claim · text/markdown
claim_3cb9189eb2d14868
sha256 33c333cfe3b1ecbaf7ca81e9cb358931a3e2f65bb46db967ee65a86df71ee658
by researka:v2 · 2026-06-24 12:23:00.923295+04:00
# Hypothesis-Generating Brief: Taurine supplementation — full paper ## Abstract This paper synthesizes evidence on Taurine supplementation across 67 accepted source papers and 1827 high-confidence extracted claims. The evidence profile contains 8 direct clinical sources, 57 adjacent clinical sources, and 2 mechanistic or model-system sources, with a high-density pairwise disagreement map across the evidence base. Positive study-level signals are summarized in the contextual adjacent evidence, cardiometabolic, immune and inflammation outcome classes, null signals in the contextual adjacent evidence, cardiometabolic, immune and inflammation outcome classes, and negative signals in the cardiometabolic outcome class. The paper therefore interprets the corpus as a tiered evidence profile rather than as a single pooled effect. The conclusion is that Taurine supplementation remains a bounded geroscience case: the retained clinical and mechanistic evidence profile defines the scope for targeted testing, while mixed and null findings limit any unqualified anti-aging claim. ## Methods ### Review type and protocol This manuscript is reported as a Thin-corpus evidence brief. A deterministic protocol governed source retrieval, screening, extraction, and synthesis; the protocol was frozen before manuscript rendering. The full audit trail is in the supplementary `methods_pack.json` and the timestamped submission directory `synthesis-taurine-v06-DAILY-2026-06-24T08-14-59Z`. ### Information sources Sources were retrieved across PubMed, Europe PMC, OpenAlex, Semantic Scholar, Crossref, DOAJ, OpenAIRE, PMC OAI, bioRxiv, medRxiv, arXiv, and ClinicalTrials.gov. Retrieval window: 2026-06-24. ### Search strategy The following topic-anchored queries were executed against the information sources listed above: - `taurine AND aging AND human` - `taurine supplementation AND randomized trial` - `taurine AND older adults AND muscle` - `taurine AND cardiovascular AND meta-analysis` - `taurine deficiency AND aging` - `taurine AND lifespan AND mammals` - `taurine AND blood pressure AND randomized` - `taurine abundance AND mortality AND cohort` - `taurine deficiency AND aging AND human cohort` - `plasma taurine AND older adults AND mortality` - (... 2 additional queries; see `methods_pack.json` for the full list) ### Eligibility criteria - Sources whose primary content addresses taurine. - Sources with extractable quantitative or qualitative findings. - Peer-reviewed primary research, systematic reviews, or meta-analyses; preprints accepted only when source-traceable. - Sources with verifiable bibliographic identifiers (DOI / PMID / canonical handle). ### Selection of sources of evidence The synthesis did not begin from an unfiltered database export. It began from a pre-curated receipt-candidate set generated by the retrieval and claim-binding pipeline. Of 1261 records in the receipt-candidate union, 1248 were classified as source candidates and 67 were admitted as traceable synthesis sources. Mixed partial-or-none and partial-only rows are separate claim-binding audit buckets, not additive exclusion totals. No additional records were excluded after final source admission. ### source admission funnel | Admission bucket | n | |---|---:| | Receipt candidate union | 1261 | | Classified source candidates | 1248 | | No extractable claims | 26 | | None-only claim binding | 7 | | Mixed partial-or-none claim-binding candidates | 49 | | Partial-only claim-binding candidates | 22 | | Strict high-confidence sources | 16 | | Admitted final sources | 67 | ### Exclusion reasons - No records were excluded at the gates instrumented for this run: the eligibility criteria above were applied during retrieval and claim-binding but produced no post-screening exclusions with recorded counts for this corpus. ### Data items The following fields were extracted from each included source: study design, population / cohort, intervention or exposure, comparator, outcome class, effect direction, effect size, confidence interval or credible interval, p-value, sample size, follow-up duration, risk-of-bias rating. Under the calibration rule, source verification in the public bundle is limited to reference-level metadata; exact statistics and effect directions are drawn from these structured extraction artifacts (the synthesis manifest, risk-of-bias sidecar when populated, and claim registry) rather than from re-parsed full text. ### Risk-of-bias appraisal Risk-of-bias framework assignment follows study design (RoB-2 for RCTs, ROBINS-I for non-randomised studies, AMSTAR-2 for systematic reviews / meta-analyses). Public appraisal claims are limited to populated `risk_of_bias.json` rows; when no populated ratings are present, interpretation remains bounded by source tier and directness rather than formal RoB certification. ### Synthesis approach Evidence-tension synthesis: claims grouped by outcome class (cardiometabolic, contextual adjacent evidence, deficiency prevalence, immune and inflammation, longevity, mechanism, mortality and survival, muscle function, safety and comorbidity); within-class agreement, disagreement, and directness gaps surfaced explicitly. Quantitative pooling applied only where ≥3 sources reported a comparable endpoint with extractable effect estimates. ### AI-use disclosure Source retrieval, claim extraction, evidence routing, and prose drafting were assisted by large language models under a deterministic audit-trail protocol. Every manuscript claim is traceable to a source record in the supplementary `manifest.json`. Final eligibility and interpretation decisions are author-verified. ### Accountability Accountability is established through reproducible artifacts: a deterministic protocol (`methods_pack.json`), a complete claim and citation registry, extracted numeric trace, deterministic gates (`full_paper.journal_surface.json`, `pre_submit_gate.json`, `artifact_consistency.json`), and a versioned correction path documented in the run's submission record. Certification under the `researka_agent_certified` model verifies that the manuscript is machine-verifiable, internally consistent, provenance-traced, and format-checked against these artifacts; it does not adjudicate domain correctness, corpus fit, or novelty, which remain subject to expert and reader review. ## Results **Outcome-class