- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05572905
Effect of Acute Bout of Exercise on Levels of PAHSA (ETAPA)
Novel Approaches to Enhance Insulin-sensitizing Effects of Exercise: Targeting PAHSA Metabolism
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Prague
-
Prague, Prague, Czechia, 10000
- 3rd faculty of medicine, Charles University
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- healthy young lean, young obese and older omnivorous men and women as defined by BMI, self-reported activity, self-reported medical history and self-reported diet assessment
- must be able to withstand repeated blood draws
- must be able to undergo abdominal fat biopsy
Exclusion Criteria:
- use of betablockers
- use of glucocorticoids
- use of non-steroidal anti-inflammatory drugs
- use of metformin in prediabetes
- use of psychiatric drugs such as selective serotonin reuptake inhibitors, serotonin and norepinephrine reuptake inhibitors, anticonvulsants and others
- oncologic malignancy
- chronic inflammatory or autoimmune diseases
- diabetes mellitus
- chronic ischemic heart disease
- cardiovascular and pulmonary disease
- renal and hepatological disease as assessed per biochemistry
- musculo-skeletal deviations limiting physical performance
- substance abuse
- other than omnivorous diet
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Basic Science
- Allocation: Non-Randomized
- Interventional Model: Crossover Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Young lean men and women
25 to 40 y.o.
participants with body mass index in range of 18.5 to 25
|
Patients after overnight fast will cycle on ergo-meter for 60 minutes.
No per-oral food intake will be allowed during the test.
Level of the intensity of exercise will be determined as individual range of heart frequency (HF), oxygen consumption (VO2) and respiratory quotient (RQ) just bellow the aerobic threshold of the given participant (close to anticipated fatmax).
These values will be obtained during maximal capacity stress test on cyclo-ergo-meter.
This maximum stress test will be performed at least one week prior to the 60 minutes exercise to eliminate potential carry-over effect.
Power output will be modulated during the 60 minutes of exercise to ensure keeping participants values of HF, RQ and VO2 in the given range.
Blood will be sampled at 5 time points with interval of 30 minutes during the exercise (0, 30, 60, 90, 120) and 24 hours post-exercise.
The same participants will be monitored while resting for 120 minutes in calm environment.
No peroral food intake will be allowed during the test.
Fasting control will take place at least one week apart of the exercise.
Blood will be sampled at 5 timepoints with interval of 30 minutes during the exercise (0, 30, 60, 90, 120) and 24 hours post-control.
|
|
Experimental: Young obese men and women
25 to 40 y.o.
participants with body mass index in range of 30 to 45.
|
Patients after overnight fast will cycle on ergo-meter for 60 minutes.
No per-oral food intake will be allowed during the test.
Level of the intensity of exercise will be determined as individual range of heart frequency (HF), oxygen consumption (VO2) and respiratory quotient (RQ) just bellow the aerobic threshold of the given participant (close to anticipated fatmax).
These values will be obtained during maximal capacity stress test on cyclo-ergo-meter.
This maximum stress test will be performed at least one week prior to the 60 minutes exercise to eliminate potential carry-over effect.
Power output will be modulated during the 60 minutes of exercise to ensure keeping participants values of HF, RQ and VO2 in the given range.
Blood will be sampled at 5 time points with interval of 30 minutes during the exercise (0, 30, 60, 90, 120) and 24 hours post-exercise.
The same participants will be monitored while resting for 120 minutes in calm environment.
No peroral food intake will be allowed during the test.
Fasting control will take place at least one week apart of the exercise.
Blood will be sampled at 5 timepoints with interval of 30 minutes during the exercise (0, 30, 60, 90, 120) and 24 hours post-control.
|
|
Experimental: Elderly men and women
65 to 80 y.o.
participants with body mass index in range of 18.5 to 30.
|
Patients after overnight fast will cycle on ergo-meter for 60 minutes.
No per-oral food intake will be allowed during the test.
