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ALLHAT

ALLHAT.

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ALLHAT

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  1. ALLHAT Fasting Glucose Levels & Incident Diabetes Mellitus in Older Non-Diabetic Adults Randomized to Three Different Classes of Antihypertensive TreatmentA Report from ALLHATJ. Barzilay, M. Alderman, B. R. Davis, J. A. Cutler, S. L. Pressel, P. K. Whelton, J. Basile, K. L. Margolis, S. T. Ong, L. S. Sadler, J. Summerson Archives of Internal Medicine – In Press

  2. Context • Elevated glucose levels have been reported with use of diuretic therapy in the treatment of hypertension. • The clinical significance of this is uncertain.

  3. Objective Among participants who are non-diabetic at baseline: • Compare the effects of 1st-step antihyper-tensive drug therapy with chlorthalidone, amlodipine, or lisinopril on fasting glucose (FG) levels and incident diabetes • Determine risks for CV and renal disease associated with elevated FG and incident diabetes in the three treatment groups.

  4. Design & Population • Post hoc analyses of ALLHAT population (hypertensive, age 55 years, >1 other CVD risk factor) • Subgroup that was nondiabetic by history at baseline, plus: • FG < 126 mg/dl, or • Random glucose <110 mg/dl • Follow-up mean 4.9 years

  5. Derivation of Cohortfor Analysis ALLHAT Total ALLHAT Participants 42,418 Randomized to C, A, or L 33,357 Nondiabetic by history 21,294 FG<126* or RG<110 mg/dl 18,411 1+ follow-up blood samples (fasting* or nonfasting) 14,005 1+ follow-up FG values* 9,802 *Duration of at least 8 hours

  6. ALLHAT Baseline Characteristics

  7. ALLHAT Fasting Glucose * * * * * p<.05 compared to chlorthalidone

  8. ALLHAT Changes in Fasting Glucose * * * * * p<.05 compared to chlorthalidone

  9. ALLHAT Follow-up Fasting Glucose126+ mg/dL * * * * * p<.05 compared to chlorthalidone

  10. ALLHAT Potential Confounders and Mediators • β-blockers decrease insulin sensitivity and therefore may increase the risk of DM. • Potassium depletion appears to be a major intervening factor between thiazide treatment and dysglycemia. • Statin therapy may decrease risk of incident DM.

  11. ALLHAT Medication at 2 Years

  12. ALLHAT Diabetes Incidence –Logistic Regressions

  13. ALLHAT Effect of Change in Fasting Glucose on ALLHAT Endpoints*(Cox Regressions Beginning at 2 Years)

  14. ALLHAT Effect of Change in Fasting Glucose on ALLHAT Endpoints*(Cox Regressions Beginning at 2 Years)

  15. ALLHAT Effect of Incident Diabetes on ALLHAT Endpoints*(Cox Regressions Beginning at 2 Years)

  16. ALLHAT Effect of Incident Diabetes on CHD& Heart Failure by Treatment Group*(Cox Regressions Beginning at 2 Years)

  17. ALLHAT Effect of Incident Diabetes on Combined CVD & ESRD by Treatment Group*(Cox Regressions Beginning at 2 Years)

  18. ALLHAT Effect of Incident Diabetes on Total Mortality by Treatment Group*(Cox Regressions Beginning at 2 Years)

  19. ALLHAT Incident Diabetes in ALLHAT – Summary • FG increased in all 3 treatment groups • Differences between treatment groups were small • For incident DM to 2 years, mean increase was 52 mg/dl • Follow-up FG and incident diabetes were highest in chlorthalidone, lowest in lisinopril • Chlorthalidone has detrimental effect on FG? • Lisinopril / amlodipine have neutral / protective effect on FG?

  20. ALLHAT Effect of FG & Incident Diabetes on Outcomes – Summary • No significant overall effect of change in FG on any of the study endpoints in the combined treatment groups or the chlorthalidone group separately • Incident DM increased risk of CHD • Statistically significant for total group & lisinopril • In chlorthalidone group, increase in risk was smallest and not significant

  21. Discussion of ALLHAT Findings • Lisinopril group: FG associated with  risk of CCHD and CCVD; incident DM associated with  risk of CHD • Lisinopril generally prevents FG • Amlodipine group: Incident DM associated with  risk of total mortality • Amlodipine does not generally raise glucose levels →Participants with FG in these groups may have been very insulin resistant and at high risk for CV events

  22. Discussion of ALLHAT Findings • Low potassium did not significant increase the odds of developing DM • Use of K supplements doubled from year 2 to year 5 • Treatment differences in FG and DM decreased at years 4 and 6 • Sustained low K+ not captured in dataset – prescription of K+ supplement may indicate this, and tends to be associated with DM • Recent review – “thiazide-induced hyperglycemia should be anticipated and prevented by measures to preserve normokalemia and total body K+”. (Zillich et al. Hypertension. 2006;48:219-224.)

