Viswanath Vishalakshi, Phiske Meghana M, Gopalani Vinay V
Department of Dermatology, Rajiv Gandhi Medical College and CSM Hospital, Kalwa, Thane Municipal Corporation, India.
Indian J Dermatol. 2013 Jul;58(4):255-68. doi: 10.4103/0019-5154.113930.
Systemic sclerosis (SSc) is a chronic, multisystem connective tissue disease with protean clinical manifestations. Recent advances in understanding the pathogenic mechanisms have led to development of target-oriented and vasomodulatory drugs which play a pivotal role in treating various dermatological manifestations. An exhaustive literature search was done using Medline, Embase, and Cochrane library to review the recent concepts regarding pathogenesis and evidence-based treatment of salient dermatological manifestations. The concept of shared genetic risk factors for the development of autoimmune diseases is seen in SSc. It is divided into fibroproliferative and inflammatory groups based on genome-wide molecular profiling. Genetic, infectious, and environmental factors play a key role; vascular injury, fibrosis, and immune activation are the chief pathogenic factors. Vitamin D deficiency has been documented in SSc and correlates with the severity of skin involvement. Skin sclerosis, Raynaud's phenomenon (RP) with digital vasculopathies, pigmentation, calcinosis, and leg ulcers affect the patient's quality of life. Immunosuppressives, biologicals, and hematopoietic stem cell transplantation are efficacious in skin sclerosis. Endothelin A receptor antagonists, calcium-channel blockers, angiotensin receptor inhibitors, prostacyclin analogs, and phosphodiesterase type 5 (PDE-5) inhibitors are the mainstay in RP and digital vasculopathies. Pigmentation in SSc has been attributed to melanogenic potential of endothelin-1 (ET-1); the role of ET 1 antagonists and vitamin D analogs needs to be investigated. Sexual dysfunction in both male and female patients has been attributed to vasculopathy and fibrosis, wherein PDE-5 inhibitors are found to be useful. The future concepts of treating SSc may be based on the gene expression signature.
系统性硬化症(SSc)是一种临床表现多样的慢性多系统结缔组织疾病。在理解其致病机制方面的最新进展已促使开发出靶向和血管调节药物,这些药物在治疗各种皮肤表现中起着关键作用。我们使用Medline、Embase和Cochrane图书馆进行了详尽的文献检索,以回顾有关发病机制的最新概念以及显著皮肤表现的循证治疗。自身免疫性疾病发展的共同遗传风险因素概念在系统性硬化症中可见。根据全基因组分子谱分析,它分为纤维增生性和炎症性两组。遗传、感染和环境因素起关键作用;血管损伤、纤维化和免疫激活是主要致病因素。系统性硬化症患者中已证实存在维生素D缺乏,且与皮肤受累的严重程度相关。皮肤硬化、伴有指端血管病变的雷诺现象(RP)、色素沉着、钙质沉着和腿部溃疡会影响患者的生活质量。免疫抑制剂、生物制剂和造血干细胞移植对皮肤硬化有效。内皮素A受体拮抗剂、钙通道阻滞剂、血管紧张素受体抑制剂、前列环素类似物和5型磷酸二酯酶(PDE - 5)抑制剂是治疗RP和指端血管病变的主要药物。系统性硬化症中的色素沉着归因于内皮素 - 1(ET - 1)的黑素生成潜能;ET - 1拮抗剂和维生素D类似物的作用有待研究。男性和女性患者的性功能障碍都归因于血管病变和纤维化,其中发现PDE - 5抑制剂有用。治疗系统性硬化症的未来概念可能基于基因表达特征。