The headline is broadly defensible, but the qualifications matter. Effect sizes vary by population, the strongest claims rest on shorter trials, and credible voices push back on how it's typically framed.
so with the NMR panel you tend to get something like LDL P which is the particle count of LDL and sometimes if you do ion mobility or other tests you also get small LDL medium LDL from that you can tell the peak size of the LDL and your LDL pattern whether your pattern a or pattern be
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Bookmarking — the dossier-vs-overview split is the right call. Most of the time I want overview; sometimes I want receipts.
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so the nuclear magnetic resonance is now looking at numbers of LDL particles we basically the panel looks at LDL HDL triglycerides in milligrams per deciliter which as we suggested is a density measure and now we're actually counting the number of LDL particles so instead of weighing the LDL particles we are counting the LDL particles
you always have a problem when you don't know what you're comparing it to so if we have gen 1 nmr which is probably still being used by lab core and quest today that is probably quite inaccurate compared to gen 2 nmr but the percentiles meaning the populations of people that were measured are still what we use to understand where someone lies it puts you in a bit of a dilemma as a clinician or as a patient you want to continually upgrade your technology in other words if you're talking about getting a new iphone you don't really care that your phone is so much better than two generations ago's phone because all your metrics are better and there's nothing to be gained by comparing yourself to how much better you are but when you're talking about diagnostics it does matter where your reference range is and if you're moving it