Audit: QRS - DHEA for Health & Longevity

Audit conducted on 09/09/2026 05:00 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. 🟢 Spot-checked every populated span against the ER; all content traces to ER text (e.g. action_3_value “DHEA-S first” is supported by ER Risk Mitigation “DHEA-S is measured first”).
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. 🟢 The ER uses no “not formally studied”/”None documented” phrasing; conflict markers and net readings are carried by the tier structure as the checklist prescribes.
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”). 🟢 No claim strengthened or softened; contraindications keep absolute framing, interactions keep caution framing.
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. 🟢 ER contraindication bullet (anti-estrogens, “Absolute contraindication”) sits in Contraindications; all “Caution/Monitor” bullets sit in Key Interactions. No modifying factors surfaced as risks.
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 ids, study names, expert names or brand names anywhere in the QRS.
1.6 The QRS does not introduce new attributions. 🟢 No attributions introduced; EndoCeutics/Life Extension funding attributions from the ER are omitted rather than reassigned.

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. 🟢 Matches the ER’s measured, evidence-first register.
2.2 The tone of the QRS is simultaneously expert, accessible, objective, and data-driven, but also empowering and encouraging 🟢 Expert, objective and data-driven; tiering and targets give the reader a usable decision frame.
2.3 The QRS reads as a trusted, knowledgeable guide rather than a prescriptive doctor 🟢 Presents evidence and reference ranges rather than instructing a patient.
2.4 The QRS avoids language that implies medical or clinical advice 🟢 No imperative clinical instructions; content is stated descriptively.
2.5 The QRS “presents information” instead of “providing guidance”, “recommending”, or “advising” 🟢 No “recommend”, “advise” or “you should” constructions.
2.6 The QRS never addresses “the reader” directly — it presents evidence, not guidance 🟢 No second-person address anywhere in the document.
2.7 The QRS is written in plain language, avoiding unnecessary medical jargon 🟢 Plain language throughout; retained acronyms (DHEA-S, HDL, PSA, CYP3A4) are decision-relevant identifiers used verbatim by the ER.
2.8 Information is presented in a concise and very compact manner 🟢 Every field is a compressed phrase; rationales, citations and effect sizes are stripped.
2.9 It DOES NOT address the reader directly 🟢 Confirmed by search: no you/your/we/our in the rendered text.
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. 🟢 Content assumes a proactive reader who will test DHEA-S, track eight biomarkers and titrate.
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. 🟢 Protocol and monitoring cadence presuppose willingness to run repeat lab panels.
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. 🟢 Not pitched at a general audience; assumes lab access and biomarker literacy.
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. 🟢 Weighting mirrors the ER: replacement and intravaginal use rated high, general longevity use rated low.
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; only “anti-doping”, which is the ER’s own term.
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. 🟢 Clinical register throughout; At-A-Glance plain-language wording is ER-verbatim and required by 7.4.

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” 🟢 Diff against [qrs_template] confirms all fixed headings, gate headings, tier labels and Monitoring column headers are byte-identical.
3.2 All “…” from the [qrs_template] are present in the the QRS. 🟢 Diff of data-qrs-var names against the template: identical set, with the repeatable marker_#/qualitative_item_# rows expanded to 1-8 and 1-7.
3.3 Spans that are not addressed in a checklist item are left unchanged 🟢 Full-file diff against the template shows changes only inside variable spans, plus the display:none on risks_medium mandated by 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 mapped to the QRS is empty; the ER contains no “None documented in human trials to date” or “Not formally studied” phrasing to carry over. The empty Medium risk tier is governed by 13.5.
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. 🟢 Protocol cell labels (“Standard replacement dose”, “Best time of day”, “Baseline biomarkers that drive the protocol”) and all eight Monitoring row labels are the ER’s bold labels verbatim.
4.3 Labels are not paraphrased, abbreviated, or invented. 🟢 No label paraphrased or invented; the Time to Effect labels are lifted from the ER’s “Time to effect” sentence.
4.4 The QRS DOES NOT use emoji indicators (no 🟩, 🟥, 🟨, etc.). Color and emphasis are conveyed through CSS and bold labels. 🟢 Unicode scan finds no emoji; the ER’s tier emoji 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. 🟢 Every field is condensed to a phrase and all rationales/citations stripped; the remaining volume (8 contraindications, 8 interactions, 8 markers, 7 qualitative items) is mandated by 8.2, 9.2, 14.2 and 15.2.

