Audit: QRS - Magnesium Bisglycinate for Health & Longevity

Audit conducted on 23/08/2026 06:44 using AI4L / Opus 5

Iterations

Summary

Items Count
Total 93
Passed 83
Failed 0
N/A 10
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. 🟢 Dose range 200–400 mg/day, 10–14% elemental, 250 mg sleep trial, 8–12 weeks, all nine biomarker targets and the cadence all trace to ER lines 376–384, 425 and 453–463.
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. 🟢 At-A-Glance keeps the ER’s hedge (“though thinly evidenced”) mirroring ER line 497; Speculative tiers retained for both benefits and risks.
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 and interactions carry the ER’s severity unchanged; benefit tiers match the ER’s own tier assignment.
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 come from the ER’s “Populations who should avoid” list; Key Interactions from the ER interaction bullets; no modifying factors were promoted into either gate.
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 identifiers, author names or brand names appear anywhere in the QRS.
1.6 The QRS does not introduce new attributions. 🟢 Only unattributed references such as “the sleep trials” and “the trial literature”, both present in ER lines 376 and 382.

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. 🟢 Sober, deflationary register matching the ER conclusion, including the diet-versus-capsule distinction.
2.2 The tone of the QRS is simultaneously expert, accessible, objective, and data-driven, but also empowering and encouraging 🟢 Quantified targets and ranges throughout, framed neutrally without alarm or promotion.
2.3 The QRS reads as a trusted, knowledgeable guide rather than a prescriptive doctor 🟢 Descriptive constructions (“where the trial literature clusters”, “As used in the sleep trials”) rather than directives.
2.4 The QRS avoids language that implies medical or clinical advice 🟢 No imperatives; protocol cells report what trials used rather than instructing.
2.5 The QRS “presents information” instead of “providing guidance”, “recommending”, or “advising” 🟢 No instance of recommend/advise/should in the QRS body.
2.6 The QRS never addresses “the reader” directly — it presents evidence, not guidance 🟢 No second-person pronouns anywhere in the document.
2.7 The QRS is written in plain language, avoiding unnecessary medical jargon 🟢 Technical terms retained only where the ER heading requires them (hypermagnesemia, eGFR); no gratuitous jargon added.
2.8 Information is presented in a concise and very compact manner 🟢 Gate and tier items are noun phrases; monitoring “Why” cells are single clauses.
2.9 It DOES NOT address the reader directly 🟢 Confirmed: no “you”/”your” in the source.
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. 🟢 Optimal functional ranges (serum magnesium 0.85–0.95 mmol/L, HbA1c ≤5.4%) rather than conventional reference cutoffs.
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-biomarker panel, home blood pressure baseline and seven qualitative trackers assume a willing, effortful reader.
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. 🟢 Red blood cell magnesium and parathyroid hormone testing are beyond general-population expectations.
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. 🟢 At-A-Glance states the key differential explicitly: “in adults eating well, the same doses move very little”.
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. 🟢 “Longevity” in the title; the phrase “anti-aging” does not occur.
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. 🟢 Terms used (“blood sugar”, “capsules”) are the ER’s own register at ER lines 168 and 499.

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 twelve fixed strings byte-identical to the template, including the template’s own unescaped “Risk & Side Effects” at line 610.
3.2 All “…” from the [qrs_template] are present in the the QRS. 🟢 68 spans present = 38 template spans with marker_#* expanded to nine rows (+24) and qualitative_item# to seven items (+6).
3.3 Spans that are not addressed in a checklist item are left unchanged 🟢 The three non-variable spans (website=”evidence_review”, website=”audit”, website=”full_review”) and the entire head/CSS block are unchanged from 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 that feeds the QRS is empty.
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 dose range”, “Reading the label correctly” and “Timing” match the ER Protocol bold labels at ER lines 376, 378 and 382.
4.3 Labels are not paraphrased, abbreviated, or invented. 🟢 All nine marker names match the ER table verbatim; Time-to-Effect labels are lifted phrases from ER line 425.
4.4 The QRS DOES NOT use emoji indicators (no 🟩, 🟥, 🟨, etc.). Color and emphasis are conveyed through CSS and bold labels. 🟢 No emoji present; the ER’s “⚠️ Conflicted” markers 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. 🟢 Every section is condensed to its minimum form — tier lines are single sentences, gate items are noun phrases, monitoring “Why” cells are single clauses, and the cadence is one sentence.

