Author:
Hauner Dagmar,Mang Anna,Donik Lara,Schederecker Florian,Meyer Dorothy,Rack Brigitte,Janni Wolfgang,Hauner Hans
Abstract
Abstract
Background
There is little evidence that dietary supplements are beneficial for patients with breast cancer; therefore, they are usually not recommended by treatment guidelines. The aim of the present analysis was to assess the prevalence of dietary supplement (DS) intake among women before and after a breast cancer diagnosis.
Methods
Participants in the SUCCESS C lifestyle intervention study, a randomized controlled trial in women with newly diagnosed intermediate- to high-risk breast cancer, completed two questionnaires on dietary supplement intake 24 months (QS1) and 48 months (QS2) after beginning the lifestyle intervention. The study was registered on 12.17.2008 under the EU Clinical Trials Register https://www.clinicaltrialsregister.eu/, trial registration number: 2008-005453-38. The questionnaires collected data on DS intake during the 5-year period prediagnosis (QS1) and in the period postdiagnosis (QS2). Multivariate logistic regression models were fitted to examine differences in DS intake between the two intervention groups. The groups were then pooled to examine differences in DS use between the prediagnostic and postdiagnostic period.
Results
A total of 320 questionnaires from 58.5% of intervention group completers and 416 questionnaires from 46.6% of low-level intervention group completers were included in the analysis. Overall, 20.2% of all respondents reported taking DS prior to their diagnosis. After a cancer diagnosis, the percentage of women taking DS significantly increased to 56.4% (p for time effect < 0.0001). No differences in DS intake between the intervention groups were observed. Single or combined preparations of vitamins and minerals/trace elements were the most frequently reported supplements. Notably, a 9-fold increase in vitamin D intake was reported postdiagnosis, where the proportion of women increased from 3.8 to 34.5%.
Conclusion
A 3-fold increase in the reported intake of dietary supplements was seen in women after a breast cancer diagnosis. These observations underscore the need to incorporate patient education surrounding the use of dietary supplements in a treatment care plan, particularly addressing the negligible benefits as well as the potential risks and treatment interactions.
Funder
Technische Universität München
Publisher
Springer Science and Business Media LLC
Reference43 articles.
1. GUIDELINE 2002/46/EG OF THE EUROPEAN PARLIAMENT AND COUNCIL of June 10. 2002 on the adaptation of laws of the legal regulation of member states relating to supplements. Official Journal of European Communities: The European Parliament and the Council of the European Union 2021 [https://eur-lex.europa.eu/legal-content/DE/TXT/PDF/?uri=CELEX:02002L0046-20170726&qid=1545903950901&from=DE
2. Verordnung über Nahrungsergänzungsmittel. (Nahrungsergänzungsmittelverordnung - NemV): Bundesministerium der Justiz und für Verbraucherschutz; [updated 2017; cited October 26, 2022. https://www.gesetze-im-internet.de/nemv/NemV.pdf.
3. Weißenborn A, Bakhiya N, Demuth I, Ehlers A, Ewald M, Niemann B, et al. Höchstmengen für Vitamine Und Mineralstoffe in Nahrungsergänzungsmitteln. J Consumer Prot Food Saf. 2018;13(1):25–39.
4. Bundesministerium für Ernährung LuV. Ergebnisbericht Teil 1: Nationale Verzehrsstudie II, die bundesweite Befragung Zur Ernährung Von Jugendlichen Und Erwachsenen. Volume 5. Contract No.: Max Rubner-Institut; 2008.
5. Bundesministerium für Ernährung LuV. Ergebnisbericht Teil 2: Nationale Verzehrsstudie II, Die bundesweite Befragung zur Ernährung von Jugendlichen und Erwachsenen: Max Rubner-Institut. 2008.