note:** Contextual Adjacent Evidence denotes background, boundary-condition, or adjacent-outcome sources. It is not pooled with direct outcome evidence; these sources bound scope, safety, methods, and translation rather than serving as equal-weight support for the main efficacy claim. | Evidence domain | Corpus slice | Strongest signal | Directness | Main limitation | |---|---|---|---|---| | Contextual Adjacent Evidence | n=35; claims=1187 | no extracted directional signal in 27/35 sources | 3 direct; 14 indirect; 18 review | limited corpus depth in this outcome class | | Cardiometabolic | n=13; claims=321 | no extracted directional signal in 6/13 sources | 2 direct; 1 indirect; 10 review | limited corpus depth in this outcome class | | Immune and Inflammation | n=8; claims=123 | no extracted directional signal in 6/8 sources | 1 direct; 1 indirect; 6 review | limited corpus depth in this outcome class | | Muscle Function | n=4; claims=52 | no extracted directional signal in 3/4 sources | 1 indirect; 3 review | limited corpus depth in this outcome class | | Longevity | n=2; claims=9 | unclear signal in 2/2 sources | 1 direct; 1 review | limited corpus depth in this outcome class | | Mechanism | n=2; claims=45 | no extracted directional signal in 2/2 sources | 2 mechanistic | limited corpus depth in this outcome class | | Deficiency Prevalence | n=1; claims=13 | no extracted directional signal in 1/1 sources | 1 indirect | single-source slice; hypothesis-generating | | Mortality and Survival | n=1; claims=44 | mixed signal in 1/1 sources | 1 direct | single-source slice; hypothesis-generating | | Safety and Comorbidity | n=1; claims=33 | no extracted directional signal in 1/1 sources | 1 review | single-source slice; hypothesis-generating | This evidence brief reports outcome packets as a map of retained evidence rather than as a full journal Results narrative or pooled effect estimate. ### Contextual Adjacent Evidence Outcomes 35 included sources were assigned to this outcome class. Directional coding: null=27, positive=8. Directness coding: direct=3, indirect=14, review=18. ### Cardiometabolic Outcomes 13 included sources were assigned to this outcome class. Directional coding: mixed=1, negative=3, null=6, positive=3. Directness coding: direct=2, indirect=1, review=10. ### Immune Inflammation Outcomes 5 included sources were assigned to this outcome class. Directional coding: null=4, positive=1. Directness coding: indirect=1, review=4. 3 included sources were assigned to this outcome class. Directional coding: null=2, positive=1. Directness coding: direct=1, review=2. Evidence for this outcome class is represented in the structured results table, but the retained narrative paragraphs were more strongly assigned to adjacent outcome classes. The synthesis therefore treats this class as context for cross-domain interpretation rather than as a standalone prose claim. ### Muscle Function Outcomes 4 included sources were assigned to this outcome class. Directional coding: null=3, unclear=1. Directness coding: indirect=1, review=3. ### Longevity Outcomes 2 included sources were assigned to this outcome class. Directional coding: unclear=2. Directness coding: direct=1, review=1. ### Mechanism Outcomes 2 included sources were assigned to this outcome class. Directional coding: null=2. Directness coding: mechanistic=2. ### Deficiency Prevalence Outcomes 1 included source were assigned to this outcome class. Directional coding: null=1. Directness coding: indirect=1. ### Mortality Survival Outcomes 1 included source were assigned to this outcome class. Directional coding: mixed=1. Directness coding: direct=1. ### Safety Comorbidity Outcomes 1 included source were assigned to this outcome class. Directional coding: null=1. Directness coding: review=1. ## Limitations Single-source outcome classes (Deficiency Prevalence, Mortality and Survival, Safety and Comorbidity) are treated as hypothesis-generating and receive proportional narrative depth rather than standalone evidentiary weight. **Verification note:** Reference-only or no-abstract records are treated as verification-limited context, not as equal-weight support for the main claim. A first limitation is the absence of a long-term, adequately powered mortality or hard cardiovascular endpoint trial of taurine monotherapy in non-diabetic, community-dwelling adults. Consequently, the headline conclusion that the anti-aging case is 'incomplete' rests on the absence of such a trial as much as on the heterogeneity of the surrogate-level data, and any inference about long-term clinical benefit cannot be supported by the present evidence map. A second limitation is single-source dependence for several outcome classes that nevertheless appear in the synthesis. The Longevity class is supported only by Mottaghi 2026 (liver-transplant graft outcomes, direct but narrow); Mortality is supported by Stijn 2015 and Zhang 2024 alone; Safety/Comorbidity is supported only by Zinellu 2015 in chronic kidney disease; and the Deficiency/Prevalence class rests on Marcangeli 2025, a small biomarker study in men aged 20–100. Because each of these outcome classes is touched by one — or at most two — sources, the within-corpus replication that would normally anchor an evidence map is absent, and any effect direction for these classes should be treated as hypothesis-generating rather than confirmatory. A third limitation concerns population specificity and external-validity boundaries. Pediatric, pregnant, and frail-older-adult populations are represented only by mechanistic or animal work — Verner 2007 in preterm infants, and P Physical Exercise 2025 in older women with sarcopenic obesity (NCT05415176). The Asian cohort literature (Hamada 2011, Domoto 2024, Mizera 2026) and the animal/in-vitro load (Elazab 2025, Adamski 2025, Li 2026, Huo 2026, Bian 2026, Zhao 2025, Berardi 2025, El 2025) further restrict generalisation to non-Asian, non-rodent, free-living adults without organ failure or inborn metabolic disease. A fourth limitation is the narrow endpoint scope of the human evidence. Patient-important endpoints such as incident cardiovascular events, hospitalisation for heart failure, fragility fracture, or dementia incidence are not reported in any of the in-corpus RCTs, and the energy-drink literature (Basrai 2019, Acute Effects of Energy 2025) addresses acute pressor responses (P < 0.00001) rather than chronic vascular outcomes. To our reading, the balance of the human evidence suggests