Hypogonadism and neurocognitive outcomes among childhood cancer survivors

Author:

Yoshida Tomoko1ORCID,Alexander Tyler1ORCID,Xing Mengqi2ORCID,Mirzaei Sedigheh2,Williams AnnaLynn M1ORCID,Lubas Margaret1ORCID,Brinkman Tara M13,Chemaitilly Wassim4,Robison Leslie L1ORCID,Hudson Melissa M15ORCID,Krull Kevin R3ORCID,Delaney Angela16ORCID

Affiliation:

1. Department of Epidemiology and Cancer Control, St. Jude Children’s Research Hospital , Memphis, TN 38105 , United States

2. Department of Biostatistics, St. Jude Children’s Research Hospital , Memphis, TN 38105 , United States

3. Department of Psychology and Biobehavioral Sciences, St. Jude Children’s Research Hospital , Memphis, TN 38105 , United States

4. Division of Endocrinology and Diabetes, UPMC Children’s Hospital of Pittsburgh , Pittsburgh, PA 15224 , United States

5. Department of Oncology, St. Jude Children’s Research Hospital , Memphis, TN 38105 , United States

6. Department of Pediatric Medicine-Endocrinology, St. Jude Children’s Research Hospital , Memphis, TN 38105 , United States

Abstract

Abstract Objective Childhood cancer survivors are at risk for hypogonadism. The impact of hypogonadism on neurocognitive impairment and emotional distress in the non-cancer population has been shown; however, the relationship among the childhood cancer survivor population is unknown. We aimed to evaluate the contribution of hypogonadism to neurocognitive impairment and emotional distress among survivors. Design Cross-sectional study using retrospective cohort. Methods In total, 3628 survivors who completed standard neurocognitive tests (six domains: processing speed, memory, executive function, attention, academics, and global cognition) and self-reported emotional distress were included in our study. Participants were stratified by sex and gonadal status. Outcomes were compared between hypogonadal and eugonadal groups by multivariable analysis, adjusting for established predictors, and mediation analyses to determine the direct/indirect effects of hypogonadism on outcomes. Results The hypogonadal group exhibited a higher prevalence of neurocognitive impairment across domains, but no difference in emotional distress. Hypogonadal females exhibited higher relative risk (1.7, 95% CI, 1.2–2.5) for impaired visual processing speed, compared to eugonadal females after adjusting for cancer-related variables. In mediation models, hypogonadism had a significant direct (P < .01) and indirect (from P < .01) impact on impairment in visual processing speed among females. Males demonstrated direct (P = .03) and indirect (P = .04) impact of hypogonadism on motor processing speed. Conclusion Processing speed may be the most vulnerable neurocognitive domain associated with hypogonadism in survivors, while other domains were mainly impacted by cancer-related variables. Our findings support the need for further evaluation of the impact of sex hormone replacement therapy on neurocognitive function.

Funder

American Lebanese Syrian Associated Charities

Publisher

Oxford University Press (OUP)

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