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Prevention of Type 2 Diabetes Mellitus by L-Arginine in Patients With Metabolic Syndrome (L-arginine)

Primary Purpose

Metabolic Syndrome, Impaired Glucose Tolerance, Insulin Resistance

Status
Completed
Phase
Phase 3
Locations
Italy
Study Type
Interventional
Intervention
L-arginine
Placebo
Sponsored by
IRCCS San Raffaele
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Metabolic Syndrome focused on measuring Metabolic Syndrome, Impaired glucose tolerance, Type 2 diabetes mellitus, Endothelial dysfunction, L-arginine, Insulin resistance

Eligibility Criteria

35 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Written informed consent must be obtained before any procedure of the study is done.
  • Male or Female aged more than 35 years.
  • Diagnosis of IGT after a standard Glucose Tolerance Test (OGTT, 75 g)
  • Moreover, in order to be considered affected by Metabolic Syndrome, they must have two or more of the following criteria:
  • Abdominal obesity (waist>120 cm for man, >88 cm for women)
  • Hypertriglyceridemia (>150 mg/dl)
  • Low HDL cholesterol (<40mg/dl in man, <50 mg/dl in woman)
  • Hypertension (>130 / >85 mmHg)

Exclusion Criteria:

  • Presence of type 1 or type 2 diabetes mellitus
  • Fasting glucose levels >126 mg/dl
  • Sitting Systolic Arterial Pressure >140mmHg, and Sitting Diastolic Arterial Pressure >90mmHg
  • Pregnancy
  • Known renal insufficiency or creatinine levels more than 1.8 mg/dl,
  • Presence of chronic hepatopathy or levels of ALT and AST more than two standard deviations from normality levels
  • Presence of malignancy
  • Abuse of alcohol or abuse substances
  • Psychiatric disorders

Sites / Locations

  • Scientific Institute San Raffaele

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Placebo Comparator

Arm Label

L-arginine

placebo

Arm Description

L-arginine (3.2 gr bid) plus lifestyle counselling vs placebo plus lifestyle counselling

placebo plus lifestyle counselling for 18 months

Outcomes

Primary Outcome Measures

To evaluate the efficacy of long term (18 months) L-Arginine therapy in preventing or delaying clinical onset of type 2 diabetes mellitus in subjects with impaired glucose tolerance (IGT) and Metabolic Syndrome.

Secondary Outcome Measures

Define if the treatment with L-arginine can ameliorate insulin sensitivity and endothelial dysfunction and find new risk profiles and candidate genes able to characterize the sub-group of patients at higher risk to develop type 2 diabetes mellitus.

Full Information

First Posted
June 9, 2009
Last Updated
June 9, 2009
Sponsor
IRCCS San Raffaele
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1. Study Identification

Unique Protocol Identification Number
NCT00917449
Brief Title
Prevention of Type 2 Diabetes Mellitus by L-Arginine in Patients With Metabolic Syndrome
Acronym
L-arginine
Official Title
Interventional Pharmacological Study With L-Arginine in the Prevention of Type 2 Diabetes Mellitus in Patients With Metabolic Syndrome
Study Type
Interventional

2. Study Status

Record Verification Date
June 2009
Overall Recruitment Status
Completed
Study Start Date
December 2005 (undefined)
Primary Completion Date
June 2009 (Actual)
Study Completion Date
June 2009 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
IRCCS San Raffaele

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Aim The principal objective of this project is: • To evaluate the efficacy of long term (18 months) L-Arginine therapy in preventing or delaying clinical onset of type 2 diabetes mellitus in subjects with impaired glucose tolerance (IGT) and Metabolic Syndrome. Secondary end points are: To define if a long term treatment with L-arginine is able to ameliorate insulin sensitivity and endothelial dysfunction in this population. To find new risk profiles and candidate genes able to define the sub-group of patients at higher risk to develop type 2 diabetes mellitus. Methodology This is a double blind, parallel, one centre study to determine if long term oral L-arginine administration is able to delay or prevent type 2 diabetes mellitus in patients with Metabolic Syndrome. Two hundred and ninety four subjects were recruited at the Cardio-Metabolic and Clinical Trials Unit of the San Raffaele Scientific Institute. One hundred and forty two patients were randomized to enter the study and assigned to two arms: oral L-arginine (6.4 g/die) or placebo, in addition to diet and physical exercise. The treatment were maintained for 18 months. Visits were performed every 3 months for clinical evaluation, blood samples, treatment supply and collection of data on adverse events. Furthermore, patients were contacted every month by telephone to evaluate the accurate continuation of the study and they were instructed to phone to the centre in case of possible adverse events. An OGTT were performed before the enter into the study and at the end of the study period. An additional OGTT were performed at an intermediate visit if fasting glucose levels were more than 126 mg/dl. A diabetic response caused the end-point of the patient. Metabolic, hormonal and endothelial activation and inflammation parameters were measured. Evaluation of endothelium-mediated and non-endothelium-mediated vasodilatation were performed by strain gauche plethysmography evaluating forearm blood at the basal state. in post-ischemic conditions and after nitroglycerine administration. Before the enter into the study, an additional blood sample were drawn for DNA extraction and candidate genes variants evaluation. Before the enter into the study and at the end of the study period, gene expression for inflammation were measured on mRNA extraction on endothelial progenitor cells.
Detailed Description
This is a double blind, parallel, one centre study to determine if long term oral L-arginine administration is able to delay or prevent type 2 diabetes mellitus in patients with IGT and Metabolic Syndrome. Two hundred and ninety four subjects were recruited at the CardioMetabolic and Clinical Trials Unit of the San Raffaele Scientific Institute. One hundred and fourty two patients were randomized to enter the study. Patients were randomly assigned to two arms: oral L-arginine (6.4 g/die) or placebo in blind scheme. The treatment were maintained for 18 months. Visits will be performed every 3 months for clinical evaluation, blood samples, treatment supply and collect data on adverse events, if any. Furthermore, patients were contacted every month by telephone to evaluate the accurate continuation of the study and they were instructed to phone to the centre in case of possible adverse events. Inclusion criteria Written informed consent must be obtained before any procedure of the study is done. Male or Female aged more than 35 years. Diagnosis of IGT after a standard Glucose Tolerance Test (OGTT, 75 g) Moreover, in order to be considered affected by Metabolic Syndrome, they must have two or more of the following criteria: Abdominal obesity (waist>120 cm for man, >88 cm for women) Hypertriglyceridemia (>150 mg/dl) Low HDL cholesterol (<40mg/dl in man, <50 mg/dl in woman) Hypertension (>130 / >85 mmHg) Exclusion criteria Presence of type 1 or type 2 diabetes mellitus Fasting glucose levels >126 mg/dl Sitting Systolic Arterial Pressure >140mmHg, and Sitting Diastolic Arterial Pressure >90mmHg Pregnancy Known renal insufficiency or creatinine levels more than 1.8 mg/dl, Presence of chronic hepatopathy or levels of ALT and AST more than two standard deviations from normality levels Presence of malignancy Abuse of alcohol or abuse substances Psychiatric disorders

