Abstract

Chemotherapy-induced peripheral neuropathy (CIPN) is a common and severe side-effect in colorectal cancer (CRC) patients. This study assessed the association between habitual dietary intake of magnesium or calcium and prevalence and severity of chronic CIPN in CRC patients receiving adjuvant chemotherapy. For this prospective cohort study, 196 CRC patients were considered. Magnesium and calcium intake was determined using a food frequency questionnaire at diagnosis, during and after chemotherapy. Chronic CIPN was assessed 12 months after diagnosis using the quality of life questionnaire CIPN20. Prevalence ratios were calculated to assess the association between magnesium or calcium intake and the prevalence of CIPN. Multivariable linear regression analysis was used to assess the association between magnesium or calcium intake and severity of CIPN. CIPN was reported by 160 (82%) patients. Magnesium intake during chemotherapy was statistically significantly associated with lower prevalence of CIPN (prevalence ratio (PR) 0.53, 95% confidence interval (CI) 0.32, 0.92). Furthermore, higher dietary intake of magnesium during (β −1.08, 95% CI −1.95, −0.22) and after chemotherapy (β −0.93, 95% CI −1.81, −0.06) was associated with less severe CIPN. No associations were found for calcium intake and the prevalence and severity of CIPN. To conclude, we observed an association between higher dietary magnesium intake and lower prevalence and severity of CIPN in CRC patients.

Highlights

  • Chemotherapy-induced peripheral neuropathy (CIPN) is a common side-effect in colorectal cancer (CRC) patients treated with oxaliplatin [1]

  • The aim of this study was to assess the association between magnesium and calcium intake and CIPN in a prospective cohort of CRC patients

  • We found that a higher magnesium intake was associated with a lower severity of chronic CIPN, whereas no association for calcium was found

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Summary

Introduction

Chemotherapy-induced peripheral neuropathy (CIPN) is a common side-effect in colorectal cancer (CRC) patients treated with oxaliplatin [1]. Oxaliplatin can cause both acute and chronic CIPN. Symptoms of chronic CIPN include distal paresthesia, tingling sensations and numbness. CIPN predominantly affects sensory nerves and can lead to long-term disability [1]. Occurrence and Nutrients 2018, 10, 398; doi:10.3390/nu10040398 www.mdpi.com/journal/nutrients. Nutrients 2018, 10, 398 severity of chronic CIPN are related to the cumulative dose and dose-intensity of the treatment [1,2,3]. Six to eight months after the end of oxaliplatin treatment, 40–60% of the patients still suffer from

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