Effect of DPP4 Inhibition on Vasoconstriction

Type 2 Diabetes Mellitus Clinical Trial

Official title:

Contribution of Neuropeptide Y (NPY) to Vasoconstriction and Sympathetic Activation in the Setting of Dipeptidyl Peptidase IV (DPP4) Inhibition

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02639637
• Other study ID #: 151133
• Status: Completed
• Phase: Phase 4
• Start date: December 2015
• Est. completion date: September 2017

Study information

• Verified date: July 2018
• Source: Vanderbilt University Medical Center
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The purpose of this study is to understand how dipeptidyl peptidase IV (DPP4) inhibition in diabetics affects hemodynamic parameters and sympathetic activation in the setting of increasing concentrations of neuropeptide Y, an endogenous peptide. The central hypothesis is that DPP4 inhibition decreases degradation of neuropeptide Y, resulting in increased vasoconstriction and sympathetic activation.

Description:

Dipeptidyl peptidase IV (DPP4) inhibitors are routinely used for the treatment of type II diabetes mellitus (T2DM). Since the prevalence of hypertension is 1.5-3 times greater in diabetics compared to sex-aged matched controls, the use of antihypertensives such as ACE inhibitors is also common in diabetics. DPP4 is involved in the degradation of multiple vasoactive peptides, one of which is neuropeptide Y. This peptide is thought to play a role in blood pressure regulation and sympathetic nervous system activation. The aim of this study is to investigate how DPP4 inhibition affects vasoconstriction in response to increasing neuropeptide Y concentrations. Additionally, the investigators want to understand how the combination of DPP4 inhibition and ACE inhibition affects vasoconstriction and sympathetic activation. Understanding the hemodynamic and neurohumoral changes associated with DPP4 and ACE inhibitors has important implications for the millions of patients with T2DM who take these drugs concurrently.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 18
• Est. completion date: September 2017
• Est. primary completion date: June 2017
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 55 Years

Eligibility

Inclusion Criteria:

Type 2 Diabetes Mellitus, as defined by one or more of the following,

• Hgb A1C =6.5%, or

• Fasting plasma glucose =126mg/dL, or

• Two hour plasma glucose =200 mg/dL following 75gr oral glucose load

For female subjects the following conditions must be met:

• Postmenopausal status for at least 1 year, or

• Status post-surgical sterilization, or

• If of childbearing potential, utilization of some form of birth control and willingness to undergo ß-HCG testing prior to drug treatment and on every study day

Exclusion Criteria:

• Type 1 diabetes.

• Poorly controlled T2DM, defined as Hgb A1C>8.7%.

• Use of anti-diabetic medications other than metformin.

• Hypertension.

• Subjects who have participated in a weight-reduction program during the last 6 months and whose weight has increased or decreased more than 5 kg over the preceding 6 months.

• Pregnancy. Breast-feeding.

• Treatment with any of the following drugs: cisapride, pimozide, terfenadine, astemizol

• Clinically significant gastrointestinal impairment that could interfere with drug absorption

• Cardiovascular disease that would pose risk for the subject to participate in the study, such as: myocardial infarction within 6 months prior to enrollment, presence of angina pectoris, significant arrhythmia, congestive heart failure (LV hypertrophy acceptable), deep vein thrombosis, pulmonary embolism, second- or third-degree AV block, mitral valve stenosis, or hypertrophic cardiomyopathy.

• Impaired hepatic function (aspartate amino transaminase [AST] and/or alanine amino transaminase [ALT] >2 x upper limit of normal range)

• Impaired renal function (eGFR< 60mL/min/1.73m2 as determined by the MDRD equation).

• History or presence of immunological or hematological disorders.

• History of pancreatitis or known pancreatic lesions.

• History of angioedema or cough while taking an ACE inhibitor.

• Hematocrit <35%.

• Treatment with anticoagulants.

• Growth hormone deficiency.

• Diagnosis of asthma requiring use of an inhaled ß-2 agonist more than 1 time per week.

• Any underlying or acute disease requiring regular medication which could possibly pose a threat to the subject or make implementation of the protocol or interpretation of the study results difficult

• Treatment with systemic glucocorticoids within the last 6 months.

• Treatment with lithium salts

• Ongoing tobacco use or recreational drug use.

