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Liver protein may explain younger women's low risk of heart disease

SANTA FE, N.M. (March 21, 1998 6:54 p.m. EST http://www.nando.net) -- New
discoveries about an enzyme that regulates cholesterol levels could help
explain one of the enduring mysteries of the sexes -- why men die younger than
women from heart disease.

Everywhere researchers have looked in the world, heart disease strikes men at
earlier ages than women.

In Western countries, where heart trouble is the biggest killer of both sexes,
men generally die from it about 10 years sooner.

Differences in traditional risk factors -- high blood pressure, smoking and
obesity, among others -- do not entirely explain this disparity, nor do the
obvious hormonal and physical differences.

However, scientists say their research into gender differences in a liver
enzyme called hepatic lipase may well explain why women typically have better
cholesterol levels than men, especially before menopause when their risk of
heart trouble is very low.

Dr. John E. Hokanson of the University of Washington in Seattle presented the
findings at an American Heart Association conference, which concluded
Saturday.

Younger women's risk is low because of their favorable lipid profiles -- the
types, not just the quantity, of cholesterol in their blood.

Cholesterol and fats called triglycerides cannot dissolve in blood.

So they are carried through the bloodstream by transport molecules called
lipoproteins, which are produced by the liver.

The liver also makes hepatic lipase, which breaks down these combinations so
the fats can be used by the body.

Most of the cholesterol is transported by low-density lipoprotein, or LDL.

This is generally called the bad cholesterol, since it deposits excess
cholesterol on the artery walls and leads to blockages.

LDL also comes in different sizes, and small, dense LDL is considered
especially harmful.

High-density lipoprotein, or HDL, is helpful, because it carries cholesterol
and fats out of the bloodstream before they harm the arteries.

The higher the proportion of HDL, the lower the risk of heart attacks.

Typically, young women have higher HDL, lower LDL and less dense LDL than do
men the same age.

Hokanson and colleagues tested 25 men and 39 premenopausal women. They ranged
in age from 21 to 59 and had normal cholesterol levels.

Hepatic lipase levels were 53 percent higher in the men.

Hokanson found that the men's higher amounts of this enzyme could explain 42
percent of the difference between the sexes in the density of the LDL they
carried.

And it could explain 97 percent of the difference between men and women in HDL
levels.

"We believe that hepatic lipase is an important modulator of HDL," said
Hokanson.

"This accounts for the difference in coronary risk lipid profiles in men and
women."

While he said this does not explain all of the difference in heart disease
risks between the sexes, it could play a significant part.

Experts think women's risk goes up after menopause because they lose the
protective effects of estrogen, the female sex hormone.

Estrogen appears to regulate the body's levels of hepatic lipase, and Hokanson
found this enzyme increases after menopause.

Hokanson said estrogen's effects on this enzyme may be one reason why hormone
replacement therapy significantly lowers older women's risk of heart attacks.

He said cholesterol-lowering drugs also may work by affecting levels of
hepatic lipase.

In the United States, 29 percent of men in their 40s have cardiovascular
disease, compared with 17 percent of women.

By the time they reach their 70s, about 70 percent of both sexes have heart
disease.

Dr. Shiriki Kumanyika of the University of Illinois at Chicago said
understanding the reasons for young women's protection could help men of all
ages, as well as older women.

"The question is: What is it about women?" she said. "Why don't they get heart
disease so soon? If we could figure that out, maybe we could give it to men."

By DANIEL Q. HANEY, AP Medical Editor

Copyright 1998 Nando.net
Copyright 1998 The Associated Press

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