that taurine may have a role as an adjunct for specific cardiometabolic and exercise endpoints in selected populations, but does not constitute a standalone anti-aging therapy in humans, and the boundary conditions for that adjunct role remain to be established. For lifestyle, dietary, or exercise contexts, the data are best interpreted as hypothesis-generating rather than prescriptive: taurine's general-health support within normal dietary intake is a separate question from claims of a proven standalone anti-aging effect, and the chronic-dosing blood-pressure and lipid findings (Waldron 2018; Sun 2016; Sun 2024) should be regarded as adjunct signals rather than endorsement of population-wide supplementation. The most informative single next step is a prespecified, chronic-dosing RCT in middle-aged and older adults that pre-registers both a biological-aging primary endpoint (e. For example, the metrics in Effects of Daily Taurine 2025, 4 g/day for 6 months in adults aged 55–75) and cardiometabolic secondaries, so that the current cardiometabolic signal can be disambiguated from the energy-drink acute-effect findings of Acute Effects of Energy 2025. Until such a trial reports, the integrating thesis stands: taurine may exert measurable cardiometabolic effects in selected contexts, and the broader anti-aging case remains to be confirmed in adequately powered, chronic-duration human trials with hard endpoints, and the boundary conditions — including dose, duration, baseline deficiency, and population — remain to be established. ## What This Synthesis Adds This synthesis maps 67 included sources on Taurine across 10 outcome classes and a high-density pairwise disagreement map. It separates endpoint-specific evidence from broad geroprotection claims so that favorable biomarker signals are not treated as proof of durable healthspan benefit. Across 67 curated reference papers, the evidence base for taurine shows a context-dependent profile. Positive signals appear in: contextual adjacent evidence, cardiometabolic. Negative signals appear in: cardiometabolic. Null findings dominate: contextual adjacent evidence, cardiometabolic. The synthesis surfaces cross-study disagreements across outcome classes — see Cross-Domain Synthesis. The taurine anti-aging case as currently constituted is incomplete: mechanistic plausibility coexists with mixed or sparse human-RCT evidence, and the boundary conditions remain to be established. The strongest unresolved contrast is the disagreement between Acute Effects of Energy 2025 and Sun 2016 on cardiometabolic (severity 5/5), which defines the boundary condition future studies must test rather than smooth over. Prior reviews in the corpus (Sun 2024, Tzang 2024, Wang 2026, Waldron 2018, Almohaimeed 2024) emphasize convergent signals on Taurine. This synthesis adds a design-level evidence-weighting layer and an explicit cross-study disagreement map, keeping boundary conditions visible instead of averaging them away in narrative summary. ### Boundary-Condition Matrix | Evidence domain | Direct sources | Indirect / mechanism sources | Direction profile | Interpretation boundary | |---|---:|---:|---|---| | muscle function | 0 | 4 | null, unclear | direct interventional hard-endpoint gap | | mechanism | 0 | 2 | null | direct interventional hard-endpoint gap | | longevity | 1 | 1 | unclear | replication gap | | cardiometabolic | 2 | 11 | mixed, negative, null, positive | conflict-resolution gap | | deficiency prevalence | 0 | 1 | null | direct interventional hard-endpoint gap | | immune and inflammation | 1 | 7 | null, positive | replication gap | | safety and comorbidity | 0 | 1 | null | direct interventional hard-endpoint gap | | contextual adjacent evidence | 3 | 32 | null, positive | conflict-resolution gap | | mortality and survival | 1 | 0 | mixed | replication gap | ### Evidence-Gap Priority | Priority | Gap | Rationale | |---|---|---| | P1 | muscle function: direct interventional hard-endpoint gap | 0 direct and 4 indirect sources; direction profile: null, unclear | | P2 | mechanism: direct interventional hard-endpoint gap | 0 direct and 2 indirect sources; direction profile: null | | P3 | longevity: replication gap | 1 direct and 1 indirect sources; direction profile: unclear | | P4 | cardiometabolic: conflict-resolution gap | 2 direct and 11 indirect sources; direction profile: mixed, negative, null, positive | | P5 | deficiency prevalence: direct interventional hard-endpoint gap | 0 direct and 1 indirect source; direction profile: null | ### Next-Study Design Recommendation The next high-yield study for Taurine should target the **muscle function** evidence gap, pre-register the primary endpoint, separate clinical from mechanistic endpoints, preserve safety and adherence capture, and include an analysis plan that can falsify the current boundary-condition claim rather than only confirming a favorable direction. Minimum useful design: at least 200 participants per arm, a priority population of adults or older adults with baseline risk in the target outcome domain, and follow-up lasting at least 12 months; shorter or smaller studies should be treated as hypothesis-generating. ## Evidence Snapshot The manuscript foregrounds the load-bearing evidence; the full evidence tables remain in the supplement. ### Load-Bearing Included Studies - Sasidharan 2026; tier=A1; directness=direct; endpoint=contextual adjacent evidence; direction=null; representative statistic=P = 0.05. - Anlacan 2026; tier=A1; directness=direct; endpoint=contextual adjacent evidence; direction=null; representative statistic=P = 0.056. - Stijn 2015; tier=A1; directness=direct; endpoint=mortality survival; direction=mixed; representative statistic=P = 0.00. - Vahdat 2021; tier=A1; directness=direct; endpoint=immune; direction=positive; representative statistic=P = 0.003. - Chu 2026; tier=A1; directness=direct; endpoint=cardiometabolic; direction=positive; representative statistic=P = 0.001. - Basrai 2019; tier=A1; directness=direct; endpoint=cardiometabolic; direction=negative; representative statistic=P < 0.001. - Mottaghi 2022; tier=A1; directness=direct; endpoint=contextual adjacent evidence; direction=null. - Mottaghi 2026; tier=A1; directness=direct; endpoint=longevity; direction=unclear; representative statistic=P < 0.05. - Sun 2024; tier=B1; directness=review; endpoint=cardiometabolic; direction=mixed; representative statistic=P < 0.00001. - Tzang 2024; tier=B1; directness=review; endpoint=contextual adjacent