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Standard panels are doing exactly the job that they were built to do, which is to catch a
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disease.
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They were never built to tell you whether you're operating anywhere close to your ceiling
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or what diseases may be coming in the future.
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So if you walked away from your last physical with a clean bill of health, but you still
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don't feel like you're operating at your best, that gap right there is exactly what these
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markers are built to close.
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Welcome to Health Decoded, your number one source for real health information with your
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host, doctor Alessi and Matt Tack.
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So you just got your annual physical.
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Your blood work came back normal, and your doctor shook your hand and said, see you next
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year.
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Everything's fine.
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But why do you still hit the wall at 2PM every single day?
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Why does the recovery from your bad night's sleep take you longer than it used to?
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Why is the number on the scale the same as five years ago, but you look and you feel different?
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Well, here's the problem, and I wanna be precise about this because this is the whole
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episode basically in one sentence.
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The standard physical is built to catch disease.
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It is not built to measure performance.
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And those are two different jobs.
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A normal fasting glucose tells your doctor you don't have diabetes right now.
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It tells you almost nothing about whether your metabolic engine is running efficiently,
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whether you're inflamed, whether your cardiovascular risk is quietly climbing.
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The panel your insurance covers is basically a floor.
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It's not a ceiling.
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And if you're a high performer or someone whose job depends on cognitive output, stamina,
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decision making under pressure, the floor is not the number you should be optimizing to.
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So today, I'm giving you the five categories of biomarkers that never make it onto a standard
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panel, but why each one matters specifically if you're operating an executive level, and what
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we actually do with the data once we have it.
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This isn't a go ask your doctor list.
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This is what we run at Ascend and exactly why we do that.
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So let's get right into it.
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So start here because this is the clearest example of normal not being optimal.
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Lipids.
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Your standard lipid panel gives you four numbers.
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Basically, total cholesterol, LDL, HDL, and triglycerides.
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Your doctor will look at the LDL.
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He'll see it's under one thirty, maybe under a 100 if you're being careful, and tell you that
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you're fine.
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But here's what that panel doesn't tell you.
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How many particles are carrying that cholesterol and how small and dense they are.
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This matters because cardiovascular risk isn't driven by how much cholesterol is floating in
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your blood.
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It's driven by how many particles are available to lodge into your arterial walls and start the
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inflammatory cascade that eventually becomes plaque.
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Think of it less like a fuel gauge and more like a traffic count.
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LDL cholesterol tells you the total volume of cargo being shipped.
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It doesn't tell you how many trucks are on the road.
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You can have a totally normal LDL number and still have a high particle count because your
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cholesterol is being packed into large number of small dense particles instead of fewer
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larger ones.
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So two patients with an identical LDL of one ten can have wildly different actual risk.
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One might have 900 particles, the other 1.
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Same cargo, total twice the trucks on the road, twice the opportunity for something to go wrong
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at an intersection.
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So that panel can't tell them apart, but an APOB can.
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So APOB, which is apolipoprotein b, is a direct count of the atherogenic particles, LDL, VLDL,
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ILDL, LPA, one number, and it is far better predictor of cardiovascular events than LDL
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cholesterol alone.
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This has been argued in cardiology for over a decade.
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It's increasingly recognized as the more accurate measure even if it's still catching on
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in mainstream primary care.
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But it's still not on the standard panel, and most of you are getting once a year.
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So why is that?
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And here's why this is specifically important.
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If you're running a company or you run a team or you're somebody who needs to perform
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cardiovascular events, they do not announce themselves.
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And we've all heard stories of people who seemingly are healthy, and their doctors say
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they're fine, and then they have a heart attack.
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There's no meeting on your calendar for this.
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There's not warning sign.
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The first sign of a heart attack is often the heart attack itself.
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And so the people who show up in the cardiologist's office with an event in their
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fifties, they over overwhelmingly, people had what would be called normal cholesterol on
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paper the year before.
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Not because the disease appeared overnight, but because nobody was measuring the marker that
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would actually have shown it developing.
