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Comparison of blood levels of factors involved in resolving inflammation in individuals with features of the metabolic syndrome versus matched healthy controls

Not Applicable
Completed
Conditions
Overweight men and women
Cardiovascular - Other cardiovascular diseases
Diet and Nutrition - Obesity
Registration Number
ACTRN12610000708055
Lead Sponsor
Professor Trevor Mori
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
All
Target Recruitment
40
Inclusion Criteria

Men and post-menopausal women not taking hormone replacement therapy, aged 20-70 years, will be recruited from the general population by newspaper advertisements. Subjects will recruited on the basis of being untreated but having features of the metabolic syndrome using the criteria of the National Cholesterol Education Program Adult Treatment Panel III (NCEP: ATP III). They will be invited to participate if they have a waist circumference >102cm for males and >88cm for females and systolic blood pressure (SBP) >130 mmHg,
Age and gender matched healthy control subjects will be recruited from the general population. Subjects will be included if in the age range 20 to 70 years with a waist circumference <102cm for males and <88cm for females and no other defining criteria for the metabolic syndrome.

Exclusion Criteria

Smokers, history of cardiovascular or peripheral vascular disease, diabetes, renal disease, liver disease or taking anti-hypertensive agents, lipid lowering drugs, aspirin or non-steroidal anti-inflammatory drugs, omega-3 fatty acids or >2 fish meals /week.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Plasma and serum anti-inflammatory resolvins and protectins[Blood samples will be taken at week 0 and at weeks 3 and 4.]
Secondary Outcome Measures
NameTimeMethod
Other anti-inflammatory metabolites are Interleukin-6 (IL-6) and C-Reactive Protein (CRP)[Blood samples will be taken at week 0 and at weeks 3 and 4.]
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