CINCA/NOMID is a rare autoinflammatory syndrome in rheumatological practice. Experience of diagnosis, management and therapy with interleukin-1 inhibitors

S. Salugina, E. S. Fedoro, A. Torgashina
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Abstract

Objective: to present the experience of diagnosis, management and therapy with interleukin-1 inhibitors (iIL1) in patients with Chronic Infantile Onset Neurologic Cutaneous Articular/Neonatal Onset Multisystem Inflammatory Disease (CINCA/NOMID) according to the Russian Federal Rheumatological Center data.Material and methods. From 2007 to 2023, eight patients were included in the study (7 men) aged 10 months to 33 years, including 3 with a disease duration of more than 10 years (13, 17 and 33 years). Genetic testing was performed in all patients and mutations in the NLRP3 gene were identified in 6 cases.Results and discussion. The age of onset of the disease ranged from 0 to 6 months. The delay in diagnosis and prescription of therapy ranged from 10 months to 33 years. All patients had the classic manifestations of CINCA/NOMID, including fever, rash, central nervous system (CNS) involvement, elevated ESR and CRP levels, 6 patients had articular manifestations, 7 had ocular manifestations and 6 had sensorineural hearing loss. Amyloidosis was detected in 1 case. All patients were prescribed iIL1. Anakinra was used in 6 patients (in 5 as the first line, in 1 as the second line therapy) with a positive response; subsequently 2 of these patients were switched to canakinumab once every 4 weeks (1 patient deteriorated and was readministered anakinra). Five patients received canakinumab (3 as first-line therapy, 2 as second-line therapy), 1 patient was switched to anakinra due to insufficient CNS response. The response to iIL1 therapy was positive in all patients, but incomplete in some of them due to the severity of the manifestations and the presence of irreversible organ damage.Conclusion. Patients with CINCA/NOMID have a severe disease and a poor prognosis. In this context, early administration of iIL1 is necessary. In the case of CNS involvement, the use of anakinra is preferable, as it is characterized by better penetration of the blood-brain barrier and is therefore more effective. Later it is possible to switch the patient to canakinumab, however, to achieve a complete response, it is sometimes necessary to increase the dose of the drug and reduce the interval between doses.
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CINCA/NOMID是风湿病学实践中一种罕见的自身炎症综合征。白细胞介素-1抑制剂的诊断、管理和治疗经验
目的:根据俄罗斯联邦风湿病中心的数据,介绍慢性婴儿期发病神经皮肤关节病/新生儿期发病多系统炎症性疾病(CINCA/NOMID)患者的诊断、管理和白细胞介素-1抑制剂(iIL1)治疗经验。从 2007 年到 2023 年,研究共纳入了 8 名患者(7 名男性),年龄在 10 个月到 33 岁之间,其中 3 名患者的病程超过 10 年(13、17 和 33 年)。所有患者均进行了基因检测,其中 6 例患者的 NLRP3 基因发生了突变。发病年龄从 0 个月到 6 个月不等。诊断和治疗延迟时间从 10 个月到 33 年不等。所有患者均有 CINCA/NOMID 的典型表现,包括发热、皮疹、中枢神经系统(CNS)受累、血沉和 CRP 水平升高,6 例患者有关节表现,7 例患者有眼部表现,6 例患者有感音神经性听力损失。1例患者出现淀粉样变性。所有患者都服用了 iIL1。6名患者使用了阿纳金拉(5名患者作为一线治疗,1名患者作为二线治疗),并取得了积极的反应;随后,其中2名患者改用卡纳库单抗,每4周一次(1名患者病情恶化,重新使用阿纳金拉)。5名患者接受了卡纳库单抗治疗(3人作为一线治疗,2人作为二线治疗),1名患者因中枢神经系统反应不足而改用阿纳金雷治疗。所有患者对iIL1治疗的反应均为阳性,但其中一些患者的反应不完全,原因是表现严重,存在不可逆的器官损伤。结论:CINCA/NOMID患者病情严重,预后不良。因此,有必要尽早使用 iIL1。在中枢神经系统受累的情况下,最好使用 Anakinra,因为它能更好地穿透血脑屏障,因此更有效。之后,患者有可能改用卡纳金单抗,但为了获得完全应答,有时需要增加药物剂量并缩短剂量间隔。
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