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. 🟢 The metadata comment is the first element after <!doctype html> (lines 2-14), before <html>.
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. 🟢 Opened and closed by bare “—” lines; the comment’s title text precedes the opening delimiter.
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. 🟢 Wrapped in an HTML comment and not duplicated by any visible element.
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. 🟢 All values trimmed; only duration: “00:03” is quoted, which is required because the value contains a colon.
5.5 The filename of the source ER is stated as “er_filename: [er_filename]” 🟢 er_filename: dhea_2026-0909-0001_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]” 🟢 qrs_prompt_version: 26.7.02 matches the version badge of QRS.md.
5.7 Creation date and time of the document is stated as “qrs_creation_date: [YYYY-MMDD-HHMM]” (e.g., 2026-0501-1430) 🟢 qrs_creation_date: 2026-0909-0444, in YYYY-MMDD-HHMM form.
5.8 The nickname of the AI used to create the document is stated as “qrs_creator_ai_nickname: [qrs_creator_ai_nickname]” 🟢 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” is a single word with no version or qualifier.
5.10 The full name of the AI used to create the document is stated as “qrs_creator_ai_fullname: [qrs_creator_ai_fullname]” 🟢 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” is nickname plus version number with no additional qualifier.
5.12 The filename of the document is stated as “qrs_filename: [filename of this document]” 🟢 qrs_filename: dhea_2026-0909-0001_Opus_QRS.html matches the file on disk.
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. 🟢 No stray whitespace or unnecessary quoting in any frontmatter value.

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 &) 🟢 DHEA for Health & Longevity - Quick Reference Sheet, with the ampersand entity-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 &) 🟢 header_topic is “DHEA for Health & Longevity”, the ER canonical_topic entity-encoded.
6.3 [header_subline_date] is set to [qrs_creation_date reformatted as MM/DD/YYYY] 🟢 header_subline_date is 09/09/2026, the MM/DD/YYYY form of qrs_creation_date 2026-0909-0444.
6.4 [header_subline_model] is set to [qrs_creator_ai_fullname] 🟢 header_subline_model is “Opus 5”, equal to qrs_creator_ai_fullname.
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 block is byte-identical to the template apart from the three variable spans; no badge, AKA line or audit stamp.

7. At-A-Glance Section

# Description Result Comments
7.1 [at_a_glance] is dense, execution-oriented summary of the ER Conclusion section 🟢 Condenses the ER Conclusion into where DHEA works, where it fails, and its drawbacks.
7.2 [at_a_glance] is no longer than 60 words 🟢 59 words.
7.3 Every fact in [at_a_glance] is supported by a distinct passage in the ER. 🟢 All five facts map to distinct Conclusion passages (adrenal decline, adrenal failure, vaginal tissue, failed capsule trials, drawbacks).
7.4 It DOES NOT use acronyms or technical classifications that require specialist knowledge, uses plain-language terms instead 🟢 No acronyms; “adrenal glands” is rendered as “the glands above the kidneys” and HDL as “protective cholesterol”.
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 effect sizes, relative risks or statistical results.

8. Contraindications

# Description Result Comments
8.1 The section is derived from the ER Key Interactions & Contraindications section 🟢 All eight items derive from the ER Key Interactions & Contraindications section.
8.2 [stop_items] represent the Contraindications from the ER 🟢 Carries the ER’s absolute contraindication (anti-estrogens) plus all seven entries of the ER’s “Populations who should avoid DHEA” list.
8.3 Individual [stop_items] are formatted as <li></li> 🟢 Eight <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. 🟢 Rationale clauses stripped (e.g. “given repeated reports of activation and mania” reduced to “Bipolar disorder”); no trailing dash 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). 🟢 Thresholds and classes preserved: PSA above 4 ng/mL, IPSS above 19, Child-Pugh Class C, “prohibited at all times”.
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 uses no ranking notation inside parentheses in this section.
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 identify populations that should avoid DHEA.
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 eight items derive from the ER Key Interactions & Contraindications section.
9.2 [caution_items] represent the Key Interactions from the ER, excluding any that are already listed as Contraindications 🟢 Covers all eight ER interaction bullets and correctly excludes the anti-estrogen bullet already listed as a contraindication.
9.3 Individual [caution_items] are formatted as <li></li> 🟢 Eight <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. 🟢 Mechanistic rationale and mitigations dropped; the ER’s em-dash constructions converted to parenthetical drug lists.
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). 🟢 Named example drugs preserved for every class (warfarin/apixaban/clopidogrel/aspirin, glipizide/glimepiride, prednisone/hydrocortisone/dexamethasone, ketoconazole/ritonavir/clarithromycin/grapefruit juice, cimetidine/ibuprofen/naproxen, soy isoflavones, pregnenolone/7-keto-DHEA/Tribulus/boron, resistance training/sauna).
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 uses no ranking notation inside parentheses in this section.
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 does identify interactions that change how DHEA is used.
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 action sets come from the ER Therapeutic Protocol section.
10.2 The three sets of [action] items cover the three most important actionable implementation aspects from the ER Protocol section 🟢 Dose, timing and the baseline biomarkers that set the dose are the three decision-bearing aspects of that section.
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 well over three 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 action fields carry ER-derived content; action_1_sub and action_3_sub are near-verbatim ER text.

