Audit: QRS - Procyanidin C1 as a Senolytic Therapy

Audit conducted on 17/09/2026 13:28 using AI4L / Opus 5

Iterations

Summary

Items Count
Total 93
Passed 87
Failed 0
N/A 6
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. 🟢 Every element traced: protocol doses (ER 386, 388, 396), time-to-effect (ER 443), contraindications (ER 350-360), interactions (ER 326-348), benefit/risk tiers, all nine monitoring targets (ER 477-487) and cadence (ER 475).
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. 🟢 “Unknown in humans” (line 497), “No biomarker confirms an effect within days” (500), “which has reported nothing” (525), “No established target; track change from own baseline” (674, 771) all mirror ER wording.
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”). 🟢 Absolute items stay absolute (malignancy item at 570 keeps “unless scheduled by the treating oncologist”); speculative tiers stay speculative.
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. 🟢 Gates draw only on the ER Key Interactions & Contraindications section; no Benefit- or Risk-Modifying Factor is surfaced as a gate or a risk.
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, NCT numbers, author names or brand names appear anywhere in the QRS.
1.6 The QRS does not introduce new attributions. 🟢 Only generic references carried from the ER (“the only registered human study”, “senolytic researchers”).

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. 🟢 Same sober, evidence-first register as the ER Conclusion.
2.2 The tone of the QRS is simultaneously expert, accessible, objective, and data-driven, but also empowering and encouraging 🟢 Presents actionable protocol, monitoring panel and qualitative tracking alongside the honest evidence gap.
2.3 The QRS reads as a trusted, knowledgeable guide rather than a prescriptive doctor 🟢 States what the studies used; no imperatives directed at a patient.
2.4 The QRS avoids language that implies medical or clinical advice 🟢 Regimens are described as study arms and researcher patterns, not prescriptions.
2.5 The QRS “presents information” instead of “providing guidance”, “recommending”, or “advising” 🟢 No “recommended”, “should”, or “advised” anywhere in the sheet.
2.6 The QRS never addresses “the reader” directly — it presents evidence, not guidance 🟢 No second-person pronouns; “track change from own baseline” avoids “your”.
2.7 The QRS is written in plain language, avoiding unnecessary medical jargon 🟢 Technical terms retained only where they are the ER’s own labels (BCL-2, CYP3A4, INR); marker names spelled out in full in the Monitoring table.
2.8 Information is presented in a concise and very compact manner 🟢 Tiers collapsed to single semicolon-separated lines; gate items reduced to the key fact.
2.9 It DOES NOT address the reader directly 🟢 Confirmed: no direct address in any span.
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. 🟢 Assumes willingness to run a 12-week regimen with laboratory monitoring.
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. 🟢 Nine-marker panel, twice-daily home blood-pressure logging, cycle scheduling.
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. 🟢 Content assumes access to laboratory testing and adherence to an episodic dosing schedule.
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. 🟢 Empty human-evidence tiers are hidden rather than dressed up; speculative tier carries the rodent and cell evidence explicitly.
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. 🟢 “anti-aging” does not appear; “late-life”, “vascular aging” and “age-related” are used instead.
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)”; “oral” / “administered orally” not “taken by mouth” / “given by mouth”; “injection” not “shot”; “adverse event” not “bad reaction”). This holds on EVERY surface, including the QRS lede — the stricter plain-language bar (see 2.7) does not license lay phrasing for route of administration. Direct quotes from sources are exempt. 🟢 Route of administration given as “oral regimen” (448, 461); lay pairings in the gates (“blood thinners”, “painkillers”) are the ER’s own bold labels carried verbatim per 4.2.

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 headings, gate headings, tier labels and table headers match the template byte-for-byte.
3.2 All “<span data-qrs-var=”NAME”>…</span>” from the [qrs_template] are present in the the QRS. 🟢 All 38 template spans present; marker_#* expanded to 1-9 and qualitative_item# to 1-7.
3.3 Spans that are not addressed in a checklist item are left unchanged 🟢 The three website= spans (evidence_review, audit, full_review) and the entire style block are byte-identical to the template.

