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Medical Forum / Diseases and Disorders / Diabetes / January 2004

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Is a good A1c enough for glycemic control?

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Quentin Grady - 29 Jan 2004 04:04 GMT
G'day G'day Folks,

 Here is a partial answer to the puzzle.

It basically says if you make it to the 5% club the risk of coronary
heart disease is still double if post prandial glucose rises above
140 mg/dL (US units) or 7.8 mmol/L for the international units.

Notice the post prandial reading is taken at 2-hour not 1-hour.

1: Arch Intern Med.  2003 Jun 9; 163(11): 1306-16.  

Clinical significance, pathogenesis, and management of postprandial
hyperglycemia.  

Gerich JE.  

Department of Medicine, University of Rochester Medical Center,
Rochester, NY, USA. mary_little@urmc.rochester.edu  

It is well established that strict glycemic control (hemoglobin A1c
<7.0%) can prevent the microvascular complications of diabetes
mellitus.

Recent studies indicate that elevated plasma glucose concentrations
are an independent and clinically significant risk factor for
cardiovascular disease in nondiabetic and diabetic individuals.

Thus, isolated postprandial hyperglycemia

(2-hour postprandial glucose level >140 mg/dL [>7.8 mmol/L])

in the face of normal fasting plasma glucose

     (<110 mg/dL [<6.1 mmol/L])

and normal hemoglobin A1c (<6.1%)

values is associated with a 2-fold increased risk of death from
cardiovascular disease.

These observations imply that more strict glycemic control is required
to prevent macrovascular disease than microvascular disease.
This review summarizes epidemiologic and experimental studies linking
postprandial hyperglycemia to cardiovascular disease and therapeutic
approaches available and in development to treat this disorder.  

Publication Types: Review Review, Academic  

PMID: 12796066 [PubMed - indexed for MEDLINE]  

Best wishes,

Signature

Quentin Grady       ^  ^  /
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"... and the blind dog was leading."

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Quentin Grady - 29 Jan 2004 04:32 GMT
This post not CC'd by email
On Thu, 29 Jan 2004 17:04:18 +1300, Quentin Grady
<quentin@paradise.net.nz> wrote:

>G'day G'day Folks,
>
>  Here is a partial answer to the puzzle.

All in all it suggests control both A1c and post prandial glucose
makes sense if it is achievable.  

Note the spelling of Hanefeld   One reference had the name misspelt as
Henefeld which made is hard to find.  <grin>

Best wishes,

1: Nutr Metab Cardiovasc Dis.  2002 Apr; 12(2): 98-107.  

Control of post-prandial hyperglycemia--an essential part of good
diabetes treatment and prevention of cardiovascular complications.  

Hanefeld M, Temelkova-Kurktschiev T.  

Center of Clinical Studies, Technical University Dresden,
Fiedlerstrasse 34, 01307 Dresden, Germany. hanefeld@gwt-tud.de  

AIM: This article reviews the relationship between the control of
post-prandial hyperglycemia and diabetes-related complications.

DATA SYNTHESIS: Hyperglycemia is a modifiable risk factor that has a
deleterious effect on the development and progression of microvascular
and macrovascular complications in patients with type 2 diabetes.

The UK Prospective Diabetes Study revealed how reductions in
hemoglobin A1c (HbA1c) correlate with a significant reduction in
all-cause mortality and the incidence of myocardial infarction.

The Diabetes Intervention Study showed that poor control of fasting
glycemia does not increase the risk of myocardial infarction or
mortality, whereas poor control of post-prandial glucose is associated
with a high all-cause mortality rate.

HbA1c is the standard measure for metabolic control and therapeutic
efficacy, but does not reflect fluctuations in glycemic control.

Plasma glucose concentrations in healthy subjects remain within a
narrow range, which suggests that the fluctuations in glucose levels
caused by inappropriate treatment may have negative consequences.

These fluctuations have been associated with acute adverse effects
(particularly excessive post-prandial hyperglycemia, pre-meal
hypoglycemia and weight gain) that counteract the positive effect of
lowering fasting plasma glucose and HbA1c.

Post-prandial hyperglycemia and spikes also have deleterious effects
on insulin secretion and sensitivity.

Prandial oral antidiabetic agents such as alpha-glucosidase inhibitors
(acarbose, miglitol) and rapidly acting insulin secretagogues
(nateglinide, repaglinide) have recently been introduced to improve
the control of post-prandial hyperglycemia.

CONCLUSION: Near-normal post-prandial glycemic control is associated
with lower rates of cardiovascular and all-cause mortality than
excessive post-challenge hyperglycemia. In addition to the aggressive
control of HbA1c and fasting plasma glucose, the strict normalisation
of postprandial hyperglycemia is an essential part of good diabetes
treatment. There is growing evidence from epidemiological and clinical
studies that this also reduces the risk of cardiovascular
complications.  

