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肾活检与免疫风湿性疾病:一项回顾性观察研究。

Kidney Biopsy and Immuno-Rheumatological Diseases: A Retrospective and Observational Study.

作者信息

Gigante Antonietta, Cianci Rosario, Villa Annalisa, Pellicano Chiara, Giannakakis Konstantinos, Rosato Edoardo, Spinelli Francesca Romana, Basile Umberto, Racco Cosimo, Di Virgilio Elena Maria, Cerbelli Bruna, Conti Fabrizio

机构信息

Department of Translational and Precision Medicine, Sapienza University of Rome, 00185 Rome, Italy.

Department of Radiological, Oncological and Pathological Sciences, Sapienza University of Rome, 00185 Rome, Italy.

出版信息

J Pers Med. 2024 Jan 13;14(1):92. doi: 10.3390/jpm14010092.

Abstract

Renal involvement is a common occurrence in patients with immuno-rheumatological diseases (IRDs). Several instances of glomerulonephritis (GN) occur in the setting of IRD and complicate the clinical course of an underlying condition. The aim of this study was to observe the spectrum of nephropathies according to age, kidney function, history of IRD at the time of biopsy, and histopathological kidney diagnosis. We evaluated data relating to 699 consecutive kidney native biopsies (female 52.1%) with a median age of 48 years (IQR 34-62) performed in adult patients collected over 15 years. The study population was divided into three groups: patients with kidney histological findings correlated to underlying IRD (Group 1), patients with kidney histological findings not correlated to underlying IRD (Group 2), and patients with kidney histological findings compatible with "de novo" IRD (absent in personal medical history) (Group 3). Kidney involvement related to IRD was found in 25.2% of patients. Group 1 was mostly represented by lupus nephritis (76.6%), with a younger age than Group 3 ( < 0.001) and by a higher percentage of females than other groups ( < 0.001). Group 3 was the most represented by microscopic polyangiitis (50.8%) when compared with the other two groups ( < 0.001). Acute nephritic syndrome ( < 0.001), acute kidney injury (AKI), and abnormal urinalysis ( < 0.001) were more represented in Group 3 than the other groups. In conclusion, IRDs are characterized by different clinical presentations and heterogeneous histological findings. Kidney biopsy remains fundamental to achieving the correct diagnosis and starting targeted therapy.

摘要

肾脏受累在免疫性风湿病(IRDs)患者中很常见。在IRDs背景下会出现几例肾小球肾炎(GN),并使基础疾病的临床病程复杂化。本研究的目的是根据年龄、肾功能、活检时的IRD病史以及肾脏组织病理学诊断来观察肾病谱。我们评估了15年间收集的成年患者连续699例肾穿刺活检的数据(女性占52.1%),中位年龄为48岁(四分位间距34 - 62岁)。研究人群分为三组:肾脏组织学结果与基础IRD相关的患者(第1组)、肾脏组织学结果与基础IRD不相关的患者(第2组)以及肾脏组织学结果符合“新发”IRD(个人病史中无)的患者(第3组)。25.2%的患者发现有与IRD相关的肾脏受累。第1组主要为狼疮性肾炎(76.6%),年龄比第3组小(<0.001),女性比例高于其他组(<0.001)。与其他两组相比,第3组中显微镜下多血管炎最为常见(50.8%)(<0.001)。第3组中急性肾炎综合征(<0.001)、急性肾损伤(AKI)和尿常规异常(<0.001)比其他组更常见。总之,IRDs具有不同的临床表现和异质性组织学结果。肾穿刺活检对于正确诊断和启动靶向治疗仍然至关重要。

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