Insights from Rare Obesity Disorders

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Insights from Rare Obesity Disorders Ashley Shoemaker, MD, MSCI Ian M. Burr Division of Pediatric Endocrinology and Diabetes

Disclosures Research funding: Zafgen, AstraZeneca, Rhythm Member, Zafgen Hypothalamic Injury Assoc. Obesity Adviory Board (2015) I will discuss off label drug use

Objectives Why syndromic obesity matters Review of the leptin-melanocortin pathway Novel treatments for POMC deficiency Lessons from pseudohypoparathyroidism

Syndromic Obesity Mendelian diseases Rare variant Large effect Effect size Common disease Rare variant Moderate effect Common disease Common variant Small effect Very rare Variant frequency Common Fig. modified from Kaiser J. Science. 2012

Common Variants Associated with Obesity Speliotes EK et al. Nat Genet. 2010

Why are rare diseases important? Syndromic obesity accounts for more than 5% of childhood obesity 625,000 children Furthers our understanding of the pathophysiology underlying common obesity Potential to develop targeted treatments

Leptin-Melanocortin Pathway Food intake Energy Expenditure MC4R PVN Mc4r - + α-msh Hypothalamus Ghsr Agrp/Npy POMC Ghrelin + Lepr Arcuate - Lepr + Leptin Stomach Adipose Tissue

Dehghani et al. Euro J Med Gen 2018 Farooqi et al. Endocrine Reviews 2006 Krude et al. Nat Genetics 1998 Leptin-Melanocortin Pathway MC4R PVN Food intake Energy Expenditure Mc4r - + α-msh Hypothalamus Ghsr Agrp/Npy POMC Ghrelin + Lepr Arcuate - Lepr + Leptin Stomach Adipose Tissue

Leptin 1994: Defects in leptin secretion cause obesity in the ob/ob mouse 1997: Congenital leptin deficiency reported in two children 1998: Leptin receptor mutation reported in humans 2002: Recombinant human leptin treats leptin deficiency Zhang et al. Nature 1994 Montague et al. Nature 1997 Clement et al. Nature 1998 Farooqi et al. JCI 2002

Dehghani et al. Euro J Med Gen 2018 Farooqi et al. Endocrine Reviews 2006 Krude et al. Nat Genetics 1998 Leptin-Melanocortin Pathway MC4R PVN Food intake Energy Expenditure Mc4r - + α-msh Hypothalamus Ghsr Agrp/Npy POMC Ghrelin + Lepr Arcuate - Lepr + Leptin Stomach Adipose Tissue

POMC POMC γ-msh ACTH β-msh βend Enzyme: Proprotein convertase 1 (PCSK1) α-msh Setmelanotide Jackson et al. Nat Genetics 1997 Philippe et al. IJO 2014 Krude et al. Nat Genetics 1998

Dehghani et al. Euro J Med Gen 2018 Farooqi et al. Endocrine Reviews 2006 Krude et al. Nat Genetics 1998 Leptin-Melanocortin Pathway MC4R PVN Food intake Energy Expenditure Mc4r - + α-msh Hypothalamus Ghsr Agrp/Npy POMC Ghrelin + Lepr Arcuate - Lepr + Leptin Stomach Adipose Tissue

Setmelanotide for POMC and LEPR Clement et al. Nature Medicine 2018

Setmelanotide - Skin changes Kuhnen et al. NEJM 2016

Setmelanotide PWS Orphan drug designation Bischof et al. J Pharmacol 2016

Common Variants Associated with Obesity Speliotes EK et al. Nat Genet. 2010

Setmelanotide for General Obesity 1856 ± 369 kcal/d 1745 ± 359 kcal/d Chen et al. JCEM 2015

Melanocortin 4 receptor Sim1 MC4R G s α MRAP2 Asai et al. Science 2013 Ramachandrappa et al. JCI 2013

Pseudohypoparathyroidism Weight Height

Pseudohypoparathyroidism Abnormal expression of G s α Plagge et al. J Endocrinol. 2008

GNAS - 20q13.2 Weinstein et al. 2009

PHP Types PPHP PHP type 1A PHP type 1B Elli et al. JCEM, 2016

Treating PHP PTH resistance Calcitriol TSH resistance Levothyroxine GHRH resistance Growth hormone LH/FSH resistance OCPs

Treating PHP NO TREATMENT FOR Obesity Cognitive impairment Subcutaneous ossifications Premature closure of the epiphyses

Why do patients with PHP become obese despite adequate hormone replacement?

Obesity is a feature of maternally inherited PHP Long et al. JCEM 2007

Melanocortin-4 Receptor G-protein coupled receptor Important role in hypothalamic control of energy balance Adipostat Food Intake Energy Expenditure MC4R Agrp/ Npy POMC

Leptin-Melanocortin Pathway Food intake Energy Expenditure MC4R PVN - Mc4r + Hypothalamus Ghsr Agrp/Npy POMC Ghrelin Lepr Arcuate + - Lepr + Leptin Stomach Adipose Tissue

MC4R Mutations Cause a Human Obesity Syndrome Farooqi et al. NEJM, 2003

PHP mouse model shows imprinting in the hypothalamus Quantification of in situ hybridization using a gnas exon-1 probe Chen, M., et al.,cell Metab, 2009.

Melanocortin 4 receptor G s camp MC4R Neuron Sympathetic Tone Energy Expenditure Food Intake Ghamari-Langroudi et al. Nature 2015

Resting Energy Expenditure is Decreased in PHP Shoemaker et al. IJO 2012 Perez et al. JCEM 2018

Hyperphagia PHP1A patients may have mild hyperphagia Breakfast buffet: 99 ± 49 vs. 63 ± 23 %REE, p= 0.01 Dinner buffet: 93 ± 22 vs. 79 ± 30 %REE, p= 0.25 Similar to MC4R deficiency (~40 kcals/kg FFM) Perez et al. JCEM 2018

HEALTH CONSEQUENCES OF OBESITY

Glucose intolerance occurs prior to onset of obesity Glucose tolerance test Insulin tolerance test Chen et al. Cell Metab, 2009.

Adults with PHP have reduced insulin sensitivity IV glucose tolerance test Mixed meal Muniyappa et al. JCEM, 2013

Children with PHP are less insulin resistant than obese controls Shoemaker unpublished data

Children vs. Adults Perez et al. JCEM, 2018 Muniyappa et al. JCEM, 2013

Children with PHP have impaired glucose tolerance 180 * * * Glucose (mg/dl) 150 120 90 * 60 0 30 60 90 120 Minutes Perez et al. JCEM, 2018

HbA1c may be decreased in PHP Hemoglobin A1c (%) 8.0 7.0 6.0 5.0 4.0 100 200 300 2h glucose (mg/dl) Perez et al. JCEM, 2018

Repurposing drugs for PHP G s Kir 7.1 K+ PDE inhibitors PDE camp AMP MC4R Neuron

Summary Understanding the pathophysiology of syndromic obesity provides opportunity for novel treatments Repurposing drugs is a viable option for orphan diseases

Acknowledgements Shoemaker Research Group Katia Perez Sachini Kahanda Rodayne Williams Kate Curley Margo Black, RN, Jenny Leshko, RN and Sarah Wright, RN Collaborators Harald Jϋppner (Massachusetts General Hospital) Christian Roth (Seattle Children s Hospital) Jennifer Abuzzahab (Minnesota Children s Hospital and Clinics) Vanderbilt Institute for Clinical and Translational Research