代谢性阑尾炎:病理生理学,临床相关性,诊断挑战和靶向治疗的观点综述。

IF 3.3 4区 医学 Q3 IMMUNOLOGY
Giuseppe Lisco, Anna De Tullio, Roberta Zupo, Marcella Prete, Giuseppina Piazzolla, Vito Racanelli, Vincenzo Triggiani
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引用次数: 0

摘要

椎体是连接韧带和肌腱与骨表面的特殊组织,经常涉及血清阴性脊柱炎。在代谢紊乱(MD)患者中也可以检测到肠炎,无论基线自身免疫性风湿病如何,这构成了真正的诊断挑战。本综述讨论了肺脏炎和代谢相关性肺脏炎的病理生理学,代谢紊乱与肺脏炎相关结果的临床相关性,充分鉴别诊断的诊断挑战,以及改善临床结果的可能治疗策略。检索PubMed/MEDLINE和Cochrane图书馆的原始文章、系统综述和元分析。根据研究的标题、摘要和全文的层次分析筛选参考文献,收集、展示和讨论。代谢相关性炎症可归因于体重过量引起的机械应力/过载,通常见于代谢紊乱(MD),如超重/肥胖合并症患者、代谢综合征(MS)和2型糖尿病(T2D)。白细胞介素1β、6、17、18和23和肿瘤坏死因子-α在引发和维持肺脏炎症中起关键作用。慢性高血糖和胰岛素抵抗会导致恶性循环,因为它们会刺激被激活的特化T细胞产生这些特定的细胞因子,从而长期维持炎性炎症。MD与更严重的临床表现、对药物治疗的反应更差以及现有血清阴性脊柱炎患者较差的骨骺结局相关。非免疫介导的代谢相关肠炎构成了真正的诊断挑战,可能低估病例和潜在的误诊。从治疗的角度来看,血糖控制的改善和体重的减轻与entheseal相关结果的改善相关。旨在减轻体重、改善血糖控制和胰岛素敏感性以及减轻炎症的药物和非药物干预是实现治疗目标的必要条件。胰高血糖素样肽1受体激动剂和钠-葡萄糖共转运蛋白2型抑制剂,必要时加用非甾体抗炎药和免疫调节剂,可能对代谢相关性肠炎患者有治疗意义。意识到代谢相关的炎症对于提高MD患者鉴别诊断的准确性和制定适当的治疗策略至关重要。然而,需要基础和临床研究来了解“降糖”药物在更好地管理代谢相关炎症中的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Metabolic-associated enthesitis: a review on pathophysiology, clinical relevance, diagnostic challenges, and perspective on target treatments.

Entheses are specialized tissues that connect ligaments and tendons to the bone surface and are frequently involved in seronegative spondyloarthritis. Enthesitis can also be detected in patients with metabolic disorders (MD), regardless of baseline autoimmune rheumatic disease, posing real diagnostic challenges. The present review discusses the pathophysiology of enthesitis and metabolic-associated enthesitis, the clinical relevance of metabolic disorders on enthesitis-related outcomes, diagnostic challenges for adequate differential diagnosis, and possible therapeutic strategies to improve clinical outcomes. PubMed/MEDLINE and the Cochrane Library were searched for original articles, systematic reviews, and meta-analyses. References were screened according to a hierarchical analysis of studies by title, abstract, and full text, collected, presented, and discussed. Metabolic-associated enthesitis is attributable to mechanical stress/overload due to weight excess typically observed in metabolic disorders (MD), such as overweight/obese comorbid patients, metabolic syndrome (MS), and type 2 diabetes (T2D). Interleukin 1β, 6, 17, 18, and 23 and tumor necrosis factor-α play a crucial role in initiating and maintaining entheseal inflammation. Chronic hyperglycemia and insulin resistance lead to a vicious circle as they stimulate, upon activated, specialized T cells to produce these specific cytokines, thus maintaining entheseal inflammation chronically. MD is associated with more severe clinical presentation, worse response to pharmacological treatments, and poor entheseal outcomes also in patients with existing seronegative spondyloarthritis. Non-immune-mediated metabolic-associated enthesitis poses a real diagnostic challenge, possibly underestimating cases and potential misdiagnoses. From a therapeutic viewpoint, glucose control improvement and weight loss are associated with relevant amelioration of entheseal-related outcomes. Pharmacological and non-pharmacological interventions aiming to reduce body weight, improve glucose control and insulin sensitivity, and attenuate inflammation are desirable to achieve the therapeutic target. Glucagon-like peptide 1 receptor agonists and sodium-glucose co-transporter type 2 inhibitors, in add-on to non-steroidal anti-inflammatory drugs and immunomodulators when necessary, may have a therapeutic rationale in patients with metabolic-associated enthesitis. Awareness of metabolic-associated enthesitis is essential to improve the accuracy of differential diagnosis in patients with MD and prescribe appropriate therapeutic strategies. However, basic and clinical research is needed to understand the role of "antihyperglycemic" agents in better managing metabolic-associated enthesitis.

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来源期刊
Immunologic Research
Immunologic Research 医学-免疫学
CiteScore
6.90
自引率
0.00%
发文量
83
审稿时长
6-12 weeks
期刊介绍: IMMUNOLOGIC RESEARCH represents a unique medium for the presentation, interpretation, and clarification of complex scientific data. Information is presented in the form of interpretive synthesis reviews, original research articles, symposia, editorials, and theoretical essays. The scope of coverage extends to cellular immunology, immunogenetics, molecular and structural immunology, immunoregulation and autoimmunity, immunopathology, tumor immunology, host defense and microbial immunity, including viral immunology, immunohematology, mucosal immunity, complement, transplantation immunology, clinical immunology, neuroimmunology, immunoendocrinology, immunotoxicology, translational immunology, and history of immunology.
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