Early menstrual cycle impacts of oestrogen and progesterone on the timing of the fertile window
article
OA: closed
CC0
⤵ 1 in-corpus citation
Abstract
STUDY QUESTION: What is the effect of oestrogen and progesterone at the beginning of the menstrual cycle in delaying entry into the fertile window? SUMMARY ANSWER: Both oestrogen and progesterone contribute to a delay in the onset of the fertile window. WHAT IS KNOWN ALREADY: Oestrogen enhances cervical mucus secretion while progesterone inhibits it. STUDY DESIGN, SIZE, DURATION: Observational study. Daily observation of 220 menstrual cycles contributed by 88 women with no known menstrual cycle disorder. PARTICIPANTS/MATERIALS, SETTING, METHODS: Women recorded cervical mucus daily and collected first-morning urine samples for analysis of oestrone-3-glucuronide, pregnanediol-3-alpha-glucuronide (PDG), FHS, and LH. They underwent serial ovarian ultrasound examinations. The main outcome measure was the timing within the cycle of the onset of the fertile window, as identified by the appearance of mucus felt or seen at the vulva. MAIN RESULTS AND THE ROLE OF CHANCE: Low oestrogen secretion and persistent progesterone secretion during the first week of the menstrual cycle both negatively affect mucus secretion. Doubling oestrogen approximately doubled the odds of entering the fertile window (OR: 1.82 95% CI=1.23; 2.69). Increasing PDG from below 1.5 to 4 µg/mg creatinine was associated with a 2-fold decrease in the odds of entering the fertile window (OR: 0.51 95% CI=0.31; 0.82). Prolonged progesterone secretion during the first week of the menstrual cycle was also statistically significantly associated with higher LH secretion. Finally, the later onset of the fertile window was associated with statistically significant persistently elevated LH secretion during the luteal phase of the previous menstrual cycle. LIMITATIONS, REASONS FOR CAUTION: This post hoc study was conducted to assess the potential impact of residual progesterone secretion at the beginning of the menstrual cycle. It was conducted on an existing data set because of the scarcity of data available to answer the question. Analysis with other datasets with similar hormone results would be useful to confirm these findings. WIDER IMPLICATIONS OF THE FINDINGS: This study provides evidence for residual progesterone secretion in the early latency phase of some menstrual cycles, which may delay the onset of the fertile window. This progesterone secretion may be supported by subtly increased LH secretion during the few days before and after the onset of menses, which may relate to follicular waves in the luteal phase. Persistent progesterone secretion should be considered in predicting the onset of the fertile window and in assessing ovulatory dysfunction. STUDY FUNDING/COMPETING INTEREST(S): The authors declare no conflicts of interest. No funding was provided for this secondary data analysis. TRIAL REGISTRATION NUMBER: N/A.
My notes (saved in your browser only)
Citation neighborhood (sparse)
Too few in-corpus citations on either side for a chart; here are the lists.
Cited by (1)
References (39)
- doi:10.36959/763/502 via openalex
- doi:10.1073/pnas.95.18.11002 via openalex
- doi:10.1093/humrep/deab049 via openalex
- doi:10.1002/uog.1891 via openalex
- W171142860 via openalex
- doi:10.1002/sim.4780100207 via openalex
- doi:10.1111/j.1552-6909.2007.000129.x via openalex
- doi:10.1016/j.ando.2010.02.021 via openalex
- doi:10.1093/humrep/dem051 via openalex
- doi:10.1093/humupd/dmr039 via openalex
- doi:10.1530/jrf.0.0850163 via openalex
- W2411014441 via openalex
- W2418160021 via openalex
- doi:10.1093/oxfordjournals.humrep.a019329 via openalex
- doi:10.4054/demres.2000.3.5 via openalex
- W6603460600 via openalex
- doi:10.1016/s0398-7620(05)84773-x via openalex
- W6649182828 via openalex
- doi:10.1016/j.fertnstert.2017.05.012 via openalex
- doi:10.1016/j.fertnstert.2023.12.009 via openalex
- doi:10.1093/hropen/hoac039 via openalex
- doi:10.1016/s0029-7844(03)00358-2 via openalex
- doi:10.1016/j.repbio.2014.03.003 via openalex
- doi:10.1053/beog.2000.0132 via openalex
- doi:10.1016/j.fertnstert.2015.01.031 via openalex
- doi:10.3389/fphys.2023.1254943 via openalex
- doi:10.1186/1477-7827-4-53 via openalex
- doi:10.1016/s0015-0282(16)46638-0 via openalex
- doi:10.1016/j.steroids.2022.108964 via openalex
- doi:10.1016/j.ejogrb.2005.07.024 via openalex
- doi:10.1016/s0015-0282(16)53821-7 via openalex
- doi:10.1126/sciadv.adg9646 via openalex
- doi:10.1186/s12958-022-00993-4 via openalex
- doi:10.1095/biolreprod.102.008425 via openalex
- doi:10.1016/s0140-6736(72)90291-7 via openalex
- doi:10.1016/j.theriogenology.2009.11.016 via openalex
- doi:10.1056/nejm199512073332301 via openalex
- doi:10.1093/humrep/deh173 via openalex
- doi:10.1016/s0188-4409(01)00323-x via openalex
Cited by (1)
Source provenance
- openalex
- last seen: 2026-05-14T06:45:28.448396+00:00
License: CC0
· commercial use OK