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And so if you're an executive, if you're in your forties or fifties with a family, if you
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have history of heart disease in your family, or you've had a normal lipid panel for a
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decade, and you would, like, actually wanna know your risk, APOB is the single highest
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value number that you're not getting.
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It actually costs almost nothing to add to a panel.
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It's just one more tube of blood.
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Run this alongside everything else you're already getting drawn, and it can completely
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change the risk picture of your current cholesterol numbers and sometimes reassure you
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when the picture looked worse than it is.
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Because sometimes doing the opposite, telling you to take action before standard panel would
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have said anything.
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Okay.
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So here's the next one.
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This is the one that I want you to pay close attention to because it's the marker most
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directly tied to the one thing you're actually probably here for, which is being able to
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perform or optimize your health.
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So energy, the two PM wall.
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Standard panels are gonna check fasting glucose.
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That's it.
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Glucose is a lagging indicator.
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By the time it's elevated, the problem has usually been developing for years.
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So here's the mechanism, and I wanna walk through it slowly because once you understand
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this, you'll actually never look at normal glucose the same.
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When you eat, especially carbohydrate heavy food, your blood sugar rises, and your pancreas
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releases insulin to move that glucose out of your bloodstream and into your cells, where it
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gets used for fuel.
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In a metabolically healthy person, that process is efficient.
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A modest amount of insulin does the job.
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Glucose comes back down cleanly and the system resets.
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In someone who's developing insulin resistance, the cells stop responding as well to insulin
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signal.
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The receptors on the cell surface become less sensitive.
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So the pancreas compensates the only way it knows how, by producing more insulin to force
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the same amount of glucose into the cells.
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And because that compensation works, at least for a while, glucose stays in normal range.
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The extra insulin is doing the heavy lifting.
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But you're now running a system under load that used to run without strain, and that
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compensation has a cost that doesn't show up on the marker that anyone's actually measuring.
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This is why fasting insulin and the calculated ratio, which we call the HOMA IR, which
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combines fasting glucose and fasting insulin into a single index, catches the problem years,
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sometimes even a decade before glucose does.
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Optimal fasting insulin is under eight micro IU per ml.
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We regularly see executive high performers, people with no visible weight problem, glucose
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sitting at a comfortable 90, with, like, a fasting insulin of, like, 15 or 18, or even
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sometimes higher, telling us that their pancreas is working overtime to keep that
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glucose looking normal on paper.
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But nobody's measuring the thing doing the compensating because it was never part of the
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panel.
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So here's why this matters.
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If you're sitting in back to back meetings, if you live on coffee, if you live on adrenaline,
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insulin resistance doesn't just predict future type two diabetes, which is the framing most
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people have heard and mentally filed under, like, someday, this is not my problem right
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now.
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It's directly tied to the energy crash you feel mid afternoon.
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The brain fog that you get in a 4PM meeting.
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The carb heavy lunch that leaves you foggy and reaching for a second coffee instead of feeling
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fueled and sharped.
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Your cells, including the ones in your brain, are becoming progressively less efficient at
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taking up glucose for fuel.
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That's the biology behind the thing you've been talking up to as just stress, or getting older,
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or needing more sleep.
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It's not that you're undisciplined, and it's not something you're gonna be able to
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caffeinate your way out of for a long term.
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It's a measurable, correctable metabolic signal that your annual physical never looked for
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because it never ran the test that would have found it.
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The third thing, inflammation.
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And these are the inflammation markers that you can't even feel.
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You don't know this is building.
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Two markers here in specific, h s c r p, which is high sensitive high sensitivity c reactive
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protein, and homocysteine.
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Neither hurts.
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Neither shows up as a symptom that you would bring to the doctor.
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Both are quietly correlated with accelerated cardiovascular and cognitive decline.
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So HSCRP is a marker of systemic low grade inflammation, Not the kind of inflammation from
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a sprained ankle where you're gonna see it, feel it, watch it resolve in a few weeks.
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That it's the kind of smoldering low level inflammation that's going on at all times from
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things like visceral fat in the abdominal region, from chronic stress physiology, poor
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sleep, gut permeability, or food sensitivity.
