Premenstrual Syndrome (PMS) Protocol
Primary Stack
Core supplements with strongest evidenceModulates dopamine and prolactin levels, helping regulate the menstrual cycle and reduce PMS symptoms
Addresses menstrual cycle-related calcium fluctuations that contribute to mood and physical symptoms
Supporting Stack
Additional supplements for enhanced resultsCofactor for serotonin and dopamine synthesis, reducing mood-related PMS symptoms
Supporting Studies (1)
Reduces bloating, headaches, and mood symptoms; often depleted in the luteal phase
How This Protocol Works
Simple Explanation
Premenstrual syndrome affects up to 90% of women to some degree, with 20-30% experiencing moderate to severe symptoms. PMS occurs in the luteal phase (after ovulation, before menstruation) and involves mood changes, bloating, breast tenderness, headaches, and fatigue. The exact cause isn't fully understood but involves hormonal fluctuations affecting neurotransmitters.
Expected timeline: Vitex takes 2-3 cycles (months) for full effect. Calcium, B6, and magnesium may show benefits within 1-2 cycles. Start supplements at least one cycle before expected benefit.
Clinical Perspective
PMS pathophysiology involves abnormal sensitivity to normal hormonal fluctuations, serotonergic dysfunction, and altered calcium/magnesium homeostasis during the luteal phase. Symptoms require prospective documentation across 2+ cycles for diagnosis. This protocol addresses neurohormonal and mineral factors.
Biomarker targets: Prospective PMS symptom diary, Daily Record of Severity of Problems (DRSP), serum prolactin (if elevated).
Protocol notes: Diagnose PMS with prospective symptom charting over 2+ cycles. Vitex contraindicated with hormonal contraceptives or dopamine agonists. Calcium: ensure adequate vitamin D for absorption. B6: do not exceed 100mg/day long-term. Consider SSRIs (luteal phase dosing) for severe PMDD. Address lifestyle: regular exercise, sleep hygiene, reduced caffeine/alcohol/sodium.