Evaluation of the Association Between Congenital Cytomegalovirus Infection and Pediatric Acute Lymphoblastic Leukemia

被引:3
|
作者
Geris, Jennifer M. [1 ,2 ]
Schleiss, Mark R. [2 ,3 ]
Hooten, Anthony J. [4 ]
Langer, Erica [4 ]
Hernandez-Alvarado, Nelmary [3 ]
Roesler, Michelle A. [1 ]
Sample, Jeannette [1 ]
Williams, Lindsay A. [1 ]
Dickens, David S. [5 ]
Mody, Rajen J. [6 ]
Ravindranath, Yaddanapudi [7 ,8 ]
Gowans, Kate L. [9 ]
Pridgeon, Matthew G. [10 ,11 ]
Spector, Logan G. [1 ]
Nelson, Heather H. [4 ,12 ]
机构
[1] Univ Minnesota, Dept Pediat, Div Epidemiol & Clin Res, 420 Delaware St SE, Minneapolis, MN 55455 USA
[2] Univ Minnesota, Inst Mol Virol, Minneapolis, MN 55455 USA
[3] Univ Minnesota, Dept Pediat, Div Pediat Infect Dis, Minneapolis, MN 55455 USA
[4] Univ Minnesota, Masonic Canc Ctr, Minneapolis, MN 55455 USA
[5] Univ Iowa, Dept Pediat, Div Hematol Oncol Bone Marrow Transplantat, Iowa City, IA 52242 USA
[6] Michigan Med, Div Hematol Oncol, Dept Pediat, Ann Arbor, MI USA
[7] Wayne State Univ, Sch Med, Dept Pediat, Div Hematol Oncol, Detroit, MI USA
[8] Childrens Hosp Michigan, Detroit, MI USA
[9] Beaumont Hlth, Dept Pediat Hematol Oncol, Royal Oak, MI USA
[10] Van Andel Res Inst, Ctr Canc & Cell Biol, Grand Rapids, MI USA
[11] Spectrum Hlth Syst, Helen DeVos Childrens Hosp, Grand Rapids, MI USA
[12] Univ Minnesota, Div Epidemiol & Community Hlth, Sch Publ Hlth, Minneapolis, MN 55455 USA
关键词
DROPLET DIGITAL PCR; VIRAL LOAD; CHILDHOOD; BLOOD; PRECURSOR; DISEASE; DNA;
D O I
10.1001/jamanetworkopen.2022.50219
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
IMPORTANCE Acute lymphoblastic leukemia (ALL) is the most common form of pediatric cancer, and a leading cause of death in children. Understanding the causes of pediatric ALL is necessary to enable early detection and prevention; congenital cytomegalovirus (cCMV) has recently been identified as a potential moderate-to-strong factor associated with risk for ALL. OBJECTIVE To compare the prevalence of cCMV infection between ALL cases and matched controls. DESIGN, SETTING, AND PARTICIPANTS In this population-based case-control study of ALL cases and matched controls, cases consisted of children aged 0 to 14 years between 1987 and 2014 with an ALL diagnosis identified through the Michigan Cancer Surveillance Program and born in Michigan on or after October 1, 1987. Cancer-free controls were identified by the Michigan BioTrust for Health and matched on age, sex, and mother's race and ethnicity. Data were analyzed from November to May 2022. EXPOSURES cCMV infection measured by quantitative polymerase chain reaction in newborn dried blood spots. MAIN OUTCOMES AND MEASURES ALL diagnosed in children aged 0 to 14 years. RESULTS A total of 1189 ALL cases and 4756 matched controls were included in the study. Bloodspots were collected from participants at birth, and 3425 (57.6%) participants were male. cCMV was detected in 6 ALL cases (0.5%) and 21 controls (0.4%). There was no difference in the odds of cCMV infection comparing ALL cases with controls (odds ratio, 1.30; 95% CI, 0.52-3.24). Immunophenotype was available for 536 cases (45.1%) and cytogenetic data for 127 (27%). When stratified by subtype characteristics, hyperdiploid ALL (74 cases) was associated with 6.26 times greater odds of cCMV infection compared with unmatched controls (95% CI, 1.44-27.19). CONCLUSIONS AND RELEVANCE In this case-control study of cCMV and pediatric ALL, cCMV was associated with increased risk of hyperdiploid ALL. These findings encourage continued research.
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页数:13
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