• Treatment with any investigational drug in the 1 month preceding the study

• Mental conditions rendering the subject unable to understand the nature, scope, or possible consequences of the study

• Inability to comply with the protocol, e.g., uncooperative attitude, inability to return for follow-up visits, and unlikelihood of completing the study

Related Conditions & MeSH terms

• Diabetes Mellitus
• Diabetes Mellitus, Type 2
• Type 2 Diabetes Mellitus

Intervention

Drug:
• Sitagliptin
Subjects will receive sitagliptin 100 mg daily for 7 days prior to one of the study days.
• Placebo
Subjects will receive a placebo capsule daily for 7 days prior to one of the study days.
• Neuropeptide Y
During the study days, neuropeptide Y will be infused through an intra-arterial line. There will be four doses of neuropeptide Y used (0.1, 0.3, 1.0, and 3.0 nmol/min) and each dose will be infused for 10 minutes.
• Enalaprilat
Ninety minutes after the last dose of neuropeptide Y, enalaprilat will be infused through the intra-arterial line at 0.33 µg/min/100mL of forearm volume. After 30 minutes, a second infusion of neuropeptide Y will begin. Similar to the previous neuropeptide infusion, four doses of neuropeptide Y will be used (0.1, 0.3, 1.0, and 3.0 nmol/min) and each dose will be infused for 10 minutes.
• Valsartan 160mg
Valsartan 160 mg/d for 7 days prior to one of the study days.

Locations

Country	Name	City	State
United States	Vanderbilt University Medical Center	Nashville	Tennessee

Sponsors (1)

Lead Sponsor	Collaborator
Vanderbilt University

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Forearm Blood Flow	Forearm blood flow measured by strain gauge plethysmography in response to 1.0 nmol/min neuropeptide Y, the highest dose that all received.	FBF measured after 5 min of the 1 nmol/min dose of neuropeptide Y on study days 1 and 2. Study days 1 and two were separated by five weeks.
Secondary	Arterial Norepinephrine	Arterial norepinephrine concentration measured by high-performance liquid chromatography.	Measured at baseline (time 0) prior to the infusion of neuropeptide Y on each study day. Study days 1 and 2 were separated by five weeks.
Secondary	Venous Norepinephrine	Venous norepinephrine concentration measured by high-performance liquid chromatography	Measured at baseline (time 0) prior to the infusion of neuropeptide Y on each study day. Study days 1 and 2 were separated by five weeks.
Secondary	NPY Metabolites	NPY (3-36) concentration measured by micro ultra-hgih pressure liquid chromatography tandem mass spectrometry.; NPY (3-36) is the degradation product of NPY by dipeptidyl peptidase 4. It was measured only in the diabetics studied.	Measured after 5 min infusion of the 1.0 nmol/min dose of neuropeptide Y on study days 1 and 2. Study days 1 and 2 were separated by five weeks.
Secondary	Insulin	Plasma insulin measured by radioimmunoassay.	Measured at baseline (time 0) of each study day prior to the infusion of neuropeptide Y. Study days 1 and 2 were separated by five weeks, a four-week washout and one-week treatment period.
Secondary	GLP-1	GLP--1 was not analyzed as subjects were studied in the fasting state.	Measured at baseline (time 0) of each study day prior to the infusion of neuropeptide Y. Study days were separated by five weeks, a four-week washout and one-week treatment period.
Secondary	Glucose	Glucose was measured by the glucose oxidase method using a YSI glucose analyzer	Measured at baseline (time 0) of each study day prior to the infusion of neuropeptide Y. Study days were separated by five weeks, a four-week washout and one-week treatment period.
Secondary	ACE Activity	ACE activity was measured using a commercially available assay (Olympus AU400/AU600, Alpco Diagnotics, Salem, NH.) The lower level of detection was 15 U/L and values below the level of detection were reported at half the level of detection.	Measured at baseline (time 0) of each study day prior to the infusion of neuropeptide Y. Study days were separated by five weeks, a four-week washout and one-week treatment period.
Secondary	DPP4 Activity	DPP4 activity was measured by detection of cleavage of a colorimetric substrate.	Measured at baseline (time 0) of each study day prior to the infusion of neuropeptide Y. Study days were separated by five weeks, a four-week washout and one-week treatment period.
Secondary	Low Frequency Variability of Blood Pressure Activity	Measured using the VITAL-GARD 450c monitor Ivy Biomedical Systems, Branford, CT, USA)	Measured at baseline (time 0) of each study day prior to the infusion of neuropeptide Y. Study days were separated by five weeks, a four-week washout and one-week treatment period.
Secondary	Arterial tPA	Measured using an ELISA.	Measured at baseline (time 0) of each study day prior to the infusion of neuropeptide Y. Study days were separated by five weeks, a four-week washout and one-week treatment period.
Secondary	Venous tPA	Measured using an ELISA. This was measured in a few subjects. After it was determined that there was no change in net t-PA release it was not measured in the remainder.	Measured at baseline (time 0) of each study day prior to the infusion of neuropeptide Y. Study days were separated by five weeks, a four-week washout and one-week treatment period.
Secondary	Mean Arterial Pressure		Measured at baseline (time 0) of each study day prior to the infusion of neuropeptide Y. Study days were separated by five weeks, a four-week washout and one-week treatment period.
Secondary	Heart Rate		Measured at baseline (time 0) of each study day prior to the infusion of neuropeptide Y. Study days were separated by five weeks, a four-week washout and one-week treatment period.