Systemic Biological Mechanisms of Neurocognitive Dysfunction in Long-Term Survivors of Childhood Hodgkin Lymphoma

Author:

Williams AnnaLynn M.1ORCID,Liu Wei2ORCID,Ehrhardt Matthew J.13ORCID,Mirzaei Salehabadi Sedigheh2ORCID,Panoskaltsis-Mortari Angela4ORCID,Phillips Nicholas S.1ORCID,Mulrooney Daniel A.13ORCID,Flerlage Jamie E.3ORCID,Yasui Yutaka1ORCID,Srivastava Deokumar2ORCID,Robison Leslie L.1ORCID,Hudson Melissa M.14ORCID,Ness Kirsten K.1ORCID,Sabin Noah D.5ORCID,Krull Kevin R.6ORCID

Affiliation:

1. 1Departments of Epidemiology and Cancer Control, St. Jude Children's Research Hospital, Memphis, Tennessee.

2. 2Department of Biostatistics, St. Jude Children's Research Hospital, Memphis, Tennessee.

3. 3Department of Oncology, St. Jude Children's Research Hospital, Memphis, Tennessee.

4. 4Departments of Pediatrics and Medicine, University of Minnesota, Minneapolis, Minnesota.

5. 5Department of Diagnostic Imaging, St. Jude Children's Research Hospital, Memphis, Tennessee.

6. 6Department of Psychology and Biobehavioral Sciences, St. Jude Children's Research Hospital, Memphis, Tennessee.

Abstract

Abstract Purpose: Hodgkin lymphoma (HL) survivors experience neurocognitive impairment despite receiving no central nervous system–directed therapy, though little is known about the underlying mechanisms. Experimental Design: HL survivors (n = 197) and age-, sex- and race/ethnicity frequency-matched community controls (n = 199) underwent standardized neurocognitive testing, and serum collection. Luminex multiplex or ELISA assays measured markers of inflammation and oxidative stress. Linear regression models compared biomarker concentrations between survivors and controls and with neurocognitive outcomes, adjusting for age, sex, race, body mass index, anti-inflammatory medication, and recent infections. Results: HL survivors [mean (SD) current age 36 (8) years, 22 (8) years after diagnosis] demonstrated higher concentrations of interleukin-6 (IL6), high-sensitivity c-reactive protein (hs-CRP), oxidized low-density lipoprotein, and glutathione peroxidase (GPx), compared with controls (P’s < 0.001). Among survivors, higher concentrations of IL6 were associated with worse visuomotor processing speed (P = 0.046). hs-CRP ≥3 mg/L was associated with worse attention, processing speed, memory, and executive function (P’s < 0.05). Higher concentrations of malondialdehyde were associated with worse focused attention and visual processing speed (P’s < 0.05). Homocysteine was associated with worse short-term recall (P = 0.008). None of these associations were statistically significant among controls. Among survivors, hs-CRP partially mediated associations between cardiovascular or endocrine conditions and visual processing speed, whereas IL6 partially mediated associations between pulmonary conditions and visuomotor processing speed. Conclusions: Neurocognitive function in long-term survivors of HL appears to be associated with inflammation and oxidative stress, both representing potential targets for future intervention trials.

Funder

National Cancer Institute

American Lebanese Syrian Associated Charities

Publisher

American Association for Cancer Research (AACR)

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