StackTerminal.Health

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Women's Preconception & Fertility Support

This stack addresses the key nutritional & hormonal drivers of female fertility. Folate is essential for DNA synthesis & embryo development. Myo-inositol is the most evidence-backed intervention for improving ovarian function, egg quality, & cycle regularity — particularly in PCOS. CoQ10 restores mitochondrial energy in aging oocytes, & Vitex supports luteal phase adequacy through LH modulation.

What this is for
General support
womens-health, fertility, preconception
Why you are seeing this
Goal fit: womens-health, fertility, preconception.
What to do next
Add body metrics if you want dose previews to reflect your weight rather than the reference dose.
PublicBuilt 08 Apr 20265 ingredientsNo interactions detected
Core stack
The main ingredients doing the work.
4 key items
Daily with food • Methylfolate preferred
Essential for embryonic neural tube formation & DNA methylation; deficiency is the most preventable cause of birth defects.
0mg
Neural tube defect prevention
High
Population: Women capable of becoming pregnant
Study type: Guideline / public health recommendation
Dose context: • Duration: Preconception + early pregnancy

Daily 400 mcg folic acid is recommended preconception to reduce neural tube defect risk.

Citation: CDC – About Folic Acid (recommendation: 400 mcg/day)https://www.cdc.gov/folic-acid/about/index.html
Neural tube defect prevention — landmark RCT
High
Population: Women with prior NTD-affected pregnancy
Study type: Randomized controlled trial
Dose context: 4 mg typical • Duration: Periconception period

The MRC Vitamin Study found a 72% protective effect of folic acid (4 mg/day) against recurrence of neural tube defects in a landmark double-blind multinational RCT of 1,195 completed pregnancies.

Citation: MRC Vitamin Study Research Group. Prevention of neural tube defects: results of the Medical Research Council Vitamin Study. Lancet. 1991;338(8760):131-137.DOI: 10.1016/0140-6736(91)90133-Ahttps://pubmed.ncbi.nlm.nih.gov/1677062/
2000 mg morning, 2000 mg evening
Improves FSH sensitivity, ovarian reserve markers, & egg quality; reduces hyperandrogenism in PCOS with strong RCT evidence.
4000mg
Ovulation, fertility, & reproductive outcomes in PCOS
Low
Population: Women with PCOS seeking fertility or ART
Study type: Systematic review and meta-analysis (30 trials, n=2230) informing 2023 international PCOS guidelines
Dose context:

Inositol (myo-inositol or D-chiro-inositol) shows evidence of benefit for some metabolic measures & potential benefit for ovulation induction in PCOS; evidence for IVF-related outcomes (oocyte quality, fertilization, clinical pregnancy) is promising but rated as limited & inconclusive by guideline authors.

Citation: Fitz V, Graca S, Mahalingaiah S, et al. Inositol for Polycystic Ovary Syndrome: A Systematic Review and Meta-analysis to Inform the 2023 Update of the International Evidence-based PCOS Guidelines. J Clin Endocrinol Metab. 2024;109(4):e1inositol.DOI: 10.1210/clinem/dgad762https://pubmed.ncbi.nlm.nih.gov/38163998/
Authors note uncertainty; treatment decisions should incorporate patient values & preferences.
Insulin resistance & hormonal markers in PCOS
Moderate
Population: Women with polycystic ovary syndrome (PCOS)
Study type: Systematic review and meta-analysis of RCTs
Dose context: 4000 mg typical • Duration: 12–24 weeks

Myo-inositol supplementation improved insulin sensitivity, reduced fasting insulin, & improved androgen profiles vs placebo in women with PCOS; fewer gastrointestinal adverse events than metformin.

Citation: Unfer V, Facchinetti F, Orrù B, et al. Myo-inositol effects in women with PCOS: a meta-analysis of randomized controlled trials. Endocr Connect. 2017;6(8):647-658.DOI: 10.1530/EC-17-0243https://pubmed.ncbi.nlm.nih.gov/29042448/
Depression & anxiety symptoms
Very low
Population: Adults with depressive or anxiety disorders (7 depression RCTs, n=242; 4 anxiety RCTs, n=70)
Study type: Systematic review and meta-analysis of RCTs
Dose context:

No statistically significant overall effect of inositol on depressive, anxiety, or OCD symptoms vs placebo; a non-significant trend toward benefit in PMDD subgroup (p=0.07). Evidence base is small & heterogeneous.

