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Menstrual cycle rhythmicity: metabolic patterns in healthy women

The menstrual cycle is an essential life rhythm governed by interacting levels of progesterone, estradiol, follicular stimulating, and luteinizing hormones. To study metabolic changes, biofluids were collected at four timepoints in the menstrual cycle from 34 healthy, premenopausal women. Serum horm...

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Autores principales: Draper, C. F., Duisters, K., Weger, B., Chakrabarti, A., Harms, A. C., Brennan, L., Hankemeier, T., Goulet, L., Konz, T., Martin, F. P., Moco, S., van der Greef, J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6167362/
https://www.ncbi.nlm.nih.gov/pubmed/30275458
http://dx.doi.org/10.1038/s41598-018-32647-0
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author Draper, C. F.
Duisters, K.
Weger, B.
Chakrabarti, A.
Harms, A. C.
Brennan, L.
Hankemeier, T.
Goulet, L.
Konz, T.
Martin, F. P.
Moco, S.
van der Greef, J.
author_facet Draper, C. F.
Duisters, K.
Weger, B.
Chakrabarti, A.
Harms, A. C.
Brennan, L.
Hankemeier, T.
Goulet, L.
Konz, T.
Martin, F. P.
Moco, S.
van der Greef, J.
author_sort Draper, C. F.
collection PubMed
description The menstrual cycle is an essential life rhythm governed by interacting levels of progesterone, estradiol, follicular stimulating, and luteinizing hormones. To study metabolic changes, biofluids were collected at four timepoints in the menstrual cycle from 34 healthy, premenopausal women. Serum hormones, urinary luteinizing hormone and self-reported menstrual cycle timing were used for a 5-phase cycle classification. Plasma and urine were analyzed using LC-MS and GC-MS for metabolomics and lipidomics; serum for clinical chemistries; and plasma for B vitamins using HPLC-FLD. Of 397 metabolites and micronutrients tested, 208 were significantly (p < 0.05) changed and 71 reached the FDR 0.20 threshold showing rhythmicity in neurotransmitter precursors, glutathione metabolism, the urea cycle, 4-pyridoxic acid, and 25-OH vitamin D. In total, 39 amino acids and derivatives and 18 lipid species decreased (FDR < 0.20) in the luteal phase, possibly indicative of an anabolic state during the progesterone peak and recovery during menstruation and the follicular phase. The reduced metabolite levels observed may represent a time of vulnerability to hormone related health issues such as PMS and PMDD, in the setting of a healthy, rhythmic state. These results provide a foundation for further research on cyclic differences in nutrient-related metabolites and may form the basis of novel nutrition strategies for women.
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spelling pubmed-61673622018-10-04 Menstrual cycle rhythmicity: metabolic patterns in healthy women Draper, C. F. Duisters, K. Weger, B. Chakrabarti, A. Harms, A. C. Brennan, L. Hankemeier, T. Goulet, L. Konz, T. Martin, F. P. Moco, S. van der Greef, J. Sci Rep Article The menstrual cycle is an essential life rhythm governed by interacting levels of progesterone, estradiol, follicular stimulating, and luteinizing hormones. To study metabolic changes, biofluids were collected at four timepoints in the menstrual cycle from 34 healthy, premenopausal women. Serum hormones, urinary luteinizing hormone and self-reported menstrual cycle timing were used for a 5-phase cycle classification. Plasma and urine were analyzed using LC-MS and GC-MS for metabolomics and lipidomics; serum for clinical chemistries; and plasma for B vitamins using HPLC-FLD. Of 397 metabolites and micronutrients tested, 208 were significantly (p < 0.05) changed and 71 reached the FDR 0.20 threshold showing rhythmicity in neurotransmitter precursors, glutathione metabolism, the urea cycle, 4-pyridoxic acid, and 25-OH vitamin D. In total, 39 amino acids and derivatives and 18 lipid species decreased (FDR < 0.20) in the luteal phase, possibly indicative of an anabolic state during the progesterone peak and recovery during menstruation and the follicular phase. The reduced metabolite levels observed may represent a time of vulnerability to hormone related health issues such as PMS and PMDD, in the setting of a healthy, rhythmic state. These results provide a foundation for further research on cyclic differences in nutrient-related metabolites and may form the basis of novel nutrition strategies for women. Nature Publishing Group UK 2018-10-01 /pmc/articles/PMC6167362/ /pubmed/30275458 http://dx.doi.org/10.1038/s41598-018-32647-0 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Draper, C. F.
Duisters, K.
Weger, B.
Chakrabarti, A.
Harms, A. C.
Brennan, L.
Hankemeier, T.
Goulet, L.
Konz, T.
Martin, F. P.
Moco, S.
van der Greef, J.
Menstrual cycle rhythmicity: metabolic patterns in healthy women
title Menstrual cycle rhythmicity: metabolic patterns in healthy women
title_full Menstrual cycle rhythmicity: metabolic patterns in healthy women
title_fullStr Menstrual cycle rhythmicity: metabolic patterns in healthy women
title_full_unstemmed Menstrual cycle rhythmicity: metabolic patterns in healthy women
title_short Menstrual cycle rhythmicity: metabolic patterns in healthy women
title_sort menstrual cycle rhythmicity: metabolic patterns in healthy women
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6167362/
https://www.ncbi.nlm.nih.gov/pubmed/30275458
http://dx.doi.org/10.1038/s41598-018-32647-0
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