Department of Clinical Neuroimmunology and Neurochemistry, Hannover Medical School, Hannover, Germany.
Curr Opin Neurol. 2012 Jun;25(3):306-15. doi: 10.1097/WCO.0b013e328352ebfe.
Connective tissue diseases can present with a wide spectrum of neurological symptoms. The present review summarizes the neurological involvement in connective tissue diseases and highlights recent findings on the diagnosis of neurological manifestations and potential underlying mechanisms.
The wide range in the prevalence of neurological manifestations in systemic lupus erythematosus (SLE) and Sjögren's syndrome reveals the necessity of clear decision algorithms for the association of neurological symptoms with a systemic autoimmune disease. For this purpose new recommendations for the diagnosis and treatment of neuropsychiatric SLE have been published. Recent studies identified potential paraclinical markers for the diagnosis of nervous system involvement in connective tissue diseases. Antiaquaporin-4 antibodies occur highly specifically in those patients with connective tissue diseases that present with symptoms typical for neuromyelitis optica.
To date there is no specific marker available to prove neurological manifestation of connective tissue diseases. However, some progress has been achieved in characterizing typical clinical features and potential disease associated autoantibodies, which may lead to a better management of these patients.
结缔组织病可表现为广泛的神经系统症状。本综述总结了结缔组织病的神经受累,并重点介绍了神经表现的诊断和潜在发病机制的新发现。
系统性红斑狼疮(SLE)和干燥综合征中神经表现的患病率差异很大,这表明需要明确的决策算法将神经系统症状与自身免疫性疾病联系起来。为此,发布了新的神经精神性 SLE 的诊断和治疗建议。最近的研究确定了潜在的临床前标记物,以诊断结缔组织病的神经系统受累。抗水通道蛋白 4 抗体在具有视神经脊髓炎典型症状的结缔组织病患者中特异性高。
目前尚无可用的特定标志物来证实结缔组织病的神经表现。然而,在描述典型的临床特征和潜在的疾病相关自身抗体方面已经取得了一些进展,这可能有助于更好地管理这些患者。