{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,4,19]],"date-time":"2026-04-19T01:34:48Z","timestamp":1776562488752,"version":"3.51.2"},"reference-count":98,"publisher":"Public Library of Science (PLoS)","issue":"1","license":[{"start":{"date-parts":[[2023,1,20]],"date-time":"2023-01-20T00:00:00Z","timestamp":1674172800000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/creativecommons.org\/licenses\/by\/4.0\/"}],"funder":[{"name":"U.S. Food and Drug Administration Orphan Products Development","award":["R01 FD-R-002568"],"award-info":[{"award-number":["R01 FD-R-002568"]}]},{"name":"U.S. Food and Drug Administration Orphan Products Development","award":["R01 FD-R-003409"],"award-info":[{"award-number":["R01 FD-R-003409"]}]},{"DOI":"10.13039\/100000071","name":"National Institute of Child Health and Human Development","doi-asserted-by":"crossref","award":["R21 HD078864"],"award-info":[{"award-number":["R21 HD078864"]}],"id":[{"id":"10.13039\/100000071","id-type":"DOI","asserted-by":"crossref"}]},{"DOI":"10.13039\/100000097","name":"National Center for Research Resources","doi-asserted-by":"crossref","award":["M01 RR00052"],"award-info":[{"award-number":["M01 RR00052"]}],"id":[{"id":"10.13039\/100000097","id-type":"DOI","asserted-by":"crossref"}]},{"DOI":"10.13039\/100000072","name":"National Institute of Dental and Craniofacial Research","doi-asserted-by":"publisher","award":["640T90DE021989-09"],"award-info":[{"award-number":["640T90DE021989-09"]}],"id":[{"id":"10.13039\/100000072","id-type":"DOI","asserted-by":"publisher"}]}],"content-domain":{"domain":["www.plosone.org"],"crossmark-restriction":false},"short-container-title":["PLoS ONE"],"abstract":"<jats:sec id=\"sec001\">\n<jats:title>Background<\/jats:title>\n<jats:p>Albright hereditary osteodystrophy (AHO) is caused by heterozygous inactivating mutations in <jats:italic>GNAS<\/jats:italic>. Patients with maternally-inherited mutations develop pseudohypoparathyroidism type 1A (PHP1A) with multi-hormone resistance and aberrant craniofacial and skeletal development among other abnormalities. Chiari malformation type 1 (CM1), a condition in which brain tissue extends into the spinal canal when the skull is too small, has been reported in isolated cases of PHP1A. It has been hypothesized to be associated with growth hormone (GH) deficiency. Given the adverse clinical sequelae that can occur if CM1 goes unrecognized, we investigated the previously undetermined prevalence of CM1, as well as any potential correlations with GH status, given the known increased prevalence of GH deficiency in PHP1A. We also investigated these metrics for low lying cerebellar tonsils (LLCT), defined as tonsillar descent less than 5 mm below the foramen magnum. In addition, we investigated possible correlations of CM1\/LLCT with advanced hand\/wrist bone ages and craniofacial abnormalities known to occur in PHP1A to determine whether premature chondrocyte differentiation and\/or aberrant craniofacial development could be potential etiologies of CM1\/LLCT through both human studies and investigations of our AHO mouse model.<\/jats:p>\n<\/jats:sec>\n<jats:sec id=\"sec002\">\n<jats:title>Methods<\/jats:title>\n<jats:p>We examined patients with PHP1A in our clinic and noticed CM1 more frequently than expected. Therefore, we set out to determine the true prevalence of CM1 and LLCT in a cohort of 54 mutation-confirmed PHP1A participants who had clinically-indicated brain imaging. We examined potential correlations with GH status, clinical features, biological sex, genotype, and hand\/wrist bone age determinations. In addition, we investigated the craniofacial development in our mouse model of AHO (<jats:italic>Gnas<\/jats:italic> E1+\/-m) by histologic analyses, dynamic histomorphometry, and micro-computerized tomographic imaging (MCT) in order to determine potential etiologies of CM1\/LLCT in PHP1A.