Obesity Clinical Trial
— INDIEXOfficial title:
Exercise Program and Diet Intervention Attenuated Inflammation Through Down-regulation of ASC Gene and Inflammatory Markers in Obese Adults
Verified date | March 2020 |
Source | University of Guadalajara |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Background: Obesity is one of the most important health problems worldwide, several factors
related to lifestyle as physical inactivity and unbalanced diets increase their development.
This condition is characterized by low-chronic inflammation by excess of adipose tissue. The
apoptosis-associated speck-like protein containing a caspase recruitment domain (ASC) protein
is part of NLRP3 inflammasome, a complex related to inflammation and metabolic alterations.
Purpose: The aim of this study was to evaluate the effect of physical exercise program on ASC
gene expression and inflammatory markers in obese adults.
Methods: 37 obese individuals were randomized to exercise-diet group or diet-group during a
4-month follow-up period. The dietary evaluation was analyzed by Nutritionist Pro software.
Body composition was evaluated by bioimpedance (InBody 370). All biochemical determinations
were analyzed by dry chemistry (Vitros 350). ASC messenger ribonucleic acid (mRNA) expression
was performed by real-time polymerase chain reaction (PCR) using Taqman probes and by the
2-ΔΔcq quantification method. Cytokine levels was performed using the Bio-PlexPro™
HumanTh17Cytokine Assays (MagPix) panel. Statistical analysis was performed with Statistical
Package for the Social Sciences (SPSS) v.22 software.
Status | Completed |
Enrollment | 37 |
Est. completion date | February 15, 2019 |
Est. primary completion date | February 15, 2019 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 25 Years to 50 Years |
Eligibility |
Inclusion Criteria: - BMI greater than 30 kg/m^2 - Sedentary individuals - Both genres - Waist circumference greater than 80 centimeters in women and greater than 90 centimeters in men Exclusion Criteria: - Pregnant or breastfeeding women - Diagnosis of any metabolic disease or cancer - Alcohol or tobacco consumption - Muscle or joint injury |
Country | Name | City | State |
---|---|---|---|
Mexico | Erika Martínez-López | Guadalajara | Jalisco |
Lead Sponsor | Collaborator |
---|---|
University of Guadalajara |
Mexico,
ASTRAND PO, RYHMING I. A nomogram for calculation of aerobic capacity (physical fitness) from pulse rate during sub-maximal work. J Appl Physiol. 1954 Sep;7(2):218-21. — View Citation
Lin CH, Chiang SL, Tzeng WC, Chiang LC. Systematic review of impact of lifestyle-modification programs on metabolic risks and patient-reported outcomes in adults with metabolic syndrome. Worldviews Evid Based Nurs. 2014 Dec;11(6):361-8. doi: 10.1111/wvn.1 — View Citation
Ozaki E, Campbell M, Doyle SL. Targeting the NLRP3 inflammasome in chronic inflammatory diseases: current perspectives. J Inflamm Res. 2015 Jan 16;8:15-27. doi: 10.2147/JIR.S51250. eCollection 2015. Review. — View Citation
Ross R, Hudson R, Stotz PJ, Lam M. Effects of exercise amount and intensity on abdominal obesity and glucose tolerance in obese adults: a randomized trial. Ann Intern Med. 2015 Mar 3;162(5):325-34. doi: 10.7326/M14-1189. — View Citation
Taniguchi S, Sagara J. Regulatory molecules involved in inflammasome formation with special reference to a key mediator protein, ASC. Semin Immunopathol. 2007 Sep;29(3):231-8. Epub 2007 Sep 6. Review. — View Citation
You T, Arsenis NC, Disanzo BL, Lamonte MJ. Effects of exercise training on chronic inflammation in obesity : current evidence and potential mechanisms. Sports Med. 2013 Apr;43(4):243-56. doi: 10.1007/s40279-013-0023-3. Review. — View Citation
