118-129"},"PeriodicalIF":0.0,"publicationDate":"2025-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143917296","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
Factors associated with development of end stage renal disease during hospitalization in patients with microscopic polyangiitis and granulomatosis with polyangiitis in a population of northwestern Colombia 哥伦比亚西北部人群显微多血管炎和肉芽肿病合并多血管炎患者住院期间终末期肾脏疾病发展的相关因素
Pub Date : 2025-01-01 DOI: 10.1016/j.rcreue.2024.12.001
Santiago Cobaleda Cano , Andrés Felipe Echeverri García , Adriana Margarita Trejos Tenorio , Javier Darío Márquez Hernández , Jhon Edwar García Rueda , Luis Fernando Pinto Peñaranda

Introduction

ANCA vasculitis has been associated with increased morbidity and mortality, high disease burden, and organ damage, especially renal.

Objectives

To determine factors associated with end-stage kidney disease at hospital discharge in microscopic polyangiitis and granulomatosis with polyangiitis patients, to characterize our population, hospitalization causes, treatment received, and complications during stay.

Materials and methods

Adults with previous or new diagnosis of microscopic polyangiitis and granulomatosis with polyangiitis who required hospitalization between January 01, 2013, and April 30, 2021, were included. Association with end-stage kidney disease development was evaluated by Pearson’s Chi2 (χ2) or Fisher’s test, and Student’s t or Mann–Whitney U test according to the nature of the variables. Exploratory multivariate models were made including factors associated with end-stage kidney disease.

Results

Forty-three patients were included, microscopic polyangiitis 55.8, and granulomatosis with polyangiitis 44.25. Twelve patients (27.9%) developed early end-stage kidney disease. High blood pressure, high urea nitrogen levels on admission, as well as pulmonary oedema, and Five Factor Score >1 entailed a higher risk. In contrast, normal kidney function on admission was a protective factor. Rapidly progressive glomerulonephritis and arterial hypertension on admission were associated with end-stage kidney disease. In adjusted exploratory models according to vasculitis type, Birmingham Vasculitis Activity Score, diffuse alveolar haemorrhage, and plasma exchange use were identified as factors to include in multivariate models in multicentre studies.