Publication Types: Review Review, Tutorial  

PMID: 12189909 [PubMed - indexed for MEDLINE]  

Signature

Quentin Grady       ^  ^  /
New Zealand,       >#,#< [
                   / \ /\    
"... and the blind dog was leading."

http://homepages.paradise.net.nz/quentin

Jenny - 29 Jan 2004 14:30 GMT
Quentin,

As long as "normal" is defined as hba1c of 6.0% or FPG of 110 mg/dl or lower
all related research is going to be contaminated by the large numbers of
people with early diabetes in the study.

The more I read, the more convinced I am that 4.7% hbaic and under 90 mg/dl
are normal and everything else is part of the diabetes continuum.

P.S. did you see the rat study just published today about maternal diet and
longevity. It dovetails all too well with the earlier finding that maternal
starvation leads to diabetes in humans.

-- Jenny  - Low Carbing for 4 years. At goal for weight. Type 2 diabetes,
hba1c 5.2.
Cut the carbs to respond to my  email address!

Low carb facts and figures, my weight-loss photos, tips, recipes,
strategies for dealing with diabetes and more at
http://www.geocities.com/jenny_the_bean/

Looking for help controlling your blood sugar?
Visit  http://www.alt-support-diabetes.org/Newly%20Diagnosed.htm

> G'day G'day Folks,
>
[quoted text clipped - 56 lines]
>
> http://homepages.paradise.net.nz/quentin
gman99 - 29 Jan 2004 15:29 GMT
> Quentin,
>
> As long as "normal" is defined as hba1c of 6.0% or FPG of 110 mg/dl or
> lower all related research is going to be contaminated by the large
> numbers of people with early diabetes in the study.

There's a whole lot of problems with most studies. Many studies are not
comprehensive enough to account for the many differen variable which also
affect CVD, eyes, kidneys..etc. Things such as lipds and blood pressure are
not always taken into account as a risk factor along with hyperglycemia.
K'neH'a'Iw - 29 Jan 2004 17:23 GMT
> Quentin,
>
> As long as "normal" is defined as hba1c of 6.0% or FPG of 110 mg/dl or lower
> all related research is going to be contaminated by the large numbers of
> people with early diabetes in the study.

I think so too, although I prefer less than 5.0% and less that
100 mg/dl as my goals.

> The more I read, the more convinced I am that 4.7% hbaic and under 90 mg/dl
> are normal and everything else is part of the diabetes continuum.

Remember it wasn't that long ago that sugar in the urine was
used to diagnose and monitor. This approach at least will be a
very aggressive and at the same time conservative approach.

Signature

K'neH'a'Iw

Uncloaking, Shields up.

t2_lurking - 29 Jan 2004 14:51 GMT
So...
could I extrapolate and say that this is even more reason for more frequent
small meals?

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Do not mail to t2_lurking (auto-delete)
============================
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> G'day G'day Folks,
>
[quoted text clipped - 48 lines]
>
> Best wishes,
K'neH'a'Iw - 29 Jan 2004 19:05 GMT
> Recent studies indicate that elevated plasma glucose concentrations
> are an independent and clinically significant risk factor for
[quoted text clipped - 12 lines]
> values is associated with a 2-fold increased risk of death from
> cardiovascular disease.

I looked to see if there was any additional statistical data but
couldn't find it. If you know where it can be found please post
a link.

I wonder how "isolated" these postprandial excursions need to be
to cause an increase in marked cardiovascular disease, every
meal, once a week, once a month?

It seems obvious that regular excursions are included but what
about occasional ones. I maintain pretty good control, but
occasionally I either get it wrong or just decide to eat things
I don't normally. I've always thought that the occasional spike
was not too bad.

Signature

K'neH'a'Iw

Uncloaking, Shields up.

Quentin Grady - 29 Jan 2004 23:11 GMT
This post not CC'd by email
On Thu, 29 Jan 2004 13:05:30 -0600, K'neH'a'Iw

>> Recent studies indicate that elevated plasma glucose concentrations
>> are an independent and clinically significant risk factor for
[quoted text clipped - 16 lines]
>couldn't find it. If you know where it can be found please post
>a link.

G'day G'day K'neH'a'Iw,

 There isn't a lot of data that is readily available.  Pubmed has a
lot of abstracts that basically say something like "In this study we
looked at why post prandial glucose excursions are important ... "

To get the details one has to pay a subscription to download a full
text or .pdf file.  No one is paying me to do so, so it isn't in my
budget.  I find it very frustrating that I have to rely on a consensus
document without being able to view the original research.

>I wonder how "isolated" these postprandial excursions need to be
>to cause an increase in marked cardiovascular disease, every
>meal, once a week, once a month?

So do.  I'll have to live with that until the full texts become free
reprints or I find some form of employment that allows me to do the
downloads.

