Heart Health and Bloodwork After 50

Your cholesterol panel, your blood pressure, Lp(a), and the bloodwork most men over 50 never get explained. What the numbers mean, which ones are worth treating, and what I track on myself.

By Gunnar · Patient experience, not medical advice · Updated August 2026

Chart of expected LDL cholesterol reduction, in the order treatment usually escalates: moderate statin 30 to 49 percent, high-intensity statin 50 to 55, ezetimibe added on top a further 25, inclisiran 48 to 52, PCSK9 antibody injection 45 to 64, the oral PCSK9 pill Lipfendra 56, and the gene-editing infusion VERVE-102 at 62 percent while still in trials. Shown separately for people who cannot take a statin: ezetimibe alone 18 percent and bempedoic acid 21 to 24.
Where these numbers come from
OptionExpected LDL-C reductionSource
Ezetimibe, on its own18%2026 ACC/AHA dyslipidemia guideline
Bempedoic acid, on its own (statin intolerance)21–24%2026 ACC/AHA dyslipidemia guideline
Ezetimibe added to a statina further 25% off what the statin leaves2026 ACC/AHA dyslipidemia guideline
Moderate-intensity statin30–49%2026 ACC/AHA guideline, Table 6
High-intensity statin50% or more; the statin class tops out at 55%2026 ACC/AHA guideline, Table 6
Inclisiran (Leqvio)48–52%2026 ACC/AHA dyslipidemia guideline
PCSK9 injection (Repatha, Praluent)45–64%2026 ACC/AHA dyslipidemia guideline
Oral PCSK9 pill (Lipfendra)56% at week 24Merck, CORALreef Lipids
Gene-editing infusion (VERVE-102, in trials)62% at the highest doseNew England Journal of Medicine
Expected reductions, not a head-to-head trial. Most of the non-statin figures were measured in people already taking a statin, so they represent what the drug adds. These reductions do not add up, they stack on a smaller and smaller number: an LDL of 200 falls to about 100 on a high-intensity statin, and to about 75 once ezetimibe is added, which is roughly 62% off in total rather than 75%. Bempedoic acid adds 17–18% when it is combined with a statin instead of used alone.

What men over 50 should know

Most men my age get one cholesterol number and no explanation. Your doctor reads out an LDL, says it looks a little high, and the visit moves on. The 2026 ACC/AHA guideline widened what that conversation is supposed to cover. It starts estimating risk at 30 rather than 40, and runs the estimate out to 30 years as well as 10. It also says every adult should have Lp(a) measured at least once, which is probably the change most likely to matter to you personally, because Lp(a) is inherited, a standard panel does not report it, and a respectable LDL can be sitting on top of a bad one.

The ladder is longer than it used to be, and the cheap rungs still do most of the work. A statin is first-line for nearly everyone who needs treating at all. Ezetimibe takes about another quarter off whatever the statin leaves behind, for roughly twenty dollars a month, and the newer drugs, the injections and now a daily PCSK9 pill, are for people who are still above goal on those or who cannot tolerate a statin. My own LDL is 56 and my ApoB is 59, and I got there through about 170 pounds of weight loss and ezetimibe, without ever taking a statin. That is not a protocol, it is just what happened to me, but it is why I get skeptical when the conversation jumps straight to the expensive rung. If you want to see where any ApoB number falls, the ApoB levels chart maps 40 to 140-plus.

Not every number on the panel is a target. Inflammation is the clearest case. hs-CRP predicts events about as well as anything else you can measure cheaply, and then ZEUS, a trial in 6,376 people who already had both heart disease and kidney disease, drove it down with an IL-6 blocker and heart attacks and strokes did not move. I read a high hs-CRP as a reason to look harder now, not as a dial to turn. The things that have actually held up in outcome trials are duller than any new marker, and I have stopped being disappointed about that.

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