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. 2016 Jul 26:22:2648-55.
doi: 10.12659/msm.896843.

Is Time an Important Problem in Management of Hypertension and Hypercholesterolemia by Using an Amlodipine-Atorvastatin Single Pill Combination?

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Is Time an Important Problem in Management of Hypertension and Hypercholesterolemia by Using an Amlodipine-Atorvastatin Single Pill Combination?

Rui Zeng et al. Med Sci Monit. .

Abstract

BACKGROUND Is the timing of dosing for amlodipine and atorvastatin important with regard to therapeutic efficacy? To answer this question, we designed an outpatient, practice-based, case-control study lasting 8 weeks. MATERIAL AND METHODS Two hundred patients were divided into 2 groups: in Group I, patients were provided with a single pill containing amlodipine/atorvastatin (5/20 mg) to be taken each night at 10 pm, and in Group II, patients were taking amlodipine (5 mg) and atorvastatin (20 mg) each morning at 7 am. RESULTS Our results indicated no obvious difference in blood pressure control between the 2 groups. Taking amlodipine at night not only lowered blood pressure, but it also provided better control during the peak blood pressure in the morning. Hypercholesterolemia control in the 2 groups was also not significantly different, taking atorvastatin in the morning was as effective as dosing at night in patients with hypercholesterolemia. While the carotid IMT, hs-CRP, and LVMI were significantly lower after treatment, no differences were found between the 2 groups. Although no obvious difference was found in adverse drug reactions between the 2 groups, compliance was much better in the single-pill group than in patients taking the 2 medications separately. CONCLUSIONS In conclusion, single-pill amlodipine-atorvastatin taken at night can lower blood pressure and reduce the morning peak blood pressure levels the next day. Additionally, this dosing method could improve patient adherence to the therapy.

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Figures

Figure 1
Figure 1
Flow diagram of this research. AML – Amlodipine; ATO – Atorvastatin.
Figure 2
Figure 2
Comparison of blood pressure before and after treatment in both groups. There was no statistically significant change in D-value except in the morning peak group. In Group I, the morning peak BP reduction in SBP and DBP at week 8 was markedly less than in Group II (P<0.05).
Figure 3
Figure 3
Comparison of serum lipid levels before and after treatment in both groups. There were no significant differences in the D-values of TC, TG, and LDL-C or HDL-C before and after 8-week treatment (P>0.05).
Figure 4
Figure 4
Comparison of hs-CRP, LVMI, and carotid -IMT before and after treatment in both groups. There were no significant differences in the D-values of hs-CRP, LVMI, and IMT before and after 8-week treatment (P>0.05).

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