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本文引用的文献

1
Disease associations with monoclonal gammopathy of undetermined significance: a population-based study of 17,398 patients.意义未明的单克隆丙种球蛋白病与疾病的关联:一项基于17398例患者的人群研究。
Mayo Clin Proc. 2009 Aug;84(8):685-93. doi: 10.4065/84.8.685.
2
Pesticide exposure and risk of monoclonal gammopathy of undetermined significance in the Agricultural Health Study.农业健康研究中农药暴露与意义未明的单克隆丙种球蛋白病风险
Blood. 2009 Jun 18;113(25):6386-91. doi: 10.1182/blood-2009-02-203471. Epub 2009 Apr 22.
3
Increased risk of monoclonal gammopathy in first-degree relatives of patients with multiple myeloma or monoclonal gammopathy of undetermined significance.多发性骨髓瘤或意义未明的单克隆丙种球蛋白病患者的一级亲属患单克隆丙种球蛋白病的风险增加。
Blood. 2009 Jul 23;114(4):785-90. doi: 10.1182/blood-2008-12-192575. Epub 2009 Jan 29.
4
Criteria for diagnosis, staging, risk stratification and response assessment of multiple myeloma.多发性骨髓瘤的诊断、分期、风险分层及疗效评估标准。
Leukemia. 2009 Jan;23(1):3-9. doi: 10.1038/leu.2008.291. Epub 2008 Oct 30.
5
Pathogenesis and progression of monoclonal gammopathy of undetermined significance.意义未明的单克隆丙种球蛋白病的发病机制与进展
Leukemia. 2008 Sep;22(9):1651-7. doi: 10.1038/leu.2008.203. Epub 2008 Jul 31.
6
Familial myeloma.家族性骨髓瘤
N Engl J Med. 2008 Jul 10;359(2):152-7. doi: 10.1056/NEJMoa0708704.
7
Multiple myeloma.多发性骨髓瘤
Blood. 2008 Mar 15;111(6):2962-72. doi: 10.1182/blood-2007-10-078022.
8
Epidemiology of the plasma-cell disorders.浆细胞疾病的流行病学
Best Pract Res Clin Haematol. 2007 Dec;20(4):637-64. doi: 10.1016/j.beha.2007.08.001.
9
Prevalence of monoclonal gammopathy of undetermined significance: study of 52,802 persons in Nagasaki City, Japan.意义未明的单克隆丙种球蛋白病的患病率:对日本长崎市52802人的研究。
Mayo Clin Proc. 2007 Dec;82(12):1474-9. doi: 10.1016/S0025-6196(11)61090-2.
10
Prevalence of monoclonal gammopathy of undetermined significance among men in Ghana.加纳男性意义未明的单克隆丙种球蛋白病患病率
Mayo Clin Proc. 2007 Dec;82(12):1468-73. doi: 10.1016/S0025-6196(11)61089-6.

意义未明的单克隆丙种球蛋白血症的流行率:一项系统性综述。

Prevalence of monoclonal gammopathy of undetermined significance: a systematic review.

机构信息

Mayo Medical School, Mayo Clinic, Rochester, MN 55905, USA.

出版信息

Mayo Clin Proc. 2010 Oct;85(10):933-42. doi: 10.4065/mcp.2010.0337. Epub 2010 Aug 16.

DOI:10.4065/mcp.2010.0337
PMID:20713974
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2947966/
Abstract

Monoclonal gammopathy of undetermined significance (MGUS) is a premalignant plasma cell disorder that is associated with a lifelong risk of multiple myeloma. We conducted a systematic review of all studies investigating the prevalence and incidence of MGUS in the online database PubMed. The review was conducted from January 6, 2009, through January 15, 2010. The following MeSH search headings were used: monoclonal gammopathy, benign and prevalence; monoclonal gammopathy, benign and incidence; paraproteinemia and prevalence; and paraproteinemia and incidence. Articles were limited to those written in English and published by January 2009. Fourteen studies that met prespecified criteria were included and systematically assessed to identify the most accurate prevalence estimates of MGUS based on age, sex, and race. On the basis of our systematic review, we estimate that the crude prevalence of MGUS in those older than 50 years is 3.2% in a predominantly white population. Studies in white and Japanese populations demonstrate a clear increase in prevalence with age. The prevalence is also affected by sex: 3.7% and 2.9% in white men and women, respectively; and 2.8% and 1.6% in Japanese men and women, respectively. Additionally, MGUS is significantly more prevalent in black people (5.9%-8.4%) than in white people (3.0%-3.6%). We conclude that MGUS is a common premalignant plasma cell disorder in the general population of those older than 50 years. The prevalence increases with age and is affected by race, sex, family history, immunosuppression, and pesticide exposure. These results are important for counseling, clinical care, and the design of clinical studies in high-risk populations.

摘要

意义未明的单克隆丙种球蛋白血症(MGUS)是一种癌前浆细胞疾病,与多发性骨髓瘤终生风险相关。我们对在线数据库 PubMed 中所有研究 MGUS 患病率和发病率的研究进行了系统回顾。该回顾于 2009 年 1 月 6 日至 2010 年 1 月 15 日进行。使用了以下 MeSH 搜索标题:单克隆丙种球蛋白血症,良性和流行率;单克隆丙种球蛋白血症,良性和发病率;副蛋白血症和流行率;和副蛋白血症和发病率。文章仅限于用英文书写并于 2009 年 1 月前发表的文章。符合预设标准的 14 项研究被包括并进行了系统评估,以根据年龄、性别和种族确定 MGUS 最准确的患病率估计值。基于我们的系统回顾,我们估计在以白人为主的人群中,50 岁以上人群的 MGUS 粗患病率为 3.2%。白人及日本人种的研究显示,患病率随年龄明显增加。患病率还受性别影响:白人男性和女性分别为 3.7%和 2.9%;日本男性和女性分别为 2.8%和 1.6%。此外,黑人(5.9%-8.4%)MGUS 的患病率明显高于白人(3.0%-3.6%)。我们得出结论,MGUS 是 50 岁以上人群中常见的癌前浆细胞疾病。患病率随年龄增长而增加,受种族、性别、家族史、免疫抑制和农药暴露的影响。这些结果对于咨询、临床护理和高危人群的临床研究设计都很重要。