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; nothing precedes it but the doctype at 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; the “QRS — Metadata” preamble precedes the opener.
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 repeated in the header, footer or 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 the value contains a colon.
5.5 The filename of the source ER is stated as “er_filename: [er_filename]” 🟢 Line 4: er_filename: magnesium_bisglycinate_2026-0823-0441_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: 2026-0823-0628.
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: magnesium_bisglycinate_2026-0823-0441_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. 🟢 All nine keys carry single-space-delimited, untrimmed-free values; quoting used only where YAML requires it.

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: “Magnesium Bisglycinate for Health & Longevity - Quick Reference Sheet”.
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: “Magnesium Bisglycinate for Health & Longevity”.
6.3 [header_subline_date] is set to [qrs_creation_date reformatted as MM/DD/YYYY] 🟢 Line 421: “08/23/2026” from qrs_creation_date 2026-0823-0628.
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’s stock subline; the ER’s “Also known as” line was 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 🟢 Compresses all three conclusion paragraphs (ER lines 497–499): tolerability rationale, who actually responds, and the diet-versus-capsule signal.
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. 🟢 Glycine binding and bowel tolerance → ER 497; responder profile → ER 499; magnesium-rich food and mortality → ER 499.
7.4 It DOES NOT use acronyms or technical classifications that require specialist knowledge, uses plain-language terms instead 🟢 No acronyms; “blood sugar” used rather than glycaemic control, “living longer” rather than all-cause mortality.
7.5 It DOES NOT cite specific trials (names, years, sample sizes, p-values) 🟢 No trial name, year, sample size or p-value appears.
7.6 It DOES NOT cite effect sizes, relative risks, or statistical results 🟢 No numeric effect estimate or confidence interval appears.

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 Magnesium Bisglycinate” list at ER lines 350–354.
8.2 [stop_items] represent the Contraindications from the ER 🟢 All five ER avoid-list entries are present, in ER order.
8.3 Individual [stop_items] are formatted as <li></li> 🟢 Five discrete <li> elements at lines 573–583.
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 mechanistic tail on myasthenia gravis (“where raised magnesium worsens muscle weakness”) is correctly stripped; no dashes carry trailing clauses.
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). 🟢 “stage 4 or worse (eGFR below 30 mL/min/1.73 m²)”, “below 50 beats per minute” and “without cardiology oversight” are 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 uses no ranking notation inside parentheses in its contraindication list.
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 five such populations, and the section is correctly populated rather than 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. 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 ten items map one-to-one onto the ER interaction bullets at lines 328–346.
9.2 [caution_items] represent the Key Interactions from the ER, excluding any that are already listed as Contraindications 🟢 All ten ER interactions present; none duplicates an entry in the Contraindications gate.
9.3 Individual [caution_items] are formatted as <li></li> 🟢 Ten discrete <li> elements at lines 591–600.
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. 🟢 The ER’s Caution/Monitor/Additive labels, mechanisms, mitigations and the Gommers et al. citation are all stripped; no trailing dash clauses remain.
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 bullet carrying a drug list keeps a representative parenthetical (e.g. “(ciprofloxacin, doxycycline)”, “(spironolactone, amiloride)”, “(omeprazole, pantoprazole)”) — trimmed for the page budget, never dropped.
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 its interaction list.
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 ten such interactions, and the section is correctly populated rather than 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. 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 trace to the ER Therapeutic Protocol bullets at lines 376, 378 and 382.
10.2 The three sets of [action] items cover the three most important actionable implementation aspects from the ER Protocol section 🟢 Dose range, elemental-versus-compound label reading (the ER’s “most frequent error”, line 427) and timing are the three decision-critical bullets.
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 Protocol section contains ten actionable bullets, well above three.
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 variables carry ER-derived content; no placeholder remains.

