Category Archives: Causes of Diabetes

Misleading “Mediterranean Diet” Headline at the Washington Post

Perhaps you read the December 17, 2008, Washington Post (online) article, “Mediterranean-Style Diet Best for Blood Sugar Control.”

The same headline was used by MedlinePlus: Trusted Health Information for You, a service of the U.S. government.  The two articles may be exactly the same.

A physician spokeswoman for the American Heart Association is quoted in the story saying that “…the best diet is a Mediterranean-type diet…”

I mention this only because the Canadian study to which she refers is not a test of the Mediterranean diet in people with diabetes.

[Did you know that some people with diabetes are offended if you call them “diabetics”?  To call them diabetics defines them by their disease.  They’re not diseases, they’re individual humans.]

There are certainly some studies indicating that the traditional Mediterranean diet may be a good one for people with diabetes, and that the Mediterranean diet can prevent type 2 diabetes, but this Canadian study is not one of them.

Steve Parker, M.D.

Reference:  Jenkins, David,  et al.  Effect of a Low-Glycemic Index or High-Cereal Fiber Diet on Type 2 Diabetes: A Randomized Trial.  Journal of the American Medical Association, 300 (2008): 2,742-2,753.

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Glycemic Index and Chronic Disease Risk (Mostly in Women)

"Would you like some high-glycemic index bread?"

"Would you like some high-glycemic index bread?"

I recently blogged about glycemic index (GI), glycemic load (GL), and glycemic diets in preparation for today’s post.

The concept of glycemic index was introduced by Jenkins et al in 1981 at the University of Toronto.

Studies investigating the association between disease risk and GI/GL have been inconsistent.  By “inconsistent,” I mean some studies have made an association in one direction or the other, and other studies have not.  Diseases possibly associated with high-glycemic diets have included diabetes, cardiovascular disease, cancer, gallbladder disease, and eye disease.

“Diet” in this post refers to a habitual way of eating, not a weight loss program.

Researchers with the University of Sydney (Sydney, Australia) identified the best-designed published research reports investigating the relationship between certain chronic diseases and glycemic index and load.  The studied diseases were type 2 diabetes, coronary heart disease, stroke, breast cancer, colorectal cancer, pancreatic cancer, endometrial cancer, ovarian cancer, gallbladder disease, and eye disease.

Methodology

Literature databases were searched for articles published between 1981 and March, 2007.  The researchers found 37 studies that enrolled 1,950,198 participants ranging in age from 24 to 76, with BMI’s averaging 23.5 to 29.  These were human prospective cohort studies with a final outcome being occurrence of a chronic disease (not its risk factors).  Twenty-five of the studies were conducted in the U.S., five in Canada, five Europe, and two in Australia.  Ninety percent of participants were women [for reasons not discussed].  Food frequency questionnaires were used in nearly all the studies.  Individual studies generated between 4 to 20 years of follow-up, and 40,129 new cases of target diseases were identified.

Associations between GI, GL, and risk of developing a chronic disease were measured as rate ratios comparing the highest with the lowest quantiles.  For example, GI and GL were measured in the study population.  The population was then divided into four groups (quartiles), reflecting lowest GI/GL to medium to highest GI/GL diets.  The lowest GI/GL quartile was compared with the highest quartile to see if disease occurrence was different between the groups.  Some studies broke the populations into tertiles, quintiles, deciles, etc.

Findings

Comparing the highest with the lowest quantiles, studies with a high GI or GL independently

  • increased the risk of type 2 diabetes by 27 (GL) or 40% (GI)
  • increased the risk of coronary heart disease by 25% (GI)
  • increased the risk of gallbladder disease by 26% (GI) or 41% (GL) [gallstones and biliary colic, I assume, but the authors don’t specify]
  • increased the risk of breast cancer by 8% (GI)
  • increased risk of all studied diseases (11) combined by 14% (GI) or 9% (GL)

Overall, high GI was more strongly associated with chronic disease than was high GL
So low-GI diets may offer greater protection against disease than low-GL diets.

Comments from the Researchers

They speculate that low-GI diets may be more protective than low-GL because the latter can include low-carb foods such as cheese and meat, and low-GI, high-carb foods.  Both eating styles will reduce glucose levels after meals while having very different effects in other areas such as pancreas beta cell function, free fatty acid levels, triglyceride levels, and effects on satiety.

High GI and high GL diets, independently of known confounders, modestly increase the risk of chronic lifestyle-related diseases, with more pronounced effects for type 2 diabetes, coronary heart disease, and gallbladder disease.

