Effect of Age and Weight Loss on Inflammation and Iron Homeostasis

NCT ID: NCT01636635

Last Updated: 2015-11-16

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

44 participants

Study Classification

INTERVENTIONAL

Study Start Date

2011-03-31

Study Completion Date

2013-11-30

Brief Summary

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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.

Detailed Description

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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.

Conditions

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Obesity Aging

Study Design

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Allocation Method

NON_RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

BASIC_SCIENCE

Blinding Strategy

NONE

Study Groups

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Young (18-45 years)

Obese young women (18-45y) undergoing calorie restriction.

Group Type ACTIVE_COMPARATOR

Calorie Restriction

Intervention Type OTHER

Intervention consists of a calorically restricted diet regime designed and administered at the Weight and Wellness Center at Tufts University

Older (>60 years)

Obese older women (\>60y) undergoing calorie restriction.

Group Type EXPERIMENTAL

Calorie Restriction

Intervention Type OTHER

Intervention consists of a calorically restricted diet regime designed and administered at the Weight and Wellness Center at Tufts University

Interventions

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Calorie Restriction

Intervention consists of a calorically restricted diet regime designed and administered at the Weight and Wellness Center at Tufts University

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Enrolling patients in the Weight and Wellness Center (WWC) at Tufts Medical Center, part of their Tufts Employees, low calorie diet (LCD) or pre-surgical low calorie diet (PS-LCD) program, or enrolling at WWC as individual patients.
* BMI in the range of 30 to 55 kg/m2.
* Either ages 18-45 or \>60.

Exclusion Criteria

* Pregnancy.
* Weight reduction greater than or equal to 3% in the past 3 months.
* Prior gastric restrictive surgery.
* Weight loss medications within the 4 weeks prior to screening.
* History of eating disorder.
* Renal disease (serum creatinine \>2mg/dl).
* Hepatic disease, except for nonalcoholic steatohepatitis (NASH).
* Celiac disease, or any kind of intestinal malabsorption disorders.
* Gastrointestinal cancer.
* Hereditary hemochromatosis, or any blood disorders.
* Chronic infectious or inflammatory disease.
* Use of immunosuppressants.
* Severe iron deficiency anemia (hemoglobin\<8 g/dl) or other conditions that would prevent them from discontinuing iron supplement use.
Minimum Eligible Age

18 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

Yes

Sponsors

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Tufts University

OTHER

Sponsor Role lead

Responsible Party

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Simin Meydani

Simin Meydani, DVM, PhD

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Simin N Meydani, DVM, PhD

Role: PRINCIPAL_INVESTIGATOR

Tufts University

Locations

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JM USDA Human Nutrition Research Center on Aging

Boston, Massachusetts, United States

Site Status

Countries

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United States

Other Identifiers

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2765

Identifier Type: -

Identifier Source: org_study_id

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