跳至主要内容
临床试验/NCT03613740
NCT03613740已完成2 期

Effect of Fucoxanthin on the Metabolic Syndrome, Insulin Sensitivity and Insulin Secretion

University of Guadalajara1 个研究点 分布在 1 个国家目标入组 28 人开始时间: 2019年9月30日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
已完成
入组人数
28
试验地点
1
主要终点
Waist Circumference (WC)

研究概览

简要总结

The Metabolic Syndrome (MS) is a cluster of cardiometabolic risk factors, which include abdominal obesity, hyperglycemia, dyslipidemia, and high blood pressure. MS is considered a serious problem to health systems due to a current inability on implementing an effective prevention and treatment program. In Mexico 73% of adult population suffers obesity or overweight, this condition triggers the best studied pathophysiological mechanism; insulin resistance, which in turn precedes the diagnosis of diabetes and cardiovascular disease, that are the main cause of general mortality in Mexico, thus the prevention and timely treatment of this condition are now a priority.

Actual pharmacological therapy is designed to control its components individually, however, there are great interest in developing new therapeutic lines that improve more than one component simultaneously and thereby increase the cost-benefit and effectiveness of the therapy. Fucoxanthin is a functional element present in seaweed species. Several studies have offered certain perspectives on its action mechanism and safety. The information available is favorable for weight control in overweight subjects, but its activity in glucose levels, lipid metabolism and blood pressure is inconsistent. It represents a natural option with great interest in this research, since it could be a new, safe and effective therapy in the MS.

The aim of this study is to evaluate the effect of fucoxanthin on the components of the MS, insulin sensitivity and insulin secretion. The investigators hypothesis is that Fucoxanthin modifies the components of the MS, insulin sensitivity and insulin secretion

详细描述

A randomized, double-blind, placebo-controlled, clinical trial will be conducted in 28 patients with MS according to the International Diabetes Federation (IDF) criteria, men and women, ages 30 to 60. Participants will be assigned randomly into two groups of 14 individuals each. Patients will receive a capsule with Fucoxanthin 12 mg or homologated placebo once a day during 90 days.

Waist circumference, fasting blood glucose, serum triglycerides, serum HDL cholesterol and blood pressure will be evaluated before and after intervention in both groups. First phase of insulin secretion (Stumvoll index), total insulin secretion (Insulinogenic index) and Insulin sensitivity (Matsuda index) will be calculated from the concentration of glucose and insulin obtained from an Oral Glucose Tolerance Test.

Data from statistical analysis will be presented through measures of central tendency and dispersion( mean and standard deviation) for quantitative variables and frequencies and percentages for qualitative variables. The qualitative variables will be analyzed through the X2 or Fisher's exact test. The intra-group analysis of the quantitative variables will be carried out by means of the Wilcoxon rank test, while the inter-group analysis with the U test of Mann Whitney and Kruskal-Wallis. Statistical significance will be considered with a p<0.05.

This protocol was approved by a local ethics committee and written informed consent will be obtained from all volunteers

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Double (Participant, Investigator)

入排标准

年龄范围
30 Years 至 60 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Diagnosed MS according to the IDF criteria:
  • - - Waist circumference: ≥80 cm (women) ≥90 cm (men), plus two or more of the following:
  • - - - - Fasting glucose ≥ 100 mg/dL
  • - - - - Triglycerides ≥150 mg/dL
  • - - - - HDL-C: Men ≤40 mg/dL, women ≤50 mg/dL
  • - - - - Blood pressure ≥130/85 mmHg
  • Body Mass Index between 25 and 34.9 kg/m²
  • No pharmacological treatment for MS
  • Stable weight during the last 3 months

排除标准

  • Pregnancy or breast-feeding
  • History of kidney or liver disease
  • Drugs or supplements consumption with proven properties that modify the behavior of the MS
  • Total cholesterol >240 mg/dL
  • Triglycerides >500mg/dL
  • Glucose ≥126 mg/dL or HbA1C ≥6.5%.
  • Hypersensitivity to Fucoxanthin

研究组 & 干预措施

Placebo

Placebo Comparator

Homologated magnesium sterate capsule, once a day before breakfast during 90 days.

