Advanced parental age as risk factor for childhood acute lymphoblastic leukemia: results from studies of the Childhood Leukemia International Consortium

被引:48
作者
Petridou, Eleni Th. [1 ,2 ]
Georgakis, Marios K. [1 ]
Erdmann, Friederike [3 ,4 ]
Ma, Xiaomei [5 ]
Heck, Julia E. [6 ]
Auvinen, Anssi [7 ]
Mueller, Beth A. [8 ,9 ]
Spector, Logan G. [10 ]
Roman, Eve [11 ]
Metayer, Catherine [12 ]
Magnani, Corrado [13 ]
Pombo-de-Oliveira, Maria S. [14 ]
Ezzat, Sameera [15 ]
Scheurer, Michael E. [16 ]
Maria Mora, Ana [17 ]
Dockerty, John D. [18 ]
Hansen, Johnni [19 ]
Kang, Alice Y. [12 ]
Wang, Rong [5 ]
Doody, David R. [8 ]
Kane, Eleanor [11 ]
Rashed, Waffa M. [20 ,21 ]
Dessypris, Nick [1 ]
Schuz, Joachim [3 ]
Infante-Rivard, Claire [22 ]
Skalkidou, Alkistis [23 ]
机构
[1] Univ Athens, Med Sch, Dept Hyg Epidemiol & Med Stat, 75 Mikras Asias Str, Athens 11527, Greece
[2] Karolinska Inst, Dept Med, Clin Epidemiol Unit, Stockholm, Sweden
[3] Int Agcy Res Canc, Sect Environm & Radiat, Lyon, France
[4] Danish Canc Soc Res Ctr, Childhood Canc Survivorship Res Grp, Unit Survivorship, Copenhagen, Denmark
[5] Yale Sch Med, Yale Comprehens Canc Ctr, Yale Sch Publ Hlth Canc Prevent & Control, Dept Chron Dis Epidemiol, New Haven, CT USA
[6] Univ Calif Los Angeles, Sch Publ Hlth, Dept Epidemiol, Los Angeles, CA 90024 USA
[7] Univ Tampere, Fac Social Sci, Tampere, Finland
[8] Fred Hutchinson Canc Res Ctr, Publ Hlth Sci Div, Seattle, WA USA
[9] Univ Washington, Sch Publ Hlth, Dept Epidemiol, Seattle, WA 98195 USA
[10] Univ Minnesota, Dept Pediat, Div Epidemiol & Clin Res, Minneapolis, MN 55455 USA
[11] Univ York, Dept Hlth Sci, Epidemiol & Canc Stat Grp, York, N Yorkshire, England
[12] Univ Calif Berkeley, Sch Publ Hlth, Berkeley, CA 94720 USA
[13] Univ Piemonte Orientale, SCDU Epidemiol Tumori, Dipartimento Med Traslazi, Novara, Italy
[14] Inst Nacl Canc, Pediat Hematol Oncol Program, Rio De Janeiro, Brazil
[15] Menoufia Univ, Natl Liver Inst, NLI SSI Collaborat Res Ctr, Dept Epidemiol & Prevent Med, Cairo, Egypt
[16] Baylor Coll Med, Texas Childrens Canc Ctr, Dept Pediat, Houston, TX 77030 USA
[17] Univ Nacl, Cent Amer Inst Studies Toxic Subst IRET, Heredia, Costa Rica
[18] Univ Otago, Dunedin Sch Med, Dept Preventat & Social Med, Dunedin, New Zealand
[19] Danish Canc Soc, Res Ctr, Copenhagen, Denmark
[20] Childrens Canc Hosp Egypt, Res Dept, Cairo, Egypt
[21] Armed Forces Coll Med, Biomed Res Dept, Cairo, Egypt
[22] McGill Univ, Fac Med, Dept Epidemiol Biostat & Occupat Hlth, Montreal, PQ, Canada
[23] Uppsala Univ, Dept Womens & Childrens Hlth, Uppsala, Sweden
关键词
Maternal age; Paternal age; Acute lymphoblastic leukemia; Childhood; Risk factors; Case-control; ADVANCED PATERNAL AGE; MATERNAL AGE; PRENATAL ORIGIN; PSYCHIATRIC-DISORDERS; CESAREAN DELIVERY; POOLED ANALYSIS; RECORD-LINKAGE; DOWN-SYNDROME; CANCER; COHORT;
D O I
10.1007/s10654-018-0402-z
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
Advanced parental age has been associated with adverse health effects in the offspring including childhood (0-14 years) acute lymphoblastic leukemia (ALL), as reported in our meta-analysis of published studies. We aimed to further explore the association using primary data from 16 studies participating in the Childhood Leukemia International Consortium. Data were contributed by 11 case-control (CC) studies (7919 cases and 12,942 controls recruited via interviews) and five nested case-control (NCC) studies (8801 cases and 29,690 controls identified through record linkage of population-based health registries) with variable enrollment periods (1968-2015). Five-year paternal and maternal age increments were introduced in two meta-analyses by study design using adjusted odds ratios (OR) derived from each study. Increased paternal age was associated with greater ALL risk in the offspring (ORCC 1.05, 95% CI 1.00-1.11; ORNCC 1.04, 95% CI 1.01-1.07). A similar positive association with advanced maternal age was observed only in the NCC results (ORCC 0.99, 95% CI 0.91-1.07, heterogeneity I (2) = 58%, p = 0.002; ORNCC 1.05, 95% CI 1.01-1.08). The positive association between parental age and risk of ALL was most marked among children aged 1-5 years and remained unchanged following mutual adjustment for the collinear effect of the paternal and maternal age variables; analyses of the relatively small numbers of discordant paternal-maternal age pairs were not fully enlightening. Our results strengthen the evidence that advanced parental age is associated with increased childhood ALL risk; collinearity of maternal with paternal age complicates causal interpretation. Employing datasets with cytogenetic information may further elucidate involvement of each parental component and clarify underlying mechanisms.
引用
收藏
页码:965 / 976
页数:12
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