Direct quotes:

. . . 90% of participants were female; therefore, the findings may not be generalizable to men.

There are plausible mechanism linking the development of certain chronic diseases with high-GI diets.  Specifically, 2 major pathways have been proposed to explain the association with type 2 diabetes risk.  First the same amount of carbohydrate from high-GI food produces higher blood glucose concentrations and a greater demand for insulin.  The chronically increased insulin demand may eventually result in pancreatic beta cell failure, and, as a consequence, impaired glucose tolerance.  Second, there is evidence that high-GI diets may directly increase insulin resistance through their effect on glycemia, free fatty acids, and counter-regulatory hormone secretion.  High glucose and insulin concentrations are associated with increased risk profiles for cardiovascular disease, including decreased concentrations of HDL cholesterol, increased glycosylated protein, oxidative status, hemostatic variables, and poor endothelial function

Low-GI and/or low-GL diets are independently associated with a reduced risk of certain chronic diseases.  In diabetes and heart disease, the protection is comparable with that seen for whole grain and high fiber intakes.  The findings support the hypothesis that higher postprandial glycemia is a universal mechanism for disease progression.

My Comments

Studies like this tend to accentuate the differences in eating styles since they compare the highest with the lowest post-prandial (after meal) glucose levels.  Most people are closer to the middle of the pack, so a person there has potentially less to gain by moving to a low-GI diet.  But still some to gain, on average, particularly in regards to avoiding type 2 diabetes and coronary heart disease.

[To be fair, many population-based studies use this same quantile technique.  It increases the odds of finding a statistically significant difference.]

Only two of the 37 studies examined coronary heart disease, the cause of heart attacks.  One study was the massive Nurses’ Health Study database with 75,521 women.  The other was the Zutphen (Netherlands) Elderly Study which examined men 64 and older.  Here’s the primary conclusion of the Zutphen authors verbatim:

Our findings do not support the hypothesis that a high-glycemic index diet unfavorably affects metabolic risk factors or increases risk for CHD [coronary heart disease] in elderly men without a history of diabetes or CHD.

So there’s nothing in the meta-analysis at hand to suggest that high-GI/GL diets promote heart disease in males in the general population.

However, the recent Canadian study in Archives of Internal Medicine found strong evidence linking CHD with high-glycemic index diets.  Although not mentioned in the text of that article, Table 3 on page 664 shows that the association is much stonger in women than in men.  Relative risk for women on a high-glycemic index/load diet was 1.5 (95% confidence interval = 1.29-1.71), and for men the relative risk was 1.06 (95% confidence interval = 0.91-1.20).  See reference below.

Nine of the 37 studies examined the occurrence of type 2 diabetes.  Only one of these studied men only – 42,759 men: the abstract is not available online and the Sydney group does not mention if high-GI or high-GL was positively associated with onset of diabetes in this cohort.  Two of the diabetes studies included both men and women, but the abstracts don’t break down the findings by sex.  [I’m trying to deduce if the major overall findings of this meta-analysis apply to men or not.]

I don’t know anybody willing to change their diet just to avoid the risk of gallstones.  It’s only after they develop symptomatic gallstones that they ask me what they can do about them.  The usual answer is surgery.

The report is well-done and seems free of commercial bias, even though several of the researchers are authors or co-authors of popular books on low-GI eating.

Steve Parker, M.D.

References:

Barclay, Alan W.; Petocz, Peter; McMillan-Price, Joanna; Flood, Victoria M.; Prvan, Tania; Mitchell, Paul; and Brand-Miller, Jennie C.  Glycemic index, glycemic load, and chronic disease risk – a meta-analysis of observational studies [of mostly women].  American Journal of Clinical Nutrition, 87 (2008): 627-637.

Brand-Miller, Jennie, et al.  “The New Glucose Revolution: The Authoritative Guide to the Glycemic Index – The Dietary Solution for Lifelong Health.”  Da Capo Press, 2006.

Mente, Andrew, et al.  A Systematic Review of the Evidence Supporting a Causal Link Between Dietary Factors and Coronary Heart DiseaseArchives of Internal Medicine, 169 (2009): 659-669.

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Societal Changes and the Increasing Rates of Type 2 Diabetes

42-16033240I ran across a thought-provoking article published a few months ago at DiabetesHealth online.  It’s a non-scientific exploration of the potential causes of “diabesity,” the combination of obesity and type 2 diabetes.

You’ll get a kick out of this especially if you’re over 40.