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Optimal would be under one milligram per liter.
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And a lot of healthy executives who are healthy on paper with a good diet, exercise, they have
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no obvious red flags, are sitting at around a two or a three or even higher.
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And so I wanna spend a minute on why specifically because this is the piece that's
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most relevant to you and most commonly missed.
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Chronic occupational stress doesn't just feel bad.
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It has a direct inflammatory signature.
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When cortisol is chronically elevated or elevated at the wrong times of day because
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sleep and stress have disrupted your normal rhythm, your immune system's regulatory signals
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are gonna become disrupted.
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Cortisol is supposed to help keep inflammation in check.
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But under chronic stress, the tissues that respond to cortisol become less sensitive to
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it.
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Similar to what we talked about earlier with insulin resistance a few minutes ago.
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Except this time, it's the hormone that's supposed to be dialing inflammation down that
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stops getting hurt.
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The result is a baseline inflammatory state that has nothing to do with your diet and
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everything to do with the way you manage your calendar.
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This is the piece that people miss because you can be doing a lot of things right on the
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nutrition side and still be inflamed because the driver isn't your food.
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It's your cortisol curve and the sleep debt that you've created.
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So why does this matter beyond inflammation is bad?
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Well, chronic low grade inflammation is now understood to be one of the core mechanisms
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behind accelerated vascular aging.
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It's actually part of how the arterial plaque forms and progresses, and increasingly, it's
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implicated in cognitive decline as well.
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Though effects on the blood brain barrier pause.
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Jeez Louise.
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Unpause.
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And increasingly, it's implicated in cognitive decline as well through effects on the blood
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brain barrier and neuroinflammatory process that will track with long term changes in
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memory and processing speed.
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This is a leading indicator.
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It's not a symptom you'll notice until the downstream event happens, such as a cardiac
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event or the cognitive change, and no one can attribute to just getting older.
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The next piece that we talked about was homocysteine, an amino acid byproduct that when
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it's elevated is independently associated with cardiovascular risk and is tied to how
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efficiently your body is running methylation.
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Methylation is a biochemical process that touches an enormous range of downstream
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function.
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Detoxification pathways, neurotransmitter production, DNA repair.
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So elevated homocysteine is often a signal of a b vitamin insufficiency or possibly a genetic
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methylation inefficiency, both of which are easily correctable once you know they're there,
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and both of which are completely invisible on a standard panel that never checks for them.
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Neither of these two markers, HSC or p or homocysteine, will ever generate a symptom that
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sends you to urgent care.
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That's exactly why they matter because that silent, measurable, pause.
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That's exactly why they matter.
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Silent, measurable, and by the time they become a felt problem, you've lost the years where
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correcting course was easiest and cheapest.
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Next, hormones.
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If your physical checked hormones at all, it probably checked one number, maybe total
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testosterone or estrogen.
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That number alone tells you almost nothing useful, and here's why.
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Testosterone in your blood exists in two functional states, bound and free.
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Bound testosterone is attached to proteins, primarily sex hormone binding globulin, or what
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we call SHBG.
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And in that bound state, it is not biologically active.
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It can't do anything at the receptor level.
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What actually matters is free testosterone, the small fraction that's unbound and available to
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your tissues.
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Along with SHBG itself, estradiol, and in a generally thorough panel, thyroid markers that
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go beyond just TSH that include free t three, free t four, because TSH alone can actually
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look normal while actual thyroid hormone conversion and availability are impaired.
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So a man can have normal total testosterone and functionally low free testosterone because SHBG
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is elevated, often driven by factors like chronic stress, liver function, age related
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changes, which bind up the hormone that would otherwise be doing the work.
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That distinction is the difference between a doctor telling you you're fine, and you
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actually knowing why you feel flat, unmotivated, or like your recovery from
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training has slowed for no obvious reason.
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Then there's body composition, and this is where I wanna correct something almost everyone
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gets wrong.
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Your weight is not a leading indicator.
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Weight is actually a lagging one.
