Lab Medicine Rounds

In this episode of “Lab Medicine Rounds,” host Justin Kreuter, M.D., speaks with Jeff Meeusen, Ph.D., assistant professor of laboratory medicine and pathology and clinical chemist in the Division of Clinical Core Laboratory Services for the Department of Laboratory Medicine and Pathology at Mayo Clinic, who discusses a forthcoming guidance document on lipid testing. 
 
Discussion includes:
00:59 Importance of guidance document for lipid testing.
03:30 Key takeaways for laboratory professionals utilizing the guidance document.
09:20 Challenges with implementing a guidance document.
12:50  Advice for others looking to join guidance committees.

What is Lab Medicine Rounds?

A Mayo Clinic podcast for laboratory professionals, physicians, and students, hosted by Justin Kreuter, M.D., assistant professor of laboratory medicine and pathology at Mayo Clinic, featuring educational topics and insightful takeaways to apply in your practice.

This is Lab Medicine
Rounds, a curated podcast

for physicians, laboratory
professionals and students.

I'm your host, Justin Kreuter

a transfusion medicine pathologist
and assistant professor

of Laboratory Medicine and
pathology at Mayo Clinic.

Today we're rounding with Dr.

Jeff Meeusen, assistant
professor of Laboratory Medicine

and pathology and clinical
Chemist in the division

of Clinical Core Laboratory
services for the Department

of Laboratory Medicine and
Pathology at Mayo Clinic.

Thanks for joining us today

Dr. Meeusen.

Yeah, thanks for having me.

I'm really looking forward to talking.

Yeah, so we've had you

on the podcast a few times before and it's

it's always wonderful to have
your perspective in on things.

One of the things that
you've done recently

that's really cool is

that you've chaired a guidance
document on lipid testing.

And so maybe for our
audience we can kick off why

why is this guidance document
on lipid testing significant?

Yeah, thanks.

I am excited to talk
about that a little bit.

So it was solicited by the Association

for Diagnostic Lab Medicine,
so formerly A A C C

or the Association for
Clinical Chemistry.

And as you know, and probably most

of our colleagues lipids have benefited

from a really big public education

public health effort over the years.

I mean, we all know

that cholesterol is something
we should watch out for.

It's on the labels for
our food, et cetera.

And there's been a lot

of documents over the
years, in fact

I'd say there's been
documents consistently issued

for like 40 years on
cholesterol and its management.

So these have been refined
from various societies.

You know, the American Heart Association

the Academy of Cardiologists,
endocrinology, even, you know

primary care and family
medicine groups have

all been working together
to build a consensus

on how to manage a patient's lipids

and thereby manage their risk
of cardiovascular disease.

But this would be the first
document they've explicitly

tried to target to diagnostic
lab medicine professionals.

So we're trying to do a step removed

from the patient treatment and management

and try to work towards
harmonization standardization

of the lipids testing side.

Wow, that's really kind
of surprising for me.

You know, it's kind of an
outsider on this to, to hear that

'cause Yeah, I mean absolutely
cholesterol, I think

I think that's one of those,
you know, know your numbers

kind of a thing.

Like you say these public
health initiatives and it

it's kind of surprising that
we have not had some kind of a

a guidance on how do we measure such a

an important number in our lives.

So

Yeah, I'll jump in right there.

Yeah. So the, the reason
we've been able to go so far

and do so well is very early on the C D C

and the N I H made very strong efforts

towards creating commutable
reference materials and working

with all the big name vendors
to make sure that the methods

for measuring cholesterol
it were very standardized.

And thanks to that

the measurements that are
performed at basically

any clinical laboratory
using any different reagents

any different big box platform

they're gonna pretty much
give you the same answer.

So that's the good news.

Nice, nice.

Okay. So yeah, you brought
up a, answered my question

I even know I had, but yeah.

Okay. So that makes sense

for why it was kind of, I
guess, baked in, if you will.

So, so what are the
important kind of takeaways

for laboratory professionals to understand

about this guidance that you've worked

on? Yeah

So by convention we've been
reporting labs in the context

of what the clinical
management documents say.

And that's a little different
than the way we typically

do things in lab medicine where
we measure a thousand people

and say normal is this, you
know, bell curve and if you're

outside of that you're abnormal.

Well the convention
that has really grown up

around lipids is that it's
almost exclusively used

in the realm of cardiovascular
risk assessment.

So then we have to give
laboratorians reference

ranges that really aren't
normal, so to speak

but desirable.

