Audit: QRS - Black Currant for Health & Longevity

Audit conducted on 15/08/2026 18:39 using AI4L / Opus 5

Iterations

Summary

Items Count
Total 93
Passed 84
Failed 0
N/A 9
Pass Rate 100.00%
  • Total = Passed + Failed + N/A
  • Pass Rate = Passed / (Passed + Failed) × 100
  • N/A items are excluded from the pass rate calculation

1. General Rules

# Description Result Comments
1.1 Every claim, magnitude, label, recommendation, and statement in the QRS is literally supported by content in the source ER. 🟢 Doses (600 mg/day, 210 mg anthocyanins, 75–150 g berries, 1–3 g/day seed oil), all 10 monitoring targets, all benefit/risk tier items, and all gate items trace verbatim or near-verbatim to the ER.
1.2 Where the ER uses cautious phrasing (“not formally studied”, “None documented in human trials to date”, “theoretical concern”, “data are limited”), the QRS uses the same phrasing. 🟢 “No established target; change from own baseline” (markers 8, 10) mirrors the ER’s own hedged wording; at-a-glance retains “less settled” and “has not held up”.
1.3 The QRS never strengthens an ER claim (e.g., “not formally studied” → “not required”) or softens one (e.g., “do not use during pregnancy” → “use with caution during pregnancy”). 🟢 Contraindications remain absolute; the ER’s Caution-level interactions remain in the Key Interactions gate, not escalated or demoted.
1.4 The QRS does not relabel an ER fact under a different decision category. A “Benefit-Modifying Factor” from ER section is not surfaced as a “Caution”; a “Risk-Modifying Factor” is not surfaced as a “Side Effect”; etc. 🟢 Contraindications derive from the ER’s “Populations who should avoid Black Currant”; Key Interactions from the ER’s seven interaction bullets; Benefits/Risks from their own ER sections. No cross-category migration.
1.5 PubMed IDs, study citations, expert names, clinical trial identifiers (NCT*), and brand names appear in the QRS only if they appear in the source ER for the same fact. 🟢 No PMIDs, no NCT identifiers, no expert names (Willems, Ohguro, Chun), and no brand names (CurraNZ, Solaray, Swanson) appear anywhere in the QRS.
1.6 The QRS does not introduce new attributions. 🟢 No sponsor, laboratory, or author attributions are present.

