Department of Rheumatology, East Surrey Hospital, Canada Avenue, Redhill, RH1 5RH, UK.
School of Medicine, Cedar House, University of Liverpool, Ashton Street, Liverpool, L69 3GE, UK.
Rheumatol Int. 2024 Jul;44(7):1219-1232. doi: 10.1007/s00296-023-05513-0. Epub 2023 Dec 21.
VEXAS (vacuoles, E1 enzyme, X-linked, autoinflammatory, somatic) syndrome is a newly discovered autoinflammatory condition characterised by somatic mutation of the UBA1 gene. The syndrome leads to multi-system inflammation affecting predominantly the skin, lungs and bone marrow.
We undertook a systematic review of the multisystem features and genotypes observed in VEXAS syndrome. Articles discussing VEXAS syndrome were included. Medline, Embase and Cochrane databases were searched. Information was extracted on: demographics, type and prevalence of clinical manifestations, genetic mutations and treatment. Meta-analysis using a random effects model was used to determine pooled estimates of serum markers.
From 303 articles, 90 were included, comprising 394 patients with VEXAS. 99.2% were male, with a mean age of 67.1 years (SD 8.5) at disease onset. The most frequent diagnoses made prior to VEXAS were: relapsing polychondritis (n = 59); Sweet's syndrome (n = 24); polyarteritis nodosa (n = 11); and myelodysplastic syndrome (n = 10). Fever was reported in 270 cases (68.5%) and weight loss in 79 (20.1%). Most patients had haematological (n = 342; 86.8%), dermatological (n = 321; 81.5%), pulmonary (n = 297; 75.4%%) and musculoskeletal (n = 172; 43.7%) involvement, although other organ manifestations of varying prevalence were also recorded. The most commonly reported mutations were "c.122T > C pMET41Thr" (n = 124), "c.121A > G pMET41Val" (n = 62) and "c.121A > C pMet41Leu" (n = 52). Most patients received glucocorticoids (n = 240; 60.9%) followed by methotrexate (n = 82; 20.8%) and IL-6 inhibitors (n = 61, 15.4%). One patient underwent splenectomy; 24 received bone marrow transplants.
VEXAS syndrome is a rare disorder affecting predominantly middle-aged men. This is the first systematic review to capture clinical manifestations, genetics and treatment of reported cases. Further studies are needed to optimise treatment and subsequently reduce morbidity and mortality.
VEXAS(空泡、E1 酶、X 连锁、自身炎症、体细胞)综合征是一种新发现的自身炎症性疾病,其特征是 UBA1 基因的体细胞突变。该综合征导致多系统炎症,主要影响皮肤、肺部和骨髓。
我们对 VEXAS 综合征观察到的多系统特征和基因型进行了系统评价。纳入了讨论 VEXAS 综合征的文章。检索了 Medline、Embase 和 Cochrane 数据库。提取的信息包括:人口统计学、临床表现的类型和流行率、基因突变和治疗。使用随机效应模型进行荟萃分析,以确定血清标志物的汇总估计值。
从 303 篇文章中,纳入了 90 篇,共 394 例 VEXAS 患者。99.2%为男性,疾病发病时的平均年龄为 67.1 岁(SD 8.5)。在 VEXAS 之前最常做出的诊断为:复发性多软骨炎(n=59);Sweet 综合征(n=24);结节性多动脉炎(n=11);和骨髓增生异常综合征(n=10)。270 例(68.5%)报告有发热,79 例(20.1%)报告有体重减轻。大多数患者有血液学(n=342;86.8%)、皮肤学(n=321;81.5%)、肺部(n=297;75.4%)和肌肉骨骼(n=172;43.7%)受累,尽管也记录了其他不同流行率的器官表现。最常报道的突变是“c.122T > C pMET41Thr”(n=124)、“c.121A > G pMET41Val”(n=62)和“c.121A > C pMet41Leu”(n=52)。大多数患者接受了糖皮质激素(n=240;60.9%),其次是甲氨蝶呤(n=82;20.8%)和 IL-6 抑制剂(n=61,15.4%)。1 名患者接受了脾切除术;24 名患者接受了骨髓移植。
VEXAS 综合征是一种罕见的疾病,主要影响中年男性。这是第一次系统评价报告病例的临床表现、遗传学和治疗。需要进一步的研究来优化治疗,从而降低发病率和死亡率。