Click here to read “50 Reasons Why Diabesity Wasn’t Prevalent 50 Years Ago.”

Steve Parker, M.D.

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High Glycemic Load and Low Grain Fiber Increase Risk of Type 2 Diabetes in Men

Minimally refined grain

Minimally refined grain

A study published in 1997 helped establish the association between glycemic load, dietary fiber, and type 2 diabetes in men.

Methodology

Over 42,000 mostly middle-aged men in the Health Professionals Follow-up Study, without diabetes at baseline, were followed over six years to see if  diet composition was related to onset of type 2 diabetes.  Food intake was determined by a questionnaire.  95% of participants were white.

Results

523 cases of type 2 diabetes developed.  Men with the highest glycemic index eating pattern were 37% more likely to develop diabetes compared to the lowest glycemic index.

Cereal (grain) fiber was inversely related to risk of diabetes.  That is, the higher the intake of grain fiber, the lower the risk of developing diabetes.

The combination of high glycemic load and low cereal fiber yielded the highest rate of diabetes.

Total dietary fiber was not associated with reduced risk of diabetes.

Fiber from fruits and vegetables was not associated with diabetes one way or the other.

As other studies found, total carbohydrate intake was not related to risk of diabetes.

Take-Home Points

These findings may or may not apply to women and non-white ethnic groups.

Grains in a minimally refined form reduced the incidence of diabetes in this population.

Diets with a high glycemic load increase the risk of diabetes, at least in men.

Elsewhere, I’ve reviewed studies indicating that, in women, both high glycemic load and high glycemic index eating increase the risk of type 2 diabetes.  Click here for details.

We must wonder if  established cases of diabetes would respond positively to diets with low glycemic load and grains in a minimally refined form.  Or is it too late?

Steve Parker, M.D.

Reference:  Salmeron, Jorge, et al.  Dietary fiber, glycemic load, and risk of NIDDM in Men.  Diabetes Care, 20 (1997): 545-550

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Filed under Carbohydrate, Causes of Diabetes, Fiber, Glycemic Index and Load

Can Diabetes Be Prevented in Older Adults?

42-15653241A study published yesterday supports the idea that even in older adults, over 65, type 2 diabetes can be prevented in most cases by healthy lifestyle choices.

Researchers examined the participants in the Cardiovascular Health Study – 4,883 men and women over 65 at baseline – over the course of 10 years.  Median age at enrollment was 73.  Participants were followed clinically for 10 years.  New cases of diabetes over 10 years: 337.  Researchers suspected, based on previous studies in younger folks, that a reduced incidence of diabetes onset would be related to:

  • physical activity levels above the median (half of people exercise less than the median, half exercise more)
  • never smoking, or minimal and years ago
  • “healthy diet,” defined as high fiber, low glycemic index foods, lower trans fats, higher polyunsaturated-to-saturated fat ratio
  • low body mass index (not overweight)
  • waist circumference under 92 cm (36.2 inches) for men and 88 cm (34.6 inches) for women
  • low to moderate alcohol use

We’ll call these “lifestyle factors.”  Participants were analyzed to see how well they fit this profile and whether or not they developed diabetes.

Results

The more each of these lifestyle factors characterized a person, the lower the risk of developing diabetes.

High physical activity and healthy diet by themselves reduced risk of diabetes by half.

Study authors estimate that healthy lifestyle choices could prevent eight or nine out of 10 cases of diabetes in older adults.

Take-Home Point

The researchers rightfully point out that their results are associations, not proof that these lifestyle factors prevent diabetes.  Given the totality of the evidence from this and other studies, I would adopt many of the low-risk lifestyle choices if I wanted to avoid diabetes.

Steve Parker, M.D.

Reference:  Mozaffarian, D., et al.  Lifestyle risk factors and new-onset diabetes mellitus in older adultsArchives of Internal Medicine, 169, (2009): 798-807.

Update April 30, 2009:

Research in younger populations has associated the following factors with prevention of type 2 diabetes:

  1. Avoid overweight, or lose weight if you are overweight (body mass index over 25)
  2. Regular physical activity
  3. Don’t start smoking, or quit if you do
  4. Pick the right parents

Some cases of diabetes are related to genetic factors beyond our control.  Having parents or close relatives with diabetes suggests that you may be genetically predisposed.  Genetics is not necessarily destiny, however.

