Determinants of Bone Mineral Density and Metabolic Syndrome in South Asian Indian Men

September 23, 2021 updated by: Drexel University
This study aims to examine the association between body composition with bone density and risk factors for cardiovascular disease and type 2 diabetes. South Asian Indians have a lower bone density and a higher likelihood to develop metabolic syndrome (MetS) compared to Caucasians. MetS is a cluster of metabolic abnormalities that predispose an individual to cardiovascular disease and type 2 diabetes. This study will understand if the metabolic and biochemical markers ( Indicators of bone building and breaking in the blood and urine, Lipids and other proteins) explain both low BMD and MetS in SAI men

Study Overview

Status

Completed

Conditions

Detailed Description

There is a rising minority population in the United States and South Asians make up the largest growing sub population. Health concerns in the minority population are several of which metabolic syndrome (MetS) and low bone mineral density (BMD) are important. Interestingly research in the past decade is beginning to suggest an interplay between bone and energy metabolism. Hormones, bone proteins and cytokines that play an important role in bone metabolism are also altered in metabolic syndrome, suggesting that both these

conditions may share a common etiology. Hence the primary question in this study would be to assess whether bone is altered in the South Asian population in the United States and whether hormones or other proteins regulating bone influence metabolic syndrome outcomes in the South Asians, specifically the South Asian Indian population. There is also an altered body composition in the South Asian Indian population with a greater visceral adiposity. Greater visceral adipose tissue (VAT) is associated in both the pathogenesis of metabolic syndrome and low BMD, possibly due to release of pro inflammatory cytokines. Interestingly several factors that are involved in the etiology of low BMD such as a greater visceral adiposity, high serum pro inflammatory cytokines, altered hormonal milieu such as low 25 hydroxy vitamin D (25OHD) and high parathyroid hormone (PTH), low osteocalcin levels, low calcium and high carbohydrate diet may share a relationship with MetS outcomes. The South Asian population has all the above-mentioned biochemical and metabolic alterations and it would be interesting to examine this in an immigrant Asian population residing in the USA. The investigators propose to examine 30 South Asian Indians between the ages of 30-50 years, using 30 resident Caucasian men as controls. Bone measures such as BMD and bone mineral content will be measured at radius, trochanter, hip and tibia and body composition including lean mass, fat mass, android fat and gynoid fat will be assessed using the Dual X ray energy absorptiometry (DXA). Biochemical measures including a complete metabolic panel, PTH, 25OHD, osteocalcin and other bone markers, and pro inflammatory cytokines will be measured in the serum. Investigators hypothesize that South Asian Indian men will have a lower BMD and higher MetS risk factors compared to age and BMI matched Caucasian men. Investigators further propose that common biochemical and metabolic alterations will underlie both low BMD and MetS outcomes in SAI population, but not in the Caucasian population. Identification of common determinants will help design a single future interventional trial that will target both MetS and bone health in the SA population

Specific Aim 1 To determine whether Bone Mineral Density (BMD) at weight-bearing and non weight-bearing sites is lower in age- and weight-matched SAI compared to white men.

It is hypothesized that SAI men will have lower BMD at weight-bearing sites compared to age and BMI-matched white men.

Specific Aim 2 To determine whether body composition influences Bone Mineral Density in SAI men.

It is hypothesized that greater abdominal adiposity, specifically visceral fat, influences BMD in SAI men compared to age- and BMI-matched white men.

Specific Aim 3 To examine the hormonal, inflammatory, and dietary determinants of Bone Mineral Density and MetS in SAI compared to white men.

It is hypothesized that the hormonal, inflammatory, and dietary determinants of both MetS and low BMD will be similar in the SAI men but not in the white men.