干预措施: Placebo (Drug)

Fucoxanthin

Experimental

12 mg Fucoxanthin capsule, once a day before breakfast during 90 days.

干预措施: Fucoxanthin (Drug)

结局指标

主要结局

Waist Circumference (WC)

时间窗: 12 weeks.

WC was measured with a flexible tape at the midline between the highest point of the iliac crest and the lowest rib in the midaxillary line.

Fasting Serum Glucose

时间窗: 12 weeks.

Fasting serum glucose concentration was measured with enzymatic/colorimetric techniques by spectrophotometry.

Triglycerides (TG)

时间窗: 12 weeks.

TG concentration was measured with enzymatic/colorimetric techniques by spectrophotometry.

High-Density Lipoprotein (HDL-C)

时间窗: 12 weeks.

Serum HDL-C concentration was measured with enzymatic/colorimetric techniques by spectrophotometry.

Systolic Blood Pressure

时间窗: 12 weeks.

Blood pressure was evaluated using a digital sphygmomanometer after a resting period of 15 min with the subject sitting; the bracelet was adjusted 3.0 cm above the fold of the elbow of the left arm.

Diastolic Blood Pressure

时间窗: 12 weeks.

Blood pressure was evaluated using a digital sphygmomanometer after a resting period of 15 min with the subject sitting; the bracelet was adjusted 3.0 cm above the fold of the elbow of the left arm.

Matsuda-DeFronzo Insulin Sensitivity Index

时间窗: 12 weeks.

The Matsuda-DeFronzo index measures whole-body insulin sensitivity from serum insulin and glucose levels during an oral glucose tolerance test (OGTT). The index is calculated with the formula: 10,000 / sqrt(\[fasting glucose (mg/dL) × fasting insulin (µU/mL)\] × \[mean glucose × mean insulin during OGTT\]). The scale ranges from 0 to infinity, with higher values indicating greater insulin sensitivity. Typical values for healthy individuals range between 2 and 10, while lower values suggest insulin resistance.

Total Insulin Secretion

时间窗: 12 weeks.

The Total Insulin Secretion is calculated as the ratio of the area under the curve (AUC) for insulin to the AUC for glucose during a 120-minute oral glucose tolerance test (OGTT). The formula is: AUC insulin / AUC glucose. AUC values are derived from concentrations measured at 0, 30, 60, 90, and 120 minutes post-ingestion of a glucose solution at week 12. Interpretation of the AUC insulin/AUC glucose ratio is as follows: values \<0.5 indicate insulin resistance, values between 0.5 and 1.0 suggest moderate insulin secretion, and values \>1.0 reflect optimal insulin secretion.

Stumvoll Index

时间窗: 12 weeks.

The Stumvoll index measures the first phase of insulin secretion, incorporates demographic data along with plasma glucose (mmol/L) and insulin (pmol/L) levels measured during an oral glucose tolerance test (OGTT). There is no universally standardized ranges, values ranges from 0 to infinity; higher values indicate a better early insulin response to glucose (first 30 minutes), reflecting more effective beta-cell function.

次要结局

  • Body Weight(12 weeks.)
  • Body Mass Index (BMI)(12 weeks.)
  • Body Fat(12 weeks.)
  • Total Cholesterol (TC)(12 weeks.)
  • Low-Density Lipoprotein (LDL-C)(12 weeks.)
  • Very-Low-Density Lipoprotein (VLDL)(12 weeks.)
  • Alanine Aminotransferase (ALT)(12 weeks.)
  • Aspartate Aminotransferase (AST)(12 weeks.)
  • Creatinin(12 weeks.)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Karina Griselda Pérez Rubio

Principal Investigator

University of Guadalajara

研究点 (1)

Loading locations...

相似试验

Effect of Fucoxanthin on the Metabolic Syndrome,... | 临床试验