Genetic and Epigenetic Defects at the GNAS Locus Lead to Distinct Patterns of Skeletal Growth but Similar Early-Onset Obesity

被引:45
作者
Hanna, Patrick [1 ,2 ]
Grybek, Virginie [1 ,2 ]
Perez de Nanclares, Guiomar [3 ]
Tran, Lea C. [4 ]
de Sanctis, Luisa [5 ]
Elli, Francesca [6 ]
Errea, Javier [3 ]
Francou, Bruno [7 ]
Kamenicky, Peter [8 ,9 ]
Linglart, Lea [9 ]
Pereda, Arrate [3 ]
Rothenbuhler, Anya [9 ,10 ]
Tessaris, Daniele [5 ]
Thiele, Susanne [11 ]
Usardi, Alessia [9 ]
Shoemaker, Ashley H. [12 ]
Kottler, Marie-Laure [4 ]
Juppner, Harald [13 ,14 ,15 ]
Mantovani, Giovanna [6 ]
Linglart, Agnes [1 ,2 ,9 ,10 ]
机构
[1] INSERM, U1169, Le Kremlin Bicetre, France
[2] Paris Sud Paris Saclay Univ, Bictre Paris Sud Hosp, Le Kremlin Bicetre, France
[3] OSI Araba Univ Hosp, BioAraba Natl Hlth Inst, Mol EpiGenet Lab, Vitoria, Spain
[4] Caen Normandy Univ, Univ Caen Normandie, Caen Univ Hosp, Mol Genet Lab,Med Sch,BioTARGEN, Caen, France
[5] Univ Torino, Regina Margherita Children Hosp, Dept Publ Hlth & Pediat Sci, Paediat Endocrinol Unit, Turin, Italy
[6] Univ Milan, Dept Clin Sci & Community Hlth, Fdn IRCCS Ca Granda Osped Maggiore Policlin Endoc, Milan, Italy
[7] Bicetre Paris Sud Hosp, APHP, Dept Mol Genet, Le Kremlin Bicetre, France
[8] Bicetre Paris Sud Hosp, APHP, Dept Endocrinol & Reprod Dis, Le Kremlin Bicetre, France
[9] Bicetre Paris Sud Hosp, APHP, Reference Ctr Rare Disorders Calcium & Phosphate, Filiere OSCAR & Platform Expertise Rare Dis Paris, Le Kremlin Bicetre, France
[10] Bicetre Paris Sud Hosp, APHP, Endocrinol & Diabet Children, Le Kremlin Bicetre, France
[11] Univ Lubeck, Div Expt Pediat Endocrinol & Diabet, Dept Pediat, Ctr Brain Behav & Metab, Lubeck, Germany
[12] Vanderbilt Univ, Med Ctr, Nashville, TN USA
[13] Massachusetts Gen Hosp, Endocrine Unit, Boston, MA 02114 USA
[14] Massachusetts Gen Hosp, Pediat Nephrol Unit, Boston, MA 02114 USA
[15] Harvard Med Sch, Boston, MA USA
基金
美国国家卫生研究院;
关键词
PSEUDOHYPOPARATHYROIDISM; PSEUDOPSEUDOHYPOPARATHYROIDISM; GNAS; EARLY-ONSET OBESITY; GROWTH; PSEUDOHYPOPARATHYROIDISM TYPE 1A; GS-ALPHA GENE; ALBRIGHT HEREDITARY OSTEODYSTROPHY; HORMONE RESISTANCE; G(S)ALPHA DEFICIENCY; INTRAUTERINE GROWTH; ENERGY-EXPENDITURE; EUROPHP NETWORK; MUTATIONS; DISORDERS;
D O I
10.1002/jbmr.3450
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Pseudohypoparathyroidism type 1A (PHP1A), pseudoPHP (PPHP), and PHP type 1B (PHP1B) are caused by maternal and paternal GNAS mutations and abnormal methylation at maternal GNAS promoter(s), respectively. Adult PHP1A patients are reportedly obese and short, whereas most PPHP patients are born small. In addition to parathyroid hormone (PTH) resistance, PHP1A and PHP1B patients may display early-onset obesity. Because early-onset and severe obesity and short stature are daily burdens for PHP1A patients, we aimed at improving knowledge on the contribution of the GNAS transcripts to fetal and postnatal growth and fat storage. Through an international collaboration, we collected growth and weight data from birth until adulthood for 306 PHP1A/PPHP and 220 PHP1B patients. PHP1A/PPHP patients were smaller at birth than healthy controls, especially PPHP (length Z-score: PHP1A -1.1 +/- 1.8; PPHP -3.0 +/- 1.5). Short stature is observed in 64% and 59% of adult PHP1A and PPHP patients. PHP1B patients displayed early postnatal overgrowth (height Z-score at 1 year: 2.2 +/- 1.3 and 1.3 +/- 1.5 in autosomal dominant and sporadic PHP1B) followed by a gradual decrease in growth velocity resulting in normal adult height (Z-score for both: -0.4 +/- 1.1). Early-onset obesity characterizes GNAS alterations and is associated with significant overweight and obesity in adults (bodey mass index [BMI] Z-score: 1.4 +/- 2.6, 2.1 +/- 2.0, and 1.4 +/- 1.9 in PPHP, PHP1A, and PHP1B, respectively), indicating that reduced Gs alpha expression is a contributing factor. The growth impairment in PHP1A/PPHP may be due to Gs alpha haploinsufficiency in the growth plates; the paternal XL alpha s transcript likely contributes to prenatal growth; for all disease variants, a reduced pubertal growth spurt may be due to accelerated growth plate closure. Consequently, early diagnosis and close followup is needed in patients with GNAS defects to screen and intervene in case of early-onset obesity and decreased growth velocity. (c) 2018 The Authors. Journal of Bone and Mineral Research Published by Wiley Periodicals, Inc. on behalf of American Society for Bone and Mineral Research (ASBMR).
引用
收藏
页码:1480 / 1488
页数:9
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