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 🟢 Mood, sexual function & skin, and bone density are exactly the three aspects named in the ER’s “Time to effect” bullet.
11.2 The sets are picked and ordered by the magnitude of the related benefit 🟢 Mood maps to the High-tier benefit “Reduced Depressive Symptoms” and is placed first; the two remaining aspects both map to Low-tier benefits.
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 names three 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 time fields populated from the ER; the windows 4-8 weeks, 3-6 months and 12 months are the ER’s own.
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 items map to headings in the ER Expected Benefits section.
12.2 Key variables are [benefits_high], [benefits_medium], [benefits_low], [benefits_speculative] 🟢 All four benefit spans present and populated.
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 item is the ER heading reduced to a phrase; no effect sizes, citations or mechanisms.
12.4 Parenthetical content — including effect sizes, sample notes, mechanistic hints, and example studies — is stripped, NOT preserved. 🟢 No parenthetical content carried through; the ER’s “Conflicted” markers and magnitudes are dropped.
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 contain items in the ER, so no span needed hiding.

13. Risks

# Description Result Comments
13.1 The section is derived from the ER Potential Risks & Side Effects section 🟢 All items map to headings in the ER Potential Risks & Side Effects section.
13.2 Key variables are [risks_high], [risks_medium], [risks_low], [risks_speculative] 🟢 All four risk spans present.
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. 🟢 Each item is the ER heading reduced to a phrase; no frequencies, effect sizes or mechanisms.
13.4 Parenthetical content — including frequencies, severity grades, sample notes, mechanistic hints, and example studies — is stripped, NOT preserved. 🟢 The “(HDL)” parenthetical in the ER heading is stripped and the term spelled out.
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’s Medium risk tier holds no items, and risks_medium carries style=”display: none” rather than empty-state text.

14. Monitoring

# Description Result Comments
14.1 The section is derived from the ER Monitoring section 🟢 Table and cadence come from the ER Monitoring Protocol & Defining Success section.
14.2 All measurable/quantifiable biomarkers from the Monitoring section are listed 🟢 All eight ER biomarker rows present (DHEA-S, total and free testosterone, estradiol, HDL cholesterol, fasting glucose and HbA1c, PSA, ALT and AST, hematocrit) with targets and rationale 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. 🟢 monitoring_cadence reproduces the ER cadence sentence, including the annual PSA in men.

15. Qualitative Assessment

# Description Result Comments
15.1 The section is derived from the ER Monitoring section 🟢 Derived from the ER’s qualitative-marker list in the Monitoring section.
15.2 All subjective/qualitative biomarkers from the Monitoring section are listed 🟢 All seven ER qualitative markers are listed in ER order.

Issues 09/09/2026 05:00

Pass rate 100.00%. No issues found.

Issues 09/09/2026 04:53

  1. 11.4 — Time-to-effect sub carries no timing: [time_2_sub] (line 519) states “Libido and sexual satisfaction is the endpoint with the most consistent trial support”, which explains nothing about the “3–6 months” value above it, duplicates qualitative_item_4’s ER source, and contains a subject-verb agreement error.

Fixes 09/09/2026 04:53

  1. 11.4 — Time-to-effect sub carries no timing: Replaced [time_2_sub] with “Sexual-function and skin changes emerge together in this window; libido has the most consistent trial support.” — this anchors the cell to the ER’s “sexual-function and skin changes at 3–6 months” statement and resolves the subject-verb agreement error.