  23. Total Mortality (%) 14.3 yrs Follow up * p< 0.05 vs no diabetes SHEP-X: Systolic Hypertension in the Elderly Program extended follow-up. Kostis, et al. Am J Cardiol. 2005;95:29-35

  24. Cardiovascular Death (%) 14.3 yrs Follow up SHEP-X: Systolic Hypertension in the Elderly Program extended follow-up. Kostis, et al. Am J Cardiol. 2005;95:29-35 * p< 0.05 vs no diabetes

  25. New diabetes and CVD risk: Verdecchia 2004 • 795 treated HTs, median FU 6 yrs. • Diuretic rx (low-mod dose HCTZ or CLTD) independently predictive of new diabetes. • Adjusted* RR (95% CI) of CVD-renal event (n=63) --BL DM, 3.57 (1.65, 7.73) --New DM, 2.92 (1.33, 6.41) • Results for specific regimens not given, & only 11% on diuretic/β blocker alone. Verdecchia et al. Hypertension 2004;43:963-69. *age, 24h SBP, LVH.

  26. Evidence from Previous Studies 15-y follow-up of 686 middle-age hypertensive adults treated with diuretic • Diabetes at baseline significantly associated with CHD--RR 2.1 (1.1, 4.1) • Incident diabetes was not significantly related with CHD—RR 1.5 (0.4, 6.0). Samuelsson O, et al. Brit Med J 1996; 313:660-63.

  27. Evidence from Previous Studies Cessation of long-term use of thiazide diuretics is associated with prompt improvement in FG levels • Suggests that diuretics lead to elevated glucose levels by mechanisms different from those associated with DM Murphy MB, et al. Lancet 1982:2(8311):1293-95.

  28. Evidence from Previous Studies Meta-analysis of ACE inhibitors & ARBs • Both decrease the risk of DM • Neither reduces the odds of mortality, CV events, or cerebrovascular events vs control therapy e.g., thiazides and beta blockers Gillespie EL, et al. Diabetes Care 2005; 28:2261-66.

  29. Strengths • ALLHAT much larger than other studies •  statistical power • Use of central biochemical laboratory • Variety of practice environments

  30. Limitations • Misclassification of incident diabetes and not identifying impaired glucose tolerance could have diluted findings • FU measures in ½ of cohort were non-fasting, and not used • Data on diabetes medication use not collected • Conclusions cannot be extrapolated beyond about 5 years • Other measures of glucose metabolism (e.g., HbA1c, insulin levels) may have been helpful

  31. Conclusions • Treatment of hypertension with chlorthalidone was associated with small initial increase in FG & increased risk of DM compared with amlodipine & lisinopril. • Differences in FG diminished over 5 years. • No corresponding increase in risk of stroke, combined CVD, total mortality or ESRD over the period of follow-up. •  risk of CHD associated with  DM not clearly identified in chlorthalidone arm

  32. Perspectives on Incident Diabetes • Assuming CCB is metabolically neutral, 85% (9.3% vs 11.0%) of DM at 4 years on chlorthalidone was not due to chlorthalidone • Lifestyle intervention remains paramount

  33. Conclusion • Neither amlodipine- nor lisinopril-based treatment led to superior outcomes for any CVD endpoint. • Both were inferior for prevention of heart failure • While clinicians need to be aware of, and monitor patients for hyperglycemia, the totality of the evidence still supports the use of thiazide diuretics as preferred agents for prevention of cardiovascular disease in hypertensive patients. • The relatively small detrimental metabolic effects of thiazide-type diuretic should not affect their preferred use in the management of hypertension.

  34. EXTRA SLIDES

  35. ALLHAT Diabetes and Hypertension Links • Common antecedents: • Obesity • Insulin resistance • Treatment of one may impact the other

  36. ALLHAT Diabetes Incidence - 4 Years -All Participants(<126 mg/dL at baseline) * * * p<.05 compared to chlorthalidone JAMA 2002;288:2981-2997

  37. BP Meds and Glucose inRandomized Clinical Trials –Diuretic vs Placebo, Diuretic vs Beta-blocker Padwal and Laupaci (Diabetes Care 27:247-256)

  38. BP Meds and Glucose inRandomized Clinical Trials –ACEI or ARB vs Placebo Padwal and Laupaci (Diabetes Care 27:247-256)

  39. BP Meds and Glucose inRandomized Clinical Trials –ACEI or ARB vs Diuretic/Beta-blocker Padwal and Laupaci (Diabetes Care 27:247-256)

  40. BP Meds and Glucose inRandomized Clinical Trials –Diuretic + Beta-blocker vs CCB vs (+) ACEI Padwal and Laupaci (Diabetes Care 27:247-256)

  41. CAVEATThe criterion for defining DM( > 125 mg/dl) was chosen not based on CVD risk (a complication not specific to DM). Rather the criterion was based on a microvascular complication specific to DM - retinopathy.

  42. ALLHAT Fasting Glucose at 4 Yearsin Nondiabetic Participants

  43. ALLHAT Diuretic Useat 2, 4, and 6 Years

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