2. Focus, Tone & Audience

# Description Result Comments
2.1 The QRS follows the tone of the ER, which is determined by the ER’s own language, phrasing, and framing. 🟢 Measured, declarative, non-promotional; mirrors the ER’s register throughout.
2.2 The tone of the QRS is simultaneously expert, accessible, objective, and data-driven, but also empowering and encouraging 🟢 Quantified protocol and monitoring cells sit alongside plain-language at-a-glance framing.
2.3 The QRS reads as a trusted, knowledgeable guide rather than a prescriptive doctor 🟢 Protocol cells describe the regimens used in the literature rather than instructing a course of action.
2.4 The QRS avoids language that implies medical or clinical advice 🟢 No imperative clinical instruction in the QRS’s own voice; the footer disclaimer is fixed template text.
2.5 The QRS “presents information” instead of “providing guidance”, “recommending”, or “advising” 🟢 No occurrence of “recommend”, “advise”, or “should” in the QRS’s own voice.
2.6 The QRS never addresses “the reader” directly — it presents evidence, not guidance 🟢 No second-person pronouns anywhere in the document body.
2.7 The QRS is written in plain language, avoiding unnecessary medical jargon 🟢 Technical terms retained (hs-CRP, P1NP, DXA, respiratory exchange ratio) are the ER’s own biomarker names and are unavoidable in the Monitoring table.
2.8 Information is presented in a concise and very compact manner 🟢 Benefit and risk tiers are semicolon-separated single lines; protocol subs are one to two clauses.
2.9 It DOES NOT address the reader directly 🟢 Confirmed by search: no “you”, “your”, or “yours”.
2.10 The target audience is health- and longevity-oriented adults who are risk-aware, proactive, and actively seeking to optimize health or apply the intervention under review. 🟢 Ten-marker monitoring panel, cadence schedule, and format-specific protocols assume a self-quantifying, proactive reader.
2.11 The target audience is willing to employ lifestyle and behavioral changes as well as follow protocols that may be inconvenient, costly, or require effort. 🟢 Retains the metabolic-cart respiratory exchange ratio measurement and DXA scanning, both effortful.
2.12 The document is NOT written for the general population, who are unwilling to employ lifestyle and behavioral changes or follow protocols that may be inconvenient, costly, or require effort. 🟢 Optimal functional ranges (fasting insulin 2–5 µIU/mL, HbA1c 4.8–5.3%) are tighter than conventional clinical cut-offs, as in the ER.
2.13 Framing, takeaways, and risk/benefit weighting throughout the document reflect this audience, including where an intervention’s signal for the average person differs from its signal for this audience. 🟢 The training-adaptation blunting concern and the endurance-training-block interaction are both surfaced, which matter specifically to this audience.
2.14 The document’s own voice frames usage in longevity terms, not “anti-aging” (e.g., “anti-aging clinics”, “anti-aging community”, “anti-aging medicine”). Proper names that contain “anti-aging” (e.g., “American Academy of Anti-Aging Medicine”) are quoted verbatim. 🟢 The string “anti-aging” does not occur; the title uses “Health & Longevity”.
2.15 The document’s own voice uses formal clinical and scientific terminology, not colloquial or consumer-grade language (e.g., “oral medication” not “pill(s)”; “injection” not “shot”; “adverse event” not “bad reaction”). Direct quotes from sources are exempt. 🟢 Formal terminology throughout; the plain-language wording in At-A-Glance (“blood-thinner”) is mandated by item 7.4 and mirrors the ER Conclusion’s own plain register.

3. Template Integrity

# Description Result Comments
3.1 The following labels and headings on the QRS are fixed and not modified: Card and section headings: “Protocol”, “Time to effect”, “Benefits”, “Risk & Side Effects”, “Monitoring”, “Qualitative Assessment”; Gate headings: “Contraindications”, “Key Interactions”; Tier labels: “High”, “Medium”, “Low”, “Speculative”; Table column headers in Monitoring: “Marker”, “Target”, “Why” 🟢 All fixed headings verified verbatim (lines 444, 484, 529, 554, 566, 588, 608, 612–614, 755) and tier labels appear as “High: / Medium: / Low: / Speculative:”.
3.2 All “” from the [qrs_template] are present in the the QRS. 🟢 69 data-qrs-var spans present, forming the complete contiguous set from page_title through qualitative_item_5; the three website= spans (evidence_review, full_review, audit) are also intact.
3.3 Spans that are not addressed in a checklist item are left unchanged 🟢 The website= spans and the empty risks_high span are untouched apart from the display rule required by item 13.5.

4. Formatting

# Description Result Comments
4.1 When the source ER section is empty, the QRS uses the ER’s own empty-state phrasing verbatim. Typical phrasings are “None documented in human trials to date” and “Not formally studied” N/A No ER section drawn on by the QRS is empty; the absent High risk tier is governed by item 13.5, not by empty-state phrasing.
4.2 Where the ER presents a bulleted item as “Label: content”, the QRS uses the ER’s bold label verbatim as the cell or row label. 🟢 “Standard sports-nutrition protocol”, “Whole-food approach”, “Seed oil approach” are the ER’s bold Protocol labels verbatim; interaction labels likewise.
4.3 Labels are not paraphrased, abbreviated, or invented. 🟢 Time-to-effect labels (“Fuel shift”, “Blood flow”, “Bone and ocular change”) use the ER’s own terms from the Practical Considerations “Time to effect” bullet.
4.4 The QRS DOES NOT use emoji indicators (no 🟩, 🟥, 🟨, etc.). Color and emphasis are conveyed through CSS and bold labels. 🟢 Search confirms no tier emoji and no ⚠️ markers; the ER’s “⚠️ Conflicted” flags were correctly stripped.
4.5 The QRS is designed to render on one A4 page. Any section that has more content in the ER than fits the per-section budget is condensed by the LLM, not extended onto a second page. 🟢 Eight Low-tier benefits are compressed into one semicolon-separated line; monitoring “why” cells are single clauses; @page A4 print rule intact.

