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免疫相关性和炎症性疾病与淋巴浆细胞淋巴瘤或华氏巨球蛋白血症的风险。

Immune-related and inflammatory conditions and risk of lymphoplasmacytic lymphoma or Waldenstrom macroglobulinemia.

机构信息

Department of Medicine, Karolinska University Hospital Solna, SE-171 76 Stockholm, Sweden.

出版信息

J Natl Cancer Inst. 2010 Apr 21;102(8):557-67. doi: 10.1093/jnci/djq043. Epub 2010 Feb 24.

Abstract

BACKGROUND

Chronic immune stimulation appears to be associated with lymphoplasmacytic lymphoma (LPL)-Waldenström macroglobulinemia (WM); however, available information is sparse. We conducted, to our knowledge, the most comprehensive study to date to evaluate associations between a personal or family history of many immune-related and/or inflammatory disorders and the subsequent risk of LPL-WM.

METHODS

We used Swedish population-based registries to identify 2470 case patients with LPL-WM, 9698 matched control subjects, and almost 30 000 first-degree relatives of either case patients or control subjects. We evaluated a wide range of autoimmune, infectious, allergic, and inflammatory conditions. We calculated odds ratios (ORs) and 95% confidence intervals (CIs) for each condition by use of logistic regression.

RESULTS

An increased risk of LPL-WM was associated with a personal history of the following autoimmune diseases: systemic sclerosis (OR = 4.7, 95% CI = 1.4 to 15.3), Sjögren syndrome (OR = 12.1, 95% CI = 3.3 to 45.0), autoimmune hemolytic anemia (OR = 24.2, 95% CI = 5.4 to 108.2), polymyalgia rheumatica (OR = 2.9, 95% CI = 1.6 to 5.2), and giant cell arteritis (OR = 8.3, 95% CI = 2.1 to 33.1). An increased risk of LPL-WM was associated with a personal history of the following infectious diseases: pneumonia (OR = 1.4, 95% CI = 1.1 to 1.7), septicemia (OR = 2.4, 95% CI = 1.2 to 4.3), pyelonephritis (OR = 1.7, 95% CI = 1.1 to 2.5), sinusitis (OR = 2.7, 95% CI = 1.4 to 4.9), herpes zoster (OR = 3.4, 95% CI = 2.0 to 5.6), and influenza (OR = 2.9, 95% CI = 1.7 to 5.0). An increased risk of LPL-WM was associated with a family history of the following autoimmune or infectious diseases: Sjögren syndrome (OR = 5.0, 95% CI = 2.1 to 12.0), autoimmune hemolytic anemia (OR = 3.8, 95% CI = 1.1 to 13.2), Guillain-Barré syndrome (OR = 4.1, 95% CI = 1.8 to 9.4), cytomegalovirus (OR = 2.7, 95% CI = 1.4 to 5.3), gingivitis and periodontitis (OR = 1.9, 95% CI = 1.3 to 2.7), and chronic prostatitis (OR = 4.3, 95% CI = 1.7 to 11.1).

CONCLUSIONS

Personal history of certain immune-related and/or infectious conditions was strongly associated with increased risk of LPL-WM. The association of both personal and family history of Sjögren syndrome and autoimmune hemolytic anemia with risk of LPL-WM indicates the potential for shared susceptibility for these conditions.

摘要

背景

慢性免疫刺激似乎与淋巴浆细胞淋巴瘤(LPL)-瓦尔登斯特伦巨球蛋白血症(WM)有关;然而,现有的信息还很有限。我们进行了迄今为止最全面的研究,以评估许多与免疫相关和/或炎症相关的疾病的个人或家族史与随后发生 LPL-WM 的风险之间的关系。

方法

我们使用瑞典基于人群的登记处来确定 2470 例 LPL-WM 病例患者、9698 名匹配的对照患者以及几乎 30000 名病例患者或对照患者的一级亲属。我们评估了广泛的自身免疫、感染、过敏和炎症疾病。我们使用逻辑回归计算了每种疾病的比值比(OR)和 95%置信区间(CI)。

结果

LPL-WM 的风险增加与以下自身免疫性疾病的个人病史相关:系统性硬化症(OR=4.7,95%CI=1.4 至 15.3)、干燥综合征(OR=12.1,95%CI=3.3 至 45.0)、自身免疫性溶血性贫血(OR=24.2,95%CI=5.4 至 108.2)、巨细胞性多肌炎(OR=2.9,95%CI=1.6 至 5.2)和巨细胞动脉炎(OR=8.3,95%CI=2.1 至 33.1)。LPL-WM 的风险增加与以下传染病的个人病史相关:肺炎(OR=1.4,95%CI=1.1 至 1.7)、败血症(OR=2.4,95%CI=1.2 至 4.3)、肾盂肾炎(OR=1.7,95%CI=1.1 至 2.5)、鼻窦炎(OR=2.7,95%CI=1.4 至 4.9)、带状疱疹(OR=3.4,95%CI=2.0 至 5.6)和流感(OR=2.9,95%CI=1.7 至 5.0)。LPL-WM 的风险增加与以下自身免疫或传染病的家族史相关:干燥综合征(OR=5.0,95%CI=2.1 至 12.0)、自身免疫性溶血性贫血(OR=3.8,95%CI=1.1 至 13.2)、格林-巴利综合征(OR=4.1,95%CI=1.8 至 9.4)、巨细胞病毒(OR=2.7,95%CI=1.4 至 5.3)、牙龈炎和牙周炎(OR=1.9,95%CI=1.3 至 2.7)和慢性前列腺炎(OR=4.3,95%CI=1.7 至 11.1)。

结论

某些与免疫相关和/或感染相关的疾病的个人史与 LPL-WM 的风险增加密切相关。干燥综合征和自身免疫性溶血性贫血的个人和家族史与 LPL-WM 风险之间的关联表明,这些疾病可能存在共同的易感性。

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