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Two people can weigh the same, wear the same size, have a completely different risk profile
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depending on where their weight is actually distributed.
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This is where a DEXA or dual energy x-ray absorptiometry test earns its place.
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It doesn't just give your body fat percentage.
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It separates visceral fat, which is around the organs, metabolically active fat that directly
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drives inflammation and insulin signaling.
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Doesn't distribute it doesn't delineate that from subcutaneous fat, which is the fat under
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the skin that is comparatively metabolically, you know, inert.
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It also gives you your lean mass, and lean mass is one of the strongest predictors we have of
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long term metabolic resilience.
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Functional independence, healthy aging, because muscle isn't just about strength, it's your
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body's largest reservoir for glucose disposal.
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Meaning, the more lean mass directly supports insulin sensitivity that we just talked about a
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few minutes ago.
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So two executives at the same weight and the same BMI can have wildly different visceral fat
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and lean mass numbers, and therefore, wildly different actual risk.
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One might be carrying most of that weight as muscle with some moderate visceral fat.
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The other person might be at the same number on the scale with high visceral fat and a
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comparatively low lean mass.
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The scale can't see that difference.
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BMI can't read that either.
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BMI is just basically a height to weight ratio, by the way, and it has no idea what tissue is
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actually making up that weight.
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The DEXA scan can see it and see it precisely.
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This is the category where most people are surprised because you you could be lifting
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three days a week, eating reasonably well, showing a normal BMI, and still be carrying
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visceral fat that's driving that exact inflammatory and metabolic picture we just
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spent the last few minutes talking about.
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It all connects.
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None of these four categories are isolated.
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They're four windows into the same underlying system.
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And now what we actually do with this data is very important because getting a number is
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cool, but it's it's pointless unless you know what to do with it.
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A number with no action attached to it is just gonna become anxiety.
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So let me walk you through how this actually plays out, and I wanna be upfront about
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something first.
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The case I'm about to describe is a composite.
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It's not a specific patient.
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It's basically a pattern that we see over and over blended into, like, a single picture, for
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example.
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And so I'm using it to show you how these pieces connect, not to hand you a protocol for
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yourself.
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That part still requires actually running your own numbers and having a physician walk through
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this with you.
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So just to be clear, this is for illustration only.
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This is not medical advice for your specific situation.
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My listeners know that by now.
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Your own protocol would depend entirely on your own labs, history, and an evaluation.
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But if any of this sounds like you, the next step would likely be testing, not a self
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diagnosis.
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So here's a picture.
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Picture this.
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A mid forties executive person comes in after completely clean annual physical.
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My doctor said everything was good.
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My glucose is normal.
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My cholesterol is acceptable.
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The doctor told me he would just report me next year.
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But this person has this constant daily wall that they hit around two to 3PM.
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They feel like they're not recovering from sleep.
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They feel like their weight has slightly been gaining even though they're working out harder
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than they have ever before.
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On paper, this is fine, but in the room, they don't feel fine.
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And so what we do, we run a panel that we talked about.
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ApoB comes back elevated, even though their LDL was comfortably sitting in the range of a
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standard panel.
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The particle count tells a different risk story than the cholesterol number did.
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Years of quietly elevated cardiovascular risk that a doctor would have no reason to flag
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because the doctor wasn't looking at that in the first place.
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Next is a fasting insulin comes back at like a 17.
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Glucose was a 91, which would have been completely unremarkable, but the 17 tells us
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that the pancreas has been compensating for a while.
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That's the mechanism behind that 2PM crash.
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The cells are less efficient at taking up glucose, including the brain.
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HSCRP comes back at a 2.4, well above the optimal one point o target.
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Diet's reasonable.
00:19:06
The driver here is almost always the existing chronic stress, chronic under sleeping, a
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stress hormone curve that never fully resets, which drives inflammatory signaling independent
00:19:18
of what's on someone's plate.
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And then the DEXA scan shows visceral fat that's elevated.
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Lean mass, adequate, but not increasing.
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So weight gain that looked minor on the scale is actually concentrated in exactly the tissue
00:19:32
that's most tied to the insulin and inflammation findings from above.
