Vineis P, Miligi L, Crosignani P, Fontana A, Masala G, Nanni O, Ramazzotti V, Rodella S, Stagnaro E, Tumino R, Viganò C, Vindigni C, Costantini A S
Servizio di Epidemiologia dei Tumori, Ospedale S Giovanni Battista e Università di Torino, via Santena 7, I-10123 Torino, Italy.
J Epidemiol Community Health. 2000 Dec;54(12):907-11. doi: 10.1136/jech.54.12.907.
The annual incidence of non-Hodgkin's lymphomas (NHL) is increasing by 3%-4% in different parts of the developed world. Excesses of NHL have been observed in populations exposed to immunosuppressants and to HIV, but these causes do not explain the increasing trends. It is suggested that delayed infection could explain NHL trends, through an impairment of the Th1/Th2 lymphocyte patterns.
In a population-based study on 1388 patients with NHL, 354 with Hodgkin's disease (HD) and 1718 healthy controls, the age of first occurrence of bacterial and viral diseases was investigated. Clinical records were perused in one centre to check the anamnestic data.
The age of occurrence of bacterial and viral diseases was significantly higher among NHL patients than in the controls. The association between later age at first bacterial or viral disease was limited to small families (OR= 1.95; 95% confidence intervals 1.26, 3.00, for age 4-8 at first infection; OR=1.91; 1.19, 3.06, for age 9+, compared with less than 4). The association was more obvious for bacterial diseases (possibly for the lower degree of misclassification). High grade lymphomas showed the strongest association. The later age of occurrence of bacterial or viral diseases in NHL patients is consistent with a higher incidence of lymphomas observed in higher social groups. No clear association was found between HD and age at first bacterial or viral diseases.
It is proposed that delayed infection could explain the increasing NHL trends, through an impairment of the Th1/Th2 lymphocyte patterns. The model of delayed infection has been proposed also to explain increasing prevalence rates of asthma.
在发达国家的不同地区,非霍奇金淋巴瘤(NHL)的年发病率正以3%-4%的速度增长。在接触免疫抑制剂和感染HIV的人群中观察到NHL发病率过高,但这些原因并不能解释其增长趋势。有人提出,延迟感染可能通过损害Th1/Th2淋巴细胞模式来解释NHL的发病趋势。
在一项基于人群的研究中,对1388例NHL患者、354例霍奇金病(HD)患者和1718名健康对照者进行了调查,以研究细菌和病毒疾病首次发生的年龄。在一个中心查阅临床记录以核对既往病史数据。
NHL患者中细菌和病毒疾病发生的年龄显著高于对照组。首次发生细菌或病毒疾病的年龄较晚之间的关联仅限于小家庭(首次感染时年龄为4-8岁,比值比[OR]=1.95;95%置信区间为1.26, 3.00;9岁及以上,OR=1.91;1.19, 3.06,与小于4岁相比)。细菌疾病的关联更为明显(可能是因为错误分类程度较低)。高级别淋巴瘤显示出最强的关联。NHL患者中细菌或病毒疾病发生较晚的年龄与在较高社会阶层中观察到的淋巴瘤发病率较高一致。未发现HD与首次细菌或病毒疾病发生的年龄之间有明确关联。
有人提出,延迟感染可能通过损害Th1/Th2淋巴细胞模式来解释NHL的增长趋势。延迟感染模型也被提出来解释哮喘患病率的上升。