Metabolic Syndrome Clinical Trial
Official title:
Evaluation of the Citotoxicity and Clicemic Control of Subject With Metabolic Syndrome Managed With Conventional Nutritional Tratment More Quinoa, Flaxseed or Borh Versus Conventional Nutrition
The Metabolic Syndrome (MS) is a set of anthropometric alterations and chronic-degenerative
diseases, such as obesity, diabetes mellitus and arterial hypertension. Each one of the
diseases and physiological alterations represents a risk factor that conditions in the medium
or long term another incapacitating or limiting disease that reduces the quality of life of
an individual.
Our country has a growing burden of morbidity and mortality due to diseases
chronic-degenerative caused, for the most part, to the unhealthy lifestyle produced by
multiple factors, such as social, economic, behavioral, environmental, among others. For this
reason, it is important to plan, design and implement strategies that reduce, mitigate or
control this public health problem in the population. The purpose of this study is to perform
a nutritional intervention that includes food such as quinoa, flaxseed or both in subjects
with metabolic syndrome and follow them up for six months. The impact of this intervention
will be carried out through the measurement of cytotoxicity and glycemic control, this is
with the micronucleus count and the estimation of glycosylated hemoglobin (Hba1c).
This document will explain in detail what is intended to be done by presenting the following
sections:
In the approach of the problem and the justification, the metabolic syndrome will be
described, its impact on the Mexican population, the interest and relevance of this research
project.
In the background will be detailed what has been said and done in the different studies
scientists regarding the consumption of quinoa and flaxseed. Methodology defines the
strategy, conditions, clinical criteria, material and epidemiological and statistical methods
for the management of subjects and information.
Status | Recruiting |
Enrollment | 90 |
Est. completion date | December 31, 2020 |
Est. primary completion date | December 31, 2020 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 30 Years to 60 Years |
Eligibility |
Inclusion Criteria: - Diagnostic of Metabolic Syndrome that meets at least one of the ATP-III criteria: - Abdominal obesity over 102cm for men and over 88cm for women - Triglycerides levels over 150mg/dl with or without treatment for dyslipidemia - c-HDL concentration under 40mg/dl for men and under 50mg/dl for women - Blood Pressure over 130/85mmHg - Fasting glucose levels over 100mg/dl with or without treatment Exclusion Criteria: - Pregnant women - Subject with other degenerative chronic diseases does not include or consider it in ATP-III criteria for Metabolic Syndrome Elimination Criteria - Subjects without oral mucosa samples - Subjects without A1c data - Subjects without addiction to treatment under 80% with quinoa, flaxseed or both and conventional diet |
Country | Name | City | State |
---|---|---|---|
Mexico | Centro Universitario de Ciencias de la Salud, Universidad de Guadalajara | Guadalajara | Jalisco |
Mexico | Hospital Civil de Guadalajara "Fray Antonio Alcalde" | Guadalajara | Jalisco |
Lead Sponsor | Collaborator |
---|---|
University of Guadalajara | Hospital Civil de Guadalajara |
Mexico,
Andreassi MG, Barale R, Iozzo P, Picano E. The association of micronucleus frequency with obesity, diabetes and cardiovascular disease. Mutagenesis. 2011 Jan;26(1):77-83. doi: 10.1093/mutage/geq077. Review. — View Citation
Berti C, Riso P, Monti LD, Porrini M. In vitro starch digestibility and in vivo glucose response of gluten-free foods and their gluten counterparts. Eur J Nutr. 2004 Aug;43(4):198-204. Epub 2004 Jan 6. — View Citation
Ezzati M, Riboli E. Behavioral and dietary risk factors for noncommunicable diseases. N Engl J Med. 2013 Sep 5;369(10):954-64. doi: 10.1056/NEJMra1203528. — View Citation
Graf BL, Poulev A, Kuhn P, Grace MH, Lila MA, Raskin I. Quinoa seeds leach phytoecdysteroids and other compounds with anti-diabetic properties. Food Chem. 2014 Nov 15;163:178-85. doi: 10.1016/j.foodchem.2014.04.088. Epub 2014 May 4. — View Citation
Hou Y, Aboukhatwa MA, Lei DL, Manaye K, Khan I, Luo Y. Anti-depressant natural flavonols modulate BDNF and beta amyloid in neurons and hippocampus of double TgAD mice. Neuropharmacology. 2010 May;58(6):911-20. doi: 10.1016/j.neuropharm.2009.11.002. Epub 2009 Nov 14. — View Citation
