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首页> 外文期刊>Progress in Artificial Intelligence >Antihypertensive Effectiveness of Perindopril Arginine and Indapamide Single-Pill Combination According to Body Mass Index: Findings from the FORSAGE Study
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Antihypertensive Effectiveness of Perindopril Arginine and Indapamide Single-Pill Combination According to Body Mass Index: Findings from the FORSAGE Study

机译:Perindopril精氨酸和吲达纳米胺单丸组合的抗高血压有效性根据体重指数:来自福尔斯研究的结果

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摘要

Introduction Overweight and obesity are increasing worldwide and are associated with an increased risk for cardiovascular disease (CVD). The aim of this study was to examine the burden of CVD risk factors among normal weight, overweight, and obese subjects with hypertension, and to evaluate the effectiveness of switching to a single-pill combination (SPC) of perindopril arginine/indapamide for blood pressure (BP) control in overweight and obese subjects treated in routine clinical practice. Methods FORSAGE was a 3-month, multicenter, observational, open-label study conducted in Russian patients with uncontrolled arterial hypertension under previous antihypertensive therapy. Subjects were switched to the full-dose perindopril arginine 10 mg/indapamide 2.5 mg SPC. BP was assessed at 2 weeks, 1 month, and 3 months, and serum creatinine and general health status at 3 months. The present post hoc analysis of the FORSAGE study results explored the effectiveness of perindopril arginine/indapamide SPC in patients with arterial hypertension with regard to baseline body mass index (BMI): normal (< 25 kg/m(2)), overweight (25 <= BMI < 30 kg/m(2)), and obese (>= 30 kg/m(2)). Results A total of 1969 patients were recruited, but BMI data were available for 1963 patients, two-thirds of whom were women. The distribution of BMI groups was as follows: < 25 kg/m(2) (16.7%), overweight (48.7%), and obese (34.7%). Overweight or obese patients had more concomitant diseases such as diabetes mellitus or history of stroke, higher BP levels, serum cholesterol and creatinine, and lower glomerular filtration rates. Switching to perindopril arginine/indapamide SPC was associated with a statistically significant reduction in BP as early as the second week of treatment. At 3 months, systolic blood pressure (SBP)/diastolic blood pressure (DBP) had decreased significantly by 39.3/18.8 mmHg in the normal BMI group, 39.8/18.8 mmHg in overweight, and 39.4/18.7 mmHg in obese groups. The magnitude of the BP reduction was independent of BMI. Achievement of target BP (< 140/90 mmHg) was good in all groups, but lower in obese subjects (70.9%) than in overweight subjects (78.1%) or those with a normal BMI (81.8%) (P < 0.0001 for both comparisons). Conclusions In subjects with uncontrolled BP on existing antihypertensive therapy, switching to perindopril arginine 10 mg/indapamide 2.5 mg was associated with statistically significant decreases in BP and higher rates of target BP achievement in all BMI groups, including more than 70% of overweight and obese patients.
机译:引言超重和肥胖在全世界正在增加,并且与心血管疾病(CVD)的风险增加有关。本研究的目的是审查正常体重,超重和肥胖受试者的CVD危险因素的负担,并评估切换到Perindoplil精氨酸/吲普米酰胺的单丸组合(SPC)的有效性进行血压(BP)在常规临床实践中治疗超重和肥胖受试者的控制。方法FORSAGE是在俄罗斯患者在先前的抗高血压治疗下进行俄罗斯患者进行的3个月,多中心,观测,开放标签研究,在俄罗斯患者中进行了不受控制的动脉高血压。将受试者切换到全剂量perindoplil精氨酸10mg /吲达咪啶2.5mg SPC。 BP在2周,1个月和3个月内评估,3个月,血清肌酐和一般健康状况。对福尔斯研究结果的目前的HOC分析结果探讨了PRINDOPRIL精氨酸/吲达曼SPC在有关基线体重指数(BMI)的动脉高压患者中的有效性:正常(<25kg / m(2)),超重(25 <= BMI <30 kg / m(2)),肥胖(> = 30kg / m(2))。结果共有1969名患者招募,但为1963名患者提供BMI数据,其中三分之二是女性。 BMI组的分布如下:<25kg / m(2)(16.7%),超重(48.7%)和肥胖(34.7%)。超重或肥胖患者具有更多伴随的疾病,例如糖尿病或中风史,较高的BP水平,血清胆固醇和肌酐,以及较低的肾小球过滤速率。切换到Perindopril精氨酸/吲达咪酰胺SPC与BP的统计学显着降低有关,早在第二周的治疗中有关。在3个月内,在正常BMI组中,39.3 / 18.8 mmHg,39.8 / 18.8 mmHg,在超重39.8 / 18.8mmHg,39.4 / 18.7mmHg,肥胖群体中的39.3 / 18.8mmHg,收缩压(SBP)/舒张压(DBP)显着下降。 BP减少的幅度与BMI无关。靶BP(<140/90 mmHg)的成就在所有群体中都很好,但肥胖受试者(70.9%)低于超重主体(78.1%)或正常BMI(81.8%)(两者P <0.0001)比较)。结论在具有不受控制的BP对现有的抗高血压治疗的受试者中,转向PerindopropliL精氨酸10mg / indapamide 2.5mg与BP的统计学显着降低有关,所有BMI组中的目标BP成就率较高有关,包括超过70%的超重和肥胖耐心。

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