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CAN STATINS HAVE A BENEFIT IN THE REDUCTION OF PLASMA KETONE BODIES IN PATIENTS WITH UNCONTROLLED TYPE 2 DIABETES MELLITUS AND MIXED HYPERLIPIDEMIA? Spyridon.

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Presentation on theme: "CAN STATINS HAVE A BENEFIT IN THE REDUCTION OF PLASMA KETONE BODIES IN PATIENTS WITH UNCONTROLLED TYPE 2 DIABETES MELLITUS AND MIXED HYPERLIPIDEMIA? Spyridon."— Presentation transcript:

1 CAN STATINS HAVE A BENEFIT IN THE REDUCTION OF PLASMA KETONE BODIES IN PATIENTS WITH UNCONTROLLED TYPE 2 DIABETES MELLITUS AND MIXED HYPERLIPIDEMIA? Spyridon Karamagkiolis 1,2, Eleni Sogka 1, Nikolaos Aggelis 1, Ourania Triantafyllou 1, Flora Koumoutsou 1, Vasiliki Mintza 1, Polyxeni Choussi 1,2 1 Department of Internal Medicine, General Hospital of Larissa, Larissa, Greece 2 Diabetes Mellitus Outpatient Clinic, General Hospital of Larissa, Larissa, Greece

2 BACKGROUND (1) In diabetic patients, high blood levels of ketone bodies are an early sign of Diabetic Ketoacidosis (DKA), a potentially life-threatening condition. DKA is a less common occurrence in patients with Type 2 Diabetes Mellitus (T2DM) in contrast to patients with Type 1 Diabetes Mellitus. DKA precipitating factors  Infection, new diagnosis of diabetes mellitus, insulin omission, myocardial infarction, abdominal crisis, trauma,pregnancy Ketone bodies : acetone, acetoacetic acid and beta – hydroxybutyrate.

3 BACKGROUND (2)

4 BACKGROUND (3)

5 OBJECTIVES To study whether treatment with statins in insulin-treated patients with uncontrolled Type 2 Diabetes Mellitus (T2DM) and Mixed Hyperlipidemia (MHL) decreases the blood levels of β-Hydroxybutyrate (B-OHB), the predominant ketone in Diabetic Ketoacidosis (DKA).

6 METHODS (1) Patients profile Total Number = 12, 8 Males - 4 Females Age = 59.5 ± 5.5 years old, BMI = 37.5 ± 5.5 Diet Rich in fat (> 40% fat,mostly saturated) Daily use of alcohol Sedentary life style Refusal to comply to medical suggestions 1.T2DM Duration 12.5 ± 3.5 years HbA1c = 12.98 ± 1.02% Antidiabetic treatment for the past year  7 patients = Basal Insulin q.d. (Glargine or Detemir) + Metformin ± DPP-4-I  5 patients = Premixed Insulin b.i.d. + Metformin ± DPP-4-i None of the subjects accepted a change in treatment or insulin dose titration No daily blood glucose (SMBG) check –Frequent insulin omission 2. Mixed Hyperlipidemia Duration 6.5 ± 2.5 years No systematic hypolipidemic treatment by choice

7 METHODS (2) At the time of the study none of the subjects were acutely ill and all declined hospital admission Capillary blood glucose and capillary blood β-OHB were measured (twice) All patients exhibited β-OHB values > 0.6 mmol/L Method used for determining capillary blood β-OHB = Test strips Abbott ® FreeStyle-Precision-β-Ketone ® Blood β-OHB normal values < 0.6 mmol/L  values 0.6 – 1.5 mmol/L and blood glucose ≥ 300 mg/dL→ Risk for DKA  values > 1.5 mmol/L and blood glucose ≥ 300 mg/d→ High Risk for DKA

8 METHODS (3) Patients agreed to follow a hypolipidemic regimen They were randomly selected to receive either Simvastatin 40 mg q.d. or Atorvastatin 20 mg q.d. 15 days later capillary blood glucose and capillary blood β-OHB were measured (twice) in an outpatient setting

9 METHODS (4) Statistical Analysis: Due to the small number of patients, the non- parametric Wilcoxon matched-pairs signed- ranks test was used. Software Program: GraphPad-InStat® (version 3.10)

