Characterization of the Incretinpathy in Type 2 Diabetes Initiated After Sixty Years Old

NCT ID: NCT00843232

Last Updated: 2011-02-04

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

24 participants

Study Classification

OBSERVATIONAL

Study Start Date

2009-07-31

Study Completion Date

2010-09-30

Brief Summary

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Type 2 diabetes (T2DM) is characterized by hyperglycemia, insulin resistance, absolute or relative insulin deficiency, hyperglucagonemia, increased hepatic glucose production, frequently accelerated gastric emptying and obesity. The known effects of the incretin hormone glucagon-like peptide-1 (GLP-1) on the metabolism are stimulation of insulin secretion, inhibition of glucagon secretion and hepatic glucose production, reduction in gastric emptying and modulation of the appetite. T2DM have disturbances in this system, providing a rationale for therapeutic use of GLP-1 in T2DM. Furthermore, GLP-1 seems to exert trophic effects on the beta-cell.

Dipeptidyl Peptidase IV (DPP-IV) inhibitors represent a new class of oral anti-hyperglycemic agents for the treatment of T2DM. The therapeutic utility of these antihyperglycemic agents rests on their ability of to increase active (intact) levels of incretin peptides, including GLP-1 and GIP.

Twenty four T2DM volunteers will be evaluated by a meal tolerance test (MTT) for incretin hormone measurements, and by the hyperglycemic clamp followed by an arginine test for assessing the beta-cell function and the acute insulin response. Others parameters as body composition and basic biochemistry will be also evaluated at Laboratory of Investigation on Metabolism and Diabetes - LIMED / State university of Campinas, Brazil.

T2DM in elderly are behaving differently. Elderly patients have no increase in liver production of glucose; when obese, have normal insulin secretion, however, display extreme resistance to its action. In non obese individuals, the concentration of glucose necessary for insulin secretion is increased and the action is standard. These findings suggest therefore that the approach should be differentiated treatment for these individuals.

Detailed Description

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Conditions

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Diabetes Mellitus, Type 2 Insulin Resistance

Study Design

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Observational Model Type

CASE_CONTROL

Study Time Perspective

CROSS_SECTIONAL

Study Groups

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Elderly T2DM

Elderly T2DM subjects 65 to 80 years old

No interventions assigned to this group

Middle-age T2DM

Middle-age T2DM subjects 35 to 50 years old

No interventions assigned to this group

Eligibility Criteria

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Inclusion Criteria

* Stable weight (\<5% variation) within the last three months
* Age: 35 to 50 years old for middle-age group, and 65 to 80 y old for elderly group
* Body mass index (BMI): 20 to 29.9kg/m2
* T2DM with diagnosis above 35 years and less than 5 years (Middle-age group)
* T2DM with diagnosis above 65 years and less than 5 years (Elderly group)
* Use of oral antidiabetic drugs (that must at stable dose within the last 3 months)
* Not have participated in any study of intervention with drugs in the last six months.

Exclusion Criteria

* Use of estrogen, progestogen, active antipsychotics and systemic corticosteroids
* Use of DPP-IV inhibitors and incretin mimetics (current or within 1 month before)
* Continuous use of insulin or glitazone
* Hepatic cirrhosis, renal failure or any clinical condition with impaired insulin sensitivity
* Smoking
* Obesity
* Uncontrolled systemic or disabling diseases
* T2DM treated by non pharmacological methods
* Patients submitted to bariatric surgery
* Latent autoimmune diabetes of the adult (positive anti-GAD antibodies)
Minimum Eligible Age

35 Years

Maximum Eligible Age

80 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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University of Campinas, Brazil

OTHER

Sponsor Role lead

Responsible Party

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University of Campinas, Brazil

Principal Investigators

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Bruno Geloneze, MD, PhD

Role: PRINCIPAL_INVESTIGATOR

LIMED (Laboratory of Investigation of Metabolism and Diabetes)/GASTROCENTRO/Univeristy of Campinas (UNICAMP)

José Carlos Pareja, MD, PhD

Role: PRINCIPAL_INVESTIGATOR

LIMED (Laboratory of Investigation of Metabolism and Diabetes)/GASTROCENTRO/Univeristy of Campinas (UNICAMP)

Carla Fiori, Nurse

Role: PRINCIPAL_INVESTIGATOR

LIMED (Laboratory of Investigation of Metabolism and Diabetes)/GASTROCENTRO/Univeristy of Campinas (UNICAMP)

Marcelo MO Lima, MD

Role: PRINCIPAL_INVESTIGATOR

LIMED (Laboratory of Investigation of Metabolism and Diabetes)/GASTROCENTRO/Univeristy of Campinas (UNICAMP)

Ana Carolina Vasques, MSNutr

Role: PRINCIPAL_INVESTIGATOR

LIMED (Laboratory of Investigation of Metabolism and Diabetes)/GASTROCENTRO/Univeristy of Campinas (UNICAMP)

Locations

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LIMED (Laboratory of Investigation of Metabolism and Diabetes)/GASTROCENTRO/Univeristy of Campinas (UNICAMP)

Campinas, São Paulo, Brazil

Site Status

Countries

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Brazil

References

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Geloneze B, de Oliveira Mda S, Vasques AC, Novaes FS, Pareja JC, Tambascia MA. Impaired incretin secretion and pancreatic dysfunction with older age and diabetes. Metabolism. 2014 Jul;63(7):922-9. doi: 10.1016/j.metabol.2014.04.004. Epub 2014 Apr 12.

Reference Type DERIVED
PMID: 24854384 (View on PubMed)

Other Identifiers

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LIMED0007

Identifier Type: -

Identifier Source: org_study_id

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