Table of Contents

January 20, 2009; 150 (2)

Articles

  • Paynter and colleagues compared cardiovascular risk prediction using a genetic variation at chromosome 9p21.3 plus conventional risk factors—such as family history of early cardiovascular disease, smoking, blood pressure, and cholesterol and C-reactive protein levels—with risk prediction using conventional risk factors alone. Using a sample of 22 129 white, female health professionals observed for a median of 10 years, the investigators found that adding genetic information to conventional risk factors did not improve the accuracy of classifying cardiovascular risk.

  • Eckman and coworkers evaluated the cost-effectiveness of genotype-guided warfarin dosing for patients with nonvalvular atrial fibrillation. For the standard base case (a man age 69 years with no contraindications to warfarin therapy and the current cost of genotyping of about $400), it costs $170 000 more per quality-adjusted life-year gained than standard warfarin dosing. At its current cost, routine genotyping before warfarin dosing is unlikely to be cost-effective.

  • High-density lipoprotein (HDL) particles are heterogeneous in size and composition. This nested case–control study found that both HDL size and particle concentration were associated with risk for coronary artery disease (CAD). Larger size was strongly associated with risk factors of the metabolic syndrome, such as triglyceride and apolipoprotein B levels. Adjustment for those factors weakened the association, suggesting that they mediate the effect of HDL particle size on CAD risk. On the other hand, HDL particle concentration seems to be an independent predictor of CAD risk.

Academia and Clinic

  • White and associates discuss the ethical principles that could guide allocation of scarce resources—including mechanical ventilators, critical care beds, and other potentially life-saving treatments—during a public health emergency. They propose an allocation strategy that incorporates several morally relevant considerations and argue for applying these principles to all patients.

Review

  • Nearly 30% of patients who undergo bariatric surgery have type 2 diabetes. Glycemic control improves rapidly after surgery for many of these patients. Gut peptides, including the incretins glucagon-like peptide-1 and glucose-dependent insulinotropic peptide, as well as ghrelin and peptide YY, mediate the enteroinsular axis. Bariatric surgery alters secretion of these gut hormones, which results in enhanced insulin secretion and sensitivity. Vetter and associates discuss the various bariatric procedures and how they alter the enteroinsular axis.

NIH Conferences

  • Vaccines for hepatitis B virus have resulted in a substantial decline in the number of new cases of acute hepatitis B in the United States, but this success has not yet been duplicated worldwide. To more closely examine this topic, the National Institutes of Health (NIH) Consensus Development Panel and others met to answer critical questions about the management of hepatitis B in adults. This consensus statement provides the Panel's answers to these questions.

  • This review supports the NIH consensus statement on the management of chronic hepatitis B in adults. Shamliyan and colleagues synthesized the evidence about effectiveness of interferon therapy, oral therapy, and various combinations with different courses of treatment. They found insufficient evidence to assess treatment effect on clinical outcomes or to determine whether selected intermediate measures are reliable surrogates of the clinical response.

Clinical Guidelines

  • About 1 million U.S. persons are living with HIV/AIDS. In this guidance statement, the American College of Physicians' Clinical Efficacy Assessment Subcommittee presents the available evidence on screening for HIV in health care settings. The statement has been endorsed by the HIV Medicine Association. The College recommends that clinicians adopt routine screening for HIV, encourage patients to be tested, and determine the need for repeat screening on an individual basis.

Editorial

  • Many common genetic variants associated with diseases have been identified, which has boosted expectations for personalized genetic prediction. In this issue, Paynter and colleagues confirm that the rs10757274 polymorphism is associated with incident cardiovacsular disease risk, but knowledge of its presence did not improve prediction of cardiovascular disease. In a separate article, Eckman and coworkers found that genotype-guided dosing based on CYP2C9 and VKORC1 was not cost-effective for patients. These 2 articles suggest that the promise of personalized genetic prediction may be exaggerated and premature.

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