TY - JOUR
T1 - Height in adolescence as a risk factor for glioma subtypes
T2 - A nationwide retrospective cohort study of 2.2 million subjects
AU - Tschernichovsky, Roi
AU - Katz, Lior H.
AU - Derazne, Estela
AU - Berliner, Matan Ben Zion
AU - Simchoni, Maya
AU - Levine, Hagai
AU - Keinan-Boker, Lital
AU - Benouaich-Amiel, Alexandra
AU - Kanner, Andrew A.
AU - Laviv, Yosef
AU - Honig, Asaf
AU - Dudnik, Elizabeth
AU - Siegal, Tali
AU - Mandel, Jacob
AU - Twig, Gilad
AU - Yust-Katz, Shlomit
N1 - Publisher Copyright:
© 2021 The Author(s) 2021. Published by Oxford University Press on behalf of the Society for Neuro-Oncology. All rights reserved. For permissions, please e-mail: [email protected].
PY - 2021/8/2
Y1 - 2021/8/2
N2 - Background: Gliomas manifest in a variety of histological phenotypes with varying aggressiveness. The etiology of glioma remains largely unknown. Taller stature in adulthood has been linked with glioma risk. The aim of this study was to discern whether this association can be detected in adolescence. Methods: The cohort included 2 223 168 adolescents between the ages of 16 and 19 years. Anthropometric measurements were collected at baseline. Incident cases of glioma were extracted from the Israel National Cancer Registry over a follow-up period spanning 47 635 745 person-years. Cox proportional hazard models were used to estimate the hazard ratio (HR) for glioma and glioma subtypes according to height, body mass index (BMI), and sex. Results: A total of 1195 patients were diagnosed with glioma during the study period. Mean (SD) age at diagnosis was 38.1 (11.7) years. Taller adolescent height (per 10-cm increase) was positively associated with the risk for glioma of any type (HR: 1.15; P =. 002). The association was retained in subgroup analyses for low-grade glioma (HR: 1.17; P =. 031), high-grade glioma (HR: 1.15; P =. 025), oligodendroglioma (HR: 1.31; P =. 015), astrocytoma (HR: 1.12; P =. 049), and a category of presumed IDH-mutated glioma (HR: 1.17; P =. 013). There was a trend toward a positive association between height and glioblastoma, however this had borderline statistical significance (HR: 1.15; P =. 07). After stratification of the cohort by sex, height remained a risk factor for men but not for women. Conclusions: The previously established association between taller stature in adulthood and glioma risk can be traced back to adolescence. The magnitude of association differs by glioma subtype.
AB - Background: Gliomas manifest in a variety of histological phenotypes with varying aggressiveness. The etiology of glioma remains largely unknown. Taller stature in adulthood has been linked with glioma risk. The aim of this study was to discern whether this association can be detected in adolescence. Methods: The cohort included 2 223 168 adolescents between the ages of 16 and 19 years. Anthropometric measurements were collected at baseline. Incident cases of glioma were extracted from the Israel National Cancer Registry over a follow-up period spanning 47 635 745 person-years. Cox proportional hazard models were used to estimate the hazard ratio (HR) for glioma and glioma subtypes according to height, body mass index (BMI), and sex. Results: A total of 1195 patients were diagnosed with glioma during the study period. Mean (SD) age at diagnosis was 38.1 (11.7) years. Taller adolescent height (per 10-cm increase) was positively associated with the risk for glioma of any type (HR: 1.15; P =. 002). The association was retained in subgroup analyses for low-grade glioma (HR: 1.17; P =. 031), high-grade glioma (HR: 1.15; P =. 025), oligodendroglioma (HR: 1.31; P =. 015), astrocytoma (HR: 1.12; P =. 049), and a category of presumed IDH-mutated glioma (HR: 1.17; P =. 013). There was a trend toward a positive association between height and glioblastoma, however this had borderline statistical significance (HR: 1.15; P =. 07). After stratification of the cohort by sex, height remained a risk factor for men but not for women. Conclusions: The previously established association between taller stature in adulthood and glioma risk can be traced back to adolescence. The magnitude of association differs by glioma subtype.
KW - BMI
KW - adolescence
KW - glioma
KW - height
KW - sex
UR - http://www.scopus.com/inward/record.url?scp=85113304749&partnerID=8YFLogxK
U2 - 10.1093/neuonc/noab049
DO - 10.1093/neuonc/noab049
M3 - Article
C2 - 33631004
AN - SCOPUS:85113304749
SN - 1522-8517
VL - 23
SP - 1383
EP - 1392
JO - Neuro-Oncology
JF - Neuro-Oncology
IS - 8
ER -