10 RESULTS (1) TablesTables –Table 1: parameters prior to treatment with statins –Table 2: parameters prior to and 15 days after initiating treatment with statins

11 Pts (n=12) GenderAgeHbA1c (%) Random BG (mg/dL) β-OHB (mmol/L) CHOL (mg/dL) TRG (mg/dL) 1F5411.83060.6248305 2F6013.73451.2237330 3F6113.53511.1256321 4F6513.23380.8241265 5M5513.33640.6230292 6M5612.93270.7250340 7M5714.03721.0246310 8M5812.12960.7237288 9M5912.83210.6251290 10M6212.53400.9260345 11M6313.03680.7258276 12M6412.93700.8280322 Pts = Patients, F = Female, M = Male, BG = Blood Glucose, β-OHB = β- Hydroxybutyrate, Chol = Cholesterol, TRG = Triglycerides

12 Pts (n=12) GenderAgeHbA1c (%) Random BG (mg/dL) β-OHB (mmol/L) 15 days after statins use Random BG (mg/dL) β-OHB (mmol/L) 1F5411.83060.6Simv 40mg 3120.4 ↓ 2F6013.73451.2Atorv 20mg 3300.8 ↓ 3F6113.53511.1Atorv 20mg 3620.7 ↓ 4F6513.23380.8Simv 40mg 3360.6 ↓ 5M5513.33640.6Simv 40mg 3470.3 ↓ 6M5612.93270.7Simv 40mg 3390.5 ↓ 7M5714.03721.0Atorv 20mg 3590.6 ↓ 8M5812.12960.7Atorv 20mg 3050.4 ↓ 9M5912.83210.6Atorv 20mg 2890.2 ↓ 10M6212.53400.9Simv 40mg 3520.4 ↓ 11M6313.03680.7Atorv 20mg 3800.3 ↓ 12M6412.93700.8Simv 40mg 3540.2 ↓

13 RESULTS (2) Blood levels of B-OHB were significantly reduced after treatment with statins in all the patients. The mean values (±SD) of blood B-OHB levels before the initiation of treatment with statins,were 0.80 ± 0.20 mmol/L; 95% confidence intervals (CI) = 0.68 – 0.94 mmol/L –[Std error = 0.05, Minimum = 0.60 mmol/L, Maximum = 1.20 mmol/L, Median = 0.75 mmol/L] The mean values of blood B-OHB levels 15 days after the introduction of statins,were 0.45 ± 0.19 mmol/L, 95% CI = 0.33 – 0.57 mmol/L –[Std error = 0.05, Minimum = 0.20 mmol/L, Maximum = 0.80 mmol/L, Median = 0.40 mmol/L] Mean Difference: 0.35 ± 0.12 mmol/L; 95% CI = 0.28 – 0.44 mmol/L, p = 0.0005 (two-tailed). –[Std error = 0.03, Minimum = 0.20 mmol/L, Maximum = 0.60 mmol/L, Median = 0.40 mmol/L]

14 RESULTS (3) In 67% (n=8) of the patients studied, blood B-OHB concentrations returned to normal levels (< 0.6 mmol/L) No statistically significant differences were noticed in relation to  Sex,  Age,  Levels of HbA1c, Blood Glucose, Cholesterol, Triglycerides,  Type of antidiabetic regimen,  Treatment with simvastatin 40 mg/d or atorvastatin 20 mg/d.

15 RESULTS (4) Study’s Disadvantages: Patients sample small in number, non randomized Absence of a control group The method for determining β-OHB levels lacks a high degree of exactitude Lack of evidence that the study’s results apply to a longer time frame (months,years).

16 CONCLUSIONS The novel finding of this study is that in patients with uncontrolled T2 Diabetes Mellitus and Mixed Hyperlipidemia, treatment with statins may reduce blood B-OHB-levels. A larger study with a control group is required to confirm these findings. Prompt initiation, appropriate titration of insulin treatment and mainly,patient compliance,remain the corner stone for the reduction of HbA1c and pathological values of β-OHB.

17 Thank you for your attention


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