Literature DB >> 29059381

Ossifications in Albright Hereditary Osteodystrophy: Role of Genotype, Inheritance, Sex, Age, Hormonal Status, and BMI.

Parissa Salemi1, Julie M Skalamera Olson2, Lauren E Dickson3, Emily L Germain-Lee1,2,3,4.   

Abstract

Context: Albright hereditary osteodystrophy (AHO) is caused by heterozygous inactivating mutations in GNAS. Depending on the parental origin of the mutated allele, patients develop either pseudohypoparathyroidism type 1A (PHP1A), with multihormone resistance and severe obesity, or pseudopseudohypoparathyroidism (PPHP), without hormonal abnormalities or marked obesity. Subcutaneous ossifications (SCOs) are a source of substantial morbidity in both PHP1A and PPHP. Objective: This study investigated the previously undetermined prevalence of SCO formation in PHP1A vs PPHP as well as possible correlations with genotype, sex, age, hormonal resistance, and body mass index (BMI). Design: This study evaluated patients with AHO for SCOs by physical examination performed by one consistent physician over 16 years. Setting: Albright Clinic, Kennedy Krieger Institute; Institute for Clinical and Translational Research, Johns Hopkins Hospital; Albright Center, Connecticut Children's Medical Center. Patients: We evaluated 67 patients with AHO (49 with PHP1A, 18 with PPHP) with documented mutations in GNAS. Main Outcome Measures: Relationships of SCOs to genotype, sex, age, hormonal resistance, and BMI.
Results: Forty-seven of 67 participants (70.1%) had SCOs. Patients with PHP1A and PPHP had similar prevalences and degrees of ossification formation. Patients with frameshift and nonsense mutations had much more extensive SCOs than those with missense mutations. Males were affected more than females. There was no correlation with hormonal status or BMI. Conclusions: There is a similar prevalence of SCOs in PHP1A and PPHP, and the extent of SCO formation correlates with the severity of the mutation. Males are affected more extensively than females, and the SCOs tend to worsen with age.
Copyright © 2017 Endocrine Society

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Year:  2018        PMID: 29059381      PMCID: PMC5761497          DOI: 10.1210/jc.2017-00860

Source DB:  PubMed          Journal:  J Clin Endocrinol Metab        ISSN: 0021-972X            Impact factor:   5.958


  53 in total

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Authors:  P Justin Tortolani; Bryan W Cunningham; Mmech Eng; Paul C McAfee; Gwen A Holsapple; Karen A Adams
Journal:  J Bone Joint Surg Am       Date:  2007-01       Impact factor: 5.284

2.  Heterozygous inactivation of Gnas in adipose-derived mesenchymal progenitor cells enhances osteoblast differentiation and promotes heterotopic ossification.

Authors:  Robert J Pignolo; Meiqi Xu; Elizabeth Russell; Alec Richardson; Josef Kaplan; Paul C Billings; Frederick S Kaplan; Eileen M Shore
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3.  Progressive osseous heteroplasia: a model for the imprinting effects of GNAS inactivating mutations in humans.

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Journal:  J Clin Endocrinol Metab       Date:  2010-04-28       Impact factor: 5.958

Review 4.  Short stature, obesity, and growth hormone deficiency in pseudohypoparathyroidism type 1a.

Authors:  Emily L Germain-Lee
Journal:  Pediatr Endocrinol Rev       Date:  2006-04

5.  The stimulatory G protein alpha-subunit Gs alpha is imprinted in human thyroid glands: implications for thyroid function in pseudohypoparathyroidism types 1A and 1B.

Authors:  Jie Liu; Beth Erlichman; Lee S Weinstein
Journal:  J Clin Endocrinol Metab       Date:  2003-09       Impact factor: 5.958

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7.  Receptor-mediated adenylyl cyclase activation through XLalpha(s), the extra-large variant of the stimulatory G protein alpha-subunit.

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8.  The imprinted signaling protein XL alpha s is required for postnatal adaptation to feeding.

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Review 9.  Physiological functions of the imprinted Gnas locus and its protein variants Galpha(s) and XLalpha(s) in human and mouse.

Authors:  Antonius Plagge; Gavin Kelsey; Emily L Germain-Lee
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10.  Genetic and epigenetic alterations in the GNAS locus and clinical consequences in Pseudohypoparathyroidism: Italian common healthcare pathways adoption.

Authors:  L de Sanctis; F Giachero; G Mantovani; G Weber; M Salerno; G I Baroncelli; M F Elli; P Matarazzo; M Wasniewska; L Mazzanti; G Scirè; D Tessaris
Journal:  Ital J Pediatr       Date:  2016-11-21       Impact factor: 2.638

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2.  Parental Origin of Gsα Inactivation Differentially Affects Bone Remodeling in a Mouse Model of Albright Hereditary Osteodystrophy.

Authors:  Patrick McMullan; Peter Maye; Qingfen Yang; David W Rowe; Emily L Germain-Lee
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3.  Different AHO phenotype in a Chinese family with a novel GNAS missense variant: a case report.

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  5 in total

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