This study will involve one single visit. The following will be conducted during this visit:

  • This visit will last for about 2 hours
  • Blood draw- Four 5 ml tubes of blood will be collected via venipuncture
  • Spot urine sample collection
  • Measurement of height, weight, blood pressure, waist circumference
  • Completion of study questionnaires
  • DXA scan

Study Type

Observational

Enrollment (Actual)

60

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Pennsylvania
      • Philadelphia, Pennsylvania, United States, 19102
        • Drexel University Nutrition Sciences Research Lab

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

20 years to 50 years (Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

Male

Sampling Method

Non-Probability Sample

Study Population

South Asians Indians are defined as those who can trace their ancestry to Bangladesh, Bhutan, India, the Maldives, Nepal, Pakistan, and Sri Lanka.

Caucasians are defined as non-Hispanic who do not belong to any other ethnic group.

Description

Inclusion Criteria:

  • South Asian Indian and Caucasian males
  • 20 and 50 years of age
  • BMI range 23 - 35 kg/m2

Exclusion Criteria:

  • An individual is unwilling to sign the informed consent document.
  • A physician states that a participant is not able to participate in the study.
  • Individuals with the presence of any acute illness in the past month.
  • Individuals with preexisting chronic medical conditions such as diabetes (type I and II), cancer, other metabolic disorders.
  • Individuals who are using medications known to influence bone, blood glucose, lipids,and blood pressure.
  • Individuals who had a history of major diseases, such as cardiac, diabetes, renal, or evidence of cancer, in the past year.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Observational Models: Other
  • Time Perspectives: Cross-Sectional

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
South Asian Indians
No intervention will be applied for any group
No intervention will be applied to any group. It is an observational study and all measurements are collected during one visit.
Other Names:
  • Observational Study
Caucasians
No intervention will be applied for any group
No intervention will be applied to any group. It is an observational study and all measurements are collected during one visit.
Other Names:
  • Observational Study

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Bone Mineral Density ( g/cm2)
Time Frame: 1 day at baseline
Baseline differences in BMD in 2 groups
1 day at baseline
Total Body fat ( kg)
Time Frame: 1 day at baseline
Using the total body scan from the DXA , fat mass will be assessed
1 day at baseline
Lean mass ( Kg)
Time Frame: 1 day at baseline
Using the total body scan from the DXA , lean mass will be assessed
1 day at baseline
Visceral adipose tissue - VAT ( kg)
Time Frame: 1 day at baseline
Using the total body scan from the DXA ,VAT mass will be assessed
1 day at baseline

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Interleukin-6 ( IL-6)- pg/mL
Time Frame: 1 day at baseline
Serum levels will be assayed
1 day at baseline
Monocyte Chemoattractant protein-1 ( MCP-1)- ng//mL
Time Frame: 1 day at baseline
Serum levels will be assayed
1 day at baseline
C- Reactive Protein ( CRP)-mg/L
Time Frame: 1 day at baseline
Serum levels will be assayed
1 day at baseline
Adiponectin- ng/mL
Time Frame: 1 day at baseline
Serum levels will be assayed
1 day at baseline
Lipid profile
Time Frame: 1 day
Serum levels of HDL, LDL, Total cholesterol and triglycerides will be assayed ( mg/dL)
1 day
Blood pressure
Time Frame: 1 day
1 day
beta-C-terminal telopeptide (CTx) - ug/L
Time Frame: 1 day
Serum levels will be assayed
1 day
Parathyroid hormone- pg/mL
Time Frame: 1 day
Serum levels will be assayed
1 day
25 hydroxy vitamin D- ng/ML
Time Frame: 1 day
Serum levels will be assayed
1 day
Osteocalcin ( total)- ng/mL
Time Frame: 1 day
Serum levels will be assayed
1 day

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Deeptha Sukumar, PhD, Drexel University

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

May 8, 2015

Primary Completion (Actual)

May 8, 2020

Study Completion (Actual)

May 8, 2021

Study Registration Dates

First Submitted

March 14, 2018

First Submitted That Met QC Criteria

July 16, 2018

First Posted (Actual)

July 26, 2018

Study Record Updates

Last Update Posted (Actual)

September 27, 2021

Last Update Submitted That Met QC Criteria

September 23, 2021

Last Verified

September 1, 2021

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

Undecided

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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