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 source ER section is empty; the empty High/Medium tiers are governed by 12.5 / 13.5, which require display:none instead.
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. 🟢 “Continuous low-dose oral regimen”, “Intermittent high-dose oral regimen”, “Best time of day”, “Time to effect” and all gate labels are the ER bold labels verbatim.
4.3 Labels are not paraphrased, abbreviated, or invented. 🟢 Monitoring marker names match the ER table verbatim; the two additional time cells label distinct facts inside the ER’s single Time-to-effect bullet, for which the ER provides no label.
4.4 The QRS DOES NOT use emoji indicators (no 🟩, 🟥, 🟨, etc.). Color and emphasis are conveyed through CSS and bold labels. 🟢 No emoji in the file; ER tier emoji and the ⚠️/⭕️ tags are 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. 🟢 Thirteen speculative benefits, five risks, nine contraindications and eleven interactions are each compressed to headline form with all rationale removed.

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.
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 “—” line 3, closing “—” 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 element repeats the YAML block.
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, which the embedded colon requires.
5.5 The filename of the source ER is stated as “er_filename: [er_filename]” 🟢 Line 4: procyanidin_c1_senolytic_2026-0917-1113_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: 26.9.11, 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: 2026-0917-1323.
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: 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) 🟢 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: 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 actual filename.
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 nine keys, including git_user and git_issue.

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 20: “Procyanidin C1 as a Senolytic Therapy - Quick Reference Sheet”; no entity encoding required.
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 415 matches the ER canonical_topic exactly.
6.3 [header_subline_date] is set to [qrs_creation_date reformatted as MM/DD/YYYY] 🟢 Line 419: 09/17/2026, from qrs_creation_date 2026-0917-1323.
6.4 [header_subline_model] is set to [qrs_creator_ai_fullname] 🟢 Line 423: 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 holds only the title and the template subline.

7. At-A-Glance Section

# Description Result Comments
7.1 [at_a_glance] is dense, execution-oriented summary of the ER Conclusion section 🟢 Lines 431-437 condense the three Conclusion paragraphs: the two-speed mechanism, the missing human data and unmeasured tissue exposure, and the modest harm profile.
7.2 [at_a_glance] is no longer than 60 words 🟢 58 words.
7.3 Every fact in [at_a_glance] is supported by a distinct passage in the ER. 🟢 Each clause maps to ER 521-525 (two-speed behaviour, broad animal record, unmeasured human tissue exposure, the five listed harms).
7.4 It DOES NOT use acronyms or technical classifications that require specialist knowledge, uses plain-language terms instead 🟢 “worn-out cells” not “senescent cells”; no acronyms, no senolytic/senomorphic classification terms.
7.5 It DOES NOT cite specific trials (names, years, sample sizes, p-values) 🟢 No trial identifiers or sample sizes.
7.6 It DOES NOT cite effect sizes, relative risks, or statistical results 🟢 No numbers at all.

8. Contraindications

# Description Result Comments
8.1 The section is derived from the ER Key Interactions & Contraindications section 🟢 Sourced from the “Populations who should avoid Procyanidin C1” list and the chemotherapy/radiotherapy bullet (ER 332, 350-360).
8.2 [stop_items] represent the Contraindications from the ER 🟢 All nine ER avoidance populations reproduced (lines 565-576); the ER’s absolute chemotherapy contraindication is carried by the malignancy item.
8.3 Individual [stop_items] are formatted as <li></li> 🟢 Nine <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. 🟢 ER trailing clauses after em-dashes (“— no reproductive toxicity or lactation data exist”, “— senescent-cell burden is low…”) are stripped; no dashes remain in any item.
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 100 × 10⁹/L”, “INR above 3.0”, “Within 14 days”, “(Child-Pugh Class C)”, “ferritin below 30 ng/mL”, “under 18 years” 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. 🟢 The ER uses no ranking notation here; thresholds are rendered as words (“above”, “below”), not bare symbols.
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 ER names nine such populations and the section is correctly populated, not empty.
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. <!– empty: ER names no population that should avoid the intervention –> 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 🟢 Sourced from ER 326-348.
9.2 [caution_items] represent the Key Interactions from the ER, excluding any that are already listed as Contraindications 🟢 All eleven interaction bullets carried; the chemotherapy/radiotherapy bullet is correctly excluded because it appears as a contraindication.
9.3 Individual [caution_items] are formatted as <li></li> 🟢 Eleven <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. 🟢 All ER mechanism sentences and “Mitigation:” clauses dropped; each item is the bold label alone.
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). 🟢 Every ER example-drug list is preserved in full (warfarin/apixaban/rivaroxaban/dabigatran, navitoclax/venetoclax, simvastatin/tacrolimus/ciclosporin, etc.).
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. 🟢 ER parentheses contain plain comma-separated drug lists only; no ranking symbols carried through.
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 ER names twelve interactions and the section is correctly populated, not empty.
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. <!– empty: ER names no interaction that changes how the intervention is used –> N/A The section is not empty.