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Metabolic Syndrome, Impaired Glucose Tolerance, Insulin Resistance, Endothelial Dysfunction
Keywords
Metabolic Syndrome, Impaired glucose tolerance, Type 2 diabetes mellitus, Endothelial dysfunction, L-arginine, Insulin resistance

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigator
Allocation
Randomized
Enrollment
142 (Actual)

8. Arms, Groups, and Interventions

Arm Title
L-arginine
Arm Type
Active Comparator
Arm Description
L-arginine (3.2 gr bid) plus lifestyle counselling vs placebo plus lifestyle counselling
Arm Title
placebo
Arm Type
Placebo Comparator
Arm Description
placebo plus lifestyle counselling for 18 months
Intervention Type
Drug
Intervention Name(s)
L-arginine
Other Intervention Name(s)
bioarginine
Intervention Description
Oral L-arginine (3.2 gr bid)for 18 months
Intervention Type
Drug
Intervention Name(s)
Placebo
Intervention Description
Oral Placebo BID for 18 months
Primary Outcome Measure Information:
Title
To evaluate the efficacy of long term (18 months) L-Arginine therapy in preventing or delaying clinical onset of type 2 diabetes mellitus in subjects with impaired glucose tolerance (IGT) and Metabolic Syndrome.
Time Frame
18 months
Secondary Outcome Measure Information:
Title
Define if the treatment with L-arginine can ameliorate insulin sensitivity and endothelial dysfunction and find new risk profiles and candidate genes able to characterize the sub-group of patients at higher risk to develop type 2 diabetes mellitus.
Time Frame
18 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
35 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Written informed consent must be obtained before any procedure of the study is done. Male or Female aged more than 35 years. Diagnosis of IGT after a standard Glucose Tolerance Test (OGTT, 75 g) Moreover, in order to be considered affected by Metabolic Syndrome, they must have two or more of the following criteria: Abdominal obesity (waist>120 cm for man, >88 cm for women) Hypertriglyceridemia (>150 mg/dl) Low HDL cholesterol (<40mg/dl in man, <50 mg/dl in woman) Hypertension (>130 / >85 mmHg) Exclusion Criteria: Presence of type 1 or type 2 diabetes mellitus Fasting glucose levels >126 mg/dl Sitting Systolic Arterial Pressure >140mmHg, and Sitting Diastolic Arterial Pressure >90mmHg Pregnancy Known renal insufficiency or creatinine levels more than 1.8 mg/dl, Presence of chronic hepatopathy or levels of ALT and AST more than two standard deviations from normality levels Presence of malignancy Abuse of alcohol or abuse substances Psychiatric disorders
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
PierMarco Piatti, MD
Organizational Affiliation
Scientific Institute San Raffaele
Official's Role
Principal Investigator
Facility Information:
Facility Name
Scientific Institute San Raffaele
City
Milan
ZIP/Postal Code
20132
Country
Italy

12. IPD Sharing Statement

Citations:
PubMed Identifier
29052766
Citation
Monti LD, Galluccio E, Villa V, Fontana B, Spadoni S, Piatti PM. Decreased diabetes risk over 9 year after 18-month oral L-arginine treatment in middle-aged subjects with impaired glucose tolerance and metabolic syndrome (extension evaluation of L-arginine study). Eur J Nutr. 2018 Dec;57(8):2805-2817. doi: 10.1007/s00394-017-1548-2. Epub 2017 Oct 20.
Results Reference
derived
PubMed Identifier
26385052
Citation
Monti LD, Galluccio E, Fontana B, Spadoni S, Comola M, Marrocco Trischitta MM, Chiesa R, Comi G, Bosi E, Piatti P. Pharmacogenetic influence of eNOS gene variant on endothelial and glucose metabolism responses to L-arginine supplementation: Post hoc analysis of the L-arginine trial. Metabolism. 2015 Nov;64(11):1582-91. doi: 10.1016/j.metabol.2015.08.015. Epub 2015 Aug 28.
Results Reference
derived

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Prevention of Type 2 Diabetes Mellitus by L-Arginine in Patients With Metabolic Syndrome

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