Effects of California Walnuts on Vascular Function in Postmenopausal Women
To determine the potential acute cardiovascular benefits of California Walnuts in postmenopausal women of ages 55-70.
Primary outcome measures:
- Vascular function
- Platelet reactivity
We hypothesize that the consumption of California walnuts will improve vascular function and platelet reactivity.
Studieoversikt
Status
Forhold
Intervensjon / Behandling
Detaljert beskrivelse
Epidemiological studies have shown that consumption of high amounts of plant foods, such as nuts, fruits and vegetables, appears to be protective against chronic diseases including heart disease, stroke, diabetes mellitus and metabolic syndrome. In recent years, numerous studies indicate that consumption of walnuts mainly containing α-linolenic acid (ALA), L-arginine and polyphenols beneficially alters vascular function and reduces inflammatory biomarkers. Recent studies have reported that consumption of walnuts is associated with beneficial effects in prevention of chronic diseases by favorably altering human serum profiles (i.e. decrease in LDL cholesterol and triglycerides and increase in HDL cholesterol and apolipoprotein A1) which are closely involved in the development of cardiovascular disease (CVD). In addition, recent reports by Dr. Ros and his colleagues indicate that addition of walnuts to a high-fat meal can improve endothelial function. This favorable influence on vasoactivity has been attributed to the antioxidant and anti-inflammatory properties of components of walnuts.
Due to their age and menopausal status, postmenopausal women in particular, are at a greater risk population for developing CVD. Males tend to show greater rates of CVD than pre-menopausal women, while women following menopause show an increase in the rates of CVD. This increase is associated with endothelial dysfunction and decreased vasodilation which are apparently expressed after menopause and become worse with age. In this study, we will define the effects of consuming California walnuts on vascular health.
We hypothesize that consumption of California walnuts, which are particularly rich in ALA, L-arginine and polyphenols, will improve endothelial function and platelet reactivity in an at-risk population of postmenopausal women 50-70 years of age.
Studietype
Registrering (Faktiske)
Fase
- Fase 1
Kontakter og plasseringer
Studiesteder
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California
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Davis, California, Forente stater, 95616
- Ragle Human Nutrition Research Center
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Deltakelseskriterier
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
Tar imot friske frivillige
Kjønn som er kvalifisert for studier
Beskrivelse
Inclusion Criteria:
- 50 to 70 years of age
- Lack of menses in the last year and FSH 23-116.3 mlU/mL
- Subject is willing and able to comply with the study protocols.
- Subject is willing to consume up to 40 g of California walnuts.
- BMI 18.5-34.9 kg/m2
- Weight ≥ 110 pounds
Exclusion Criteria:
- BMI ≥ 35 kg/m2
- Weight <110 pounds
- Diabetes
- Taking anticoagulation medication including NSAIDs
- Blood pressure ≥ 160/90 mm Hg
- PFA-100 readings 10 % outside of normal reference range (normal reference range for ADP-Collagen: 71-118 sec; Epinephrine-Collagen: 94-193 sec).
- Renal or liver disease
- Heart disease, which includes cardiovascular events and Stroke
- Cushing's syndrome
- Chronic/routine high intensity exercise
- Inability to properly place or wear the PAT probes or abnormal measurements on pre-screening PAT
- Abnormal Liver, CBC or CMP (laboratory values outside the reference range) if determined to be clinically significant.
- History of cancer
- History of psychiatric disorders i.e. schizophrenia or bi-polar or depression treated with antidepressants within the last 1 year.
- Use of MAOI inhibitor within the last 1 year (e.g. phenelzine (Nardil), tranylcypromine (Parnate), etc)
- Malabsorption
- Anxiety medications
- Routine use of prescription drugs or over-the counter medications, which may potentially modulate the outcome of this study; including antibiotics, aspirin and aspirin-containing formulations, COX-2 inhibitors, antihistamines, corticosteroids, ACE-inhibitors, and beta-blockers.
- Asthma (can be worsened by mild to moderate food allergies).
- Indications of substance or alcohol abuse within the last 3 years
- Use of multivitamin/mineral supplements
- Use of herbal or plant-based supplements; omega-3 fatty acids, and fish oils in the past 3-6 months.
- Nut allergies
- Soy-derived supplements
- Soy/soy products consumption > 2 servings/week
- Hormone replacement therapy
- Alcohol consumption > 1 drink/day (i.e. 1 bottle of beer, ½ glass of wine, and 1 shot of hard liquor)
- Fruit consumption ≥ 3 cups (6 servings)/day
- Vegetable consumption ≥ 4 cups (8 servings)/day
- Grain consumption ≥ 8 oz/day
- Meat and Beans ≥ 7 oz/day
- Fatty Fish ≥ 3 times/week
- Milk ≥ 5 cups/day
- Oil ≥ 8 tsp/day
- Coffee/tea ≥ 3 cups/day
- Dark chocolate ≥ 3 oz/day
Studieplan
Hvordan er studiet utformet?
Designdetaljer
- Primært formål: Grunnvitenskap
- Tildeling: Randomisert
- Intervensjonsmodell: Crossover-oppdrag
- Masking: Ingen (Open Label)
Våpen og intervensjoner
Deltakergruppe / Arm |
Intervensjon / Behandling |
|---|---|
|
Eksperimentell: 5 g of walnuts
|
Consumption of 5 g of walnuts.
Consumption of 20 g of walnuts.
Consumption of 30 g of walnuts.
Consumption of 40 g of walnuts.
|
|
Eksperimentell: 20 g of walnuts
|
Consumption of 5 g of walnuts.
Consumption of 20 g of walnuts.
Consumption of 30 g of walnuts.
Consumption of 40 g of walnuts.
|
|
Eksperimentell: 30 g of walnuts
|
Consumption of 5 g of walnuts.
Consumption of 20 g of walnuts.
Consumption of 30 g of walnuts.
Consumption of 40 g of walnuts.
|
|
Eksperimentell: 40 g of walnuts
|
Consumption of 5 g of walnuts.
Consumption of 20 g of walnuts.
Consumption of 30 g of walnuts.
Consumption of 40 g of walnuts.
|
Hva måler studien?
Primære resultatmål
Resultatmål |
Tidsramme |
|---|---|
|
Peripheral Arterial Tonometry (PAT)
Tidsramme: 2 and 4 hours
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2 and 4 hours
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Samarbeidspartnere og etterforskere
Sponsor
Samarbeidspartnere
Etterforskere
- Hovedetterforsker: Robert M. Hackman, PhD, University of California, Davis
Studierekorddatoer
Studer hoveddatoer
Studiestart
Primær fullføring (Faktiske)
Studiet fullført (Faktiske)
Datoer for studieregistrering
Først innsendt
Først innsendt som oppfylte QC-kriteriene
Først lagt ut (Anslag)
Oppdateringer av studieposter
Sist oppdatering lagt ut (Anslag)
Siste oppdatering sendt inn som oppfylte QC-kriteriene
Sist bekreftet
Mer informasjon
Begreper knyttet til denne studien
Nøkkelord
Ytterligere relevante MeSH-vilkår
Andre studie-ID-numre
- 200917508-1
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