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Psychiatric disorders in offspring of childhood or adolescent central nervous system tumor survivors: a national cohort study

BACKGROUND: Children experience a higher risk of psychiatric problems when their parents are diagnosed with cancer. However, the psychological effect among offspring who are born after parental cancer diagnosed in childhood or adolescence is unknown. We aimed to investigate the risk of psychiatric d...

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Autores principales: Huang, Wuqing, Sundquist, Kristina, Sundquist, Jan, Ji, Jianguang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7877351/
https://www.ncbi.nlm.nih.gov/pubmed/33135321
http://dx.doi.org/10.1002/cam4.3591
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author Huang, Wuqing
Sundquist, Kristina
Sundquist, Jan
Ji, Jianguang
author_facet Huang, Wuqing
Sundquist, Kristina
Sundquist, Jan
Ji, Jianguang
author_sort Huang, Wuqing
collection PubMed
description BACKGROUND: Children experience a higher risk of psychiatric problems when their parents are diagnosed with cancer. However, the psychological effect among offspring who are born after parental cancer diagnosed in childhood or adolescence is unknown. We aimed to investigate the risk of psychiatric disorders in children of survivors with childhood or adolescent central nervous system (CNS) tumors. METHODS: By combining several nationwide Swedish registers, we identified all children who had at least one parent previously diagnosed with CNS tumor below the age of 20. Five children without parental CNS tumor were randomly selected for the matching. Cox proportional hazards model was used to calculate hazard ratios (HRs) with 95% confidence interval (CI). RESULTS: The incidence rate of psychiatric disorders was 8.46 per 1000 person‐years in children of CNS tumor survivors, whereas the rate was 7.47 in the matched comparisons, yielding an adjusted HR of 1.10 (95% CI = 0.94, 1.28). Boys of survivors had a higher risk of psychiatric disorders (adjusted HR = 1.29, 95% CI = 1.04, 1.59). The risk of the specific types of psychiatric disorders in children of tumor survivors was comparable with that in the matched comparisons, except for mental retardation. Children of survivors experienced 2.36 times higher risk of mental retardation (95% CI = 1.21, 4.58), mainly of mild mental retardation (adjusted HR = 2.99, 95% CI = 1.40, 6.38). CONCLUSION: Children of survivors with CNS tumor in early life did not experience a significantly increased risk of overall psychiatric disorders, with the exception of an elevated risk of mental retardation that was mainly mild.
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spelling pubmed-78773512021-02-18 Psychiatric disorders in offspring of childhood or adolescent central nervous system tumor survivors: a national cohort study Huang, Wuqing Sundquist, Kristina Sundquist, Jan Ji, Jianguang Cancer Med Clinical Cancer Research BACKGROUND: Children experience a higher risk of psychiatric problems when their parents are diagnosed with cancer. However, the psychological effect among offspring who are born after parental cancer diagnosed in childhood or adolescence is unknown. We aimed to investigate the risk of psychiatric disorders in children of survivors with childhood or adolescent central nervous system (CNS) tumors. METHODS: By combining several nationwide Swedish registers, we identified all children who had at least one parent previously diagnosed with CNS tumor below the age of 20. Five children without parental CNS tumor were randomly selected for the matching. Cox proportional hazards model was used to calculate hazard ratios (HRs) with 95% confidence interval (CI). RESULTS: The incidence rate of psychiatric disorders was 8.46 per 1000 person‐years in children of CNS tumor survivors, whereas the rate was 7.47 in the matched comparisons, yielding an adjusted HR of 1.10 (95% CI = 0.94, 1.28). Boys of survivors had a higher risk of psychiatric disorders (adjusted HR = 1.29, 95% CI = 1.04, 1.59). The risk of the specific types of psychiatric disorders in children of tumor survivors was comparable with that in the matched comparisons, except for mental retardation. Children of survivors experienced 2.36 times higher risk of mental retardation (95% CI = 1.21, 4.58), mainly of mild mental retardation (adjusted HR = 2.99, 95% CI = 1.40, 6.38). CONCLUSION: Children of survivors with CNS tumor in early life did not experience a significantly increased risk of overall psychiatric disorders, with the exception of an elevated risk of mental retardation that was mainly mild. John Wiley and Sons Inc. 2020-11-01 /pmc/articles/PMC7877351/ /pubmed/33135321 http://dx.doi.org/10.1002/cam4.3591 Text en © 2020 The Authors. Cancer Medicine published by John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Clinical Cancer Research
Huang, Wuqing
Sundquist, Kristina
Sundquist, Jan
Ji, Jianguang
Psychiatric disorders in offspring of childhood or adolescent central nervous system tumor survivors: a national cohort study
title Psychiatric disorders in offspring of childhood or adolescent central nervous system tumor survivors: a national cohort study
title_full Psychiatric disorders in offspring of childhood or adolescent central nervous system tumor survivors: a national cohort study
title_fullStr Psychiatric disorders in offspring of childhood or adolescent central nervous system tumor survivors: a national cohort study
title_full_unstemmed Psychiatric disorders in offspring of childhood or adolescent central nervous system tumor survivors: a national cohort study
title_short Psychiatric disorders in offspring of childhood or adolescent central nervous system tumor survivors: a national cohort study
title_sort psychiatric disorders in offspring of childhood or adolescent central nervous system tumor survivors: a national cohort study
topic Clinical Cancer Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7877351/
https://www.ncbi.nlm.nih.gov/pubmed/33135321
http://dx.doi.org/10.1002/cam4.3591
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