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The newspaper of The Johns Hopkins University May 5, 2008 | Vol. 37 No. 33
 
Study Ties Obesity, Inflammatory Proteins to Heart Failure Risk

By David March
Johns Hopkins Medicine

Heart specialists at Johns Hopkins and elsewhere report what is believed to be the first wide- scale evidence linking severe overweight to prolonged inflammation of heart tissue and the subsequent damage leading to failure of the body's blood-pumping organ.

The latest findings from the Multiethnic Study of Atherosclerosis, to be published May 6 in the Journal of the American College of Cardiology, appear to nail down yet one more reason for the estimated 72 million obese American adults to be concerned about their health, say scientists who conducted the research.

"The biological effects of obesity on the heart are quite profound," said senior study investigator Joao Lima. "Even if obese people feel otherwise healthy, there are measurable and early chemical signs of damage to their heart beyond the well-known implications for diabetes and high blood pressure."

Lima said that there is now "even more reason for them to lose weight, increase their physical activity and improve their eating habits."

In the latest study, researchers conducted tests and tracked the development of heart failure in an ethnically diverse group of nearly 7,000 men and women, ages 45 to 84, who were enrolled in the MESA study that started in 2000.

Of the 79 who have developed congestive heart failure so far, 35 (44 percent) were physically obese, having a body mass index of 30 or greater. And on average, obese participants were found to have higher blood levels of interleukin 6, C-reactive protein and fibrinogen, key immune system proteins involved in inflammation, than nonobese adults.

A near doubling of average interleukin 6 levels alone accounted for an 84 percent greater risk of developing heart failure in the study population.

The researchers from five universities across the United States also found alarming links between inflammation and the dangerous mix of heart disease risk factors known as the metabolic syndrome. Its combined risk factors for heart disease and diabetes — high blood pressure, elevated blood-glucose levels, excess abdominal fat, abnormal cholesterol levels and particularly obesity — double a person's chances of developing heart failure.

"More practically, physicians need to monitor their obese patients for early signs of inflammation in the heart and to use this information in determining how aggressively to treat the condition," said Lima, a professor of medicine and radiology at the Johns Hopkins School of Medicine and its Heart Institute.

All MESA study participants, who will be followed through to 2012, had no pre-existing symptoms of heart disease. Upon enrollment, they all underwent a physical exam, including weight and body measurements, blood analysis and an MRI scan to assess heart function.

"Our results showed that when the effects of other known disease risk factors — including race, age, sex, diabetes, high blood pressure, smoking, family history and blood cholesterol levels — were statistically removed from the analysis, inflammatory chemicals in the blood of obese participants stood out as key predictors of who got heart failure," Lima said.

The chemicals are all known to be part of the body's defensive response to disease. They are well-recognized for producing symptoms that stem from the widening of small blood vessels, including redness and fever, and the release of immune system cells that make blood vessels leak fluid into surrounding tissue, causing swelling and cell death. The inflammatory process eventually leads to cell damage and the buildup of scar tissue near the damaged areas.

In obese participants, interleukin 6, a chemical that activates white blood cells and drives inflammation, was higher than in nonobese participants.

Similarly, a near tripling of average levels of C-reactive protein in study participants increased the chance of heart failure by 36 percent.

C-reactive protein levels are widely known to rise dramatically and speed up the early stages of inflammation when cells swell up with fluid, leading to widespread arterial damage.

One-fifth-higher-than-average blood levels of fibrinogen, best known for its role in blood clotting but also a major player in muscle scarring, bumped up the risk of heart failure by 37 percent.

When the scientists removed the effects of the inflammatory protein levels from their statistical analysis, the heightened risk from obesity disappeared.

"What this tells us," said lead researcher Hossein Bahrami, "is that both obesity and the inflammatory markers are closely tied to each other and to heart failure."

Each year, nearly 300,000 Americans die from heart failure.

Bahrami says study results also point to inflammation as a possible catalyst in metabolic syndrome. Increased blood levels of albuminuria, a chemical more known for its association with impaired kidney function and metabolic syndrome, boosted risk of a progressively weakening heart nearly tenfold among MESA participants.

Bahrami, a senior cardiology research fellow at Johns Hopkins, said, "The basic evidence is building the case that inflammation may be the chemical route by which obesity targets the heart, and that inflammation may play an important role in the increased risk of heart failure in obese people, especially those with the metabolic syndrome."

He notes that previous studies, also done at Johns Hopkins, have shown that even moderate exercise to lose abdominal fat dramatically offsets the harmful effects of metabolic syndrome on heart function.

Bahrami says the team's next steps are to determine how, over a longer timeframe, heart function changes with levels of inflammatory markers, and to see if alterations to the immune system proteins halts or speeds up disease.

MESA is funded by the National Heart, Lung and Blood Institute, a member of the National Institutes of Health.

Other Johns Hopkins investigators involved in this study were David Bluemke and Moyses Szklo. Co-authors were Richard Kronmal, University of Washington; Alain Bertoni, Wake Forest University; Donald Lloyd-Jones, Northwestern University; and Eyal Shahar, University of Arizona.

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