| 1 |
Partly verified |
Full text not readStored summary read |
N01 · Evidence conditionSelected isolated-component question and original gradeRequired |
The selected existing record is liver-fat reduction from Mankai or green tea alone, grade ?, with a note that individual component effects were not separated. Subclaim score, status and axes are absent and are not filled with parent C with 46 points. |
Only corresponding stored-summary information is recorded. Detailed original material is unread and review of existing content remains incomplete. Separate subclaim score, status, axes and direct isolated-component effects are absent from the original material. Review of existing content remains incomplete. |
Mankai or green-tea wording, note and grade, and the parent dietary verdict |
Record updates distinguishing isolated-component and bundled-diet questions. This is a proposal; no new investigation, calculation or trial is conducted here. |
| 2 |
Partly verified |
Full text not readStored summary read |
N02 · Evidence conditionBoundary between the bundled diet and component attributionRequired |
The original text records results for a package of foods and meat restriction. Its overall descriptions of Mankai, green tea, walnuts and meat restriction are not transferred into efficacy of any one component. |
Only corresponding stored-summary information is recorded. Detailed original material is unread and review of existing content remains incomplete. Direct comparisons changing only Mankai or green tea, component-specific effects and interactions are not linked. Review of existing content remains incomplete. |
Simultaneously changed components, factor separation and isolated comparisons |
Propose follow-up research separating component attribution from the bundled pattern. No product or diet instructions are produced. This is a proposal; no new investigation, calculation or trial is conducted here. |
| 3 |
Partly verified |
Full text not readStored summary read |
N03 · Evidence conditionPhysical activity common to all three groupsRequired |
The original account allocated 294 participants to healthy-diet guidance, MED and green-MED, all undertaking a physical-activity program. Activity is not recast as unique to green-MED or as an isolated-component effect. |
Only corresponding stored-summary information is recorded. Detailed original material is unread and review of existing content remains incomplete. Activity specifications, group implementation, contact and actual exposure by period are unverified. Review of existing content remains incomplete. |
Common exposures in all groups and actual implementation |
Propose follow-up material distinguishing common exposures from dietary differences. Exercise instructions are not written. This is a proposal; no new investigation, calculation or trial is conducted here. |
| 4 |
Partly verified |
Full text not readStored summary read |
N04 · Evidence conditionWalnuts common to both MED groupsRequired |
The study condition that both MED groups received 28 g/day walnuts is preserved. The green-MED versus conventional-MED difference is not explained as a walnut-only effect or as walnuts added only in green-MED. |
Only corresponding stored-summary information is recorded. Detailed original material is unread and review of existing content remains incomplete. Actual walnut adherence, correspondence with other foods and isolated comparisons are unverified. Review of existing content remains incomplete. |
Common and different food exposures by group |
Propose follow-up material disclosing common foods and different components. No intake guidance is provided. This is a proposal; no new investigation, calculation or trial is conducted here. |
| 5 |
Partly verified |
Full text not readStored summary read |
N05 · Evidence conditionStudy exposures added in green-MEDRequired |
Green-MED jointly added 3-4 cups/day green tea, 100 g/day frozen Mankai and greater restriction of red and processed meat. These figures are study conditions, not individual products, recommended amounts or doses establishing isolated efficacy. |
Only corresponding stored-summary information is recorded. Detailed original material is unread and review of existing content remains incomplete. Actual adherence, component and product specifications, meat-restriction amounts and individual exposures are unverified. Review of existing content remains incomplete. |
Simultaneous planned and actual green-tea, Mankai and meat-restriction exposures |
Propose follow-up material separating planned from actual component exposures. No dose or energy conversions are produced. This is a proposal; no new investigation, calculation or trial is conducted here. |
| 6 |
Unverified |
Full text not readStored summary read |
N06 · Evidence conditionDirect material for Mankai aloneRequired |
The current stored summary concerns the DIRECT-PLUS bundled pattern. Direct liver-fat trials of Mankai alone are not linked in the preserved citation list, and the bundled-group -38.9% is not used as an isolated effect. |
Information currently required is unverified in the stored summary. Mankai-only trials, formulations, exposure, direct comparisons, effects, CIs and denominators are not linked. Review of existing content remains incomplete. |
Isolated formulation, comparator, population, outcome and denominators |
Propose follow-up research separating the isolated-component study specification. No hypothetical reports or effects are created. This is a proposal; no new investigation, calculation or trial is conducted here. |
| 7 |
Unverified |
Full text not readStored summary read |
N07 · Evidence conditionDirect material for green tea aloneRequired |
The current stored summary concerns a bundled diet including green tea. Direct liver-fat trials of green tea alone are not linked, and bundled results are not recast as green-tea treatment of fatty liver. |