Conclusion

88% of patients had renal involvement and 27.9% developed end-stage kidney disease. Rapidly progressive glomerulonephritis and arterial hypertension on hospital admission were associated with early development of end-stage kidney disease while normal renal function on admission was a protective factor for this outcome.
anca血管炎与发病率和死亡率增加、疾病负担高和器官损害(尤其是肾脏)有关。目的确定显微镜下多血管炎和肉芽肿合并多血管炎患者出院时终末期肾病的相关因素,以确定我们的人群、住院原因、接受的治疗和住院期间的并发症。材料和方法纳入2013年1月1日至2021年4月30日期间住院治疗的既往或新诊断为显微镜下多血管炎和肉芽肿病合并多血管炎的成年人。根据变量的性质,采用Pearson χ2检验或Fisher检验、Student t检验或Mann-Whitney U检验来评价与终末期肾病发展的相关性。建立了包括终末期肾病相关因素在内的探索性多变量模型。结果纳入43例患者,镜下多血管炎55.8例,肉芽肿合并多血管炎44.25例。12例患者(27.9%)发展为早期终末期肾病。入院时高血压、高尿素氮水平、肺水肿和五因子评分(5 Factor Score >1)的风险较高。相反,入院时正常的肾功能是一个保护因素。入院时迅速进展的肾小球肾炎和动脉高血压与终末期肾脏疾病相关。在根据血管炎类型调整的探索性模型中,伯明翰血管炎活动评分、弥漫性肺泡出血和血浆置换使用被确定为多中心研究中多变量模型的因素。结论88%的患者有肾脏受累,27.9%的患者有终末期肾脏疾病。入院时迅速进展的肾小球肾炎和动脉高血压与终末期肾病的早期发展有关,而入院时正常的肾功能是这一结果的保护因素。
{"title":"Factors associated with development of end stage renal disease during hospitalization in patients with microscopic polyangiitis and granulomatosis with polyangiitis in a population of northwestern Colombia","authors":"Santiago Cobaleda Cano ,&nbsp;Andrés Felipe Echeverri García ,&nbsp;Adriana Margarita Trejos Tenorio ,&nbsp;Javier Darío Márquez Hernández ,&nbsp;Jhon Edwar García Rueda ,&nbsp;Luis Fernando Pinto Peñaranda","doi":"10.1016/j.rcreue.2024.12.001","DOIUrl":"10.1016/j.rcreue.2024.12.001","url":null,"abstract":"<div><h3>Introduction</h3><div>ANCA vasculitis has been associated with increased morbidity and mortality, high disease burden, and organ damage, especially renal.</div></div><div><h3>Objectives</h3><div>To determine factors associated with end-stage kidney disease at hospital discharge in microscopic polyangiitis and granulomatosis with polyangiitis patients, to characterize our population, hospitalization causes, treatment received, and complications during stay.</div></div><div><h3>Materials and methods</h3><div>Adults with previous or new diagnosis of microscopic polyangiitis and granulomatosis with polyangiitis who required hospitalization between January 01, 2013, and April 30, 2021, were included. Association with end-stage kidney disease development was evaluated by Pearson’s Chi<sup>2</sup> (<em>χ</em><sup>2</sup>) or Fisher’s test, and Student’s <em>t</em> or Mann–Whitney <em>U</em> test according to the nature of the variables. Exploratory multivariate models were made including factors associated with end-stage kidney disease.</div></div><div><h3>Results</h3><div>Forty-three patients were included, microscopic polyangiitis 55.8, and granulomatosis with polyangiitis 44.25. Twelve patients (27.9%) developed early end-stage kidney disease. High blood pressure, high urea nitrogen levels on admission, as well as pulmonary oedema, and Five Factor Score &gt;1 entailed a higher risk. In contrast, normal kidney function on admission was a protective factor. Rapidly progressive glomerulonephritis and arterial hypertension on admission were associated with end-stage kidney disease. In adjusted exploratory models according to vasculitis type, Birmingham Vasculitis Activity Score, diffuse alveolar haemorrhage, and plasma exchange use were identified as factors to include in multivariate models in multicentre studies.</div></div><div><h3>Conclusion</h3><div>88% of patients had renal involvement and 27.9% developed end-stage kidney disease. Rapidly progressive glomerulonephritis and arterial hypertension on hospital admission were associated with early development of end-stage kidney disease while normal renal function on admission was a protective factor for this outcome.</div></div>","PeriodicalId":101099,"journal":{"name":"Revista Colombiana de Reumatología (English Edition)","volume":"32 1","pages":"Pages 16-26"},"PeriodicalIF":0.0,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143444557","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
Erdheim-Chester disease, an uncommon non-Langerhans cell histiocytosis and its association with Sjögren's syndrome Erdheim-Chester病,一种罕见的非朗格汉斯细胞组织细胞增多症及其与Sjögren综合征的关系