5. Metadata

# Description Result Comments
5.1 The metadata is placed inside a single HTML comment that is the first element after “<!doctype html>” and before any other comment, head, or body content. 🟢 Lines 2–14, immediately after the doctype on line 1.
5.2 Inside that HTML comment the YAML block is delimited by a line “—” opening and a line “—” closing. Text before the opening “—” is permitted but is not parsed as YAML. 🟢 Opening “—” at line 3, closing “—” at line 13.
5.3 The metadata is not visible in any rendered view of the QRS and is not surfaced by any other element on the sheet. 🟢 Enclosed in an HTML comment; no metadata value is echoed into the body.
5.4 All frontmatter values are trimmed: no leading or trailing whitespace, no surrounding quotes unless the value contains a colon, bracket, or leading special character that requires YAML quoting. 🟢 Only duration: "00:03" is quoted, correctly so because it contains a colon.
5.5 The filename of the source ER is stated as “er_filename: [er_filename]” 🟢 Line 4: er_filename: black_currant_2026-0825-1601_Opus_ER.md.
5.6 Version of the QRS.md file used to create the document is stated as “qrs_prompt_version: [Version of QRS.md]” 🟢 Line 5: qrs_prompt_version: 26.7.02, matching the QRS.md version badge.
5.7 Creation date and time of the document is stated as “qrs_creation_date: [YYYY-MMDD-HHMM]” (e.g., 2026-0501-1430) 🟢 Line 6: qrs_creation_date: 2026-0815-1832.
5.8 The nickname of the AI used to create the document is stated as “qrs_creator_ai_nickname: [qrs_creator_ai_nickname]” 🟢 Line 7: qrs_creator_ai_nickname: Opus.
5.9 The nickname of the AI is just a single word model name without version, etc. (e.g., Opus, Sonnet, Grok, Gemini, ChatGPT) 🟢 “Opus” — single word, no version.
5.10 The full name of the AI used to create the document is stated as “qrs_creator_ai_fullname: [qrs_creator_ai_fullname]” 🟢 Line 8: qrs_creator_ai_fullname: Opus 5.
5.11 The full name of the AI consists of the [qrs_creator_ai_nickname] and the model version number and no additional qualifier (e.g., Opus 4.6, Sonnet 3.2, Grok 4.5, Gemini 3.1, ChatGPT 5.4) 🟢 “Opus 5” — nickname plus version, no qualifier.
5.12 The filename of the document is stated as “qrs_filename: [filename of this document]” 🟢 Line 9 matches the file on disk: black_currant_2026-0825-1601_Opus_QRS.html.
5.13 All frontmatter values are trimmed: no leading or trailing whitespace, no surrounding quotes unless the value contains a colon, bracket, or leading special character that requires YAML quoting. 🟢 Re-verified across all ten keys; no stray whitespace or unnecessary quoting.