Information currently required is unverified in the stored summary. Green-tea-only trials, formulations, components, exposure, comparisons, effects, CIs and denominators are not linked. Review of existing content remains incomplete. |
Isolated formulation, comparator, population, outcome and denominators |
Propose follow-up research distinguishing isolated components from bundled diets. No intake or treatment instructions are given. This is a proposal; no new investigation, calculation or trial is conducted here. |
| 8 |
Partly verified |
Full text not readStored summary read |
N08 · Evidence conditionActual population of the parent trialRequired |
The original text describes 294 adults with abdominal obesity or dyslipidemia. Findings are not extended into isolated-component efficacy in selected liver-disease patients or everyone. |
Only corresponding stored-summary information is recorded. Detailed original material is unread and review of existing content remains incomplete. Age, sex, baseline liver fat and disease, recruitment and group allocation and analysis denominators are unverified. Review of existing content remains incomplete. |
Abdominal obesity or dyslipidemia, eligibility and denominators |
Propose follow-up material distinguishing populations and application boundaries for isolated and bundled questions. This is a proposal; no new investigation, calculation or trial is conducted here. |
| 9 |
Partly verified |
Full text not readStored summary read |
N09 · Evidence conditionDifferent conventional-MED and healthy-diet-guidance contrastsRequired |
The parent classification fields identify healthy-diet guidance as the comparator, while weight-adjusted P=.035 describes green-MED versus conventional MED. Effects, P values and comparator exposures from different contrasts are not mixed. |
Only corresponding stored-summary information is recorded. Detailed original material is unread and review of existing content remains incomplete. Exact contrast-specific estimates, denominators and correspondence of whole diets and contact are unverified. Review of existing content remains incomplete. |
Three-group exposures, denominators and comparison specifications |
Propose follow-up material with disclosed comparator-specific study specifications. This is a proposal; no new investigation, calculation or trial is conducted here. |
| 10 |
Partly verified |
Full text not readStored summary read |
N10 · Evidence conditionIntrahepatic-fat MRS and isolated-component resultsRequired |
S01 describes 18-month change in intrahepatic fat by proton MRS. Imaging findings are not transferred into direct clinical treatment results for Mankai or green tea alone, or into other MRI-PDFF trials. |
Only corresponding stored-summary information is recorded. Detailed original material is unread and review of existing content remains incomplete. MRS acquisition, reading, location, units, eligibility criteria and isolated-comparison findings are unverified. Review of existing content remains incomplete. |
Proton-MRS definitions, units, time points and directness |
Propose follow-up material separating measurement methods from component attribution. This is a proposal; no new investigation, calculation or trial is conducted here. |
| 11 |
Partly verified |
Full text not readStored summary read |
N11 · Evidence conditionProportional reductions and absolute or between-group effectsRequired |
Green-MED -38.9%, MED -19.6% and HDG -12.2% are original proportional intrahepatic-fat reductions. They are not recast as absolute percentage points, isolated-component effects, between-group differences or CIs, or new relative or absolute calculations. |
Only corresponding stored-summary information is recorded. Detailed original material is unread and review of existing content remains incomplete. Group original values, variances, exact comparative effects and CIs, within-person calculations and denominators are unverified. Review of existing content remains incomplete. |
Group proportional changes, denominators and estimates |
Propose follow-up material separating units and scope of reported estimates. No new calculations are produced. This is a proposal; no new investigation, calculation or trial is conducted here. |
| 12 |
Partly verified |
Full text not readStored summary read |
N12 · Evidence conditionWeight-adjusted P values and causal component attributionRequired |
Weight-adjusted green-MED versus MED P=.035 and similar weight-loss wording concern a bundled-diet comparison. Possibilities beyond weight change do not establish causal effects of Mankai or green tea alone. |
Only corresponding stored-summary information is recorded. Detailed original material is unread and review of existing content remains incomplete. Exact adjusted models, coefficients and CIs, weight-analysis denominators and separate mediation or component effects are unverified. Review of existing content remains incomplete. |
Adjusted models, contrasts, weight changes and effects |
Propose follow-up research separating weight change from component attribution. This is a proposal; no new investigation, calculation or trial is conducted here. |
| 13 |
Partly verified |
Full text not readStored summary read |
N13 · Evidence conditionHistorical wording of a small standardized effectRequired |
The parent text describes a small standardized effect versus conventional MED. No new standardized values or CIs, isolated-component magnitudes or grades are created from that wording. |
Only corresponding stored-summary information is recorded. Detailed original material is unread and review of existing content remains incomplete. Exact standardized estimates, variances, specifications, CIs and relevance thresholds are unverified. Review of existing content remains incomplete. |
Original standardized estimates, denominators and interpretation specifications |
Propose follow-up records separating reported effects from the historical scope of verdict interpretation. This is a proposal; no new investigation, calculation or trial is conducted here. |
| 14 |
Partly verified |