So if we were to measure a
hundred people, I would say

about half of us are actually
above desirable cholesterol

concentrations, especially
depending on where you live

in the United States and your lifestyle.

But what we were trying
to now establish and

and unfortunately there was
a little bit of a disparity

from lab to lab, clinic to clinic.

Some people would still list
the normal reference range

and some people would say
the desirable concentration

which is less than a
hundred mgs per deciliter

L D L cholesterol, less
than 200 mgs per deciliter

total cholesterol.

So we tried to provide a little
guidance around that area.

And then there's two other
really big issues that have been

coming up in very recent
years and that is around

low density lipoprotein cholesterol.

So typically

and this is the convention
because of the A M A

panel. So

This is the L D L cholesterol, right?

Okay. L

D L cholesterol, which is
the bad cholesterol, right?

So we can't just measure
cholesterol and gauge your risk.

You have to measure your cholesterol

and your H D L cholesterol

which is the good cholesterol
that's known to be protective.

And the L D L cholesterol, it turns out

is what has a propensity to get clogged

in the arteries causing
cardiovascular disease.

And since the 1970s that
L D L cholesterol has

been calculated rather than measured.

And we do that by taking
your total cholesterol

subtracting the H D L
cholesterol and then we put

in a fudge factor for all the other kinds

of cholesterol by taking your
triglycerides divided by five.

Sounds like a lot of my math course.

Okay. You got the fudge factor in there.

Yes.

And that's okay.

And it worked well for
many, many years because

every lab is reporting it that way.

And we all understood there
were some potential limitations

the patient needed to be
fasting 'cause that'll

keep your triglycerides lower.

And so the fudge factor has
less of an effect, so to speak

or is less relevant.

Other, other aspects that
were important as you

couldn't use this if a person
had hyper hypertriglyceridemia

for other reasons, but
more modern techniques now

have been developed and a
couple of new equations, one out

of Johns Hopkins University,
it's referred to colloquially

as the extended Martin equation,
allows for triglycerides up

to about 800 mgss per deciliter.

And another equation developed
at N I H referred to often

as the Sampson equation
because of the first author

the publication was on also
can account for that elevation

of triglycerides.

And they do a fairly similar job

in estimating L D L cholesterol

And, and is there, so the

the evolution of L D L is,
we are still calculating it

but there have been new math
for how we do that calculation.

And so was that guidance document

did that kind of provide some guidance

over which equation or in
what context, which equation?

Absolutely. And so
there's two parts there.

I'm glad you mentioned.

We're still calculating it most

of the time we're still calculating it.

However, there are now methods

for measuring L D L cholesterol
on the big blocks platforms.

They have varying degrees
of precision and accuracy

and most of the time
they don't do any better

than the calculation as long

as your triglycerides are
within a normal range.

So it's often been a reflex test

in most institutions now that
we have new calculations.

And so our guidance document
is basically saying either

of those two calculations that
have been widely published

and and worked on

and reviewed and evaluated
would be acceptable.

So we need to phase

out the Friedewald equation, which is the

the fudge factor of trig over
five that's been universally

I'd say implemented for many decades.

And then the second aspect
of that, so we're phrasing

out Friedewald now we have new
equations that do a decent job

throughout a big majority
of the hypertriglyceridemia.

In other situations, fasting, non-fasting

it might obviate the need

for the directly measured
L D L cholesterol

which is also routinely ordered

because it does just as good a job

in now much wider range of situations.

So those are our two,
one is a recommendation

that you need to use a modern equation.

And two is now we less

of a recommendation
and more of a statement

that we should consider reevaluating when

we use the measured L D L cholesterol.

So as you talk about that, you know

my next question I usually kind of think

about what kind of
challenges do you anticipate

with implementing this guidance?

And it sounds like with
that, you know, there's

there is some interaction

with clinical colleagues
and education to, to happen

particularly with that second
point that you mentioned

about when are we actually
ordering a measured L D L and

and so can you kind of walk us

through kind of what
challenges or what kind

of discussions you guys were having

as a group with coming up with that?

Absolutely. So oftentimes

that measured L D L is
built in as a reflex.

If your triglyceride happens
to be over this threshold

then we're just gonna do a measure.

And we were speaking with
our clinical colleagues

and this actually helped us
discover an underlying issue.

That was another recommendation we made.

Oftentimes the L D L
cholesterol is simply reported

and it might've been calculated

or it might've been measured

but it's not clearly distinguished

in the medical record which
method was used particularly

in these reflex cases.