6. Page Title & Header

# Description Result Comments
6.1 [page_title] is set to the [canonical_topic] of the ER frontmatter followed by “ - Quick Reference Sheet” (e.g., “Intervention - Quick Reference Sheet”). The [canonical_topic] is HTML-entity-encoded as needed (e.g., &amp; for &) 🟢 Line 22: “Black Currant for Health & Longevity - Quick Reference Sheet”, matching canonical_topic with the ampersand encoded.
6.2 [header_topic] is set to the [canonical_topic] of the ER frontmatter, with HTML entities encoded as needed (e.g., &amp; for &) 🟢 Line 417: “Black Currant for Health & Longevity”.
6.3 [header_subline_date] is set to [qrs_creation_date reformatted as MM/DD/YYYY] 🟢 Line 421: “08/15/2026”, correctly derived from qrs_creation_date 2026-0815-1832.
6.4 [header_subline_model] is set to [qrs_creator_ai_fullname] 🟢 Line 425: “Opus 5”.
6.5 No additional header content appears: no badge, version stamp, AKA / alternate names line, source-AI attribution, audit date, or QRS variant marker. 🟢 Header contains only the title and the template subline; the ER’s “Also known as” line was correctly not carried over.

7. At-A-Glance Section

# Description Result Comments
7.1 [at_a_glance] is dense, execution-oriented summary of the ER Conclusion section 🟢 Condenses all four Conclusion paragraphs: format framing, fuel-shift finding, performance uncertainty, vascular split, and the two named harms.
7.2 [at_a_glance] is no longer than 60 words 🟢 Exactly 60 words, verified by script.
7.3 Every fact in [at_a_glance] is supported by a distinct passage in the ER. 🟢 Each clause maps to a distinct ER Conclusion sentence (food first; week-long fuel shift; unsettled performance; artery widening supported / blood pressure not; enamel and seed-oil harms).
7.4 It DOES NOT use acronyms or technical classifications that require specialist knowledge, uses plain-language terms instead 🟢 No acronyms; “blood-thinner”, “artery widening”, “tooth enamel”, “fuel use” are all lay terms.
7.5 It DOES NOT cite specific trials (names, years, sample sizes, p-values) 🟢 No trial names, years, sample sizes, or p-values.
7.6 It DOES NOT cite effect sizes, relative risks, or statistical results 🟢 No numeric effect estimates; the only quantity is “about a week”.

8. Contraindications

# Description Result Comments
8.1 The section is derived from the ER Key Interactions & Contraindications section 🟢 All four items come from that section’s “Populations who should avoid Black Currant” list.
8.2 [stop_items] represent the Contraindications from the ER 🟢 All four ER avoid-list entries are present, none added.
8.3 Individual [stop_items] are formatted as <li></li> 🟢 Lines 557–561: four <li> elements inside the stop_items span.
8.4 Items are as concise as possible. No trailing explanations, no elaborations, no mechanistic rationale, no attributions, no citations, no study details. No content after an em-dash, en-dash, or hyphen-dash (e.g., “— dose reduction required”, “— reduced efficacy”) — these trailing clauses are stripped. Just the key fact. 🟢 The ER’s trailing “— seed oil in particular” on the bleeding-disorder entry was correctly stripped; no other trailing clauses remain.
8.5 Parenthetical qualifiers from the ER bullet — time windows, severity classes, threshold values, clinical staging — ARE preserved as part of the item, kept as concise as possible (shortened or trimmed where needed to fit the one-page budget, but never dropped entirely). 🟢 “below 50 × 10⁹/L”, “above 3.0”, “within 14 days”, and “irreversible” (MAOI class qualifier) all retained.
8.6 When the ER uses ranking notation inside parens (e.g., “>” for severity ordering) that depends on an explanatory phrase to interpret, normalize the items to a plain comma-separated list rather than carrying through the bare symbol. N/A The ER’s avoid-list uses no ranking notation inside parentheses.
8.7 The section is left empty ONLY IF the ER’s Key Interactions & Contraindications section identifies no population, condition, or scenario for which the intervention should be avoided, deferred, or used only under specialist supervision. 🟢 The section is populated, and the ER does name populations that should avoid the intervention.
8.8 If the section is left empty, an HTML comment inside the [stop_items] span records the ER basis for the absence, naming or quoting the ER text relied on. E.g. N/A The section is not empty.