Full text not readStored summary read |
N14 · Evidence conditionRetention and eligible MRS have different denominatorsRequired |
The original 294 randomized participants, 89.8% retention at 18 months and 78% eligible follow-up MRS are preserved separately. The original 22% without eligible MRS is not recast as 22% trial attrition or exact participant counts. |
Only corresponding stored-summary information is recorded. Detailed original material is unread and review of existing content remains incomplete. Group retention, MRS eligibility and missingness, reasons, and selected and analysis denominators are unverified. Review of existing content remains incomplete. |
Randomization, retention, imaging eligibility and group missingness |
Propose follow-up material distinguishing retention from imaging-analysis eligibility. No new count or rate calculations are produced. This is a proposal; no new investigation, calculation or trial is conducted here. |
| 15 |
Unverified |
Full text not readStored summary read |
N15 · Evidence conditionMissing imaging, analysis populations and sensitivity analysesRequired |
Imaging missingness reflected in 78% eligible MRS is recorded as a limitation of the parent verdict. It is not used as proof that everyone completed imaging or as ITT evidence for an isolated-component effect. |
Information currently required is unverified in the stored summary. ITT or PP, imaging-missingness handling, imputation, sensitivity analyses and baseline associations are unverified. Review of existing content remains incomplete. |
Missing-data handling, ITT or PP, selection and estimate stability |
Propose follow-up material distinguishing missingness from analysis specifications. This is a proposal; no new investigation, calculation or trial is conducted here. |
| 16 |
Partly verified |
Full text not readStored summary read |
N16 · Evidence conditionRandomization and assessment maskingRequired |
The original S01 design is a three-arm 18-month randomized lifestyle trial. The design label does not establish allocation concealment or participant, imaging-reader or analyst masking. |
Only corresponding stored-summary information is recorded. Detailed original material is unread and review of existing content remains incomplete. Sequence generation, concealment, reading and analysis masking, and group contact and expectations are unverified. Review of existing content remains incomplete. |
Allocation, concealment, MRS reading, contact and expectations |
Propose follow-up material disclosing lifestyle exposures and imaging-assessment conditions. This is a proposal; no new investigation, calculation or trial is conducted here. |
| 17 |
Unverified |
Full text not readStored summary read |
N17 · Evidence conditionActual diets, activity and other concurrent exposuresRequired |
Activity common to all three groups, walnuts common to both MED groups and added green-MED components are recorded as originally described. This is not interpreted as a trial isolating components without actual adherence or concurrent-management differences. |
Information currently required is unverified in the stored summary. Group energy intake, whole diets, activity, medications, management and individual adherence are unverified. Review of existing content remains incomplete. |
Food, weight, activity and management adherence material |
Propose follow-up material distinguishing common from different exposures. No diet or weight-management instructions are given. This is a proposal; no new investigation, calculation or trial is conducted here. |
| 18 |
Partly verified |
Full text not readStored summary read |
N18 · Evidence conditionRegistration identifier and access to actual plansRequired |
The original evidence and citation lists identify NCT03020186. The identifier and historical parent registration verification do not establish current registration reading or isolated-component plans before recruitment. |
Only corresponding stored-summary information is recorded. Detailed original material is unread and review of existing content remains incomplete. Recruitment and registration timing, protocol, SAP, outcome and component hierarchy, and changes remain unread. Review of existing content remains incomplete. |
Original registration identifier, protocol, SAP and changes |
Propose follow-up material distinguishing the preserved identifier from actual plan access. This is a proposal; no new investigation, calculation or trial is conducted here. |
| 19 |
Unverified |
Full text not readStored summary read |
N19 · Evidence conditionMultiple contrasts and analysis hierarchyRequired |
Multiple bundled-diet contrasts and weight-adjusted analyses are not prespecified primary results for isolated components. Parent MRS classification fields are not used as an isolated-effect hierarchy. |
Information currently required is unverified in the stored summary. Pre-recruitment contrasts, outcomes, subgroup analyses, multiplicity, adjustment and SAP are unverified. Review of existing content remains incomplete. |
Plans for three groups, time points, outcomes and subgroup analyses |
Propose follow-up material distinguishing all contrasts from component questions. This is a proposal; no new investigation, calculation or trial is conducted here. |
| 20 |
Partly verified |
Full text not readStored summary read |
N20 · Evidence conditionThe same trial and absence of linked isolated-component replicationRequired |
S01 DIRECT-PLUS includes the same trial's 294 participants, three groups, multiple exposures and time points. Groups, components, registration identifiers and other liver-fat sheets are not added as new independent trials, participants or isolated-component replication. |
Only corresponding stored-summary information is recorded. Detailed original material is unread and review of existing content remains incomplete. Separate direct Mankai-only or green-tea-only trials and independent-family relationships are not linked. Review of existing content remains incomplete. |