>It seems obvious that regular excursions are included but what
>about occasional ones. I maintain pretty good control, but
>occasionally I either get it wrong or just decide to eat things
>I don't normally. I've always thought that the occasional spike
>was not too bad.

IMHO the occasional spike isn't too bad.  Occasional can all too
easily drift into habitual.  So long as we understand the difference.

I find it easier to make decisions when I have very simple rules.
Here are my current ones, subject to update at any moment.

The CVD risk for early stage diabetics or those A1c below 6.1% and
frequent excursions at 2-hours over 140 mg/dL (7.8 mmol/L) is about
double that for non-diabetics.  That is actually quite a good risk
level.  

For those that have A1c of about 7% the risk is IIRC about four times
that for non-diabetics. (I'd need to check those figures) Put simply
the people in this group would appear to be twice as well off as those
whose A1c is higher.  

People who are obese but exercise have half the mortality rate of
those who have ideal weight but live sedentary lifestyles. (5 years
study a few thousand people.)  Put simply there is a reasonable chance
that one risk offsets the other.  Getting together a long term study
for a small select group who exercise vigorous but have this IGT
hyperglycemic profile might be a bit daunting.

Uncontrolled T2 diabetics have a risk of CHD over four times that of
non-diabetics.

People think of diabetes as an error of blood glucose metabolism.  In
practice it is an error in fat metabolism, protein and carbohydrate
metabolism.  As the worst excesses of blood glucose are dealt with
there rapidly becomes a point where dealing with the lipid imbalance
becomes more important.  My simplistic approach has been to follow
triglyceride:HDL ratio.  Dealing with inflammation and blood pressure
also rapidly assume centre stage.

Best wishes,
Signature

Quentin Grady       ^  ^  /
New Zealand,       >#,#< [
                   / \ /\    
"... and the blind dog was leading."

http://homepages.paradise.net.nz/quentin

K'neH'a'Iw - 31 Jan 2004 04:57 GMT
> G'day G'day K'neH'a'Iw,

> IMHO the occasional spike isn't too bad.  Occasional can all too
> easily drift into habitual.  So long as we understand the difference.

How do you define occasional? I am currently at sorta
once a week. I can reduce it if I believe that that
there is  a benefit.

> The CVD risk for early stage diabetics or those A1c below 6.1% and
> frequent excursions at 2-hours over 140 mg/dL (7.8 mmol/L) is about
> double that for non-diabetics.  That is actually quite a good risk
> level.  

My recent A1c's have been 5% or less, how do you
define frequent?

> People who are obese but exercise have half the mortality rate of
> those who have ideal weight but live sedentary lifestyles. (5 years
> study a few thousand people.)

OK, I'm now simply overweight and sedentary.

> Uncontrolled T2 diabetics have a risk of CHD over four times that of
> non-diabetics.

How do your define uncontrolled?

> People think of diabetes as an error of blood glucose metabolism.  In
> practice it is an error in fat metabolism, protein and carbohydrate
> metabolism.  

I think of it as carbohydrate intolerance. Where does
the fat and protein metabolism come in?

> As the worst excesses of blood glucose are dealt with
> there rapidly becomes a point where dealing with the lipid imbalance
> becomes more important.

In my case I tried that and am now taking Lipitor, it
seems to be working. The lipid problem seems to be
genetic. My grandmother lasted to 99 years 6 months
with a total cholesterol of 300+

> My simplistic approach has been to follow
> triglyceride:HDL ratio.

 Doing good there 93/64 at my last test.

> Dealing with inflammation

OK, how do you do that? I'm doing lots of fresh/frozen
vegetables and aspirin therapy.

> and blood pressure

This is a weak point I'm at the high point of
acceptable for non-diabetics pushing 140/80

--
K'neH'a'Iw

Uncloaking, Shields up.
Quentin Grady - 31 Jan 2004 11:38 GMT
This post not CC'd by email
On Fri, 30 Jan 2004 22:57:15 -0600, K'neH'a'Iw

>> G'day G'day K'neH'a'Iw,
>
>> IMHO the occasional spike isn't too bad.  Occasional can all too
>> easily drift into habitual.  So long as we understand the difference.
>
>How do you define occasional?

G'day G'day K'neH'a'Iw,

 I don't make the definitions ... thank goodness.  Every so often
groups of learned people get together to refine the definition of
diabetes.  Now you have to ask yourself, why would they do that?

There is nothing to be gained from a definition that doesn't lead to
practical decision making in some way.

>I am currently at sorta
>once a week. I can reduce it if I believe that that
>there is  a benefit.

We all take some risk ... living is a risky business.  

I'd like you to think about what you are asking.  How likely is it
there is a study where people have one spike a week and where their
rate of complications over five or ten years is compared with another
group who have two spikes per week.  Complications are often assessed
as a rate over ten years.  I don't think anyone has the detailed sort
of information you are seeking.

