Anderson L A, Pfeiffer R M, Landgren O, Gadalla S, Berndt S I, Engels E A
Centre for Public Health, Queen's University Belfast, Northern Ireland, UK.
Br J Cancer. 2009 Mar 10;100(5):822-8. doi: 10.1038/sj.bjc.6604935.
Autoimmune conditions are associated with an elevated risk of lymphoproliferative malignancies, but few studies have investigated the risk of myeloid malignancies. From the US Surveillance Epidemiology and End Results (SEER)-Medicare database, 13 486 myeloid malignancy patients (aged 67+ years) and 160 086 population-based controls were selected. Logistic regression models adjusted for gender, age, race, calendar year and number of physician claims were used to estimate odds ratios (ORs) for myeloid malignancies in relation to autoimmune conditions. Multiple comparisons were controlled for using the Bonferroni correction (P<0.0005). Autoimmune conditions, overall, were associated with an increased risk of acute myeloid leukaemia (AML) (OR 1.29) and myelodysplastic syndrome (MDS, OR 1.50). Specifically, AML was associated with rheumatoid arthritis (OR 1.28), systemic lupus erythematosus (OR 1.92), polymyalgia rheumatica (OR 1.73), autoimmune haemolytic anaemia (OR 3.74), systemic vasculitis (OR 6.23), ulcerative colitis (OR 1.72) and pernicious anaemia (OR 1.57). Myelodysplastic syndrome was associated with rheumatoid arthritis (OR1.52) and pernicious anaemia (OR 2.38). Overall, autoimmune conditions were not associated with chronic myeloid leukaemia (OR 1.09) or chronic myeloproliferative disorders (OR 1.15). Medications used to treat autoimmune conditions, shared genetic predisposition and/or direct infiltration of bone marrow by autoimmune conditions, could explain these excess risks of myeloid malignancies.
自身免疫性疾病与淋巴增殖性恶性肿瘤风险升高相关,但很少有研究调查其与髓系恶性肿瘤的风险。从美国监测、流行病学及最终结果(SEER)-医疗保险数据库中,选取了13486例髓系恶性肿瘤患者(年龄≥67岁)和160086例基于人群的对照。采用经性别、年龄、种族、日历年份和医生诊疗次数校正的逻辑回归模型,估计自身免疫性疾病与髓系恶性肿瘤相关的比值比(OR)。使用Bonferroni校正(P<0.0005)控制多重比较。总体而言,自身免疫性疾病与急性髓系白血病(AML,OR 1.29)和骨髓增生异常综合征(MDS,OR 1.50)风险增加相关。具体而言,AML与类风湿关节炎(OR 1.28)、系统性红斑狼疮(OR 1.92)、风湿性多肌痛(OR 1.73)、自身免疫性溶血性贫血(OR 3.74)、系统性血管炎(OR 6.23)、溃疡性结肠炎(OR 1.72)和恶性贫血(OR 1.57)相关。骨髓增生异常综合征与类风湿关节炎(OR 1.52)和恶性贫血(OR 2.38)相关。总体而言,自身免疫性疾病与慢性髓系白血病(OR 1.09)或慢性髓系增殖性疾病(OR 1.15)无关。用于治疗自身免疫性疾病的药物、共同的遗传易感性和/或自身免疫性疾病对骨髓的直接浸润,可能解释了这些髓系恶性肿瘤的额外风险。