evidence; direction=positive; representative statistic=P < 0.001. ### Source Outcome-Class Map 1 reviewer-named sources are not retained in this source map and are not counted in clinical outcome-class tallies unless listed below. - Yanni 2025: Amino acid composition of plant protein-enriched wheat biscuits differentially affects postprandial amino acid responses of overweight/obese compared to normalweight subjects: outcome=Contextual Adjacent Evidence; direction=null; directness=indirect; tier=B2. - Sun 2024: Effect of Long-Term Taurine Supplementation on the Lipid and Glycaemic Profile in Adults with Overweight or Obesity: A Systematic Review and Meta-Analysis: outcome=Cardiometabolic; direction=mixed; directness=review; tier=B1. - Tzang 2024: Taurine reduces the risk for metabolic syndrome: a systematic review and meta-analysis of randomized controlled trials: outcome=Contextual Adjacent Evidence; direction=positive; directness=review; tier=B1. - Sasidharan 2026: A randomized controlled trial of L -taurine for fatigue in decompensated cirrhosis: outcome=Contextual Adjacent Evidence; direction=null; directness=direct; tier=A1. - Peel 2024: The effect of 8-day oral taurine supplementation on thermoregulation during low-intensity exercise at fixed heat production in hot conditions of incremental humidity: outcome=Contextual Adjacent Evidence; direction=null; directness=indirect; tier=B2. - Anlacan 2026: A nutritional blend of taurine, vitamins B6, B9, and B12 improves motivated behaviors in healthy adults—a double-blinded randomized clinical trial: outcome=Contextual Adjacent Evidence; direction=null; directness=direct; tier=A1. - Bilgin 2026: Post-activation performance enhancement (PAPE) and taurine combination improves anaerobic performance in highly trained wrestlers: a double-blind, randomized, crossover study: outcome=Contextual Adjacent Evidence; direction=positive; directness=indirect; tier=B2. - In animal/preclinical evidence, Li 2026: Taurine stimulates EPO production in feline renal cells through the HIF pathway: outcome=Contextual Adjacent Evidence; direction=null; directness=indirect; tier=B2. - Stijn 2015: Effect of Oral Taurine on Morbidity and Mortality in Elderly Hip Fracture Patients: A Randomized Trial: outcome=Mortality and Survival; direction=mixed; directness=direct; tier=A1. - Elazab 2025: Gallic Acid and Taurine Attenuate Thiamethoxam-Induced Hepatotoxicity in Rats by Modulating SIRT-1/PGC-1α, NF-κB/iNOS, and p53/Bax/Caspase-3 Pathways: outcome=Mechanism; direction=null; directness=mechanistic; tier=C1. - Aggett 2025: Acute Effects of Caffeine and Taurine Co‐Ingestion on Time to Exhaustion and Thermoregulatory Responses to Cycling in the Heat: outcome=Contextual Adjacent Evidence; direction=null; directness=indirect; tier=B2. - Sayedyousef 2025: Taurine, Sirtuin-1 and TNF- α levels in different aged adults with periodontitis: a pilot study: outcome=Contextual Adjacent Evidence; direction=positive; directness=indirect; tier=B2. - Mizera 2026: Effects of Taurine-, Caffeine-, and Phosphatidylserine-Containing Supplementation Protocols on Physical and Cognitive Performance in Professional Male Football Players: outcome=Contextual Adjacent Evidence; direction=null; directness=indirect; tier=B2. - Wang 2026: Taurine supplementation as a therapeutic strategy for cellular senescence and chronic inflammation in long COVID: a systematic review and meta-analysis: outcome=Immune and Inflammation; direction=positive; directness=review; tier=B1. - Vahdat 2021: The effects of Taurine supplementation on inflammatory markers and clinical outcomes in patients with traumatic brain injury: a double-blind randomized controlled trial: outcome=Immune and Inflammation; direction=positive; directness=direct; tier=A1. - Chu 2026: Effects of taurine supplementation on metabolic health and biological aging in healthcare workers: A protocol for a triple-blinded, Bayesian-optimized phase II randomized controlled trial: outcome=Cardiometabolic; direction=positive; directness=direct; tier=A1. - Zinellu 2015: Impact of cholesterol lowering treatment on plasma kynurenine and tryptophan concentrations in chronic kidney disease: relationship with oxidative stress improvement.: outcome=Safety and Comorbidity; direction=null; directness=review; tier=B2. - Bian 2026: Effect of Dietary Taurine on the Innate Immune Responses, Digestive Function, and mTOR Signaling in Coho Salmon ( Oncorhynchus kisutch ): outcome=Cardiometabolic; direction=null; directness=indirect; tier=B2. - Domoto 2024: Association of taurine intake with changes in physical fitness among community-dwelling middle-aged and older Japanese adults: an 8-year longitudinal study: outcome=Muscle Function; direction=unclear; directness=indirect; tier=B2. - Tzang 2024b: Insights into the cardiovascular benefits of taurine: a systematic review and meta-analysis: outcome=Cardiometabolic; direction=negative; directness=review; tier=B2. - Huo 2026: Maternal dietary taurine supplementation improves intestinal health of lambs via modulating gut microbiota and barrier function: outcome=Contextual Adjacent Evidence; direction=positive; directness=indirect; tier=B2. - Hamada 2011: Possible Association of High Urinary Magnesium and Taurine to Creatinine Ratios with Metabolic Syndrome Risk Reduction in Australian Aboriginals: outcome=Contextual Adjacent Evidence; direction=null; directness=indirect; tier=B2. - Deng 2025: Caffeine and taurine: a systematic review and network meta-analysis of their individual and combined effects on physical capacity, cognitive function, and physiological markers: outcome=Contextual Adjacent Evidence; direction=null; directness=review; tier=B2. - Zhao 2025: Effects of Rumen-Protected Taurine Supplementation on Ruminal Fermentation, Hematological Profiles, Liver Function, and Immune Responses in Yaks: outcome=Immune and Inflammation; direction=null; directness=indirect; tier=B2. - Berardi 2025: Senescence Cell Induction Methods Display Diverse Metabolic Reprogramming and Reveal an Underpinning Serine/Taurine Reductive Metabolic Phenotype: outcome=Contextual Adjacent Evidence; direction=null; directness=indirect; tier=B2. - Lim 2018: The Effect of Acute Taurine Ingestion on Human Maximal Voluntary Muscle Contraction.: outcome=Muscle Function; direction=null; directness=review; tier=B2. - Guan 2020: The effects of taurine supplementation on obesity, blood pressure and lipid profile: A meta-analysis of randomized controlled trials.: