TY - JOUR
T1 - Are higher pre-diagnosis follicle stimulating hormone levels associated with long-term prostate cancer risk?
AU - Dymanus, Kyle
AU - Howard, Lauren E.
AU - Oyekunle, Taofik
AU - De Hoedt, Amanda M.
AU - Labadzhyan, Artak
AU - Polascik, Thomas
AU - Freedland, Stephen J.
AU - Klaassen, Zachary
N1 - Funding Information:
This research received funding from Ferring Pharmaceuticals Inc.
Publisher Copyright:
© 2022 Wiley Periodicals LLC.
PY - 2022/12/1
Y1 - 2022/12/1
N2 - Background: Follicle stimulating hormone (FSH) is a pituitary hormone that helps regulate testosterone homeostasis. Although it is generally accepted that FSH levels increase with LHRH-agonist therapy for prostate cancer (PC), the specific impact of FSH levels on risk of PC diagnosis is largely unknown. The objective of this study was to perform a population-level analysis to assess the association between FSH levels and PC diagnosis. Methods: All men (n = 386,018) who had a pre-PC diagnosis FSH level and complete data were identified within the Veterans Affairs Health System between 1999 and 2018. The association between FSH level and time from FSH test to PC diagnosis was tested using stratified Cox proportional hazards models. Multivariable models were adjusted for age, year, race, body mass index, and Charlson comorbidity index. Due to nonproportional hazards over time, time to PC was modeled separately: ≤4 years after an FSH test and >4 years following an FSH test. Results: Median age at first FSH level was 64 years (interquartile range [IQR]: 54–72), median year of FSH was 2010 (IQR: 2005–2014), and 70% of the cohort was white. Median follow-up was 76 months (IQR: 38–126) during which 17,519 men (4.5%) were diagnosed with PC. On multivariable analysis, in the first 4 years after FSH test, there was no association between FSH and time to PC diagnosis. Starting from 4 years after FSH test, on multivariable analysis, a higher FSH level was associated with lower risk of PC with continuous modeling, but found no association with log continuous and categorical modeling. Conclusions: In this population-level study among male veterans receiving an FSH test for an unknown clinical indication, associations between FSH levels and PC risk were inconsistent and likely driven by selection bias and confounding variables. Future studies should consider different study designs.
AB - Background: Follicle stimulating hormone (FSH) is a pituitary hormone that helps regulate testosterone homeostasis. Although it is generally accepted that FSH levels increase with LHRH-agonist therapy for prostate cancer (PC), the specific impact of FSH levels on risk of PC diagnosis is largely unknown. The objective of this study was to perform a population-level analysis to assess the association between FSH levels and PC diagnosis. Methods: All men (n = 386,018) who had a pre-PC diagnosis FSH level and complete data were identified within the Veterans Affairs Health System between 1999 and 2018. The association between FSH level and time from FSH test to PC diagnosis was tested using stratified Cox proportional hazards models. Multivariable models were adjusted for age, year, race, body mass index, and Charlson comorbidity index. Due to nonproportional hazards over time, time to PC was modeled separately: ≤4 years after an FSH test and >4 years following an FSH test. Results: Median age at first FSH level was 64 years (interquartile range [IQR]: 54–72), median year of FSH was 2010 (IQR: 2005–2014), and 70% of the cohort was white. Median follow-up was 76 months (IQR: 38–126) during which 17,519 men (4.5%) were diagnosed with PC. On multivariable analysis, in the first 4 years after FSH test, there was no association between FSH and time to PC diagnosis. Starting from 4 years after FSH test, on multivariable analysis, a higher FSH level was associated with lower risk of PC with continuous modeling, but found no association with log continuous and categorical modeling. Conclusions: In this population-level study among male veterans receiving an FSH test for an unknown clinical indication, associations between FSH levels and PC risk were inconsistent and likely driven by selection bias and confounding variables. Future studies should consider different study designs.
KW - FSH
KW - follicle stimulating hormone
KW - prostate cancer
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U2 - 10.1002/pros.24429
DO - 10.1002/pros.24429
M3 - Article
C2 - 35981148
AN - SCOPUS:85135877803
SN - 0270-4137
VL - 82
SP - 1558
EP - 1563
JO - Prostate
JF - Prostate
IS - 16
ER -