<\/jats:p>\n<\/jats:sec>\n<jats:sec id=\"sec003\">\n<jats:title>Results<\/jats:title>\n<jats:p>In our cohort of PHP1A, the prevalence of CM1 is 10.8%, which is at least 10-fold higher than in the general population. If LLCT is included, the prevalence increases to 21.7%. We found no correlation with GH status, biological sex, genotype, or hand\/wrist bone age. Through investigations of our <jats:italic>Gnas<\/jats:italic> E1+\/-m mice, the correlate to PHP1A, we identified a smaller cranial vault and increased cranial dome angle with evidence of hyperostosis due to increased osteogenesis. We also demonstrated that there was premature closure of the spheno-occipital synchondrosis (SOS), a cartilaginous structure essential to the development of the cranial base. These findings lead to craniofacial abnormalities and could contribute to CM1 and LLCT development in PHP1A.<\/jats:p>\n<\/jats:sec>\n<jats:sec id=\"sec004\">\n<jats:title>Conclusion<\/jats:title>\n<jats:p>The prevalence of CM1 is at least 10-fold higher in PHP1A compared to the general population and 20-fold higher when including LLCT. This is independent of the GH deficiency that is found in approximately two-thirds of patients with PHP1A. In light of potential serious consequences of CM1, clinicians should have a low threshold for brain imaging. Investigations of our AHO mouse model revealed aberrant cranial formation including a smaller cranium, increased cranial dome angle, hyperostosis, and premature SOS closure rates, providing a potential etiology for the increased prevalence of CM1 and LLCT in PHP1A.<\/jats:p>\n<\/jats:sec>","DOI":"10.1371\/journal.pone.0280463","type":"journal-article","created":{"date-parts":[[2023,1,20]],"date-time":"2023-01-20T18:34:59Z","timestamp":1674239699000},"page":"e0280463","update-policy":"https:\/\/doi.org\/10.1371\/journal.pone.corrections_policy","source":"Crossref","is-referenced-by-count":5,"title":["Prevalence of Chiari malformation type 1 is increased in pseudohypoparathyroidism type 1A and associated with aberrant bone development"],"prefix":"10.1371","volume":"18","author":[{"given":"Neetu","family":"Krishnan","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Patrick","family":"McMullan","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Qingfen","family":"Yang","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Alexzandrea N.","family":"Buscarello","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-5727-610X","authenticated-orcid":true,"given":"Emily L.","family":"Germain-Lee","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"340","published-online":{"date-parts":[[2023,1,20]]},"reference":[{"issue":"2","key":"pone.0280463.ref001","doi-asserted-by":"crossref","first-page":"193","DOI":"10.1677\/JOE-07-0544","article-title":"Physiological functions of the imprinted Gnas locus and its protein variants Galpha(s) and XLalpha(s) in human and mouse","volume":"196","author":"A Plagge","year":"2008","journal-title":"J Endocrinol"},{"issue":"8","key":"pone.0280463.ref002","doi-asserted-by":"crossref","first-page":"476","DOI":"10.1038\/s41574-018-0042-0","article-title":"Diagnosis and management of pseudohypoparathyroidism and related disorders: first international Consensus Statement","volume":"14","author":"G Mantovani","year":"2018","journal-title":"Nat Rev Endocrinol"},{"issue":"4","key":"pone.0280463.ref003","doi-asserted-by":"crossref","first-page":"865","DOI":"10.1016\/j.ecl.2018.07.011","article-title":"Pseudohypoparathyroidism","volume":"47","author":"A Linglart","year":"2018","journal-title":"Endocrinol Metab Clin North Am"},{"issue":"4","key":"pone.0280463.ref004","doi-asserted-by":"crossref","first-page":"537","DOI":"10.1097\/MOP.0000000000000783","article-title":"Management of pseudohypoparathyroidism","volume":"31","author":"EL Germain-Lee","year":"2019","journal-title":"Curr Opin Pediatr"},{"key":"pone.0280463.ref005","unstructured":"Haldeman-Englert CR, Hurst ACE, Levine MA. 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