So one

of our other statements we put
in there is you have to state

if it was calculated or
measured, which is consistent

with best practice lab
medicine in general.

And then somewhere you have to
state which equation you use

since it's no longer
this universal equation.

And I think we spent a lot of
time building consensus there.

I was fortunate to have
a few clinicians as well

as laboratorians on our
writing committee panel.

Fasting is gonna be a new thing too

because the new equations
can handle trigs now.

We don't have to be so
prescriptive about fasting.

Oh

Okay. Which is a big boon
to the lab workflow I think.

So what about, is there any
impact for the patients?

I mean, you know, when I
get my cholesterol checked

I gotta be fasting for
some time period before

I I go and do this.

Is now that we're measuring things

does does this change that that game?

Absolutely. So that's
the other big takeaway.

Now that we've got new
calculations that can

accommodate high levels
of triglyceride fasting

is really less of a strong requirement.

Unfortunately, you know
how workflows work.

If we show up at our
doctor and he says, oh

it's been a while since I
had your cholesterol stop

by the lab on your way
out, well you're gonna show

up at the lab or they're
gonna ask when you last ate

and they're gonna turn you away maybe

if you haven't fasted overnight.

And so now we're gonna be able to offer

so our recommendation is you
should offer a lipid panel

for non-fasting and then simply add

as a result whether or not
the patient was fasting.

And either way you can
calculate L D L cholesterol

and really get the
patient the care they need

without the inconvenience
of coming back later.

So if I can paraphrase you, it's with, now

with this calculated
eating isn't gonna really

change my number in any way.

Correct. Because L D L is much more

of a stable analyte over time.

It's just the fact that
we've been calculating it

and triglycerides have been
confounder in old equation.

Absolutely correct.

I should have started with that.

Cholesterol doesn't
fluctuate with a a meal.

It's pretty, it, you can only change that

with long-term dietary
trends or, or medication.

So fasting doesn't affect your cholesterol

it does affect your triglycerides

which is part of the equation
to calculate your cholesterol.

That's wonderful.

You're bringing me back to medical school

the very important lessons
and reminding me with

with that in mind of, of kind of learning.

One of the reasons I wanted to invite you

and I think it's great for our
community to kind of be aware

of your guidance document.

We'll of course, you know

put this in the show notes and link below

but also just for
professionals in our community

perhaps young professionals
just getting started.

You know, I think this is
an awesome opportunity to

maybe peek behind the curtain
and understand how these

how these things get made.

So I, I was wondering if
you could kind of reflect on

on your experience kind
of chairing this guidance

what advice do you have for others

in our community that,
you know, maybe have not

yet participated with their
societies in this way?

Or maybe they are starting to get engaged

with their societies, but
you know, kind of shy away

from maybe taking on this
kind of a, an assignment.

Do you have any kind

of thoughts or advice for
the young professional?

Absolutely. Yeah.

So like everything else in
life, it takes a great team

and I'm very fortunate
we have another lipid

focused clinical chemist right here, Mayo

who's my colleague, Leslie Donato

she co-chaired this committee with me.

We brought in some great lipid
experts and had a good bunch

of chemists as well as
physicians speaking specific.

And so that, that way
we got a, a wide range

of perspectives and we're
able to build consensus.

And now speaking specifically

to maybe people that are
earlier in their career

just like with your academic publications

you're not necessarily
making an expert statement

from your own personal standing

but everything you do has
to be backed up by data.

So there was a lot more literature review

than maybe I expected at first.

I would liken it

to like a book chapter
or a, or a view article.

A lot of, lot of studying
up on the latest literature

but then you can make these
statements substantiated

by evidence in the, in the public record

in the peer reviewed literature.

So it's been very rewarding

great experience and I highly
recommend getting involved.

Wow. Yeah, I I, I hear the
teamwork component in there

and I hear the, you know,
surprise, maybe it's some

of the work and effort that,
that, that goes into it.

But I, I think as you're pointing out

that's really a hallmark
of scholarly work and

and kind of the, the
reason that we are in the

the type of work that we, that we are.

Yeah.

Well, this has been awesome.

Thank you so much for joining us today.

Absolutely. Thanks for having me.

Nice talking with you.

So we've been rounding with Dr.

Meeusen about the the new lipid
testing guidance document.

And to our listeners, thank
you for joining us today.

We invite you to share your thoughts

and suggestions by email
to MCLeducation@mayo.edu.

If you've enjoyed this podcast

please subscribe until
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We encourage you to continue
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