As promised I’m posting results of the n=1 experiment wrt. lipid medication. No changes in diet or exercise or other lifestyle factors, sleep, level of stress insofar as I can tell (low), supplements. The only med change has been the addition of 80mg/day of telmisartan for two weeks (first 20mg/day for 4 weeks, followed by 4 weeks of 40mg/day, before the final 2 weeks of 80mg/day that I have continued on with to this day). This test (4) keeps pitavastatin 4mg/day but adds a combined pill Brillo EZ of 180mg/day + 10mg/day ezetimibe.
So the tests are as follows - each intervention roughly 6 weeks with no washout period:
(1)pitavastatin 4mg/day alone (switched from atorvastatin 10mg/day)
(2)pitavastatin 4mg/day + bempedoic acid 180mg/day
(3)pitavastatin 4mg/day + ezetimibe 10mg/day
(4)pitavastatin 4mg/day + bempedoic acid 180mg/day + ezetimibe 10mg/day - CURRENT TEST ON 10/28/25.
This test (4) has been of a drug regimen that has been ongoing since the initiation on 08/09/25.
Pitavastatin 4mg/day alone vs pitavastatin 4mg/day + bempedoic acid 180mg/day vs pitavastatin 4mg/day + ezetimibe 10mg/day vs pitavastatin 4mg/day + bempedoic acid 180mg/day + ezetimibe 10mg/day
Pita alone - 5 months; Pita + BA - 39 days.
Legend: Pita alone - PA; Pita + BA - P+BA; Pita + ezetimibe P+EZ
Total Cholesterol: PA - 228 mg/dL; P+BA - 208 mg/dL; P+EZ - 195 mg/dL; P+BA+EZ - 178 mg/dL
LDL-C Calc: PA - 123 mg/dL ; P+BA - 110 mg/dL; P+EZ - 99 mg/dL; P+BA+EZ - 91 mg/dL
Trig: PA - 93 mg/dL ; P+BA - 62 mg/dL; P+EZ - 82 mg/dL; P+BA+EZ - 62 mg/dL
HDL: PA - 89 mg/dL ; P+BA - 87 mg/dL; P+EZ - 81 mg/dL; P+BA+EZ - 75 mg/dL
Not exactly thrilling results. It brings me (just) under the cutoff values for hyperlipidemia as specified by the UCLA lab range. Each additional drug brings down the values by just a few points (if any - see trigs!). To say the results are underwhelming given the arsenal of drugs deployed is a depressing understatement. I’m not impressed.
Unfortunately it also represents the end of the road for me for easily available LLT drugs I have on hand. I am aware that the next currently available drug class I might add in order to crush LDL/ApoB further would be PCSK9i. However, call me excessively paranoid, but I continue to be worried by the MR AD signal for PCSK9i. That said, I’m not absolutely excluding that I might use a PCSK9i in the future. Meanwhile I am eagerly awaiting the whole slew of LLT drugs that should be coming online in the not too distant future, fingers crossed.