# Cardiometabolic Health in Adolescents of South Asian Ancestry - the CHAriSmA study

> **NIH NIH R01** · JOHNS HOPKINS UNIVERSITY · 2022 · $901,813

## Abstract

Project Summary/Abstract
South Asians (SA), the fastest growing major ethnic group in the U.S., are also at greater type 2 diabetes (T2DM) and
cardiovascular disease (CVD) risk at relatively lower body mass index (BMI) compared to those of European and African
ancestry. The mechanism(s) underlying this increased cardiometabolic risk remain undefined. We are submitting this
research proposal in response to an NIH program announcement (PA-17-021) requesting proposals addressing health
disparities in NIDDK diseases. The increased cardiometabolic risk in SA Americans represent an understudied and
disparate risk. Mostly adult, associative studies performed outside the U.S. indicate that SA have higher % body fat,
visceral adiposity, and abdominal adiposity for a given BMI than other ethnic groups. These studies have also found
increased insulin resistance and dyslipidemia as well as decreased insulin-mediated glucose disposal (inversely
proportional to visceral fat) and β-cell function in SA adults. We propose to study SA adolescents, in order to elucidate
early mechanistic changes underlying their increased cardiometabolic risk. Given the unique fat distribution of SA, we
propose to define ectopic fat deposition and test for altered fat metabolism and β-cell insulin secretion in SA adolescents
in the U.S. We will use cutting-edge, innovative techniques, including MRI/MRS, mathematical modeling of free fatty
acid (FFA) kinetics, and the glucose-potentiated arginine test (GPA) to measure insulin secretory capacity, methods not
previously used in SA adolescents. We have assembled a highly experienced, multi-institutional (CNMC, CHOP, NIH),
and multi-disciplinary team with a track record of successful collaboration, to perform a cross-sectional study of 12-21
year old adolescents and young adults of SA ancestry (n=50), BMI ≥ 85%ile, compared to adolescents of European
ancestry (White) (n=50) and African American (AA) ancestry (n=50) of comparable age, sex, and BMI %ile. AA
individuals are known to also have increased cardiometabolic risk but have decreased visceral adiposity, making them a
unique comparison group. Aims: 1. To examine ancestry-related differences in body fat distribution (by MRI/MRS), FFA
flux (by 3-hour oral glucose tolerance test and Minimal Model of fatty acid kinetics), and to compare the relationships
between visceral adiposity and FFA flux among ancestral groups. 2. To examine ancestry-related differences in β-cell
insulin secretory capacity (by GPA), and compare the relationship between FFA flux and insulin secretory capacity
among groups. 3. To compare CVD and T2DM risk factors and vascular end organ injury (aortic pulse wave velocity)
among the three groups, and test for ancestry-related differences in the relationships between FFA flux and
cardiometabolic risk profile. Exploratory Aim: to compare adipocyte-derived exosomal microRNAs involved in insulin
signaling among the groups, and measure their association with β-cell insulin...

## Key facts

- **NIH application ID:** 10428356
- **Project number:** 5R01DK115648-05
- **Recipient organization:** JOHNS HOPKINS UNIVERSITY
- **Principal Investigator:** SHEELA NATESH MAGGE
- **Activity code:** R01 (R01, R21, SBIR, etc.)
- **Funding institute:** NIH
- **Fiscal year:** 2022
- **Award amount:** $901,813
- **Award type:** 5
- **Project period:** 2018-09-04 → 2024-06-30

## Primary source

NIH RePORTER: https://reporter.nih.gov/project-details/10428356

## Citation

> US National Institutes of Health, RePORTER application 10428356, Cardiometabolic Health in Adolescents of South Asian Ancestry - the CHAriSmA study (5R01DK115648-05). Retrieved via AI Analytics 2026-05-23 from https://api.ai-analytics.org/grant/nih/10428356. Licensed CC0.

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