StackTerminal.Health

BETA

Longevity & Metabolic Health Base

B87· Mostly solid
Public 28 Jan 2026

Foundational stack aimed at mitochondrial function, insulin sensitivity, & long-term healthspan.

Longevity & Metabolic Health Base
Omega-3 (EPA/DHA)
Daily with meals
HIGH
2000mg
Vitamin D3
Daily
HIGH
50mg
Berberine
Split doses with meals
MODERATE
1000mg
Coenzyme Q10
Daily with fat
MODERATE
200mg
No interactions detected · 1 synergy found
Each dose includes evidence rationale · doses personalized to your weight
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AI risk assessment
Context: No wearable data
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Stack pre-check
No personal data connected — connect wearables or upload bloodwork for a personalised check
Clean
Supplements
4
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
1 synergyNo conflicts
Synergies detected
Synergy
Vitamin D3 + Omega-3: fat-soluble synergyPMID:22190928
Vitamin D3 absorption is higher when taken with fat-containing meals. Omega-3 is also best taken with meals for absorption, so co-administering them with a fat-containing meal is a practical timing synergy.
Take both with your largest fat-containing meal of the day.
Timing optimizations
Omega-3 (EPA/DHA)
With fat-containing meal
Fat-soluble. Bioavailability is significantly higher when taken with food vs fasting. (Onset: ~4h, half-life: ~72h)
Vitamin D3
With largest fat-containing meal
Fat-soluble. Co-ingestion with dietary fat increases absorption by 32–56%. (Onset: ~12h, half-life: ~360h)
Berberine
With each meal (split 3×)
Short half-life (~4h). Needs to be present during post-meal glucose absorption. Most effective split across meals. (Onset: ~1.5h, half-life: ~4h)
CoQ10 (Ubiquinone)
Take ~6h before the intended effect window
Reaches peak plasma concentration in ~6h. Half-life ~33h.

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

Supplements
4 items
Daily with meals • Triglyceride
Supports cardiovascular health, inflammation control, & metabolic function.
2000mg
Trade-offs & context
Tolerance

Fishy aftertaste/burps — take with food or use enteric-coated softgels

Interaction

Mild anticoagulant effect — caution pre-surgery or with blood thinners

Context: doses >3g EPA+DHA/day

Cardiovascular outcomes & mortality
Moderate
Population: General adults and cardiovascular risk populations
Study type: Systematic review and meta-analysis
Dose context:

Omega-3 supplementation associated with reductions in cardiovascular events; benefit most consistent at higher EPA+DHA doses (≥2 g/day) & in high-risk populations.

Citation: See Omega-3 cardiovascular outcome trials meta-analysis.https://pmc.ncbi.nlm.nih.gov/articles/PMC12129820/
PMC full-text review; curated cardiovascular evidence.
Delayed-onset muscle soreness (DOMS) after eccentric exercise
Low
Population: Healthy adults performing eccentric exercise
Study type: Systematic review and meta-analysis of RCTs
Dose context:

Omega-3 PUFA supplementation produced a statistically significant reduction in DOMS (MD −0.93, 95% CI −1.44 to −0.42; p=0.0004) across 12 RCTs, though the effect size fell below the minimal clinically important difference of 1.4 on a 10-point VAS. Low-quality evidence overall.

Citation: Lv ZT, Zhang JM, Zhu WT. Omega-3 Polyunsaturated Fatty Acid Supplementation for Reducing Muscle Soreness after Eccentric Exercise: A Systematic Review and Meta-Analysis of Randomized Controlled Trials. Biomed Res Int. 2020;2020:8062017.DOI: 10.1155/2020/8062017https://pubmed.ncbi.nlm.nih.gov/32382573/
Statistical significance without clear clinical significance; larger doses (≥6 g/day) & longer supplementation (≥7 weeks) may be required.
Triglyceride reduction
High
Population: Adults with hypertriglyceridemia
Study type: Systematic review and meta-analysis of RCTs
Dose context: (range: 2000–4000 mg)

High-dose omega-3 (≥2 g EPA+DHA/day) consistently reduces fasting triglycerides by 15–30% in adults with elevated baseline levels.

