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孕期中期的肌醇、D-手性肌醇、叶酸和锰:一项初步调查。

Myo-inositol, D-chiro-inositol, folic acid and manganese in second trimester of pregnancy: a preliminary investigation.

作者信息

Malvasi A, Casciaro F, Minervini M M, Kosmas I, Mynbaev O A, Pacella E, Monti Condesnitt V, Creanza A, Di Renzo G C, Tinelli A

机构信息

Department of Obstetrics and Gynecology, Santa Maria Hospital, Bari, Italy.

出版信息

Eur Rev Med Pharmacol Sci. 2014;18(2):270-4.

Abstract

DESIGN AND PURPOSE

The supplemental administration of myo-inositol, D-chiro-inositol, folic acid and manganese (MDFM) was tested in a prospective, randomized, double-blind, placebo controlled clinical trial, pilot study, to test the hypothesis that its supplemental administration in the second trimester of pregnancy would improve glucose and glycemic parameters and blood pressure.

SUBJECTS AND METHODS

Non-obese uniparous healthy pregnant women between 13th and 24th week of pregnancy were divided into two groups: group I, control group with placebo, and the group II, women in treatment with myo-inositol, D-chiro-inositol, folic acid and manganese. The main outcome measures were the comparative analysis of the parameters analyzed at time 0, after 30 days and 60 days; secondary outcome measure was the overall analysis of investigated parameters.

RESULTS

24 women were allocated to receive MDFM and 24 the placebo. The two groups did not significantly differ for demographic, lipidic and glycemic parameter and blood pressure. After 30 days, significantly lower cholesterol (p = 0.0001), significantly lower LDL (p = 0.0013), lower TG (p < 0.0001) and lower glycemia (p = 0.0021) were observed all favoring group II. No significant difference was observed for HDL, diastolic and systolic blood pressure. After 60 days, significant difference was observed for cholesterol (p = 0.0001), LDL (p = 0.0001), HDL (p = 0.0001), TG (p = 0.0001), glycemia (p = 0.0064), all favoring the group treated with MDFM. No significant differences were observed for systolic (p = 0.12) and diastolic blood pressure (p = 0.42). When examining for overall differences between the two groups, a significant difference was observed for examined parameters at time 0 and at time 60; cholesterol (p = 0.0001), LDL (p = 0.0001), HDL (p = 0.047), TG (p = 0.0001) and glycemia (p = 0.019) were reduced in the MDFM group. A significant reduction was also observed in group II for systolic blood pressure after 60 days of intervention (p = 0.0092), but not for diastolic blood pressure (p = 0.29).

CONCLUSIONS

MDFM administration after 30 days in pregnancy improved glycemic and lipidic parameters, with significant gain after 60 days, without affecting diastolic blood pressure levels.

摘要

设计与目的

在一项前瞻性、随机、双盲、安慰剂对照的临床试验(试点研究)中,对肌醇、D-手性肌醇、叶酸和锰(MDFM)的补充给药进行了测试,以检验其在妊娠中期补充给药可改善血糖和血糖参数及血压这一假设。

受试者与方法

妊娠13至24周的非肥胖单胎健康孕妇被分为两组:第一组为安慰剂对照组,第二组为接受肌醇、D-手性肌醇、叶酸和锰治疗的女性。主要观察指标是对在0天、30天和60天后分析的参数进行比较分析;次要观察指标是对所研究参数的整体分析。

结果

24名女性被分配接受MDFM,24名接受安慰剂。两组在人口统计学、脂质和血糖参数及血压方面无显著差异。30天后,观察到胆固醇显著降低(p = 0.0001)、低密度脂蛋白显著降低(p = 0.0013)、甘油三酯降低(p < 0.0001)和血糖降低(p = 0.0021),所有这些均有利于第二组。高密度脂蛋白、舒张压和收缩压方面未观察到显著差异。60天后,在胆固醇(p = 0.0001)、低密度脂蛋白(p = 0.0001)、高密度脂蛋白(p = 0.0001)、甘油三酯(p = 0.0001)、血糖(p = 0.0064)方面观察到显著差异,所有这些均有利于接受MDFM治疗的组。收缩压(p = 0.12)和舒张压(p = 0.42)未观察到显著差异。在检查两组之间的总体差异时,在0天和60天时观察到所检查参数存在显著差异;MDFM组的胆固醇(p = 0.0001)、低密度脂蛋白(p = 0.0001)、高密度脂蛋白(p = 0.047)、甘油三酯(p = 0.0001)和血糖(p = 0.019)降低。在干预60天后,第二组的收缩压也观察到显著降低(p = 0.0092),但舒张压未降低(p = 0.29)。

结论

妊娠30天后给予MDFM可改善血糖和脂质参数,60天后有显著改善,且不影响舒张压水平。

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