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

Author:

Geris Jennifer M.12,Schleiss Mark R.23,Hooten Anthony J.4,Langer Erica4,Hernandez-Alvarado Nelmary3,Roesler Michelle A.1,Sample Jeannette1,Williams Lindsay A.1,Dickens David S.5,Mody Rajen J.6,Ravindranath Yaddanapudi7,Gowans Kate L.8,Pridgeon Matthew G.910,Spector Logan G.1,Nelson Heather H.411

Affiliation:

1. Division of Epidemiology and Clinical Research, Department of Pediatrics, University of Minnesota, Minneapolis

2. Institute for Molecular Virology, University of Minnesota, Minneapolis

3. Division of Pediatric Infectious Diseases, Department of Pediatrics, University of Minnesota, Minneapolis

4. Masonic Cancer Center, University of Minnesota, Minneapolis

5. Division of Hematology/Oncology/Bone Marrow Transplantation, Department of Pediatrics, University of Iowa, Iowa City

6. Division of Hematology-Oncology, Department of Pediatrics, Michigan Medicine, Ann Arbor

7. Division of Hematology/Oncology, Department of Pediatrics, Wayne State University School of Medicine, and Children’s Hospital of Michigan, Detroit

8. Department of Pediatric Hematology/Oncology, Beaumont Health, Royal Oak, Michigan

9. Center for Cancer and Cell Biology, Van Andel Research Institute, Grand Rapids, Michigan

10. Helen DeVos Children’s Hospital, Spectrum Health System, Grand Rapids, Michigan

11. Division of Epidemiology and Community Health, University of Minnesota School of Public Health, Minneapolis

Abstract

ImportanceAcute 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.ObjectiveTo compare the prevalence of cCMV infection between ALL cases and matched controls.Design, Setting, and ParticipantsIn 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.ExposurescCMV infection measured by quantitative polymerase chain reaction in newborn dried blood spots.Main Outcomes and MeasuresALL diagnosed in children aged 0 to 14 years.ResultsA 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 RelevanceIn this case-control study of cCMV and pediatric ALL, cCMV was associated with increased risk of hyperdiploid ALL. These findings encourage continued research.

Publisher

American Medical Association (AMA)

Subject

General Medicine

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