00:19:37
Same root cause, four different numbers.
00:19:39
That's the part I want you to sit with because these four findings aren't four separate
00:19:43
problems.
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They're one metabolic picture showing up in four places.
00:19:48
The protocol that follows isn't just fix the APOB, then fix insulin, then fix CRP, as like
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four separate projects.
00:19:57
It's targeted resistance training, restructured eating, within a window to rebuild sensitivity
00:20:03
to insulin, which improves the visceral fat picture, which lowers the inflammatory load
00:20:08
alongside specific nutritional support, and where may be warranted direct treatment for the
00:20:14
particle count.
00:20:15
One coordinated protocol because one underlying pattern produced all of the four numbers.
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That's the difference between functional medicine and just conventional medicine.
00:20:25
A result with no interpretation attached to it is not useful, no matter how sophisticated the
00:20:30
test that generated it.
00:20:32
A result connected to other three results with a plan built around the pattern instead of each
00:20:37
marker targeted in isolation, that's what changes trajectory.
00:20:42
And I'd point out, none of this required any guessing.
00:20:45
Every step in the protocol maps directly back to a specific number.
00:20:49
That's the whole difference between optimization and generic advice.
00:20:54
Generic advice is eat better, sleep more, manage your stress.
00:20:58
Although that's true, it's basically useless because it doesn't tell you which lever matters
00:21:02
the most for your physiology.
00:21:04
A real panel will tell you exactly where to spend your limited time and attention.
00:21:09
So let's bring it all together.
00:21:11
Five categories that your annual physical almost certainly did not check.
00:21:15
One, advanced lipid markers, specifically APO B, instead of stopping at total cholesterol and
00:21:20
LDL.
00:21:21
Two, fasting insulin and HOMA IR, instead of just glucose.
00:21:27
Three, h s c r p and homocysteine, the inflammation that you can't feel until it's
00:21:32
already cost you some years.
00:21:34
Four, a full hormone panel, not just total testosterone, plus a DEXA scan for real body
00:21:40
composition instead of a number on a scale.
00:21:43
Every one of these is measurable right now with existing validated tests, and none of this is
00:21:49
experimental or fringe.
00:21:51
Every one of these, when it's off, has a specific actionable next step attached to it.
00:21:57
It's not a vague eat better, move more advice that leaves you exactly where you started.
00:22:04
So here's the test I give you to walk away with.
00:22:07
If you've had a physical this year, pull the results back up and ask yourself honestly, did
00:22:11
it check for any of these five?
00:22:13
For almost everyone listening, the answer is probably no.
00:22:16
That's not a failure of your doctor.
00:22:18
Standard panels are doing exactly the job that they were built to do, which is to catch a
00:22:22
disease.
00:22:23
They were never built to tell you whether you're operating anywhere close to your ceiling
00:22:27
or what diseases may be coming in the future.
00:22:30
So if you walked away from your last physical with a clean bill of health, but you still
00:22:34
don't feel like you're operating at your best, that gap right there is exactly what these
00:22:38
markers are built to close.
00:22:41
If you're ever interested, links in the show notes if you wanna see what a comprehensive
00:22:44
panel actually looks like.
00:22:46
Thank you again for tuning in to Health Decoded.
00:22:49
I'm doctor Alessi.
00:22:50
And if this was valuable, please share this with someone who needs to hear it.
00:22:53
That's how we're able to help more people and spread the word of functional health.
00:22:58
Doctor Alessi, I'll see you on the next one.
00:23:02
Thank you for tuning in to Health Decoded, where we break down the truth about all things
00:23:07
health and empower you to take charge of your well-being.
00:23:10
If you found value in today's episode, please subscribe, leave a review, and share it with
00:23:16
someone who needs to hear this.
00:23:18
For more resources, personalized support, or to have your questions answered live on the show,
00:23:23
visit Ascend Functional Health and head to the contact page to connect with us directly.
00:23:27
Until next time, stay curious, stay empowered, and remember your health is in your hands.

