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Thymus Involution across the Human Menstrual Cycle
Biorxiv : the Preprint Server for Biology
|August 1, 2026
Summary
Human thymus size fluctuates across the menstrual cycle, influenced by reproductive hormones like estradiol and progesterone. Hormonal birth control use also impacts these dynamic changes in thymus involution.
Area of Science:
- Immunology
- Endocrinology
- Human Physiology
Background:
- Thymic involution is traditionally viewed as a linear, age-related process.
- Animal studies indicate hormone-dependent thymus size fluctuations during reproductive cycles.
- Translational evidence in humans regarding menstrual cycle-related thymus dynamics is limited.
Purpose of the Study:
- To investigate dynamic changes in thymus size across the human menstrual cycle.
- To assess the association between thymus size variations and fluctuations in estradiol and progesterone levels.
- To determine the influence of hormonal contraception on menstrual cycle-related thymus size changes.
Main Methods:
- An observational, repeated-measures study utilizing quantitative computed tomography (qCT).
- Assessments were conducted during menses and the early luteal phase within the same menstrual cycle.
- Mixed-effects models analyzed associations between cycle phase, hormone levels, hormonal contraceptive status, and thymus size.
Main Results:
- Estradiol levels increased from menses to the early luteal phase, irrespective of hormonal contraceptive use.
- Thymus size differed significantly between hormonal contraceptive users and non-users, with larger volumes in non-users.
- Thymic involution from menses to the early luteal phase was observed in 66.7% of non-users versus 37.5% of users; estradiol and progesterone interacted in predicting thymus size.
Conclusions:
- This study provides the first human evidence of short-term, dynamic changes in thymus involution across the menstrual cycle.
- Reproductive hormones (estradiol, progesterone) and hormonal contraception influence these thymus size fluctuations.
- Findings suggest potential implications for sex differences in immune regulation and inflammatory diseases.
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