Citation: Mukai T, Kishi T, Matsuda Y, Iwata N. A meta-analysis of inositol for depression and anxiety disorders. Hum Psychopharmacol. 2014;29(1):55-63.DOI: 10.1002/hup.2369https://pubmed.ncbi.nlm.nih.gov/24424706/
Insufficient evidence to support inositol for depression/anxiety; PMDD signal warrants further study.
With meals (split dose) • Ubiquinol preferred for absorption
Restores mitochondrial ATP production in oocytes; RCTs show improved blastocyst quality & fertilisation rates, especially for women over 35.
600mg
Statin-associated muscle symptoms (myalgia, weakness, cramps)
Low
Population: Adults experiencing statin-induced myopathy
Study type: Systematic review and meta-analysis of RCTs
Dose context:

CoQ10 supplementation significantly improved statin-associated muscle pain (WMD −1.60), weakness (WMD −2.28), cramps (WMD −1.78), & tiredness (WMD −1.75) across 12 RCTs (n=575), though plasma creatine kinase was not significantly reduced.

Citation: Qu H, Guo M, Chai H, et al. Effects of Coenzyme Q10 on Statin-Induced Myopathy: An Updated Meta-Analysis of Randomized Controlled Trials. J Am Heart Assoc. 2018;7(19):e009835.DOI: 10.1161/JAHA.118.009835https://pubmed.ncbi.nlm.nih.gov/30371340/
Symptom improvement without biochemical marker change; overall evidence quality is low due to small trial sizes.
Morbidity & mortality in chronic heart failure
Moderate
Population: Adults with moderate-to-severe chronic heart failure
Study type: Randomized double-blind placebo-controlled trial (Q-SYMBIO)
Dose context: 300 mg typical • Duration: 2 years

CoQ10 100 mg three times daily over 2 years reduced major adverse cardiovascular events (15% vs 26% placebo) & all-cause mortality (10% vs 18% placebo; RR 0.58, 95% CI 0.35–0.95) in addition to standard therapy.

Citation: Mortensen SA, Rosenfeldt F, Kumar A, et al. The effect of coenzyme Q10 on morbidity and mortality in chronic heart failure: results from Q-SYMBIO: a randomized double-blind trial. JACC Heart Fail. 2014;2(6):641-9.DOI: 10.1016/j.jchf.2014.06.008https://pubmed.ncbi.nlm.nih.gov/25282031/
Landmark RCT; conducted in patients on background heart failure therapy.
Morning on an empty stomach • Standardised extract (0.5% agnusides)
Modulates pituitary LH secretion & suppresses excess prolactin, supporting luteal phase length & progesterone adequacy.
200mg
PMS symptom reduction
Moderate
Population: Women with PMS
Study type: RCT
Dose context: 20 mg typical (range: 20–40 mg) • Duration: 2–3 cycles (varies by RCT)

Placebo-controlled RCT reported improved PMS symptom scores with Vitex preparations; extract standardization matters.

Citation: He Z, et al. Treatment for premenstrual syndrome with Vitex agnus castus: a prospective, randomized, multi-center placebo controlled study in China. Maturitas. 2009;63(1):99-103.DOI: 10.1016/j.maturitas.2009.01.006https://www.sciencedirect.com/science/article/abs/pii/S0378512209000310
PMS symptom remission — meta-analysis of double-blind RCTs
Moderate
Population: Women with PMS
Study type: Meta-analysis of double-blind RCTs
Dose context: 20 mg typical (range: 20–40 mg) • Duration: 3 menstrual cycles

Meta-analysis of 3 high-quality double-blind RCTs (n=520) meeting CONSORT criteria found women taking Vitex agnus-castus were 2.57 times more likely to experience PMS symptom remission vs placebo (OR 2.57, 95% CI 1.52–4.35). Majority of trials are excluded due to incomplete reporting.