9. Key Interactions

# Description Result Comments
9.1 The section is derived from the ER Key Interactions & Contraindications section 🟢 All seven items map one-to-one onto the ER’s seven interaction bullets.
9.2 [caution_items] represent the Key Interactions from the ER, excluding any that are already listed as Contraindications 🟢 The MAOI entry is retained because the ER lists reversible-inhibitor caution separately from the irreversible-inhibitor contraindication; no item duplicates a stop_item.
9.3 Individual [caution_items] are formatted as <li></li> 🟢 Lines 569–578: seven <li> elements inside the caution_items span.
9.4 Items are as concise as possible. No trailing explanations, no elaborations, no mechanistic rationale, no attributions, no citations, no study details. No content after an em-dash, en-dash, or hyphen-dash (e.g., “— dose reduction required”, “— reduced efficacy”) — these trailing clauses are stripped. Just the key fact. 🟢 Each item is the ER’s bold label plus its drug list; all “Caution./Monitor.” verdicts, mechanisms, and mitigations were stripped.
9.5 Parenthetical qualifiers from the ER bullet — example drug lists, time windows, severity classes, threshold values, clinical staging — ARE preserved as part of the item, kept as concise as possible (shortened or trimmed where needed to fit the one-page budget, but never dropped entirely). 🟢 All named drug lists preserved; the OTC entry trims “fish oil sold as a supplement drug in some markets” to “fish oil”, a permitted shortening.
9.6 When the ER uses ranking notation inside parens (e.g., “>” for severity ordering) that depends on an explanatory phrase to interpret, normalize the items to a plain comma-separated list rather than carrying through the bare symbol. N/A The ER’s interaction bullets use plain comma-separated drug lists with no ranking notation.
9.7 The section is left empty ONLY IF the ER’s Key Interactions & Contraindications section identifies no interaction, additive effect, or exposure that changes how the intervention is used. 🟢 The section is populated, and the ER identifies seven such interactions.
9.8 If the section is left empty, an HTML comment inside the [caution_items] span records the ER basis for the absence, naming or quoting the ER text relied on. E.g. N/A The section is not empty.

10. Protocol

# Description Result Comments
10.1 The section is derived from the ER Protocol section 🟢 All three cells come from the ER Therapeutic Protocol section’s first three bullets.
10.2 The three sets of [action] items cover the three most important actionable implementation aspects from the ER Protocol section 🟢 The three delivery formats — standardised extract, whole food, seed oil — are the ER’s three distinct actionable regimens; the remaining bullets are modifiers, not standalone protocols.
10.3 If less that three distinct actionable implementation aspects are mentioned in the ER the unused sets are left empty and made invisible, not filled with placeholder text or empty-state phrasing. N/A The ER provides three distinct actionable aspects; all three sets are used.
10.4 All used [action_#label], [action#value], [action#_sub] items are filled with meaningful content derived from the ER Protocol section. 🟢 All nine cells populated; doses (600 mg/day for 7 days, 75–150 g, 1–3 g/day) and qualifiers (35% anthocyanin, 210 mg anthocyanins, 150–500 mg GLA) match the ER exactly.

11. Time to Effect

# Description Result Comments
11.1 The three sets of [time] items cover the three most important time-to-effect aspects from the ER 🟢 Fuel shift (~7 days), blood flow / enzyme inhibition (2 hours), and bone / ocular change (6–24 months) are the three aspects in the ER’s “Time to effect” bullet.
11.2 The sets are picked and ordered by the magnitude of the related benefit 🟢 time_1 maps to the sole High-tier benefit (fat oxidation), time_2 to a Medium-tier benefit (vascular function), time_3 to Low-tier benefits (bone, glaucoma).
11.3 If less that three distinct time-to-effect aspects are mentioned in the ER the unused sets are left empty and made invisible, not filled with placeholder text or empty-state phrasing. N/A The ER provides at least three distinct time-to-effect aspects; all three sets are used.
11.4 All used [time_#label], [time#value], [time#_sub] items are filled with meaningful content derived from the ER. 🟢 All nine cells populated and traceable to the ER’s Practical Considerations “Time to effect” bullet.
11.5 If the ER does not provide any information on time to effect, the section is removed completely from the Protocol Panel N/A The ER does provide time-to-effect information, so the section is correctly retained.

