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意义未明的单克隆丙种球蛋白病

Monoclonal gammopathy of undetermined significance.

作者信息

Kyle Robert A, Rajkumar S Vincent

机构信息

Division of Hematology, Mayo Clinic, 200 First Street SW, Rochester, MN 55905, USA.

出版信息

Clin Lymphoma Myeloma. 2005 Sep;6(2):102-14. doi: 10.3816/CLM.2005.n.036.

Abstract

Monoclonal gammopathy of undetermined significance (MGUS) is characterized by the presence of a monoclonal protein (M-protein) without evidence of multiple myeloma (MM), Waldenstrom's macroglobulinemia (WM), amyloidosis (AL), or a related plasma cell proliferative disorder. Agarose gel electrophoresis followed by immunofixation is recommended for recognition of an M-protein. Monoclonal gammopathy of undetermined significance is found in approximately 3% of persons > 70 years of age and in about 1% of those > 50 years old. In a series of 1384 patients from Southeastern Minnesota in whom MGUS was diagnosed at Mayo Clinic from 1960 through 1994, the risk of progression was 1% per year. This risk of progression continued even after > or = 25 years of a stable M-protein. The risk for developing MM, WM, or AL was increased 25-fold, 46-fold, and 8.4-fold, respectively. The concentration of the serum M-protein, abnormal serum free light-chain ratio, and the presence an immunoglobulin (Ig)M or an IgA M-protein were risk factors for progression. The presence of a urine M-protein or the reduction of > or = 1 uninvolved immunoglobulins was not a risk factor for disease progression. Patients must be monitored for progressive disease throughout their lives. Variants of MGUS consist of IgM MGUS, biclonal gammopathies, triclonal gammopathies, idiopathic Bence Jones (light-chain) proteinuria, and IgD MGUS. Monoclonal gammopathy of undetermined significance may be associated with many disorders, including lymphoproliferative diseases, leukemia, von Willebrand's disease, connective tissue diseases, and neurologic disorders. Epidemiologic and statistical methods must be used to evaluate these associations.

摘要

意义未明的单克隆丙种球蛋白病(MGUS)的特征是存在单克隆蛋白(M蛋白),但无多发性骨髓瘤(MM)、华氏巨球蛋白血症(WM)、淀粉样变性(AL)或相关浆细胞增殖性疾病的证据。推荐采用琼脂糖凝胶电泳继以免疫固定法来识别M蛋白。意义未明的单克隆丙种球蛋白病在70岁以上人群中约3%可发现,在50岁以上人群中约1%可发现。在1960年至1994年于梅奥诊所诊断为MGUS的明尼苏达州东南部的1384例患者系列中,进展风险为每年1%。即使在M蛋白稳定≥25年后,这种进展风险仍持续存在。发生MM、WM或AL的风险分别增加了25倍、46倍和8.4倍。血清M蛋白浓度、异常血清游离轻链比值以及存在免疫球蛋白(Ig)M或IgA M蛋白是进展的危险因素。存在尿M蛋白或≥1种未受累免疫球蛋白减少不是疾病进展的危险因素。患者一生中必须监测是否有疾病进展。MGUS的变异型包括IgM MGUS、双克隆丙种球蛋白病、三克隆丙种球蛋白病、特发性本-周蛋白(轻链)蛋白尿和IgD MGUS。意义未明的单克隆丙种球蛋白病可能与许多疾病相关,包括淋巴增殖性疾病、白血病、血管性血友病、结缔组织疾病和神经系统疾病。必须采用流行病学和统计学方法来评估这些关联。

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