Level of the intensity of exercise will be determined as individual range of heart frequency (HF), oxygen consumption (VO2) and respiratory quotient (RQ) just bellow the aerobic threshold of the given participant (close to anticipated fatmax).
These values will be obtained during maximal capacity stress test on cyclo-ergo-meter.
This maximum stress test will be performed at least one week prior to the 60 minutes exercise to eliminate potential carry-over effect.
Power output will be modulated during the 60 minutes of exercise to ensure keeping participants values of HF, RQ and VO2 in the given range.
Blood will be sampled at 5 time points with interval of 30 minutes during the exercise (0, 30, 60, 90, 120) and 24 hours post-exercise.
The same participants will be monitored while resting for 120 minutes in calm environment.
No peroral food intake will be allowed during the test.
Fasting control will take place at least one week apart of the exercise.
Blood will be sampled at 5 timepoints with interval of 30 minutes during the exercise (0, 30, 60, 90, 120) and 24 hours post-control.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Assessment of PAHSA levels and its changes in response to exercise and fasting in cohorts differing in age and fat mass
Time Frame: 2 years
|
PAHSA levels [nmol/l] in serum sampled at pre-set time-points during control and intervention visits (including exercise session or plain fasting) and in subcutaneous abdominal white adipose tissue will be assessed by quantitative targeted lipidomic analysis. Absolute and fold-change of PAHSA in plasma induced by experimental intervention (exercise, fasting) will be compared among individual cohorts. |
2 years
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Correlation of PAHSA levels with anthropometry and clinical characteristics
Time Frame: 2 years
|
Basal levels of PAHSA and its changes in response to interventions will be correlated with anthropometric parameters (age, weight, fat mass) and parameters of physical fitness.
Fat mass will be assessed by dual energy X-ray absorptiometry.
Intercohort matching of obese and elderly subjects based on fat mass will be improved throughout the recruitment phase by utilization of fat mass assessment on two distinct certified bioimpedance instruments.
Cohort physical fitness will be calculated as average from individual VO2max values obtained from maximum ergometry testing.
Intercohort matching of young lean and young obese men and women will be based on age.
|
2 years
|
|
Correlation of PAHSA with various indexes of insulin sensitivity
Time Frame: 2 years
|
Basal levels of PAHSA and its changes in response to interventions will be correlated with indices of muscle insulin sensitivity (MISI), hepatic insulin resistance (HIRI), adipose tissue insulin resistance (Adipo-IR) and homeostatic model assessment of insulin resistance (HOMA-IR).
Values for measurement will be obtained by biochemical analysis of blood sampled during 5-point oral glucose tolerance test.
|
2 years
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Lenka Rossmeislová, PhD, 3rd Faculty of Medicine of Charles University in Prague
Publications and helpful links
General Publications
- Brezinova M, Kuda O, Hansikova J, Rombaldova M, Balas L, Bardova K, Durand T, Rossmeisl M, Cerna M, Stranak Z, Kopecky J. Levels of palmitic acid ester of hydroxystearic acid (PAHSA) are reduced in the breast milk of obese mothers. Biochim Biophys Acta Mol Cell Biol Lipids. 2018 Feb;1863(2):126-131. doi: 10.1016/j.bbalip.2017.11.004. Epub 2017 Nov 14.
- Paluchova V, Oseeva M, Brezinova M, Cajka T, Bardova K, Adamcova K, Zacek P, Brejchova K, Balas L, Chodounska H, Kudova E, Schreiber R, Zechner R, Durand T, Rossmeisl M, Abumrad NA, Kopecky J, Kuda O. Lipokine 5-PAHSA Is Regulated by Adipose Triglyceride Lipase and Primes Adipocytes for De Novo Lipogenesis in Mice. Diabetes. 2020 Mar;69(3):300-312. doi: 10.2337/db19-0494. Epub 2019 Dec 5.
Helpful Links
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Estimated)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- NU21-01-00469
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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