Background/Objective Polycystic ovary syndrome (PCOS) is one of the most common endocrinopathies during reproductive age, affecting up to 25% of women worldwide. The aim of this study was to evaluate the efficacy of Time Restricted Eating (TRE) as an alternative to traditional hormonal therapy in patients with PCOS.
Methods A prospective, longitudinal, comparative clinical study was conducted. A total of 16 patients, diagnosed with PCOS, were divided into three groups to assess combined and isolated treatment options. Two groups underwent a 90-day Time Restricted Eating protocol with measurements at day 0 and 90 for ovary follicle count, luteinizing hormone, follicle stimulating Hormone, estradiol, progesterone, total testosterone, free testosterone, fasting insulin and glucose. Results were compared to a control group undergoing traditional hormonal treatment.
Results Ultrasonographic assessment of left and right ovary, showed a significant reduction in FC for the TRE group (36.67 ± 12.81 % and 41.79 ± 3.76, respectively). Metabolic and hormonal markers also showed an important reduction: HOMA-IR (11.7 ± 8.47 %), GLU (5.06 ± 0.91 %), INS (11.87 ± 6.93 %), FT (54.92 ± 10.01%), TT (3.96 ± 1.48%) LH (22.67 ± 3.24%) and FSH (23.53 ± 6.84 %).
Conclusions A 90-day TRE intervention is a safe and reliable treatment option when compared to standard Oral Contraceptive (OC) therapy, especially for the improvement of hyperandrogenism, metabolic and hormonal parameters in patients with PCOS.
Competing Interest StatementThe authors have declared no competing interest.
Clinical TrialNCT06031753
Funding StatementThis study did not receive any funding
Author DeclarationsI confirm all relevant ethical guidelines have been followed, and any necessary IRB and/or ethics committee approvals have been obtained.
Yes
The details of the IRB/oversight body that provided approval or exemption for the research described are given below:
Ethics committee/IRB of ABC Medical Centre, Mexico City gave ethical approval for this work
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Yes
I understand that all clinical trials and any other prospective interventional studies must be registered with an ICMJE-approved registry, such as ClinicalTrials.gov. I confirm that any such study reported in the manuscript has been registered and the trial registration ID is provided (note: if posting a prospective study registered retrospectively, please provide a statement in the trial ID field explaining why the study was not registered in advance).
Yes
I have followed all appropriate research reporting guidelines, such as any relevant EQUATOR Network research reporting checklist(s) and other pertinent material, if applicable.
Yes
Data AvailabilityAll data produced in the present study are available upon reasonable request to the authors
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