Cargando…
Evaluation of the Association Between Congenital Cytomegalovirus Infection and Pediatric Acute Lymphoblastic Leukemia
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 p...
Autores principales: | , , , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Medical Association
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9856744/ https://www.ncbi.nlm.nih.gov/pubmed/36622672 http://dx.doi.org/10.1001/jamanetworkopen.2022.50219 |
_version_ | 1784873707896832000 |
---|---|
author | Geris, Jennifer M. Schleiss, Mark R. Hooten, Anthony J. Langer, Erica Hernandez-Alvarado, Nelmary Roesler, Michelle A. Sample, Jeannette Williams, Lindsay A. Dickens, David S. Mody, Rajen J. Ravindranath, Yaddanapudi Gowans, Kate L. Pridgeon, Matthew G. Spector, Logan G. Nelson, Heather H. |
author_facet | Geris, Jennifer M. Schleiss, Mark R. Hooten, Anthony J. Langer, Erica Hernandez-Alvarado, Nelmary Roesler, Michelle A. Sample, Jeannette Williams, Lindsay A. Dickens, David S. Mody, Rajen J. Ravindranath, Yaddanapudi Gowans, Kate L. Pridgeon, Matthew G. Spector, Logan G. Nelson, Heather H. |
author_sort | Geris, Jennifer M. |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-9856744 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Medical Association |
record_format | MEDLINE/PubMed |
spelling | pubmed-98567442023-02-03 Evaluation of the Association Between Congenital Cytomegalovirus Infection and Pediatric Acute Lymphoblastic Leukemia Geris, Jennifer M. Schleiss, Mark R. Hooten, Anthony J. Langer, Erica Hernandez-Alvarado, Nelmary Roesler, Michelle A. Sample, Jeannette Williams, Lindsay A. Dickens, David S. Mody, Rajen J. Ravindranath, Yaddanapudi Gowans, Kate L. Pridgeon, Matthew G. Spector, Logan G. Nelson, Heather H. JAMA Netw Open Original Investigation 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. American Medical Association 2023-01-09 /pmc/articles/PMC9856744/ /pubmed/36622672 http://dx.doi.org/10.1001/jamanetworkopen.2022.50219 Text en Copyright 2023 Geris JM et al. JAMA Network Open. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the CC-BY License. |
spellingShingle | Original Investigation Geris, Jennifer M. Schleiss, Mark R. Hooten, Anthony J. Langer, Erica Hernandez-Alvarado, Nelmary Roesler, Michelle A. Sample, Jeannette Williams, Lindsay A. Dickens, David S. Mody, Rajen J. Ravindranath, Yaddanapudi Gowans, Kate L. Pridgeon, Matthew G. Spector, Logan G. Nelson, Heather H. Evaluation of the Association Between Congenital Cytomegalovirus Infection and Pediatric Acute Lymphoblastic Leukemia |
title | Evaluation of the Association Between Congenital Cytomegalovirus Infection and Pediatric Acute Lymphoblastic Leukemia |
title_full | Evaluation of the Association Between Congenital Cytomegalovirus Infection and Pediatric Acute Lymphoblastic Leukemia |
title_fullStr | Evaluation of the Association Between Congenital Cytomegalovirus Infection and Pediatric Acute Lymphoblastic Leukemia |
title_full_unstemmed | Evaluation of the Association Between Congenital Cytomegalovirus Infection and Pediatric Acute Lymphoblastic Leukemia |
title_short | Evaluation of the Association Between Congenital Cytomegalovirus Infection and Pediatric Acute Lymphoblastic Leukemia |
title_sort | evaluation of the association between congenital cytomegalovirus infection and pediatric acute lymphoblastic leukemia |
topic | Original Investigation |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9856744/ https://www.ncbi.nlm.nih.gov/pubmed/36622672 http://dx.doi.org/10.1001/jamanetworkopen.2022.50219 |
work_keys_str_mv | AT gerisjenniferm evaluationoftheassociationbetweencongenitalcytomegalovirusinfectionandpediatricacutelymphoblasticleukemia AT schleissmarkr evaluationoftheassociationbetweencongenitalcytomegalovirusinfectionandpediatricacutelymphoblasticleukemia AT hootenanthonyj evaluationoftheassociationbetweencongenitalcytomegalovirusinfectionandpediatricacutelymphoblasticleukemia AT langererica evaluationoftheassociationbetweencongenitalcytomegalovirusinfectionandpediatricacutelymphoblasticleukemia AT hernandezalvaradonelmary evaluationoftheassociationbetweencongenitalcytomegalovirusinfectionandpediatricacutelymphoblasticleukemia AT roeslermichellea evaluationoftheassociationbetweencongenitalcytomegalovirusinfectionandpediatricacutelymphoblasticleukemia AT samplejeannette evaluationoftheassociationbetweencongenitalcytomegalovirusinfectionandpediatricacutelymphoblasticleukemia AT williamslindsaya evaluationoftheassociationbetweencongenitalcytomegalovirusinfectionandpediatricacutelymphoblasticleukemia AT dickensdavids evaluationoftheassociationbetweencongenitalcytomegalovirusinfectionandpediatricacutelymphoblasticleukemia AT modyrajenj evaluationoftheassociationbetweencongenitalcytomegalovirusinfectionandpediatricacutelymphoblasticleukemia AT ravindranathyaddanapudi evaluationoftheassociationbetweencongenitalcytomegalovirusinfectionandpediatricacutelymphoblasticleukemia AT gowanskatel evaluationoftheassociationbetweencongenitalcytomegalovirusinfectionandpediatricacutelymphoblasticleukemia AT pridgeonmatthewg evaluationoftheassociationbetweencongenitalcytomegalovirusinfectionandpediatricacutelymphoblasticleukemia AT spectorlogang evaluationoftheassociationbetweencongenitalcytomegalovirusinfectionandpediatricacutelymphoblasticleukemia AT nelsonheatherh evaluationoftheassociationbetweencongenitalcytomegalovirusinfectionandpediatricacutelymphoblasticleukemia |