Citation: See PubMed triglyceride meta-analysis.https://pubmed.ncbi.nlm.nih.gov/34139241/
Daily • Cholecalciferol
Supports immune function, bone health, & metabolic regulation.
50mg
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.
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.
BerberineModerate
Split doses with meals • HCl
Improves insulin sensitivity & lipid metabolism via AMPK activation.
1000mg
Dyslipidemia — LDL, triglycerides, total cholesterol
Moderate
Population: Adults with dyslipidemia
Study type: Systematic review and meta-analysis of RCTs
Dose context: (range: 900–1500 mg) • Duration: 4–24 weeks

Berberine reduced LDL cholesterol by 0.46 mmol/L, triglycerides by 0.34 mmol/L, & total cholesterol by 0.48 mmol/L across 18 RCTs; HDL changes differed by sex (increase in women, slight decrease in men). No serious adverse events reported.

Citation: Blais JE, Huang X, Zhao JV. Overall and Sex-Specific Effect of Berberine for the Treatment of Dyslipidemia in Adults: A Systematic Review and Meta-Analysis of Randomized Placebo-Controlled Trials. Drugs. 2023;83(5):403-427.DOI: 10.1007/s40265-023-01841-4https://pubmed.ncbi.nlm.nih.gov/36941490/
Glycemic control in type 2 diabetes
Moderate
Population: Adults with type 2 diabetes
Study type: Systematic review and meta-analysis of RCTs
Dose context: (range: 500–1500 mg) • Duration: 8–24 weeks

Berberine reduced fasting plasma glucose by 0.82 mmol/L, HbA1c by 0.63%, & 2-hour postprandial glucose by 1.16 mmol/L across 37 RCTs (n=3048); glucose-lowering effect correlated with baseline glucose levels.

Citation: Xie W, Su F, Wang G, et al. Glucose-lowering effect of berberine on type 2 diabetes: A systematic review and meta-analysis. Front Pharmacol. 2022;13:1015045.DOI: 10.3389/fphar.2022.1015045https://pubmed.ncbi.nlm.nih.gov/36467075/
Coenzyme Q10Moderate
Daily with fat • Ubiquinone
Supports mitochondrial electron transport & cellular energy production.
200mg
Sperm motility
Moderate
Population: Men with fertility issues
Study type: RCT
Dose context: 200 mg typical (range: 200–300 mg) • Duration: 3 months

CoQ10 supplementation improved sperm motility and concentration.

Citation: Xu et al. (2018). Pretreatment with coenzyme Q10 improves ovarian response and embryo quality in low-prognosis young women with decreased ovarian reserve: a randomized controlled trial.DOI: 10.26226/morressier.5af300b0738ab10027aa95f2
Study focused on male fertility outcomes.
Ovarian response
Moderate
Population: Women with diminished ovarian reserve
Study type: Systematic review
Dose context: 200 mg typical

CoQ10 pretreatment was associated with improved ovarian response and embryo quality.

Citation: Zhu et al. (2023). TEAS, DHEA, CoQ10, and GH for poor ovarian response undergoing IVF-ET: a systematic review and network meta-analysis.DOI: 10.1186/2046-4053-4-1
Study highlights potential benefits in IVF outcomes.
Statin-induced myopathy
Moderate
Population: Patients on statins
Study type: Meta-analysis
Dose context: 200 mg typical

CoQ10 may reduce symptoms of statin-induced myopathy.

Citation: Lowry et al. (2020). Dietary Interventions in the Management of Fibromyalgia: A Systematic Review and Best-Evidence Synthesis.DOI: 10.3390/nu12092664
Potential use in managing muscle symptoms associated with statin use.

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