Karaman A, Aydin H, Geçkinli B, Çetinkaya A, Karaman S. DNA damage is increased in lymphocytes of patients with metabolic syndrome. Mutat Res Genet Toxicol Environ Mutagen. 2015 Apr;782:30-5. doi: 10.1016/j.mrgentox.2015.03.009. Epub 2015 Mar 13. — View Citation
León-Muñoz LM, Guallar-Castillón P, López García E, Banegas JR, Gutiérrez-Fisac JL, Rodríguez-Artalejo F. Relationship of BMI, waist circumference, and weight change with use of health services by older adults. Obes Res. 2005 Aug;13(8):1398-404. — View Citation
Peñarrieta JM, Alvarado JA, Akesson B, Bergenståhl B. Total antioxidant capacity and content of flavonoids and other phenolic compounds in canihua (Chenopodium pallidicaule): an Andean pseudocereal. Mol Nutr Food Res. 2008 Jun;52(6):708-17. doi: 10.1002/mnfr.200700189. — View Citation
Rajesha J, Murthy KN, Kumar MK, Madhusudhan B, Ravishankar GA. Antioxidant potentials of flaxseed by in vivo model. J Agric Food Chem. 2006 May 31;54(11):3794-9. — View Citation
Ranilla LG, Apostolidis E, Genovese MI, Lajolo FM, Shetty K. Evaluation of indigenous grains from the Peruvian Andean region for antidiabetes and antihypertension potential using in vitro methods. J Med Food. 2009 Aug;12(4):704-13. doi: 10.1089/jmf.2008.0122. — View Citation
Stewart LK, Soileau JL, Ribnicky D, Wang ZQ, Raskin I, Poulev A, Majewski M, Cefalu WT, Gettys TW. Quercetin transiently increases energy expenditure but persistently decreases circulating markers of inflammation in C57BL/6J mice fed a high-fat diet. Metabolism. 2008 Jul;57(7 Suppl 1):S39-46. doi: 10.1016/j.metabol.2008.03.003. — View Citation
Voss S, Hesse A, Zimmermann DJ, Sauerbruch T, von Unruh GE. Intestinal oxalate absorption is higher in idiopathic calcium oxalate stone formers than in healthy controls: measurements with the [(13)C2]oxalate absorption test. J Urol. 2006 May;175(5):1711-5. — View Citation
* Note: There are 12 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Changes in the number of micronuceli after 24 weeks | The number of micronuclei will be evaluated at baseline at 12 weeks and 24 weeks with Schmidt technique by Giemsa/wright and the entered values reflect the number of micronuclei at week 24 | 24 weeks | |
Primary | Changes in fasting glucose levels after 24 weeks of intervention with an added diet with quinoa or flaxseed or both or conventional diet | The fasting glucose levels will be evaluated at baseline, at 12 weeks and 24 weeks with enzymatic/colorimetric techniques and the entered values reflect the fasting glucose level at 24 weeks | 24 weeks | |
Primary | Changes in glycosylated hemoglobin (A1C) after 24 weeks of intervention with an added diet with quinoa or flaxseed or both or conventional diet | Glycosylated hemoglobin will be evaluated at baseline, at 12 weeks and 24 weeks by high-pressure liquid chromatography (HPLC) and the entered values reflect the glycosylated hemoglobin at 24 weeks | 24 weeks | |
Secondary | Body Weight | The body weight will be measured at baseline, at 12 weeks and 24 weeks with a bioimpedance balance and the entered values reflect the body weight at 24 weeks | 24 weeks | |
Secondary | Body Mass Index | Body Mass Index will be calculated at baseline, 12 weeks and 24 weeks with the Quetelet index formula and the entered values reflect the body mass index at 24 weeks | 24 weeks | |
Secondary | Waist Circumference | Waist circumference will be evaluated at baseline and at 24 weeks with a flexible tape | 24 weeks | |
Secondary | Total Cholesterol | Total cholesterol levels will be evaluated at baseline and 24 weeks by enzymatic/colorimetric techniques and the entered values reflect the total cholesterol level at 24 weeks | 24 weeks | |
Secondary | Triglycerides levels | Triglycerides levels will be evaluated at baseline and 24 weeks with enzymatic/colorimetric techniques and the entered values reflect the triglycerides level at 24 weeks | 24 weeks | |
Secondary | High Density Lipoprotein | c-HDL levels will be evaluated at baseline and 24 weeks with enzymatic/colorimetric techniques and the entered values reflect the c-HDL level at 24 weeks | 24 weeks | |
Secondary | Low Density Lipoproteins | c-LDL levels will be evaluated at baseline and 24 weeks with enzymatic/colorimetric techniques and the entered values reflect the c-LDL level at 24 weeks | 24 weeks | |
Secondary | Blood pressure | Blood pressure will be measured at baseline and 24 weeks with a digital sphygmomanometer and the entered values reflect the blood pressure at 24 weeks | 24 weeks |
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