-Steve

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Lipid Overload as the Cause of Type 2 Diabetes

An up-and-coming theory to explain type 2 diabetes suggests that abnormal lipid metabolism, not glucose/sugar metabolism, is the primary metabolic defect.  Roger H. Unger, M.D., writes about this in the March 12, 2008, issue of the Journal of the American Medical Association.

Early in the writing of this blog entry, I realized it is much too technical for many readers.  I’m writing this to solidify my own understanding of a new theory.  If you are not interested in physiology, you can quit reading now. 

Still with me? 

Definitions and Physiology

Diabetes is defined by high blood glucose (sugar) levels. 

The lipid family includes triglycerides (fats and oils), sterols (e.g., cholesterol), and phospholipids (e.g., lecithin, a major cell membrane component).  Fats are almost entirely composed of trigylcerides.  When fats are broken down, fatty acids are produced.  On the other hand, fatty acids can be joined together, along with glycerol, to form triglycerides. 

Glycogen is a storage form of glucose in liver and muscle tissue. 

Insulin is a protein hormone produced by pancreatic beta cells.  Insulin:

  1. lowers blood glucose levels by driving glucose into cells 
  2.  inhibits breakdown of glycogen into glucose
  3. inhibits formation of new glucose molecules by the body
  4. stimulates glycogen formation
  5. promotes storage of triglycerides in fat cells (i.e., lipogenesis, fat accumulation)
  6. promotes formation of fatty acids (triglyceride building blocks) by the liver
  7. inhibits breakdown of stored triglycerides
  8. supports protein synthesis. 

Fatty acids in muscle tissue block the uptake of glucose from the bloodstream by muscle cells.  Fatty acids in liver tissue impair the ability of insulin to suppress breakdown of glycogen into glucose, and impair the ability of insulin to suppress production of new glucose molecules.  In other words, an “excessive fatty acid” environment in liver and muscle tissue promotes elevated glucose levels.

Got that?  [This is very difficult material.]  Now on to . . .

 The Lipocentric Theory of Type 2 Diabetes

Type 2 diabetes may be caused by:

  1. Eating too many calories, leading to…
  2. High insulin levels, leading to…
  3. Stimulation of fat production, leading to…
  4. Increased body fat, leading to…
  5. Deposition of lipids in cells where they don’t belong (that is, not in fat cells), leading to…
  6. Resistance to insulin’s effects on glucose metabolism, leading to…
  7. Lipid accumulation in pancreatic beta cells, damaging them, leading to…
  8. Elevated blood glucose levels, i.e., diabetes.

Perhaps the key to understanding this is to know that “insulin resistance” refers to insulin having less ability to suppress glucose production by the liver, or less ability of various tissues to soak up circulating glucose.  Insulin resistance thereby leads to elevated glucose levels.  But insulin’s effect of “producing fats” (lipogenesis) continues unabated.  Excessive fats, actually fatty acids, accumulate not only in fat cells, but also in liver cells, muscle cells, pancreatic beta cells, and others.  This lipid overload can damage those cells.

If This Theory Is Correct, So What?

Steps #1 and 2 of the lipocentric theory involve excessive caloric intake and high circulating insulin levels, leading to problems down the road.  So overweight people should restrict calories and try to lose at least a modest amount of weight.  Particularly if already having type 2 diabetes or prone to it.

And what about people with type 2 diabetes who have insulin resistance and have poorly controlled glucose levels?  Most of these have high insulin levels already, contributing to a fat-producing state.  Adding more insulin, by injection, would not seem to make much sense.  The extra insulin would bring glucose levels down, but might also cause lipid overload with associated cellular damage.  Effective clinical strategies according to Dr. Unger would include 1) caloric restriction, which helps reduce weight, high insulin levels, and fat production, and 2) if #1 fails, add anti-diabetic drugs that reduce caloric intake (exenatide?), that reduce lipid overload (which drug?), or that do both.  Dr. Unger suggests consideration of bariatric surgery, for caloric restriction and cure of diabetes.

Compared with dietary fats and proteins, carbohydrates generally cause higher circulating insulin levels.  And type 2 diabetics taking insulin shots need higher doses for higher intakes of carbohydrate. So it makes sense to me to consider preferential reduction of carbohydrate intake if someone is going to reduce caloric intake.

Dr. Unger and I agree that reduction of excessive food intake and excess body fat is critically important for overweight people with type 2 diabetes.

Steve Parker, M.D.

References: Unger, Roger H.  Reinventing Type 2 Diabetes: Pathogenesis, Treatment, and Prevention.  Journal of the American Medical Association, 299 (2008): 1185-1187.

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