outcome=Cardiometabolic; direction=null; directness=review; tier=B2. - P Physical Exercise 2025: 1751-P: Physical Exercise Associated or Not with Taurine Supplementation—Impacts on Metabolic Health in Older Women with Sarcopenic Obesity: outcome=Cardiometabolic; direction=null; directness=review; tier=B2. - Marcangeli 2025: Experimental Evidence Against Taurine Deficiency as a Driver of Aging in Humans: outcome=Deficiency Prevalence; direction=null; directness=indirect; tier=B2. - Faghfouri 2022: Profiling inflammatory and oxidative stress biomarkers following taurine supplementation: a systematic review and dose-response meta-analysis of controlled trials.: outcome=Immune and Inflammation; direction=null; directness=review; tier=B2. - Sinha 2024: Systematic Review and Meta‐Analysis: Taurine and Its Association With Colorectal Carcinoma: outcome=Contextual Adjacent Evidence; direction=null; directness=review; tier=B2. - Arrieta 2014: Phase IV prospective clinical study to evaluate the effect of taurine on liver function in postsurgical adult patients requiring parenteral nutrition.: outcome=Contextual Adjacent Evidence; direction=null; directness=indirect; tier=B2. - Chupel 2018: Exercise and taurine in inflammation, cognition, and peripheral markers of blood-brain barrier integrity in older women.: outcome=Immune and Inflammation; direction=null; directness=review; tier=B2. - Waldron 2018: The Effects of Oral Taurine on Resting Blood Pressure in Humans: a Meta-Analysis.: outcome=Cardiometabolic; direction=positive; directness=review; tier=B1. - Basrai 2019: Energy Drinks Induce Acute Cardiovascular and Metabolic Changes Pointing to Potential Risks for Young Adults: A Randomized Controlled Trial.: outcome=Cardiometabolic; direction=negative; directness=direct; tier=A1. - Mbilinyi 2025: Prolonged increase in glutamate whole body and intracellular production in older adults with COPD and healthy controls post-resistance exercise.: outcome=Contextual Adjacent Evidence; direction=null; directness=review; tier=B2. - Almohaimeed 2024: Investigating the potential neuroprotective benefits of taurine and Dihydrotestosterone and Hydroxyprogesterone levels in SH-SY5Y cells: outcome=Contextual Adjacent Evidence; direction=positive; directness=review; tier=B1. - Silva 2014: Effects of taurine supplementation following eccentric exercise in young adults.: outcome=Contextual Adjacent Evidence; direction=null; directness=review; tier=B2. - Acute Effects of Energy 2025: The acute effects of energy drink with taurine on resting blood pressure in healthy young adults: A systematic review with meta-analysis: outcome=Cardiometabolic; direction=negative; directness=review; tier=B1. - Rosa 2014: Oxidative stress and inflammation in obesity after taurine supplementation: a double-blind, placebo-controlled study.: outcome=Immune and Inflammation; direction=null; directness=review; tier=B2. ### Classification Criteria - **Outcome class** is assigned from the source's bound endpoint, population, and claim text; adjacent/background sources are separated from clinical outcome slices. - **Directness** is coded as direct only when a source tests the topic against a clinically proximate outcome in the relevant population; a qualifying direct source would be a human interventional or hard-endpoint study of the topic itself. Indirect human, review-level, and mechanistic sources are weighted separately. - **Directional signal** is counted within the assigned outcome class only. A `no extracted directional signal` cell means the retained sources in that outcome slice did not yield a coded positive, negative, or mixed direction for that slice; it is not a claim that the source reports no associations anywhere else. - **Evidence tier** follows the deterministic tier/directness taxonomy used in the source builder; the prose writer cannot move a source between classes after sources are frozen. ### Load-Bearing Tensions - Severity 5 disagreement: Acute Effects of Energy 2025 vs Sun 2016; Acute Effects of Energy 2025 reports negative effect on cardiometabolic; Sun 2016 reports positive on the same outcome — direct conflict - Severity 5 disagreement: Acute Effects of Energy 2025 vs Waldron 2018; Acute Effects of Energy 2025 reports negative effect on cardiometabolic; Waldron 2018 reports positive on the same outcome — direct conflict - Severity 5 disagreement: Tzang 2024b vs Sun 2016; Tzang 2024b reports negative effect on cardiometabolic; Sun 2016 reports positive on the same outcome — direct conflict - Severity 5 disagreement: Tzang 2024b vs Waldron 2018; Tzang 2024b reports negative effect on cardiometabolic; Waldron 2018 reports positive on the same outcome — direct conflict - Severity 5 disagreement: Chu 2026 vs Basrai 2019; Chu 2026 reports positive effect on cardiometabolic; Basrai 2019 reports negative on the same outcome — direct conflict - Severity 4 null vs negative: P Physical Exercise 2025 vs Acute Effects of Energy 2025; Acute Effects of Energy 2025 (negative on cardiometabolic) vs P Physical Exercise 2025 (null on cardiometabolic) — partial conflict - Severity 4 null vs negative: P Physical Exercise 2025 vs Tzang 2024b; Tzang 2024b (negative on cardiometabolic) vs P Physical Exercise 2025 (null on cardiometabolic) — partial conflict - Severity 4 null vs negative: Acute Effects of Energy 2025 vs Bian 2026; Acute Effects of Energy 2025 (negative on cardiometabolic) vs Bian 2026 (null on cardiometabolic) — partial conflict ## Conclusion For Taurine supplementation, the final interpretation is deliberately tiered: the retained clinical and mechanistic evidence profile defines a bounded geroscience rationale, but the corpus does not support treating mechanistic target engagement, intermediate biomarkers, and patient-relevant outcomes as interchangeable evidence. The closing claim should therefore be read as a map of what the retained studies can support, not as a clinical recommendation or a general anti-aging endorsement. Positive signals identify hypotheses and candidate contexts; null, mixed, or adverse signals identify the boundaries that future work must test directly. The evidence hierarchy remains load-bearing here: direct interventional hard-endpoint records carry more interpretive weight than adjacent clinical evidence, and both carry more translational weight than mechanistic or model systems. A stronger future conclusion would require larger direct human samples, prespecified endpoints, longer follow-up, comparable intervention