Correlation of Several Formulas to Evaluate Insulin Sensitivity With the Predicted M Index

November 4, 2020 updated by: Manuel González Ortiz, University of Guadalajara

Correlation of Several Formulas to Evaluate Insulin Sensitivity With the Predicted M Index (PREDIM) in Healthy Individuals

Recently, an index based on the oral insulin sensitivity index with glucose (OGIS) has been proposed in combination with anthropometric variables, called PREDIcted M (PREDIM), however, there is no evidence of the correlation of this with respect to the various indices (McAuley, Belfiore, Cederholm, Avignon, Matsuda, Gutt, Stumvoll, HOMA-IR (Homeostatic Model Assessment for Insulin Resistance), ISI (Insulin Sensitivity Index), Raynaud, QUICKI (The quantitative insulin sensitivity check index), FIRI (Fasting Insulin Resistance Index), Bennett, TyG (triglycerides and glucose index)) in healthy patients.

Study Overview

Status

Completed

Conditions

Detailed Description

Analytical cross-sectional study with 25 healthy patients of both genders (male and female) from 30 to 60 years old, residents of the metropolitan area of Guadalajara.

They will be operated on for a 3-hour oral glucose tolerance test. The insulin sensitivity will be calculated with the PREDIM, Matsuda, McAuley, Belfiore, Cederholm, Avignon, Gutt, Stumvoll, HOMA-IR, ISI, Raynaud, QUICKI, FIRI, Bennett and TyG indexes.

This protocol is already approved by the local ethics committee and written informed consent it's going to be obtained from all volunteers.

The statistical analysis will be presented with measures of central tendency and dispersion, mean and standard deviation. The nominal variables in numbers and percentages. The Kolmogorov-Smirnov test will be performed to determine if the variables follow a normal distribution. To correlate the formulas used to evaluate the insulin sensitivity with the PREDIcted M (PREDIM) technique, the Pearson or Spearman correlation will be used according to the distribution.

Study Type

Observational

Enrollment (Actual)

25

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Jalisco
      • Guadalajara, Jalisco, Mexico, 44340
        • Intstituto de Terapeútica Experimental y Clínica. Centro Universitario de Ciencias de la Salud. Universidad de Guadalajara

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

28 years to 58 years (Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

Patients of both sexes who are not sedentary or who participate in heavy physical activities and residents of the metropolitan area of Guadalajara.

Description

Inclusion Criteria:

  • Both genres
  • Age 30 to 60 years
  • BMI <25 kg / m2,
  • Patients who are not sedentary or who participate in heavy physical activities
  • Stable weight in the last 3 months

Exclusion Criteria:

  • Blood pressure >120/80 mmHg
  • Glucose >100 mg/dL
  • Postprandial glucose >140 mg/dL
  • Cholesterol >200 mg/dL
  • Triglycerides >150 mg/dL
  • Smoking
  • Women with polycystic ovarian syndrome
  • History of metabolic, cardiovascular, thyroid, renal, pancreatic and/or arterial hypertension
  • Use of medications that modify insulin sensitivity (corticosteroids)
  • Previous surgery or infection
  • Symptoms of vomiting and/or excessive nausea

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Observational Models: Other
  • Time Perspectives: Cross-Sectional

Cohorts and Interventions

Group / Cohort
Healthy individuals
Cross-Sectional. No intervention. Patients of both sexes who are not sedentary or who participate in heavy physical activities and residents of the metropolitan area of Guadalajara

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Insulin Sensitivity With PREDIM (PREDIcted M) Index
Time Frame: Baseline

With the results of the oral glucose tolerance test at baseline, insulin sensitivity was calculated with the PREDIM index.

Insulin sensitivity was calculated with PREDIM index: A + B × log_e (OGIS) + C × log_e (IMC) + D × log_e (2hGlu) + log_e (INSf). A higher result is better.

In the formula A=2.8846219; B=0.5208520; OGIS=1/2 x (B + sqrt (Bˆ2 + 4 x p5 x p6 (G120 - Gcl) x Cl OGTT)); C=-0.8223363; D=-0.4191242; E=-0.2427896; INSf=fasting insulin.

Baseline
Insulin Sensitivity With McAuley Index
Time Frame: Baseline

With the results of the oral glucose tolerance test at baseline, insulin sensitivity was calculated with the McAuley index.

Insulin sensitivity was calculated with McAuley index: e[2.63-0.28 In(Insulin minute 0) - 0.31 In(Triglycerides minute 0)]. A lower result is better.

Baseline
Insulin Sensitivity With Belfiore Index
Time Frame: Baseline

With the results of the oral glucose tolerance test at baseline, insulin sensitivity was calculated with the Belfiore index.

Insulin sensitivity was calculated with Belfiore index: 2/((glucose minute 0/glucose minute 120) (Insulin minute 0/Insulin minute 120))+1. A higher result is better.

Baseline
Insulin Sensitivity With Cederholm Index
Time Frame: Baseline

With the results of the oral glucose tolerance test at baseline, insulin sensitivity was calculated with the Cederholm index.

