[Epidemiological, clinical, and biochemical characteristics of patients in the LUPUS-IMMex cohort].

Mario Cesar Ocampo-Torres, Francisco Martin Bravo-Rojas, Aida Martínez-Badajoz, Ramiro Hernández-Vásquez, Astrid Asminda Ramírez-Pérez, Adolfo Camargo-Coronel, Miguel Ángel Vázquez-Zaragoza, Eleonor Luna-Peña, Fabiola Pazos-Pérez, Juan Carlos H Hernández-Rivera
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Abstract

Background: Systemic lupus erythematosus (SLE) is a chronic autoimmune disease that can affect multiple organs and body systems.

Objective: To describe the sociodemographic, clinical, and biochemical characteristics of the Lupus-IMMS-Mexico (LUPUS-IMMex) patient cohort from a tertiary-level center.

Material and methods: Observational descriptive study of 160 patients with diagnosis of SLE belonging to the aforementioned cohort. Various variables were analyzed at the time of diagnosis. For quantitative variables, normality tests were applied, followed by measures of central tendency and dispersion according to their distribution. For categorical variables, frequencies and percentages were calculated.

Results: 81.87% of the patients were female, with a median age at diagnosis of 28 years. 18.12% had a family history of SLE, and concurrently with SLE, 32.50% had hypertension, and 11.25% had antiphospholipid syndrome. The most common clinical manifestation was joint involvement (68.12%), renal (49.37%) and hematological (43.75%) manifestations.

Conclusions: SLE affects millions globally. Lack of awareness leads to delayed diagnoses, suboptimal management, and diminished quality of life. After analyzing 160 patients with SLE, their clinical, socioeconomic, and therapeutic characteristics are largely like other cohorts, with differences attributable to ethnic and geographical influences. Informing patients about SLE and providing reliable resources are essential for self-care. Awareness promotes research, therapies, and enhances medical care and the lives of patients globally.

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[LUPUS-IMMex队列中患者的流行病学、临床和生化特征]
背景:系统性红斑狼疮(SLE系统性红斑狼疮(SLE)是一种可影响多个器官和身体系统的慢性自身免疫性疾病:描述一家三级医疗中心的狼疮-IMM-墨西哥(LUPUS-IMMex)患者群的社会人口学、临床和生化特征:观察性描述研究:对上述患者队列中诊断出系统性红斑狼疮的 160 名患者进行观察。对诊断时的各种变量进行了分析。对于定量变量,采用正态性检验,然后根据其分布情况进行中心倾向和离散度测量。对于分类变量,则计算了频率和百分比:81.87%的患者为女性,确诊年龄中位数为 28 岁。18.12%的患者有系统性红斑狼疮家族史,32.50%的患者有高血压,11.25%的患者有抗磷脂综合征。最常见的临床表现是关节受累(68.12%)、肾脏受累(49.37%)和血液系统受累(43.75%):结论:系统性红斑狼疮影响着全球数百万人。结论:系统性红斑狼疮影响着全球数百万人,由于缺乏认识,导致诊断延误、治疗效果不佳和生活质量下降。在对160名系统性红斑狼疮患者进行分析后发现,他们的临床、社会经济和治疗特征与其他群体的患者基本相似,但由于种族和地理位置的影响而存在差异。让患者了解系统性红斑狼疮并提供可靠的资源对于自我护理至关重要。提高患者的认识可以促进研究和治疗,改善医疗服务和全球患者的生活。
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[Epidemiological, clinical, and biochemical characteristics of patients in the LUPUS-IMMex cohort]. [Health-related quality of life in Mexican women with obesity]. [Knowledge and quality of life in chronic kidney disease and peritoneal dialysis]. [Analysis of the unicentric registry of the Infarction Code program: retrospective cohort]. [BIRADS 0 patient reclassification in a first-level of care unit].
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