12. Benefits

# Description Result Comments
12.1 The section is derived from the ER Expected Benefits section 🟢 All 14 items are the ER’s benefit headings, in the ER’s own tier grouping and order.
12.2 Key variables are [benefits_high], [benefits_medium], [benefits_low], [benefits_speculative] 🟢 All four spans present (lines 531, 534, 538, 545).
12.3 Items are as concise as possible. No explanations, no elaborations, no effect sizes, no qualifiers, no attributions, no citations, no study details, no mechanistic explanations, etc. Just the key fact. 🟢 Headings only; no Magnitude figures, mechanisms, or “⚠️ Conflicted” qualifiers carried through.
12.4 Parenthetical content — including effect sizes, sample notes, mechanistic hints, and example studies — is stripped, NOT preserved. 🟢 No parentheses appear in any benefit item.
12.5 If no items of a specific sub-section (high, medium, low, speculative) are present the respective is set to “display=none”, not filled with “None documented in human trials to date” or similar empty-state phrasing. N/A All four benefit tiers have items in the ER, so no tier required hiding.

13. Risks

# Description Result Comments
13.1 The section is derived from the ER Potential Risks & Side Effects section 🟢 All seven items are the ER’s risk headings in the ER’s tier grouping and order.
13.2 Key variables are [risks_high], [risks_medium], [risks_low], [risks_speculative] 🟢 All four spans present (lines 590, 591, 595, 599).
13.3 Items are as concise as possible. No explanations, no elaborations, no effect sizes, no qualifiers, no attributions, no citations, no study details, no mechanistic explanations, etc. Just the key fact. 🟢 Headings only; Magnitude figures and the “⚠️ Conflicted” flag on additive blood pressure lowering were stripped.
13.4 Parenthetical content — including frequencies, severity grades, sample notes, mechanistic hints, and example studies — is stripped, NOT preserved. 🟢 No parentheses appear in any risk item.
13.5 If no items of a specific sub-section (high, medium, low, speculative) are present the respective is set to “display=none”, not filled with “None documented in human trials to date” or similar empty-state phrasing. 🟢 The ER has no High-tier risk; line 590 correctly renders <span data-qrs-var="risks_high" style="display: none"></span> with no empty-state text.

14. Monitoring

# Description Result Comments
14.1 The section is derived from the ER Monitoring section 🟢 Table and cadence both come from the ER Monitoring Protocol & Defining Success section.
14.2 All measurable/quantifiable biomarkers from the Monitoring section are listed 🟢 All 10 ER table rows present in ER order: blood pressure, hs-CRP, fasting glucose, fasting insulin, HbA1c, INR, intraocular pressure, serum P1NP, DXA T-score, respiratory exchange ratio; targets match the ER verbatim.
14.3 [monitoring_cadence] is populated with the monitoring cadence/frequency derived from the ER Monitoring section. It is not left with placeholder text or empty. 🟢 Lines 746–749 condense the ER’s two cadence paragraphs, retaining baseline, 1 and 4 weeks, 6 months, 3 months, 6–12 months, 2 weeks after seed-oil change, and 24 months.

15. Qualitative Assessment

# Description Result Comments
15.1 The section is derived from the ER Monitoring section 🟢 All five items come from the ER’s “Qualitative markers worth tracking alongside the labs” list.
15.2 All subjective/qualitative biomarkers from the Monitoring section are listed 🟢 All five ER qualitative bullets present verbatim and in ER order (lines 758–774).

Issues 15/08/2026 18:39

Pass rate 100.00%. No issues found.