>> The CVD risk for early stage diabetics or those A1c below 6.1% and
>> frequent excursions at 2-hours over 140 mg/dL (7.8 mmol/L) is about
[quoted text clipped - 3 lines]
>My recent A1c's have been 5% or less, how do you
>define frequent?

I don't.  The people who wrote the paper must had some working
definition as part of their experimental procedure.  Sorry, I don't
have the cash to read the full text.  I can guess for you.  
If I did, I think it meant most days of the week.

>> People who are obese but exercise have half the mortality rate of
>> those who have ideal weight but live sedentary lifestyles. (5 years
>> study a few thousand people.)
>
>OK, I'm now simply overweight and sedentary.

Sedentary is definitely not good.  Sorry.   I think the point of the
experiment was to compare the effects of being overweight and leading
a sedentary lifestyle independently.  They are so often co-related
that this was a pretty bold question to ask and try to find an answer.
The answer they found sure gave me a wake up call.  Sedentary is twice
as bad as obesity as a killer.  

>> Uncontrolled T2 diabetics have a risk of CHD over four times that of
>> non-diabetics.
>
>How do your define uncontrolled?

This time there are working definitions. That doesn't mean they are
internationally agreed or that the figures are applicable to testing
done in different labs.  Poor control would appear to be an A1c
greater than 8.0

1: South Med J.  2002 Jan;95(1):72-7.  

Role of exercise for type 2 diabetic patient management.  

Pigman HT, Gan DX, Krousel-Wood MA.  

Office of Performance Improvement, Veterans Affairs Medical Center,
New Orleans, LA 70031, USA.  

BACKGROUND: Exercise is integral to the management of type 2 diabetes.
Unfortunately, the majority of adults with type 2 diabetes do not
engage in regular exercise.

METHODS: Three hundred patients with type 2 diabetes were randomly
selected from a patient pool of diabetic patients encountered in 1996
at the Department of Veterans Affairs Medical Center in New Orleans,
Louisiana. Medical records from October 1996 to June 1999 were
reviewed. Information about exercise, alcohol intake, smoking,
medications, laboratory results, and other variables was extracted
from medical records. Patients with mean glycosylated hemoglobin
(HbA1c) < 8.0 (good diabetic control) were compared with those who had
poor diabetic control (mean (HbA1c) > or = 8.0). The effect of
exercise in the management of type 2 diabetes was assessed.

RESULTS: After adjustment for other variables, patients without
exercise had an odds ratio of 2.71 (95% CI, 1.38-5.32) for poor
diabetic control compared with patients with exercise.

CONCLUSIONS: These findings suggest that exercise by itself is
important for type 2 diabetes management.  

PMID: 11827248 [PubMed - indexed for MEDLINE]  

>> People think of diabetes as an error of blood glucose metabolism.  In
>> practice it is an error in fat metabolism, protein and carbohydrate
>> metabolism.  
>
>I think of it as carbohydrate intolerance. Where does
>the fat and protein metabolism come in?

In the early stages of Metabolic Syndrome (Syndrome X) blood glucose
levels stay relatively normal but the liver loses the plot and fails
to switch of fat production when food is eaten.  

>> As the worst excesses of blood glucose are dealt with
>> there rapidly becomes a point where dealing with the lipid imbalance
[quoted text clipped - 9 lines]
>
>  Doing good there 93/64 at my last test.

Both those figures look excellent.  

In countries using mmol/L, the optimal cut-points were
1.47 mmol/L for triglyceride,
1.8 in SI units for the triglyceride–HDL cholesterol ratio,
and 109 pmol/L for insulin.

In countries using mg/dL the optimal cut-points were
130 mg/dL for triglyceride,
3.0 for the triglyceride–HDL cholesterol ratio,
and 109 pmol/L for insulin.

IMHO the trick to face up to whatever personal challenge we have.  In
the first instance that means having these things tested then tackling
them in earnest.

>> Dealing with inflammation
>
>OK, how do you do that? I'm doing lots of fresh/frozen
>vegetables and aspirin therapy.

Well that is a good start.  Think also improving omega-3 to omega-6
ratio. Put simply ... eat fish or FREE RANGE meat. Eat berries,
include cocoa in your diet.  Use turmeric and ginger.  Eat salads or
some other vegetables RAW.  RAW foods are a source of MSM, methyl
sulphonyl methane, which is anti-inflammatory.  Even boiling
evaporates MSM.

>> and blood pressure
>
>This is a weak point I'm at the high point of
>acceptable for non-diabetics pushing 140/80

Think anti-inflammatory.  

Best wishes,

Signature

Quentin Grady       ^  ^  /
New Zealand,       >#,#< [
                   / \ /\    
"... and the blind dog was leading."

http://homepages.paradise.net.nz/quentin

 
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