Insulin sensitivity was calculated with Cederholm index: (75000+(Glucose minute 0- Glucose minute 120) x 19 x weight) / ((AUC Glucose/18) x log (AUC insulin/120)). A lower result is better.

In the formula AUC=area under the curve.

Baseline
Insulin Sensitivity With Avignon Index
Time Frame: Baseline

With the results of the oral glucose tolerance test at baseline, insulin sensitivity was calculated with the Avignon index.

Insulin sensitivity was calculated with Avignon index: ((0.137 x Sib) + Si2h)/2. A higher result is better.

In the formula Sib=10ˆ8 / ((insulin minute 0) x (glucose minute 0) x (VD=150 ml/kg of Body weight)); Si2h=10ˆ8 / ((insulin minute 120) x (glucose minute 120) x (VD=150 ml/kg of Body weight)).

Baseline
Insulin Sensitivity With Matsuda Index
Time Frame: Baseline

With the results of the oral glucose tolerance test at baseline, insulin sensitivity was calculated with the Matsuda index.

Insulin sensitivity was calculated with Matsuda index: [10,000 / √glucose minute 0 x insulin minute 0) (mean glucose (OGTT) x mean insulin OGTT)]. A higher result is better.

In the formula OGTT: oral glucose tolerance test.

Baseline
Insulin Sensitivity With Gutt Index
Time Frame: Baseline

With the results of the oral glucose tolerance test at baseline, insulin sensitivity was calculated with the Gutt index.

Insulin sensitivity was calculated with Gutt index: ((75000 + (Glucose minute 0 - Glucose minute 120) x 0.10 x m) / (120 x Glucose mean x log Insulin mean). A higher result is better. A lower result is better.

In the formula m=body weight

Baseline
Insulin Sensitivity With Stumvoll Index
Time Frame: Baseline

With the results of the oral glucose tolerance test at baseline, insulin sensitivity was calculated with the Stumvoll index.

Insulin sensitivity was calculated with Stumvoll index: 0.156 - 0.0000459 × Insulin minute 120 - 0.000321 × Insulin minute 0 - 0.00541 × Glucose minute 120. A lower result is better.

Baseline
Insulin Sensitivity With HOMA-IR (Homeostatic Model Assessment for Insulin Resistance) Index
Time Frame: Baseline

With the results of the oral glucose tolerance test at baseline, insulin sensitivity was calculated with the HOMA-IR index.

Insulin sensitivity was calculated with HOMA-IR index: (Glucose minute 0) (Insulin minute 0) / 22.5. A lower result is better.

Baseline
Insulin Sensitivity With ISI (Insulin Sensitivity Index) Index
Time Frame: Baseline

With the results of the oral glucose tolerance test at baseline, insulin sensitivity was calculated with the ISI index.

Insulin sensitivity was calculated with ISI index: 10000 / (Insulin minute 0) (Glucose minute 0). A lower result is better.

Baseline
Insulin Sensitivity With Raynaud Index
Time Frame: Baseline

With the results of the oral glucose tolerance test at baseline, insulin sensitivity was calculated with the Raynaud index.

Insulin sensitivity was calculated with Raynaud index: 40 / (Fasting insulin). a lower result is better.

Baseline
Insulin Sensitivity With QUICKI (The Quantitative Insulin Sensitivity Check Index) Index
Time Frame: Baseline

With the results of the oral glucose tolerance test at baseline, insulin sensitivity was calculated with the QUICKI index.

Insulin sensitivity was calculated with QUICKI index: 1 / (log fasting insulin) + (log fasting glucose). A lower result is better.

Baseline
Insulin Sensitivity With FIRI (Fasting Insulin Resistance Index) Index
Time Frame: Baseline

With the results of the oral glucose tolerance test at baseline, insulin sensitivity was calculated with the FIRI index.

Insulin sensitivity was calculated with FIRI index: (Fasting Insulin) x (Fasting Glucose) / 25. A lower result is better.

Baseline
Insulin Sensitivity With Bennett Index
Time Frame: Baseline

With the results of the oral glucose tolerance test at baseline, insulin sensitivity was calculated with the Bennett index.

Insulin sensitivity was calculated with Bennett index: 1 / (log Fasting insulin) x (log Fasting glucose). A lower result is better.

Baseline
Insulin Sensitivity With TyG (Triglycerides and Glucose Index) Index
Time Frame: Baseline

With the results of the oral glucose tolerance test at baseline, insulin sensitivity was calculated with the TyG index.

Insulin sensitivity was calculated with TyG index: [ln (Triglycerides) x (Fasting Glucose) / 2]. A lower result is better.

Baseline

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Manuel Gonzalez Ortiz, PhD, Intstituto de Terapeútica Experimental y Clínica. Universidad de Guadalajara.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

February 1, 2019

Primary Completion (Actual)

February 28, 2020

Study Completion (Actual)

February 28, 2020

Study Registration Dates

First Submitted

July 3, 2019

First Submitted That Met QC Criteria

July 3, 2019

First Posted (Actual)

July 8, 2019

Study Record Updates

Last Update Posted (Actual)

December 3, 2020

Last Update Submitted That Met QC Criteria

November 4, 2020

Last Verified

November 1, 2020

More Information

Terms related to this study

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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