10. Protocol

# Description Result Comments
10.1 The section is derived from the ER Protocol section 🟢 Drawn from ER Therapeutic Protocol bullets at 386, 388, 390 and 396.
10.2 The three sets of [action] items cover the three most important actionable implementation aspects from the ER Protocol section 🟢 The two competing dosing regimens plus timing are the only directly executable parameters in the ER protocol; half-life and polymorphism bullets are explanatory.
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 supplies three or more 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. 🟢 Lines 446-485: labels are ER bold labels, values are ER doses/schedules, subs carry the ER’s own caveats.

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 🟢 The ER’s Time-to-effect bullet (443) contains exactly three facts: unknown in humans, rodent change over 2-4 months, human skin measurement at 6 and 12 weeks.
11.2 The sets are picked and ordered by the magnitude of the related benefit 🟢 Leads with the overarching human unknown, then the rodent survival/function findings (the largest claimed benefit), then the smaller skin endpoints.
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 Three distinct aspects exist; 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. 🟢 Lines 492-528; values “Unknown in humans”, “2-4 months”, “6 and 12 weeks” all match ER 443.
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 provides 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 🟢 Tiers map to ER 150-224.
12.2 Key variables are [benefits_high], [benefits_medium], [benefits_low], [benefits_speculative] 🟢 All four spans present at lines 536-555.
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. 🟢 Each ER heading reduced to its headline claim; no magnitudes, confidence intervals or study counts carried over.
12.4 Parenthetical content — including effect sizes, sample notes, mechanistic hints, and example studies — is stripped, NOT preserved. 🟢 No parentheses in either benefits span.
12.5 If no items of a specific sub-section (high, medium, low, speculative) are present the respective <SPAN> is set to “display=none”, not filled with “None documented in human trials to date” or similar empty-state phrasing. 🟢 benefits_high and benefits_medium are empty with style="display: none" (lines 536-537), matching the ER’s empty High and Medium tiers.

13. Risks

# Description Result Comments
13.1 The section is derived from the ER Potential Risks & Side Effects section 🟢 Tiers map to ER 246-306.
13.2 Key variables are [risks_high], [risks_medium], [risks_low], [risks_speculative] 🟢 All four spans present at lines 623-639.
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. 🟢 All five Low and all five Speculative risks reduced to headline form; risk ratios and absorption percentages dropped.
13.4 Parenthetical content — including frequencies, severity grades, sample notes, mechanistic hints, and example studies — is stripped, NOT preserved. 🟢 No parentheses in either risks span.
13.5 If no items of a specific sub-section (high, medium, low, speculative) are present the respective <SPAN> is set to “display=none”, not filled with “None documented in human trials to date” or similar empty-state phrasing. 🟢 risks_high and risks_medium are empty with style="display: none" (lines 623-624), matching the ER’s empty High and Medium tiers.

14. Monitoring

# Description Result Comments
14.1 The section is derived from the ER Monitoring section 🟢 Table and cadence taken from ER Monitoring Protocol & Defining Success (475-487).
14.2 All measurable/quantifiable biomarkers from the Monitoring section are listed 🟢 All nine ER biomarker rows are present in order with matching targets and rationales.
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 784-788 reproduce the ER cadence including the anticoagulant clotting-time advance and the four-week home blood-pressure log.

15. Qualitative Assessment

# Description Result Comments
15.1 The section is derived from the ER Monitoring section 🟢 Taken from the qualitative-marker list at ER 491-497.
15.2 All subjective/qualitative biomarkers from the Monitoring section are listed 🟢 All seven ER qualitative markers are present verbatim (lines 796-822).

Issues 17/09/2026 13:28

Pass rate 100.00%. No issues found.