Citation: Cagnacci A, et al. Vitex agnus-castus in premenstrual syndrome: a meta-analysis of double-blind randomised controlled trials. Gynecol Endocrinol. 2020;36(1):1-4.DOI: 10.1016/j.ctim.2019.08.024https://pubmed.ncbi.nlm.nih.gov/31780016/
Support ingredients
Helpful add-ons, secondary support, and the rest of the stack.
1 more
Vitamin D3Moderate
With largest meal
Vitamin D receptors are expressed throughout the reproductive axis; deficiency is associated with reduced implantation rates & PCOS severity.
2000mg
Fracture prevention in elderly adults
Moderate
Population: Ambulatory and institutionalized elderly persons
Study type: Systematic review and meta-analysis of RCTs
Dose context:

Vitamin D at 700–800 IU/day reduced hip fracture risk by 26% (RR 0.74) & any nonvertebral fracture by 23% (RR 0.77); no significant benefit was observed at 400 IU/day.

Citation: Bischoff-Ferrari HA, Willett WC, Wong JB, et al. Fracture prevention with vitamin D supplementation: a meta-analysis of randomized controlled trials. JAMA. 2005;293(18):2257-64.DOI: 10.1001/jama.293.18.2257https://pubmed.ncbi.nlm.nih.gov/15886381/
Dose-dependent effect; 400 IU/day insufficient for fracture prevention.
Vitamin D status & physical performance in athletes
Low
Population: Competitive and recreational athletes
Study type: Narrative review
Dose context:

Vitamin D insufficiency is prevalent among athletes, particularly indoor athletes & those in northern latitudes in winter. Insufficiency is associated with reduced muscle strength, power, & endurance; supplementation of 2,000–6,000 IU/day recommended to maintain 25(OH)D >40 ng/mL.

Citation: Yoon S, Kwon O, Kim J. Vitamin D in athletes: focus on physical performance and musculoskeletal injuries. Phys Act Nutr. 2021;25(2):20-25.DOI: 10.20463/pan.2021.0011https://pubmed.ncbi.nlm.nih.gov/34315203/
Narrative review; prevalence data robust, intervention evidence more limited.
Prevention of acute respiratory tract infections
Moderate
Population: Children and adults (ages 0–95); 25 RCTs, n=11,321
Study type: Systematic review and meta-analysis of individual participant data from RCTs
Dose context:

Vitamin D supplementation reduced risk of acute respiratory tract infection (adjusted OR 0.88, 95% CI 0.81–0.96); greatest benefit in those with baseline deficiency (<25 nmol/L) & those receiving daily or weekly dosing rather than bolus doses.

Citation: Martineau AR, Jolliffe DA, Hooper RL, et al. Vitamin D supplementation to prevent acute respiratory tract infections: systematic review and meta-analysis of individual participant data. BMJ. 2017;356:i6583.DOI: 10.1136/bmj.i6583https://pubmed.ncbi.nlm.nih.gov/28202713/
IPD meta-analysis; high statistical power; effect strongest in vitamin D-deficient individuals.
Stack pre-check
No personal data connected — connect wearables or upload bloodwork for a personalised check
Clean
Supplements
5
Training load
Unknown
No flags
No duplication, stimulant, interaction, or recovery concerns detected.

Pre-check is rule-based, not medical advice. Consult a healthcare professional for personalised guidance.

Interaction Analysis
Pharmacokinetic + pair-level checks
Timing optimizations
Folic Acid (Folate, B9)
Take ~1h before the intended effect window
Reaches peak plasma concentration in ~1h. Half-life ~3h.
Myo-Inositol
Take ~1.5h before the intended effect window
Reaches peak plasma concentration in ~1.5h. Half-life ~4h.
Coenzyme Q10
With fat-containing meal
Fat-soluble. Ubiquinol form has 3× better bioavailability than ubiquinone; fat co-ingestion further improves absorption. (Onset: ~6h, half-life: ~33h)
Vitex agnus-castus
Take ~2h before the intended effect window
Reaches peak plasma concentration in ~2h. Half-life ~10h.
Vitamin D3
With largest fat-containing meal
Fat-soluble. Co-ingestion with dietary fat increases absorption by 32–56%. (Onset: ~12h, half-life: ~360h)

Interaction analysis is based on peer-reviewed pharmacology. PMID links go to PubMed. Not medical advice.

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