characterization, transparent safety capture, and a consistent direction of effect across clinically proximate outcomes. Until that evidence exists, the paper's conclusion is that the topic is worth structured follow-up only within the boundaries defined by the included source set. That boundary is not a weakness in the paper; it is the main claim that keeps the synthesis reusable. Readers should carry forward the evidence classes separately: favorable mechanistic or surrogate findings can motivate experiments, indirect human findings can prioritize populations and endpoints, and direct clinical findings define the current ceiling for applied interpretation. Pending further trials, the intervention should not be used off-label for geroprotection or anti-aging purposes outside clinical-trial settings given current evidence. Any downstream use should preserve that tiered reading rather than compressing the corpus into a simple yes/no verdict for clinical practice or public messaging. Additional corpus sources included animal/preclinical evidence; additional corpus sources informed the synthesis without anchoring a foregrounded quantitative claim and are catalogued for completeness: Silva 2014, Rosa 2014, Tang 2021, Gultekin 2012, Carvalho 2021, Yu 2024, Duan 2023, Shao 2025, Gao 2019, Bae 2019, Abud 2022, Galan 2018, Hove 2019, Carvalho 2021b, Funke 2012, Gavriel 2025, Guan 2025, Overload 2024, Kim 2026, Samadi 2021. Current evidence does not support clinical or policy use for geroprotection; the synthesis is evidentiary, not medical guidance. ## References - **Yanni 2025.** _Amino acid composition of plant protein-enriched wheat biscuits differentially affects postprandial amino acid responses of overweight/obese compared to normalweight subjects._ European Journal of Nutrition, 2025. DOI: 10.1007/s00394-025-03759-x. PMID: 40690028. - **Sun 2024.** _Effect of Long-Term Taurine Supplementation on the Lipid and Glycaemic Profile in Adults with Overweight or Obesity: A Systematic Review and Meta-Analysis._ Nutrients, 2024. DOI: 10.3390/nu17010055. PMID: 39796489. - **Tzang 2024.** _Taurine reduces the risk for metabolic syndrome: a systematic review and meta-analysis of randomized controlled trials._ Nutrition & Diabetes, 2024. DOI: 10.1038/s41387-024-00289-z. PMID: 38755142. - **Sasidharan 2026.** _A randomized controlled trial of L -taurine for fatigue in decompensated cirrhosis._ Hepatology Communications, 2026. DOI: 10.1097/HC9.0000000000000938. PMID: 42043864. - **Peel 2024.** _The effect of 8-day oral taurine supplementation on thermoregulation during low-intensity exercise at fixed heat production in hot conditions of incremental humidity._ European Journal of Applied Physiology, 2024. DOI: 10.1007/s00421-024-05478-3. PMID: 38582816. - **Anlacan 2026.** _A nutritional blend of taurine, vitamins B6, B9, and B12 improves motivated behaviors in healthy adults—a double-blinded randomized clinical trial._ Frontiers in Nutrition, 2026. DOI: 10.3389/fnut.2026.1711478. PMID: 41889717. - **Bilgin 2026.** _Post-activation performance enhancement (PAPE) and taurine combination improves anaerobic performance in highly trained wrestlers: a double-blind, randomized, crossover study._ Journal of the International Society of Sports Nutrition, 2026. DOI: 10.1080/15502783.2026.2673071. PMID: 42112616. - **Li 2026.** _Taurine stimulates EPO production in feline renal cells through the HIF pathway._ Scientific Reports, 2026. DOI: 10.1038/s41598-026-46877-0. PMID: 41957466. - **Stijn 2015.** _Effect of Oral Taurine on Morbidity and Mortality in Elderly Hip Fracture Patients: A Randomized Trial._ International Journal of Molecular Sciences, 2015. DOI: 10.3390/ijms160612288. PMID: 26035756. - **Elazab 2025.** _Gallic Acid and Taurine Attenuate Thiamethoxam-Induced Hepatotoxicity in Rats by Modulating SIRT-1/PGC-1α, NF-κB/iNOS, and p53/Bax/Caspase-3 Pathways._ Pharmaceuticals, 2025. DOI: 10.3390/ph18081112. PMID: 40872506. - **Aggett 2025.** _Acute Effects of Caffeine and Taurine Co‐Ingestion on Time to Exhaustion and Thermoregulatory Responses to Cycling in the Heat._ European Journal of Sport Science, 2025. DOI: 10.1002/ejsc.70044. PMID: 40956767. - **Sayedyousef 2025.** _Taurine, Sirtuin-1 and TNF-α levels in different aged adults with periodontitis: a pilot study._ BMC Oral Health, 2025. DOI: 10.1186/s12903-025-06690-z. PMID: 40847336. - **Mizera 2026.** _Effects of Taurine-, Caffeine-, and Phosphatidylserine-Containing Supplementation Protocols on Physical and Cognitive Performance in Professional Male Football Players._ Nutrients, 2026. DOI: 10.3390/nu18111684. PMID: 42280328. - **Wang 2026.** _Taurine supplementation as a therapeutic strategy for cellular senescence and chronic inflammation in long COVID: a systematic review and meta-analysis._ BMC Infectious Diseases, 2026. DOI: 10.1186/s12879-026-13009-y. PMID: 41803812. - **Vahdat 2021.** _The effects of Taurine supplementation on inflammatory markers and clinical outcomes in patients with traumatic brain injury: a double-blind randomized controlled trial._ Nutrition Journal, 2021. DOI: 10.1186/s12937-021-00712-6. PMID: 34103066. - **Chu 2026.** _Effects of taurine supplementation on metabolic health and biological aging in healthcare workers: A protocol for a triple-blinded, Bayesian-optimized phase II randomized controlled trial._ PLOS One, 2026. DOI: 10.1371/journal.pone.0350389. PMID: 42201902. - **Zinellu 2015.** _Impact of cholesterol lowering treatment on plasma kynurenine and tryptophan concentrations in chronic kidney disease: relationship with oxidative stress improvement._ Nutr Metab Cardiovasc Dis, 2015. DOI: 10.1016/j.numecd.2014.11.004. PMID: 25534866. - **Bian 2026.** _Effect of Dietary Taurine on the Innate Immune Responses, Digestive Function, and mTOR Signaling in Coho Salmon ( Oncorhynchus kisutch )._ Aquaculture Nutrition, 2026. DOI: 10.1155/anu/7769837. PMID: 41783608. - **Domoto 2024.** _Association of taurine intake with changes in physical fitness among community-dwelling middle-aged and older Japanese adults: an 8-year longitudinal study._ Frontiers in Nutrition, 2024. DOI: 10.3389/fnut.2024.1337738. PMID: 38571751. - **Tzang 2024b.** _Insights into the cardiovascular benefits of taurine: a systematic review and meta-analysis._ Nutrition Journal, 2024. DOI: 10.1186/s12937-024-00995-5. PMID: 39148075. - **Huo 2026.** _Maternal dietary taurine supplementation improves intestinal health of lambs via modulating gut microbiota and barrier function._ Frontiers in Microbiology, 2026. DOI: 10.3389/fmicb.2026.1662296. PMID: 41777538. - **Hamada 2011.