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Elevated C-Reactive Protein and Subsequent Patient-Reported Cognitive Problems in Older Breast Cancer Survivors: The Thinking and Living With Cancer Study

  • Judith E. Carroll
  • , Zev M. Nakamura
  • , Brent J. Small
  • , Xingtao Zhou
  • , Harvey J. Cohen
  • , Tim A. Ahles
  • , Jaeil Ahn
  • , Traci N. Bethea
  • , Martine Extermann
  • , Deena Graham
  • , Claudine Isaacs
  • , Heather S.L. Jim
  • , Paul B. Jacobsen
  • , Brenna C. Mcdonald
  • , Sunita K. Patel
  • , Kelly Rentscher
  • , James Root
  • , Andrew J. Saykin
  • , Danielle B. Tometich
  • , Kathleen Van Dyk
  • Wanting Zhai, Elizabeth C. Breen, Jeanne S. Mandelblatt
  • University of California at Los Angeles
  • University of North Carolina at Chapel Hill
  • University of South Florida
  • Georgetown University
  • Duke University
  • Memorial Sloan-Kettering Cancer Center
  • Moffitt Cancer Center
  • National Institutes of Health
  • Indiana University-Purdue University Indianapolis
  • City of Hope National Med Center

Research output: Contribution to journal › Article › peer-review

39 Scopus citations

Abstract

PURPOSETo examine longitudinal relationships between levels of C-reactive protein (CRP) and cognition in older breast cancer survivors and noncancer controls.METHODSEnglish-speaking women age ≥ 60 years, newly diagnosed with primary breast cancer (stage 0-III), and frequency-matched controls were enrolled from September 2010 to March 2020; women with dementia, neurologic disorders, and other cancers were excluded. Assessments occurred presystemic therapy/enrollment and at annual visits up to 60 months. Cognition was measured using the Functional Assessment of Cancer Therapy-Cognitive Function and neuropsychological testing. Mixed linear effect models tested for survivor-control differences in natural log (ln)-transformed CRP at each visit. Random effect-lagged fluctuation models tested directional effects of ln-CRP on subsequent cognition. All models controlled for age, race, study site, cognitive reserve, obesity, and comorbidities; secondary analyses evaluated if depression or anxiety affected results.RESULTSThere were 400 survivors and 329 controls with CRP specimens and follow-up data (average age of 67.7 years; range, 60-90 years). The majority of survivors had stage I (60.9%), estrogen receptor-positive (87.6%) tumors. Survivors had significantly higher adjusted mean ln-CRP than controls at baseline and 12-, 24-, and 60-month visits (all P <.05). Higher adjusted ln-CRP predicted lower participant-reported cognition on subsequent visits among survivors, but not controls (P interaction =.008); effects were unchanged by depression or anxiety. Overall, survivors had adjusted Functional Assessment of Cancer Therapy-Cognitive Function scores that were 9.5 and 14.2 points lower than controls at CRP levels of 3.0 and 10.0 mg/L. Survivors had poorer neuropsychological test performance (v controls), with significant interactions with CRP only for the Trails B test.CONCLUSIONLongitudinal relationships between CRP and cognition in older breast cancer survivors suggest that chronic inflammation may play a role in development of cognitive problems. CRP testing could be clinically useful in survivorship care.

Original languageEnglish
Pages (from-to)295-306
Number of pages12
JournalJournal of Clinical Oncology
Volume41
Issue number2
DOIs
StatePublished - 10 Jan 2023

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

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