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 🟢 Blood pressure and glucose, sleep, and tissue repletion — exactly the three horizons given at ER line 425.
11.2 The sets are picked and ordered by the magnitude of the related benefit 🟢 Blood pressure and glucose (High tier, the ER’s “best-quantified benefit”, line 463) first, sleep (High tier) second, repletion (Medium tier) third.
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 supplies three distinct time-to-effect horizons.
11.4 All used [time_#label], [time#value], [time#_sub] items are filled with meaningful content derived from the ER. 🟢 All nine time variables populated; subs trace to ER lines 425 and 451.
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 at line 425.

12. Benefits

# Description Result Comments
12.1 The section is derived from the ER Expected Benefits section 🟢 All fourteen items map to ER benefit headings at lines 158–242.
12.2 Key variables are [benefits_high], [benefits_medium], [benefits_low], [benefits_speculative] 🟢 All four spans present and populated at lines 540–563.
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 tier is a semicolon-separated list of bare ER headings; no magnitude, mechanism or author name carried over.
12.4 Parenthetical content — including effect sizes, sample notes, mechanistic hints, and example studies — is stripped, NOT preserved. 🟢 No parentheses appear in any benefits tier.
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 ER benefit tiers contain items, 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 seven items map to ER risk headings at lines 266–308.
13.2 Key variables are [risks_high], [risks_medium], [risks_low], [risks_speculative] 🟢 All four spans present and populated at lines 612–629.
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. 🟢 Bare ER headings only; the 11–37% event rates, risk ratio and Epworth figures are all omitted.
13.4 Parenthetical content — including frequencies, severity grades, sample notes, mechanistic hints, and example studies — is stripped, NOT preserved. 🟢 No parentheses appear in any risks tier; the ER’s “(dangerously high blood magnesium)” gloss is stripped.
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. N/A All four ER risk tiers contain items, so no span needed hiding.

14. Monitoring

# Description Result Comments
14.1 The section is derived from the ER Monitoring section 🟢 Table and cadence both drawn from the ER Monitoring Protocol & Defining Success section at lines 451–463.
14.2 All measurable/quantifiable biomarkers from the Monitoring section are listed 🟢 All nine ER biomarker rows present with matching optimal ranges, in ER order.
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 764–768 carry both the 8–12 week / 6–12 month schedule and the earlier-checkpoint exception from ER line 451.

15. Qualitative Assessment

# Description Result Comments
15.1 The section is derived from the ER Monitoring section 🟢 Sourced from the qualitative marker list at ER lines 467–473.
15.2 All subjective/qualitative biomarkers from the Monitoring section are listed 🟢 All seven ER qualitative markers present, in ER order.

Issues 23/08/2026 06:44

Pass rate 100.00%. No issues found.

Issues 23/08/2026 06:36

  1. 2.8 — Redundant time-to-effect sub-lines: time_1_sub “Changes emerged over 8–12 weeks in the trials.” (line 503) and time_2_sub “Sleep and bowel effects appear within days.” (line 514) merely restate time_1_value “8–12 weeks” and time_2_value “Within days”, adding no information while consuming one-page budget.

Fixes 23/08/2026 06:36

  1. 2.8 — Redundant time-to-effect sub-lines: Replaced time_1_sub “Changes emerged over 8–12 weeks in the trials.” with “The two outcomes with the clearest quantified response; both need a pre-start baseline.” and time_2_sub “Sleep and bowel effects appear within days.” with “Bowel effects appear on the same timescale.”, so neither sub-line restates its own value cell.