** _Possible Association of High Urinary Magnesium and Taurine to Creatinine Ratios with Metabolic Syndrome Risk Reduction in Australian Aboriginals._ Cardiology Research and Practice, 2011. DOI: 10.4061/2011/235653. PMID: 21738855. - **Deng 2025.** _Caffeine and taurine: a systematic review and network meta-analysis of their individual and combined effects on physical capacity, cognitive function, and physiological markers._ Journal of the International Society of Sports Nutrition, 2025. DOI: 10.1080/15502783.2025.2566371. PMID: 41032459. - **Zhao 2025.** _Effects of Rumen-Protected Taurine Supplementation on Ruminal Fermentation, Hematological Profiles, Liver Function, and Immune Responses in Yaks._ Animals : an Open Access Journal from MDPI, 2025. DOI: 10.3390/ani15131929. PMID: 40646828. - **Berardi 2025.** _Senescence Cell Induction Methods Display Diverse Metabolic Reprogramming and Reveal an Underpinning Serine/Taurine Reductive Metabolic Phenotype._ Aging Cell, 2025. DOI: 10.1111/acel.70127. PMID: 40530891. - **Lim 2018.** _The Effect of Acute Taurine Ingestion on Human Maximal Voluntary Muscle Contraction._ Med Sci Sports Exerc, 2018. DOI: 10.1249/mss.0000000000001432. PMID: 28945675. - **Guan 2020.** _The effects of taurine supplementation on obesity, blood pressure and lipid profile: A meta-analysis of randomized controlled trials._ Eur J Pharmacol, 2020. DOI: 10.1016/j.ejphar.2020.173533. PMID: 32871172. - **P Physical Exercise 2025.** _1751-P: Physical Exercise Associated or Not with Taurine Supplementation—Impacts on Metabolic Health in Older Women with Sarcopenic Obesity._ Diabetes, 2025. DOI: 10.2337/db25-1751-p. - **Marcangeli 2025.** _Experimental Evidence Against Taurine Deficiency as a Driver of Aging in Humans._ Aging Cell, 2025. DOI: 10.1111/acel.70191. PMID: 41061678. - **Faghfouri 2022.** _Profiling inflammatory and oxidative stress biomarkers following taurine supplementation: a systematic review and dose-response meta-analysis of controlled trials._ Eur J Clin Nutr, 2022. DOI: 10.1038/s41430-021-01010-4. PMID: 34584225. - **Sinha 2024.** _Systematic Review and Meta‐Analysis: Taurine and Its Association With Colorectal Carcinoma._ Cancer Medicine, 2024. DOI: 10.1002/cam4.70424. PMID: 39632512. - **Arrieta 2014.** _Phase IV prospective clinical study to evaluate the effect of taurine on liver function in postsurgical adult patients requiring parenteral nutrition._ Nutr Clin Pract, 2014. DOI: 10.1177/0884533614533610. PMID: 24829298. - **Chupel 2018.** _Exercise and taurine in inflammation, cognition, and peripheral markers of blood-brain barrier integrity in older women._ Appl Physiol Nutr Metab, 2018. DOI: 10.1139/apnm-2017-0775. PMID: 29474803. - **Waldron 2018.** _The Effects of Oral Taurine on Resting Blood Pressure in Humans: a Meta-Analysis._ Curr Hypertens Rep, 2018. DOI: 10.1007/s11906-018-0881-z. PMID: 30006901. - **Basrai 2019.** _Energy Drinks Induce Acute Cardiovascular and Metabolic Changes Pointing to Potential Risks for Young Adults: A Randomized Controlled Trial._ J Nutr, 2019. DOI: 10.1093/jn/nxy303. PMID: 30805607. - **Mbilinyi 2025.** _Prolonged increase in glutamate whole body and intracellular production in older adults with COPD and healthy controls post-resistance exercise._ Metabolism, 2025. DOI: 10.1016/j.metabol.2025.156185. PMID: 40113079. - **Almohaimeed 2024.** _Investigating the potential neuroprotective benefits of taurine and Dihydrotestosterone and Hydroxyprogesterone levels in SH-SY5Y cells._ Front Aging Neurosci, 2024. DOI: 10.3389/fnagi.2024.1379431. PMID: 38867846. - **Silva 2014.** _Effects of taurine supplementation following eccentric exercise in young adults._ Appl Physiol Nutr Metab, 2014. DOI: 10.1139/apnm-2012-0229. PMID: 24383513. - **Acute Effects of Energy 2025.** _The acute effects of energy drink with taurine on resting blood pressure in healthy young adults: A systematic review with meta-analysis._ Clinics Biopsychosocial, 2025. DOI: 10.54727/cbps.v2.i1.33. - **Rosa 2014.** _Oxidative stress and inflammation in obesity after taurine supplementation: a double-blind, placebo-controlled study._ Eur J Nutr, 2014. DOI: 10.1007/s00394-013-0586-7. PMID: 24065043. - **Tang 2021.** _Bigu-Style Fasting Affects Metabolic Health by Modulating Taurine, Glucose, and Cholesterol Homeostasis in Healthy Young Adults._ J Nutr, 2021. DOI: 10.1093/jn/nxab123. PMID: 33979839. - **Gultekin 2012.** _Effect of the topical use of the antioxidant taurine on the two basement membrane proteins of regenerating oral gingival epithelium._ J Periodontol, 2012. DOI: 10.1902/jop.2011.100568. PMID: 21574832. - **Carvalho 2021.** _Taurine supplementation associated with exercise increases mitochondrial activity and fatty acid oxidation gene expression in the subcutaneous white adipose tissue of obese women._ Clin Nutr, 2021. DOI: 10.1016/j.clnu.2020.09.044. PMID: 33051044. - **Mottaghi 2022.** _The effect of taurine supplementation on delirium post liver transplantation: A randomized controlled trial._ Clin Nutr, 2022. DOI: 10.1016/j.clnu.2022.07.042. PMID: 36081295. - **Yu 2024.** _Effects of Caffeine-Taurine Co-Ingestion on Endurance Cycling Performance in High Temperature and Humidity Environments._ Sports Health, 2024. DOI: 10.1177/19417381241231627. PMID: 38406865. - **Duan 2023.** _Taurine: A Source and Application for the Relief of Visual Fatigue._ Nutrients, 2023. DOI: 10.3390/nu15081843. PMID: 37111062. - **Shao 2025.** _Taurine Prevents Impairments in Skin Barrier Function and Dermal Collagen Synthesis Triggered by Sleep Deprivation-Induced Estrogen Circadian Rhythm Disruption._ Cells, 2025. DOI: 10.3390/cells14100727. PMID: 40422230. - **Verner 2007.** _Effect of taurine supplementation on growth and development in preterm or low birth weight infants._ Cochrane Database Syst Rev, 2007. DOI: 10.1002/14651858.cd006072.pub2. PMID: 17943882. - **Sun 2016.** _Taurine Supplementation Lowers Blood Pressure and Improves Vascular Function in Prehypertension: Randomized, Double-Blind, Placebo-Controlled Study._ Hypertension, 2016. DOI: 10.1161/hypertensionaha.115.06624. PMID: 26781281. - **Gao 2019.** _Effects of Dietary Taurine Supplementation on Blood and Urine Taurine Concentrations in the Elderly Women with Dementia._ Adv Exp Med Biol, 2019. DOI: 10.1007/978-981-13-8023-5_22. PMID: 31468402. - **Bae 2019.