JM USDA Human Nutrition Research Center on Aging
Boston, Massachusetts, 02111, United States
NCT Number: NCT01636635
The purpose of this study is to evaluate the effect of aging and weight loss on iron status and immune response in obese women. Iron deficiency and immune impairment are two of the numerous complications of obesity. The central hypothesis is that obesity-induced inflammation causes lower iron status through decreased iron absorption and availability in young and older obese women. Furthermore, the investigators hypothesize that this can be corrected with weight loss in both young and older obese women.
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Notify Me18 year and older
Female
Interventional
Not applicable
Boston, Massachusetts, 02111, United States
Obese individuals have chronic inflammation, higher risk of iron deficiency, and impaired immune response. These are conditions seen also with aging, but it is unknown to what extent they may be further impacted by obesity in the elderly. With this study the investigators aim to establish the mechanism by which weight loss may reduce inflammation and enhance iron status in young and older obese adults through the peptide hormone hepcidin, which regulates iron homeostasis. The investigators also aim to identify a possible link between iron homeostasis and immune response through hepcidin, which has been implicated in T cell mediated immunity. The investigators hypothesize that obesity-induced inflammation causes dysregulation of hepcidin expression leading to lower iron status through decreased iron absorption and availability in young and older adults. Furthermore, the investigators hypothesize that hepcidin dysregulation, and thus iron status can be mitigated with weight loss in both young and older obese adults. This hypothesis will be tested in obese young and older women undergoing weight loss through calorie restriction. Change in iron status, inflammation, and hepcidin will be determined before and after weight loss. Further, the impact of inflammatory environment of obesity on peripheral blood mononuclear cell hepcidin, ferroportin, intracellular iron, and T cell function in young and older adults will be determined. This study will address two important public health problems, i.e. obesity and iron deficiency and will be an important step toward the identification of strategies to enhance health of obese young and older adults.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Intervention consists of a calorically restricted diet regime designed and administered at the Weight and Wellness Center at Tufts University
Time frame: Baseline and 12-16 weeks
The investigators will determine the change in hepcidin at baseline and after 12-16 weeks of calorie restriction.
Time frame: Baseline and 12-16 weeks
The investigators will determine the change in inflammation at baseline and after 12-16 weeks of calorie restriction.
Time frame: Baseline and 12-16 weeks
The investigators will determine the change in iron status at baseline and after 12-16 weeks of calorie restriction.
Time frame: Baseline and 12-16 weeks
Time frame: Baseline and 12-16 weeks
Time frame: Baseline and 12-16 weeks
Time frame: Baseline and 12-16 weeks
After stimulation with ConA, PHA and anti-CD3/CD28
Tufts University
Other
Effect of Age and Weight Loss on Obesity-related Inflammation and Iron Homeostasis in Women
Acronym: HEP
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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