Glucose Homeostasis in Pseudohypoparathyroidism



Status:Not yet recruiting
Conditions:Endocrine, Endocrine
Therapuetic Areas:Endocrinology
Healthy:No
Age Range:6 - 50
Updated:3/30/2019
Start Date:May 2019
End Date:January 1, 2021
Contact:Ashley H Shoemaker, MD
Email:ashley.h.shoemaker@vumc.org
Phone:615-343-8116

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Glucose Homeostasis and Beta Cell Function in Pseudohypoparathyroidism

It is increasingly recognized that Pseudohypoparathyroidism type 1A (PHP1A) is associated
with an increased risk of type 2 diabetes but the mechanism is unknown. In this pilot study
we will assess β-cell function in patients with PHP1A and pseudopseudohypoparathyroidism
PPHP.

Pseudohypoparathyroidism type 1A (PHP1A) is a rare, genetic disorder caused by impaired
stimulatory G-protein signaling due to heterozygous mutations in the gene, GNAS. The most
severe form of the disease, PHP1A occurs when a GNAS mutation is inherited on the
preferentially expressed maternal allele. A less severe form of the disease,
pseudopseudohypoparathyroidism (PPHP), occurs when a GNAS mutation is inherited on the
paternal allele. Clinically, PHP1A is characterized by multi-hormone resistance, cognitive
impairment and early-onset obesity while PPHP has a mild phenotype without multi-hormone
resistance. It is increasingly recognized that PHP1A is associated with an increased risk of
type 2 diabetes but the mechanism is unknown. Glucose homeostasis and diabetes risk has not
been studied in PPHP. As part of the parent K23 award, we investigated glucose tolerance in
children with PHP1A. In contrast to the adult literature, we found that children with PHP1A
had greater insulin sensitivity than matched controls. When challenged with an oral glucose
load, however, children with PHP1A had persistent hyperglycemia and 25% met criteria for
impaired glucose tolerance. The goal of this proposal is to quantify β-cell function in
PHP1A. It is plausible that these individuals have a) impaired β-cell function, b)
differences in insulin sensitivity, and c) impaired incretin function. Thus, in this pilot
study we will definitively assess one of these, β-cell function, using the frequently sampled
intravenous glucose tolerance test in patients with PHP1A and PPHP (aim 1). We will also
assess oral glucose tolerance over time by bringing back children and young adults with PHP1A
from our original cohort for repeat glucose tolerance testing (aim 2). The ultimate goal is
to rigorously define glucose homeostasis defects in PHP1A in order to design and conduct an
intervention study for glucose intolerance and type 2 diabetes in PHP1A.

Inclusion Criteria:

1. Diagnosis of PHP1A/PPHP

2. Age between 6 and 50 years old

Controls will be matched based on:

1. Gender

2. Race

3. Age (±2 years if <25 years old or ±5 years if ≥25 years old)

4. BMI (±2 kg/m2)

5. Diabetes status

Exclusion Criteria:

1. Treatment with appetite-altering drug or initiation of a new weight loss program in
the past 3 months

2. Type 1 diabetes

3. Type 2 diabetes treated with insulin or GLP-1 receptor agonists or A1c >9%at their
most recent clinic visit

4. Pregnant or lactating women
We found this trial at
1
site
1211 Medical Center Dr
Nashville, Tennessee 37232
(615) 322-5000
Principal Investigator: Ashley Shoemaker, M.D.
Phone: 615-343-8116
Vanderbilt Univ Med Ctr Vanderbilt University Medical Center (VUMC) is a comprehensive healthcare facility dedicated...
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