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Are dietary and serum advanced glycation end-products related to inflammation and oxidation biomarkers in breast cancer patients: a follow-up study

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Abstract

Purpose

This study is aimed at evaluating the relationship between dietary and serum advanced glycation end-products (AGEs) with serum inflammatory and oxidative stress biomarkers in breast cancer (BC).

Methods

A sample of BC patients was followed for 12 months (March 2020–January 2022). Three-day food consumption record and serum samples were taken before surgery (T1), before chemotherapy (T2), at the 6th month of chemotherapy (T3), and at the 12th month of chemotherapy (T4). Dietary AGE intake was represented by carboxymethyl lysine (dCML). Serum levels of CML, inflammation, and oxidation biomarkers were determined with biochemical blood tests. The results were compared according to human epidermal growth factor receptor-2 (HER2) status.

Results

Thirty-two women with BC and 32 age and body mass index-matched healthy women participated. No significant correlation was found between dCML and serum CML, inflammatory or oxidative stress biomarkers at T1, T2, and T4. A weak positive correlation was demonstrated between dCML and serum malondialdehyde levels (rho=0.355, p=0.046) at T3. The serum CML, inflammation, and oxidation biomarker levels of the HER2− group were significantly higher than those of the HER2+ group at T1.

Conclusion

This study suggests that there is limited correlation between dCML and serum inflammation and oxidative stress biomarkers in BC patients. Inflammation and oxidative biomarker levels appear to decline with treatment although dietary and serum AGE levels show not a corresponding significant decline. The HER2− subtype appears to be associated with higher dietary and serum AGEs and higher inflammatory and oxidative stress biomarkers.

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Acknowledgements

We would like to thank the women that have participated in this research. We would like to thank Turkish Society of Medical Oncology for supporting the research and Dr. Ahmad Qasim AL-KHATTAT for his valuable support in writing the manuscript.

Data availability

This manuscript is based on data of SBA’s PhD dissertation. The datasets of the current study are available from the corresponding author on reasonable request.

Funding

This research was supported by Turkish Society of Medical Oncology (Grant no. TTOD-2019-47).

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Authors and Affiliations

Authors

Contributions

SBA, MA, and NR designed the study. SBA, MA, FA, MMB, MG, and HCA were responsible for the clinical data extraction. SBA and NR wrote the first draft of the manuscript. MA and NR reviewed and revised the manuscript. All authors read and approved the final manuscript.

Corresponding author

Correspondence to Neslişah Rakıcıoğlu.

Ethics declarations

Ethics approval and consent to participate

Ethical approval for this study was obtained from the Ethics Committee of Necmettin Erbakan University, Konya, Turkey (2019/1866, 17 May 2019). All procedures performed in studies involving human participants were in accordance with the ethical standards of the institutional and/or national research committee and with the 1964 Helsinki declaration and its later amendments or comparable ethical standards. Informed consent was obtained from all individual participants included in the study.

Consent for publication

Participants consented to having their data published.

Competing interests

The authors declare no competing interests.

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Alkan, Ş.B., Artaç, M., Aksoy, F. et al. Are dietary and serum advanced glycation end-products related to inflammation and oxidation biomarkers in breast cancer patients: a follow-up study. Support Care Cancer 31, 334 (2023). https://doi.org/10.1007/s00520-023-07772-w

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