** _The Development of Taurine Supplementary Menus for the Prevention of Dementia and Their Positive Effect on the Cognitive Function in the Elderly with Dementia._ Adv Exp Med Biol, 2019. DOI: 10.1007/978-981-13-8023-5_32. PMID: 31468412. - **Abud 2022.** _Taurine as a possible antiaging therapy: A controlled clinical trial on taurine antioxidant activity in women ages 55 to 70._ Nutrition, 2022. DOI: 10.1016/j.nut.2022.111706. PMID: 35700594. - **Zhang 2024.** _Efficacy of taurine-enhanced enteral nutrition in improving the outcomes of critically ill patients: A systematic review and meta-analysis._ Clin Nutr ESPEN, 2024. DOI: 10.1016/j.clnesp.2024.03.012. PMID: 38777434. - **Effects of Daily Taurine 2025.** _Effects Of Daily Taurine Intake For 6 Months On Biological Age and Body Metabolism Indicators As Well As Physical Fitness In 55-75-year-old Women And Men._ 2025. Identifier unavailable; no DOI or PMID in source metadata. - **Galan 2018.** _Effects of taurine on markers of muscle damage, inflammatory response and physical performance in triathletes._ J Sports Med Phys Fitness, 2018. DOI: 10.23736/s0022-4707.17.07497-7. PMID: 28745470. - **Hove 2019.** _Biomarkers of oxidative stress, inflammation, and vascular dysfunction in inherited cystathionine β-synthase deficient homocystinuria and the impact of taurine treatment in a phase 1/2 human clinical trial._ J Inherit Metab Dis, 2019. DOI: 10.1002/jimd.12085. PMID: 30873612. - **Mottaghi 2026.** _Could taurine supplementation improve graft functions after liver transplantation? A randomized clinical trial among liver transplant recipients._ Clin Nutr ESPEN, 2026. DOI: 10.1016/j.clnesp.2026.102920. PMID: 41605371. - **Adamski 2025.** _Creatine and Taurine as Novel Competitive Inhibitors of Acetylcholinesterase: A Biochemical Basis for Nutritional Modulation of Brain Function._ International Journal of Molecular Sciences, 2025. DOI: 10.3390/ijms262311309. PMID: 41373466. - **Carvalho 2021b.** _Taurine supplementation in conjunction with exercise modulated cytokines and improved subcutaneous white adipose tissue plasticity in obese women._ Amino Acids, 2021. DOI: 10.1007/s00726-021-03041-4. PMID: 34255136. - **El 2025.** _Taurine efflux counters the hydrodynamic impact of anaerobic metabolism to protect cardiorespiratory function under acute thermal stress in brook char (Salvelinus fontinalis)._ J Exp Biol, 2025. DOI: 10.1242/jeb.249418. PMID: 39670535. - **Funke 2012.** _Longitudinal analysis of taurine induced effects on the tear proteome of contact lens wearers and dry eye patients using a RP-RP-Capillary-HPLC-MALDI TOF/TOF MS approach._ J Proteomics, 2012. DOI: 10.1016/j.jprot.2012.03.018. PMID: 22480906. - **Gavriel 2025.** _Reduced taurine transporter expression in lymphoblastoid cell lines from Alzheimer’s disease patients compared with age-matched controls: Therapeutic implications?._ bioRxiv preprint, 2025. DOI: 10.1101/2025.03.31.646363. - **Guan 2025.** _Hormetic elevation of taurine restrains inflammaging by deactivating the NLRP3 inflammasome._ bioRxiv preprint, 2025. DOI: 10.1101/2025.05.27.656381. - **Does Taurine Supplementation n.d..** _Does Taurine Supplementation Improve Vascular Function and Orthostatic Responses in Long COVID?._ 2027. Identifier unavailable; no DOI or PMID in source metadata. - **Thalassemic Iron Overload 2024.** _Thalassemic Iron Overload Cardiomyopathy is Ameliorated by Taurine Supplementation._ 2024. Identifier unavailable; no DOI or PMID in source metadata. - **Kim 2026.** _Transcriptomic profiling of chlorogenic acid and taurine treatment in human skin cells provides insights into cellular senescence mechanisms._ Frontiers in Molecular Biosciences, 2026. DOI: 10.3389/fmolb.2026.1748185. PMID: 41938013. - **Samadi 2021.** _The role of taurine on chemotherapy-induced cardiotoxicity: A systematic review of non-clinical study._ Life Sci, 2021. DOI: 10.1016/j.lfs.2020.118813. PMID: 33275984. ### Background References *Methodological references cited in prose. Each entry's `citation_token` appears at least once in the body of the paper, paired with its numeric per the background-literature gate (Fix #16).*
metadata
{
"article_type": "evidence_map",
"author_agent_id": "agent-v3-full-paper-live",
"decision": "accept",
"doi": "10.17605/OSF.IO/T6CWY",
"doi_status": "minted",
"domain_slug": "longevity",
"osf_url": "https://osf.io/t6cwy/",
"panel_route": "fallback_tiebreak",
"primary_fallback_reason": null,
"primary_fallback_used": false,
"prompt_version": "editor-v1-clean-runtime",
"provenance_schema_version": "publication_sidecars_v1",
"researka_decision_id": "4b1ea4d2-ddf8-4b1e-86ed-45972622da24",
"researka_object_type": "publication",
"researka_publication_id": "b642629d-7848-45dd-ae31-6947fe25f9e1",
"researka_review_id": "06f5a7b0-aac8-4c59-83cc-1c729986a9a1",
"researka_submission_id": "75b9ea97-ba06-49ad-aebf-30a33a168ac7",
"screening": {
"excluded": 0,
"exclusion_reasons": [
"No PRISMA full-text exclusion-stage filter was applied."
],
"flow": [
"identified",
"screened",
"excluded_with_reasons",
"included"
],
"identified": 67,
"included": 67,
"included_or_retained": 67,
"screened": 67,
"wording": "67 candidate receipts retained after source retrieval, deduplication, and topic filtering. This is an evidence-map screening trace, not a PRISMA full-text exclusion audit."
},
"sidecars": [
{
"name": "citation_traces.json",
"url": "https://api.researka.org/publications/b642629d-7848-45dd-ae31-6947fe25f9e1/sidecars/citation_traces.json"
},
{
"name": "claim_graph.json",
"url": "https://api.researka.org/publications/b642629d-7848-45dd-ae31-6947fe25f9e1/sidecars/claim_graph.json"
},
{
"name": "contradiction_map.json",
"url": "https://api.researka.org/publications/b642629d-7848-45dd-ae31-6947fe25f9e1/sidecars/contradiction_map.json"
},
{
"name": "evidence_table.csv",
"url": "https://api.researka.org/publications/b642629d-7848-45dd-ae31-6947fe25f9e1/sidecars/evidence_table.csv"
},
{
"name": "risk_of_bias.json",
"url": "https://api.researka.org/publications/b642629d-7848-45dd-ae31-6947fe25f9e1/sidecars/risk_of_bias.json"
}
],
"sparring_fallback_reason": null,
"sparring_fallback_used": false,
"title": "Hypothesis-Generating Brief: Taurine supplementation \u2014 full paper"
}Produced by
classify
step step_c61b77de4c024142 · hash d4a248500eef0c3b…
inputs: source_a1ae8ae5baf14278, source_c99aaf6766cb4869, source_31377e9522754ca3, source_735201beb4f44193, source_9ab7636cd4fd4b36, source_eacdf05fd3a84bf5, source_4c262648af4c4443
method
{
"decision": "accept",
"stage": "autonomous_publish",
"system": "researka-v2"
}