Plenya

Medicine 2.0 vs. Medicine 3.0 — alarm or detector

By Dr. Getúlio Amaral Filho··2 min
Medicine 2.0 vs. Medicine 3.0 — alarm or detector

TL;DR

The medicine that treated your father is not the medicine that will treat you. The difference lies in when it acts.

For our team at Plenya, the difference between Medicine 2.0 and Medicine 3.0 is the difference between a fire alarm and a smoke detector.

The alarm sounds when it is already burning. The detector sounds when the smoke begins.

Medicine 2.0 — the one we learned in school, the one practiced in most Brazilian offices — is built for act two. Treating established disease. Choosing the right drug, performing the right surgery, giving the right treatment at the moment everything is already happening.

Medicine 3.0 does not replace 2.0. Through The ACTS Method (Activity, Alimentation & Smart Adjuncts · Clinical Optimization · Tending Mind, Body & Bonds · Sleep, Rhythm & Recovery) we apply at Plenya, it adds act one. It looks for the smoke before the flame. It works with biomarkers that move five, ten, twenty years before the diagnosis — fasting insulin, ApoB, hs-CRP, homocysteine, VO₂ max, grip strength.

Comparative table between Medicine 2.0 (alarm — asks "what is the diagnosis?", works with symptoms and abnormal labs, acts on established disease) and Medicine 3.0 (detector — asks "am I on the path?", works with ApoB, hs-CRP, VO₂ max, fasting insulin, grip strength, homocysteine, acts within the silent window). Adapted from Attia P, Outlive 2023.
Comparative table between Medicine 2.0 (alarm — asks "what is the diagnosis?", works with symptoms and abnormal labs, acts on established disease) and Medicine 3.0 (detector — asks "am I on the path?", works with ApoB, hs-CRP, VO₂ max, fasting insulin, grip strength, homocysteine, acts within the silent window). Adapted from Attia P, Outlive 2023.

Each of these biomarkers has solid literature behind it. ApoB, according to the Sniderman and colleagues review in 2019 (JAMA Cardiology), predicts atherosclerotic risk better than LDL-C because it measures the actual count of atherogenic particles — and begins to drift before total cholesterol moves. VO₂ max, in the Mandsager study (JAMA Netw Open 2018), is the most powerful prognostic marker of all-cause mortality ever studied — stronger than smoking. The American Heart Association (Ross 2016) argues that cardiorespiratory fitness should be treated as a vital sign. hs-CRP, along the line of Ridker's CANTOS trial (NEJM 2017), connects subclinical inflammation to hard cardiovascular endpoints.

Ricardo, 52, had an annual checkup. Every test "normal." Almost died of a heart attack in a parking lot. None of the six markers that were outside the optimal range appeared on the conventional panel. The alarm only sounded once the fire had already started.

The question that matters, in our team's reading, is not "do I have a disease?" It is: "am I on its path?"

Excerpt from Chapter 1 of the book BEFORE — The silent window between normal and optimal — a decade where health is decided.

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