Pub Date : 2025-01-01 DOI: 10.1016/j.rcreue.2024.11.002
Alejandra Espinosa Trujillo , Francisco Brañas Fernández , Aitor Abuín Blanco , Robustiano Pego Reigosa , María Rodríguez Rodríguez
Erdheim Chester disease (ECD) is a rare non-Langerhans cell histiocytosis. It is characterized by the infiltration of various organs and tissues by foamy histiocytes with a heterogeneous clinical course that varies from mild forms to disseminated forms with progressive and lethal behaviour. The case of a patient who presented with a cerebellar syndrome associated with autoimmune pathology is presented. In the course of the disease, refractoriness to glucocorticoids and clinical manifestation with bone involvement in the form of symmetrical osteosclerosis of long bones were determining factors for suspicion of this entity. We reviewed scientific articles through the PubMed metasearch engine with the keywords “erdheim chester disease”, “erdheim chester and nervous system”, and “autoimmunity and erdheim chester disease”, selecting those with greater emphasis on clinical presentation with neurological involvement and associated autoimmune pathology. Advances in the pathogenesis of ECD have allowed us to understand the nature of the disease, as well as the use of targeted therapies. It is interesting to keep this entity in mind, as well as the pathologies with which it is frequently associated, with the objective of an early diagnosis and a better clinical approach.
Erdheim Chester病(ECD)是一种罕见的非朗格汉斯细胞组织细胞增多症。其特点是泡沫组织细胞浸润各种器官和组织,其临床病程不同,从轻度形式到弥散性形式,具有进行性和致死性行为。病例的病人谁提出了小脑综合征与自身免疫病理提出。在病程中,糖皮质激素的难治性和长骨对称性骨硬化累及骨骼的临床表现是怀疑该疾病的决定性因素。我们通过PubMed元搜索引擎,检索关键词为“埃尔德海姆切斯特病”、“埃尔德海姆切斯特病与神经系统”和“自身免疫与埃尔德海姆切斯特病”的科学文章,选择那些更强调神经系统受累和相关自身免疫病理的临床表现的文章。在ECD发病机制方面的进展使我们能够了解疾病的性质,以及靶向治疗的使用。有趣的是,要记住这个实体,以及与它经常相关的病理,目的是早期诊断和更好的临床方法。
{"title":"Erdheim-Chester disease, an uncommon non-Langerhans cell histiocytosis and its association with Sjögren's syndrome","authors":"Alejandra Espinosa Trujillo ,&nbsp;Francisco Brañas Fernández ,&nbsp;Aitor Abuín Blanco ,&nbsp;Robustiano Pego Reigosa ,&nbsp;María Rodríguez Rodríguez","doi":"10.1016/j.rcreue.2024.11.002","DOIUrl":"10.1016/j.rcreue.2024.11.002","url":null,"abstract":"<div><div>Erdheim Chester disease (ECD) is a rare non-Langerhans cell histiocytosis. It is characterized by the infiltration of various organs and tissues by foamy histiocytes with a heterogeneous clinical course that varies from mild forms to disseminated forms with progressive and lethal behaviour. The case of a patient who presented with a cerebellar syndrome associated with autoimmune pathology is presented. In the course of the disease, refractoriness to glucocorticoids and clinical manifestation with bone involvement in the form of symmetrical osteosclerosis of long bones were determining factors for suspicion of this entity. We reviewed scientific articles through the PubMed metasearch engine with the keywords “erdheim chester disease”, “erdheim chester and nervous system”, and “autoimmunity and erdheim chester disease”, selecting those with greater emphasis on clinical presentation with neurological involvement and associated autoimmune pathology. Advances in the pathogenesis of ECD have allowed us to understand the nature of the disease, as well as the use of targeted therapies. It is interesting to keep this entity in mind, as well as the pathologies with which it is frequently associated, with the objective of an early diagnosis and a better clinical approach.</div></div>","PeriodicalId":101099,"journal":{"name":"Revista Colombiana de Reumatología (English Edition)","volume":"32 1","pages":"Pages 90-94"},"PeriodicalIF":0.0,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143444525","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
Strategies for organizing rheumatology consultations 组织风湿病会诊的策略
Pub Date : 2025-01-01 DOI: 10.1016/j.rcreue.2024.11.006
Juan Fernando Rivadeneira Jácome, Lara Montserrat González García

