The kidney in rheumatological disorders

L. Lightstone, H. Beckwith
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Abstract

Many rheumatological conditions have systemic effects. Antibody production, complement activation, and protein deposition can all result in damage to the kidney, sometimes with devastating sequelae. Systemic lupus erythematosus—lupus nephritis is clinically evident in up to 75% of patients with systemic lupus erythematosus (SLE), and endstage renal disease is seen in 5 to 10% of patients at 10 years. Proteinuria is the most common clinical presentation, closely followed by nonvisible haematuria and tubular abnormalities. Patients with active lupus nephritis often have features of active SLE. The gold standard for lupus nephritis diagnosis is a renal biopsy, with treatment related to histopathological features observed. Adjunctive immunosuppressive agents such as rituximab and tacrolimus are emerging as increasingly important lupus nephritis therapies. Systemic sclerosis is a multiorgan connective tissue disease. Most renal manifestations are clinically silent. By contrast, the scleroderma renal crisis is characterized by accelerated-phase hypertension and impaired renal function. It carries a high mortality risk. Rheumatoid arthritis can affect the kidneys in many ways, most commonly by causing amyloid A amyloidosis. This presents with proteinuria, often severe enough to cause nephrotic syndrome, with 50% progressing to endstage renal failure after 5 years (90% at 10 years). Renal vasculitis, mesangiocapillary glomerulonephritis, and mesangial IgA proliferative glomerulonephritis are also described. Gold and penicillamine (now rarely used) can cause proteinuria, sometimes with nephrotic syndrome. Renal involvement in Sjögren’s syndrome is generally mild, but up to a quarter of patients develop acute or chronic kidney disease, typically with evidence of tubular dysfunction. Glomerular abnormalities are rare and the most common histological abnormality is tubulointerstitial nephritis. Drug nephrotoxicity—conventional antirheumatics and over-the-counter nonsteroidal anti-inflammatory drugs are used exceptionally widely in the community and are nephrotoxic. Their almost ubiquitous use, especially during intercurrent illnesses, means they are frequent contributors to acute and chronic kidney damage.
风湿病中的肾脏
许多风湿病有全身影响。抗体的产生、补体的激活和蛋白质的沉积都会对肾脏造成损害,有时还会带来毁灭性的后遗症。系统性红斑狼疮-狼疮性肾炎在高达75%的系统性红斑狼疮(SLE)患者中临床表现明显,10年终末期肾病见于5%至10%的患者。蛋白尿是最常见的临床表现,其次是不可见的血尿和肾小管异常。活动性狼疮性肾炎患者通常具有活动性SLE的特征。狼疮性肾炎诊断的金标准是肾活检,治疗与观察组织病理学特征有关。辅助免疫抑制剂如利妥昔单抗和他克莫司正在成为越来越重要的狼疮性肾炎治疗。系统性硬化症是一种多器官结缔组织疾病。大多数肾脏表现在临床上是无症状的。相反,硬皮病肾危象的特点是期高血压加速和肾功能受损。它有很高的死亡风险。类风湿性关节炎可以通过多种方式影响肾脏,最常见的是引起淀粉样蛋白A淀粉样变性。表现为蛋白尿,通常严重到足以引起肾病综合征,50%在5年后进展为终末期肾衰竭(10年后90%)。肾血管炎,系血管毛细血管肾小球肾炎,系膜IgA增生性肾小球肾炎也被描述。金和青霉胺(现在很少使用)可引起蛋白尿,有时伴有肾病综合征。Sjögren综合征的肾脏受累通常是轻微的,但多达四分之一的患者会出现急性或慢性肾脏疾病,通常伴有肾小管功能障碍。肾小球异常是罕见的,最常见的组织学异常是小管间质性肾炎。药物肾毒性——传统的抗风湿药和非处方非甾体抗炎药在社区中被广泛使用,并且具有肾毒性。它们几乎无处不在的使用,尤其是在并发疾病期间,意味着它们经常导致急性和慢性肾损伤。
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