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Change in ASC mRNA Expression | The polymorphonuclear cells were separated using Dextran treatment from peripheral blood samples. Subsequently, TRIzol® reagent was using according to the manufacturer´s instructions. The complementary DNA (cDNA) synthesis was performed according to standard techniques. Quantitative real-time PCR was performed using TaqMan® probes in Light Cycler 96 equipment considering standards PCR conditions to analyze ASC mRNA relative expression by 2-??cq method. The amplification reactions were performed in duplicate using ß-Actin gene as constitutive gene to normalized the samples. |
Mean change from baseline (0 Month) to end of treatment at 4th Month. | |
Primary | Change in Pro-inflammatory and Anti-inflammatory Cytokines | The pro-inflammatory and anti-inflammatory cytokines quantification were using Bio-Plex Pro™ Human cytokine Standard 17-Plex, Group I kit following the supplier's instructions, and the read was immediately by MAGPIX™ analyzer. | Mean change from baseline (0 Month) to end of treatment at 4th Month. | |
Primary | Change in Astrand-rhyming Submaximal Test | The Astrand-rhyming submaximal test was performed as described by Astrand. | Mean change from baseline (0 Month) to end of treatment at 4th Month. | |
Secondary | Changes in Height | Height in meters using a stadiometer. | At the baseline (0 Month) and 1st month, 2nd month, 3th month and the 4th month. 1st month, 2nd month, 3th month and the 4th month. | |
Secondary | Changes in Weight | The weight was measured in kilograms on InBody 370. | At the baseline (0 Month) and 1st month, 2nd month, 3th month and the 4th month. | |
Secondary | Changes in Body Mass Index (BMI) | Weight and height were be combined to report BMI in kg/m^2 | At the baseline (0 Month) and 1st month, 2nd month, 3th month and the 4th month. | |
Secondary | Changes in Waist Circumference | Waist circumference was measured at the narrowest point between the edge of the inner rib and the iliac crest, with the participant in an abducted and relaxed position, after expiration using a Lufkin Executive® tape. | At the baseline (0 Month) and 1st month, 2nd month, 3th month and the 4th month. | |
Secondary | Changes in Fat Mass | The Fat Mass was measured in kilograms by electrical bioimpedance on InBody 370. | At the baseline (0 Month) and 1st month, 2nd month, 3th month and the 4th month. | |
Secondary | Changes in Musculoskeletal Mass | The musculoskeletal mass was measured in kilograms by electrical bioimpedance on InBody 370. | At the baseline (0 Month) and 1st month, 2nd month, 3th month and the 4th month. | |
Secondary | Changes in Serum Glucose | It was measured in mg/dL using a dry chemistry system in Vitros 350 equipment. | At the baseline (0 Month) and 1st month, 2nd month, 3th month and the 4th month. | |
Secondary | Changes in Serum Insulin | Were determined through Insulin Model ELISA kit following the supplier's instructions. | At the baseline (0 Month), 3th month and the 4th month. | |
Secondary | Changes in homeostatic model assessment - insulin resistance (HOMA-IR) | Serum glucose and Insulin levels were be combined to report HOMA-IR calculated as described by Matthews. | At the baseline (0 Month), 3th month and the 4th month. | |
Secondary | Changes in Total Cholesterol | It was measured in mg/dL using a dry chemistry system in Vitros 350 equipment. | At the baseline (0 Month) and 1st month, 2nd month, 3th month and the 4th month. | |
Secondary | Changes in High-density lipoprotein (c-HDL) | It was measured in mg/dL using a dry chemistry system in Vitros 350 equipment. | At the baseline (0 Month) and 1st month, 2nd month, 3th month and the 4th month. | |
Secondary | Changes in Atherogenic Index | Serum total cholesterol and c-HDL were be combined to report atherogenic index, calculated through formula [Total cholesterol (mg/dL) / HDL-c (mg/dL)]. | At the baseline (0 Month) and 1st month, 2nd month, 3th month and the 4th month. |
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