Journal Article

Early postnatal soluble FGFR3 therapy prevents the atypical development of obesity in achondroplasia

Sarrazy, Vincent, Dumas, Karine, Salles, Jean-Pierre, Garcia, Stephanie, Sore, Sophie, Gual, Philippe, Saint-Laurent, Celine, Authier, Florence, Tran, Albert, Gouze, Elvire, Gennero, Isabelle

2018

Overview

Achondroplasia is a rare genetic disease is characterized by abnormal bone development and early obesity. While the bone aspect of the disease has been thoroughly studied, early obesity affecting approximately 50% of them during childhood has been somewhat neglected. It nevertheless represents a major health problem in these patients, and is associated to life-threatening complications including increasing risk of cardiovascular pathologies. We have thus decided to study obesity in patients and to use the mouse model to evaluate if soluble FGFR3 therapy, an innovative treatment approach for achondroplasia, could also impact the development of this significant complication. To achieve this, we have first fully characterized the metabolic deregulations in these patients by conducting a longitudinal retrospective study, in children with achondroplasia Anthropometric, densitometric measures as well as several blood parameters were recorded and compared between three age groups ranging from [0-3], [4-8] and [9-18] years old. Our results show unexpected results with the development of an atypical obesity with preferential fat deposition in the abdomen that is remarkably not associated with classical complications of obesity such as diabetes or hypercholosterolemia. Because it is not associated with diabetes, the atypical obesity has not been studied in the past even though it is recognized as a real problem in these patients. These results were validated in a murine model of achondroplasia (Fgfr3ach/+) where similar visceral adiposity was observed. Unexpected alterations in glucose metabolism were highlighted during high-fat diet. Glucose, insulin or lipid levels remained low, without the development of diabetes. Very interestingly, in achondroplasia mice treated with soluble FGFR3 during the growth period (from D3 to D22), the development of these metabolic deregulations was prevented in adult animals (between 4 and 14 weeks of age). The lean-over-fat tissues ratio was restored and glucose metabolism showed normal levels. Treating Fgfr3ach/+ mice with soluble FGFR3 during the growth period, prevented the development of these metabolic deregulations in adult animals and restored lean-over-fat tissues ratio as well as glucose metabolism in adult animals. This study demonstrate that achondroplasia patients develop an atypical obesity with preferential abdominal obesity not associated with classical complications. These results suggest that achondroplasia induces an uncommon metabolism of energy, directly linked to the FGFR3 mutation. These data strongly suggest that this common complication of achondroplasia should be included in the clinical management of patients. In this context, sFGFR3 proved to be a promising treatment for achondroplasia by normalizing the biology at different levels, not only restoring bone growth but also preventing the atypical visceral obesity and some metabolic deregulations.

• Publisher: Public Library of Science,Public Library of Science (PLoS)
• Subject: Achondroplasia / Adipose tissue / Adolescent / Age / Animal models / Animal tissues / Animals / Anthropometry / Biology and Life Sciences / Biomarkers / Blood Glucose / Bone growth / Cardiovascular diseases / Care and treatment / Child / Child, Preschool / Children / Complications / Complications and side effects / Densitometers / Deregulation / Diabetes / Diabetes mellitus / Disease / Disease Models, Animal / Dwarfism / Endocrinology and metabolism / Energy metabolism / Female / Fibroblast growth factor receptors / Fibroblasts / Genetic aspects / Glucose / Glucose metabolism / Growth factors / Health aspects / Health risks / High fat diet / Human health and pathology / Humans / Infant / Infant, Newborn / Insulin / Life Sciences / Lipid Metabolism / Male / Medical innovations / Medicine and Health Sciences / Mesenchymal Stem Cells / Metabolism / Mice / Mice, Transgenic / Mutation / Normalizing / Obesity / Patients / Pediatrics / People and Places / Phosphatase / Receptor, Fibroblast Growth Factor, Type 3 / Risk factors / Rodents / Sabatier, Paul (1854-1941) / Santé publique et épidémiologie / Secondary Prevention / Stem cells / Therapy