Introduction

The prevalence of rheumatic disease in the general population is approximately 10%. At the same time, there has been an increase in the workload of rheumatology services, particularly concerning consultations. Many health institutions have limited the duration of rheumatology consultation to about 15 min. This article demonstrates the need to lengthen the duration rheumatology consultations.

Objective

The goal of this work is to review the literature about the standards for the duration of rheumatology consultations and to propose new organizational strategies in this regard.

Materials and methods

A narrative review of the current literature related to care standards in rheumatology consultations was carried out, including the wide variety of diagnostic procedures, which decisively influence the duration of these consultations.

Results and discussion

Organizational strategies are proposed, based on classifying consultations into first, second, and follow-up visits, with a specific daily number, and giving more time to the first two types of consultations. Although this planning implies greater effort on the part of administrative staff, it will undoubtedly result in a better quality of care for rheumatology patients.
风湿病在普通人群中的患病率约为10%。与此同时,风湿病服务的工作量有所增加,特别是在咨询方面。许多卫生机构将风湿病咨询的时间限制在15 分钟左右。这篇文章论证了延长风湿病会诊时间的必要性。目的回顾风湿病会诊时间标准的相关文献,并在此方面提出新的组织策略。材料和方法对风湿病会诊护理标准的当前文献进行了叙述性回顾,包括各种诊断程序,这些程序对会诊的持续时间有决定性的影响。结果和讨论提出了组织策略,将会诊分为第一次、第二次和随访,每天有特定的次数,并给予前两种类型的会诊更多的时间。虽然这一规划意味着行政人员需要付出更大的努力,但它无疑会提高风湿病患者的护理质量。
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引用次数: 0
Serum interleukin-41 concentrations are decreased in women with rheumatoid arthritis and are not affected by menopausal status, disease activity, or medication 类风湿关节炎妇女血清白细胞介素-41浓度降低,且不受绝经状态、疾病活动或药物的影响
Pub Date : 2025-01-01 DOI: 10.1016/j.rcreue.2025.02.002
Dhuha F.N. Bani-Wais , Ali H. Ad’hiah

Introduction

Rheumatoid arthritis (RA) is an autoimmune inflammatory disorder characterized by immunobiological homeostasis. The recently discovered cytokine interleukin-41 (IL-41) is among the immunobiological components suggested to have modulatory effects in RA and has shown up-regulated levels in patients. However, IL-41 has not been explored during the pre- (PRM) and post-menopausal (POM) periods in women with RA, and its relationship to disease activity and medications has not been well studied.

Materials and methods

In this case–control study, serum IL-41 concentrations were quantified in 120 women with RA (70 PRM and 50 POM) and 110 control women using an enzyme-linked immunosorbent assay kit. Thirty patients were newly diagnosed (ND) and 90 patients were on treatment with etanercept (a tumor necrosis factor inhibitor; TNF) plus methotrexate (MD).

Results

Median IL-41 concentrations (interquartile range) were significantly lower in RA patients than in control women (49.8 [32.5–79.5] vs. 104.7 [76.9–134.6] pg/mL; probability <.001). As indicated by the area under the curve, .827, IL-41 showed reliable discrimination between RA patients and HC. IL-41 concentrations stratified by menopausal status (PRM vs. POM), disease activity score 28 (<3.2 vs. ≥3.2), and medication (ND vs. MD) showed no significant difference in each stratum.

