2015
DOI: 10.2217/clp.15.37
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Effects of Armolipid Plus on small dense LDL particles in a sample of patients affected by familial combined hyperlipidemia

Abstract: Aim The aim of this study was to test small dense LDL changes with Armolipid Plus treatment in patients with familial combined hyperlipidemia (FCHL). Methods After 4 weeks, 30 patients with FCHL were included in an 8-week, randomized, double-blind study and were taking, in addition to the standard diet, either placebo or Armolipid Plus. Results The placebo group showed no statistically significant differences in the studied parameters; instead, in the Armolipid Plus group, statistically significant reducti… Show more

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Cited by 17 publications
(11 citation statements)
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“…In the meta-analysis by Ho et al, oral treatment with 100 mg/day of coenzyme Q10 decreased SBP by 11 mmHg and DBP by 7 mmHg in subjects with HT [36]. However, the dose of coenzyme Q10 tested is 30 mg and higher than other NCs [37], and in part this explains its possible BP-lowering effect. However, CoQ10 has shown to significantly lower both SBP and DBP also in patients receiving conventional antihypertensive drugs [13] and in patients with isolated systolic hypertension [38].…”
Section: Discussionmentioning
confidence: 99%
“…In the meta-analysis by Ho et al, oral treatment with 100 mg/day of coenzyme Q10 decreased SBP by 11 mmHg and DBP by 7 mmHg in subjects with HT [36]. However, the dose of coenzyme Q10 tested is 30 mg and higher than other NCs [37], and in part this explains its possible BP-lowering effect. However, CoQ10 has shown to significantly lower both SBP and DBP also in patients receiving conventional antihypertensive drugs [13] and in patients with isolated systolic hypertension [38].…”
Section: Discussionmentioning
confidence: 99%
“…An additional 7 studies were excluded because of a lack of a controlled design for Armolipid Plus ® administration (n = 3) or lack of blinding (n = 4). Finally, 12 studies were eligible and included in the meta-analysis [26][27][28][29][30][31][32][33][34][35][36][37]. The study selection process is shown in Figure 1.…”
Section: Flow and Characteristics Of The Included Studiesmentioning
confidence: 99%
“…Follow-up periods ranged between 4 weeks and 12 months. All selected trials were designed with parallel groups and were multicenter [29,35,37] or single-center [26][27][28][30][31][32][33][34]36] clinical studies. Enrolled subjects were patients in primary prevention for CVD [28][29][30]32,36], patients with documented coronary artery disease (CAD) [33], with a metabolic syndrome [26,30,[34][35][36], or with a good status of health [28,37].…”
Section: Flow and Characteristics Of The Included Studiesmentioning
confidence: 99%
“…The results showed that Armolipid Plus® significantly decreased the LDL score compared with baseline and with the placebo group. Whilst mean LDL size significantly increased in the Armolipid Plus® group from baseline, there was no difference compared to placebo [122]. In another placebo-controlled trial, 147 individuals with metabolic syndrome were randomized into two groups, the intervention group received one tablet daily of Armolipid Plus® whilst the control group received a placebo tablet (microcrystalline cellulose, iron oxide brown) for 24 weeks.…”
Section: Armolipid Plus®mentioning
confidence: 97%