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Associations between childhood height and morphologically different variants of melanoma in adulthood

AIM OF THE STUDY: Melanoma subtypes have different aetiological characteristics. Child height is positively associated with adult melanoma; however, a clarification of associations with specific melanoma variants is necessary for an improved understanding of risk factors underlying the histologic en...

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Autores principales: Meyle, Kathrine Damm, Gamborg, Michael, Hölmich, Lisbet Rosenkrantz, Baker, Jennifer Lyn
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Science Ltd 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5068922/
https://www.ncbi.nlm.nih.gov/pubmed/27640136
http://dx.doi.org/10.1016/j.ejca.2016.08.002
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author Meyle, Kathrine Damm
Gamborg, Michael
Hölmich, Lisbet Rosenkrantz
Baker, Jennifer Lyn
author_facet Meyle, Kathrine Damm
Gamborg, Michael
Hölmich, Lisbet Rosenkrantz
Baker, Jennifer Lyn
author_sort Meyle, Kathrine Damm
collection PubMed
description AIM OF THE STUDY: Melanoma subtypes have different aetiological characteristics. Child height is positively associated with adult melanoma; however, a clarification of associations with specific melanoma variants is necessary for an improved understanding of risk factors underlying the histologic entities. This study investigated associations between childhood height and future development of cutaneous melanoma variants. METHOD: A cohort study of 316,193 individuals from the Copenhagen School Health Records Register, with measured heights at ages 7–13 years who were born from 1930 to 1989. Melanoma cases were identified via linkage to the national Danish Cancer Registry and subdivided into subtypes. Cox proportional hazards regressions were performed. RESULTS: A total of 2223 cases of melanoma distributed as 60% superficial spreading melanoma (SSM), 27.5% melanoma not otherwise specified (NOS), 8.5% nodular melanoma (NM), and 2% lentigo maligna melanoma (LMM). The remaining rare melanoma forms were not analysed. Childhood height was positively and significantly associated with SSM, melanoma NOS, and NM, but not LMM, in adulthood. Per height z-score at age 13 years, the hazard ratios were 1.20 (95% confidence intervals [CI]: 1.13–1.27) for SSM, 1.19 (95% CI: 1.09–1.29) for melanoma NOS, and 1.21 (95% CI: 1.04–1.41) for NM. Further, growth patterns were linked to the melanoma variants with persistently tall children having an increased risk of developing SSM, melanoma NOS, or NM. CONCLUSION: Childhood height is positively associated with the majority of the melanoma variants. These results suggest that the underlying processes contributing to childhood height and growth patterns interconnect early-life events with the predisposition to melanomagenesis in adulthood.
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spelling pubmed-50689222016-11-03 Associations between childhood height and morphologically different variants of melanoma in adulthood Meyle, Kathrine Damm Gamborg, Michael Hölmich, Lisbet Rosenkrantz Baker, Jennifer Lyn Eur J Cancer Original Research AIM OF THE STUDY: Melanoma subtypes have different aetiological characteristics. Child height is positively associated with adult melanoma; however, a clarification of associations with specific melanoma variants is necessary for an improved understanding of risk factors underlying the histologic entities. This study investigated associations between childhood height and future development of cutaneous melanoma variants. METHOD: A cohort study of 316,193 individuals from the Copenhagen School Health Records Register, with measured heights at ages 7–13 years who were born from 1930 to 1989. Melanoma cases were identified via linkage to the national Danish Cancer Registry and subdivided into subtypes. Cox proportional hazards regressions were performed. RESULTS: A total of 2223 cases of melanoma distributed as 60% superficial spreading melanoma (SSM), 27.5% melanoma not otherwise specified (NOS), 8.5% nodular melanoma (NM), and 2% lentigo maligna melanoma (LMM). The remaining rare melanoma forms were not analysed. Childhood height was positively and significantly associated with SSM, melanoma NOS, and NM, but not LMM, in adulthood. Per height z-score at age 13 years, the hazard ratios were 1.20 (95% confidence intervals [CI]: 1.13–1.27) for SSM, 1.19 (95% CI: 1.09–1.29) for melanoma NOS, and 1.21 (95% CI: 1.04–1.41) for NM. Further, growth patterns were linked to the melanoma variants with persistently tall children having an increased risk of developing SSM, melanoma NOS, or NM. CONCLUSION: Childhood height is positively associated with the majority of the melanoma variants. These results suggest that the underlying processes contributing to childhood height and growth patterns interconnect early-life events with the predisposition to melanomagenesis in adulthood. Elsevier Science Ltd 2016-11 /pmc/articles/PMC5068922/ /pubmed/27640136 http://dx.doi.org/10.1016/j.ejca.2016.08.002 Text en © 2016 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Research
Meyle, Kathrine Damm
Gamborg, Michael
Hölmich, Lisbet Rosenkrantz
Baker, Jennifer Lyn
Associations between childhood height and morphologically different variants of melanoma in adulthood
title Associations between childhood height and morphologically different variants of melanoma in adulthood
title_full Associations between childhood height and morphologically different variants of melanoma in adulthood
title_fullStr Associations between childhood height and morphologically different variants of melanoma in adulthood
title_full_unstemmed Associations between childhood height and morphologically different variants of melanoma in adulthood
title_short Associations between childhood height and morphologically different variants of melanoma in adulthood
title_sort associations between childhood height and morphologically different variants of melanoma in adulthood
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5068922/
https://www.ncbi.nlm.nih.gov/pubmed/27640136
http://dx.doi.org/10.1016/j.ejca.2016.08.002
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