Conclusions

In contrast to previous studies, serum IL-41 concentrations were significantly decreased in the present cohort of women with RA. These concentrations were not affected by menopausal status, disease activity, or medication. Data from the current study suggest that IL-41 is involved in the pathophysiology of RA.
类风湿性关节炎(RA)是一种以免疫生物学稳态为特征的自身免疫性炎症性疾病。最近发现的细胞因子白细胞介素-41 (IL-41)被认为是在RA中具有调节作用的免疫生物学成分之一,并且在患者中显示出上调水平。然而,IL-41在RA患者的绝经前(PRM)和绝经后(POM)期间尚未被研究,其与疾病活动和药物的关系也尚未得到很好的研究。材料与方法在本病例对照研究中,采用酶联免疫吸附测定试剂盒对120例RA患者(70例PRM和50例POM)和110例对照患者的血清IL-41浓度进行定量分析。30例新诊断(ND)患者,90例患者接受依那西普(肿瘤坏死因子抑制剂;TNF)加甲氨蝶呤(MD)。结果RA患者IL-41浓度中位数(四分位数范围)显著低于对照组(49.8 [32.5-79.5]vs. 104.7 [76.9-134.6] pg/mL;概率& lt;措施)。曲线下面积显示,0.827,IL-41在RA和HC患者之间具有可靠的区分。按绝经状态(PRM vs. POM)、疾病活动度评分28分(<3.2 vs.≥3.2)和用药(ND vs. MD)分层的IL-41浓度在各阶层中无显著差异。结论与以往的研究相比,本研究中RA女性患者血清IL-41浓度显著降低。这些浓度不受绝经状态、疾病活动或药物的影响。目前的研究数据表明IL-41参与了RA的病理生理过程。
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引用次数: 0
Therapeutic evidence of mepolizumab in eosinophilic granulomatosis with polyangiitis: A scoping review mepolizumab治疗嗜酸性肉芽肿病合并多血管炎的证据:一项范围审查
Pub Date : 2025-01-01 DOI: 10.1016/j.rcreue.2024.11.008
Eduardo Tuta-Quintero , Isabella Perna-Reyes , Juan Olivella-Gómeza , Daniela Rodríguez-Fraile , Juan C. Santacruz , Andrea A. Mayorga-Borja , John Londoño
Mepolizumab (MPZ) is a therapeutic option for eosinophilic granulomatosis with polyangiitis (EGPA). However, the evidence on its efficacy, effectiveness, and safety is limited. Our results included 17 full-text articles evaluating the use of MPZ in patients diagnosed with EGPA, 47% (8/17) of the documents were case reports, 18% (3/17) retrospective cohort studies, 12% (2/17) clinical trials, and 6% corresponded to a prospective cohort (1/17), ambispective cohort (1/17), case series (1/17), and pilot study (1/17). The most frequently used dose of MPZ was 300 mg/month, described in 59% (10/17) of the included manuscripts. The decrease in the Birmingham Vasculitis Activity Score, reduction in the dose of corticosteroids, and modulation in the number of eosinophils in the blood were the variables most used to determine the clinical effect in patients. Finally, 10 clinical trial records were included describing the design, conduct, and administration of the ongoing studies. The use of MPZ in patients with EGPA shows a reduction in the Birmingham Vasculitis Activity Score, saving oral corticosteroids and modulating blood hypereosinophilia. The adverse events described were mild and moderate in all the included studies.
Mepolizumab (MPZ)是嗜酸性肉芽肿病合并多血管炎(EGPA)的治疗选择。然而,关于其功效、有效性和安全性的证据是有限的。我们的研究结果包括17篇评估MPZ在诊断为EGPA的患者中的应用的全文文章,其中47%(8/17)为病例报告,18%(3/17)为回顾性队列研究,12%(2/17)为临床试验,6%对应于前瞻性队列(1/17)、双视角队列(1/17)、病例系列(1/17)和试点研究(1/17)。在纳入的文献中,59%(10/17)的文献描述了MPZ最常用的剂量为300 mg/月。伯明翰血管炎活动度评分的降低、皮质类固醇剂量的减少和血液中嗜酸性粒细胞数量的调节是决定患者临床效果的最常用变量。最后,纳入了10项临床试验记录,描述了正在进行的研究的设计、实施和管理。在EGPA患者中使用MPZ可降低伯明翰血管炎活动评分,节省口服皮质类固醇并调节血液嗜酸性粒细胞增多症。在所有纳入的研究中,描述的不良事件为轻度和中度。
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引用次数: 0
Consensus for risk management in the prescription of biologic therapies or targeted synthetic antirheumatic drugs: Colombian Association of Rheumatology 2023 生物疗法或靶向合成抗风湿药物处方风险管理共识:哥伦比亚风湿病学会2023
Pub Date : 2025-01-01 DOI: 10.1016/j.rcreue.2024.11.005
Elías Gonzalo Forero Illera , Andrés Ricardo Fernández Aldana , Daniel Gerardo Fernández Ávila , Edwin Antonio Jáuregui Cuartas , Gloria Vásquez , Monique Chalem , Wilson Bautista Molano
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引用次数: 0
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Revista Colombiana de Reumatología (English Edition)
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