Relationships among reports, groups, time points and independent trials |
Propose separate research with the same component study specification. No new totals or independence certification are produced. This is a proposal; no new investigation, calculation or trial is conducted here. |
| 21 |
Unverified |
Full text not readStored summary read |
N21 · Evidence condition18 months and clinical liver-disease eventsRequired |
18 months is the parent bundled-diet imaging-study duration. The original text records absence of clinical liver-disease events and independent confirmation trials. Long-duration imaging changes do not establish liver-disease treatment or prevention by isolated components. |
Information currently required is unverified in the stored summary. Persistence after stopping, clinical events and long-term isolated-component findings are not linked. Review of existing content remains incomplete. |
Imaging surrogates, persistence and clinical outcomes |
Propose follow-up research distinguishing imaging from clinical outcomes. This is a proposal; no new investigation, calculation or trial is conducted here. |
| 22 |
Unverified |
Full text not readStored summary read |
N22 · Evidence conditionApplication to other populations, foods and productsRequired |
Direct material concerns the bundled pattern in the selected adults. Findings are not extended into isolated efficacy for ordinary green tea, other Mankai products, other diets, liver-disease patients or every population. |
Information currently required is unverified in the stored summary. Identity, exposures and direct liver-fat or clinical material for other populations and products are not linked. Review of existing content remains incomplete. |
Direct material by eligibility, disease, formulation and exposure |
Propose separate material for questions with different populations or products. No intake or treatment instructions are given. This is a proposal; no new investigation, calculation or trial is conducted here. |
| 23 |
Partly verified |
Full text not readStored summary read |
N23 · Evidence conditionMixed funding and product-related rolesRequired |
Original wording of public support, California Walnut Commission support, the PI's disclosed Hinoman advisory role and funders' reported lack of involvement in design or analysis is preserved. This is not recast as complete current role or COI verification or isolated-efficacy certification. |
Only corresponding stored-summary information is recorded. Detailed original material is unread and review of existing content remains incomplete. Original funder-role disclosures, products or free support, employee authorship, advisory scope and complete COI material are unverified. Review of existing content remains incomplete. |
Original funding, advisory, product-support, employee-authorship and COI material |
Propose follow-up material distinguishing support types from roles. This is a proposal; no new investigation, calculation or trial is conducted here. |
| 24 |
Unverified |
Full text not readStored summary read |
N24 · Harm-information gaps supplementing the efficacy tableSafety and gaps concerning individuals and productsSupplementary |
Parent safety is unknown, and the original text states that adverse-event ascertainment was not central to the efficacy report. Nut-allergy, caffeine-sensitivity and disease-suitability wording is not used as event rates or isolated-product safety. |
Information currently required is unverified in the stored summary. Event definitions, collection, group denominators, discontinuation and isolated-component, long-term and vulnerable-population harms are unverified. Review of existing content remains incomplete. |
Harm-event collection, exposures, denominators and discontinuation |
Propose follow-up material directly collecting safety information. No diet, liver-disease or weight-management instructions are provided. This is a proposal; no new investigation, calculation or trial is conducted here. |
| 25 |
Partly verified |
Full text not readStored summary read |
N25 · Evidence conditionOriginal grades, axes, languages, dates and correctionsRequired |
Parent C with 46 points, B/S/R1/I1/E~/B1, unrecorded precision, four false flags and empty override reasons, and the subclaim ? and note are preserved. Korean and English text, 2026-09-07 and empty correction and deliberation values are original records, not inherited as subclaim scores or a current completed review. |
Only corresponding stored-summary information is recorded. Detailed original material is unread and review of existing content remains incomplete. Subclaim score, status and axes, new corrections and external comparisons were not produced or performed. Review of existing content remains incomplete. |
Separation of parent C with 46 points, subclaim ? and historical original values |
Update records distinguishing original values, production dates and correction events. This is a proposal; no new investigation, calculation or trial is conducted here. |
| 26 |
Partly verified |
Full text not readStored summary read |
N26 · Evidence conditionHistorical verification and actual summary readingRequired |
Historical full-text, registration and scoring verification is retained as original history. This production used stored summaries and bibliography; papers, registration, protocol, SAP and COI material were unread and access was not attempted. External source links were not tested. |
Only corresponding stored-summary information is recorded. Detailed original material is unread and review of existing content remains incomplete. Detailed historical verification, original-material acquisition, external reading and content review remain pending. Review of existing content remains incomplete. |
Scope of historical review, unread material and links |
Update content distinguishing history from actual access events. This is a proposal; no new investigation, calculation or trial is conducted here. |