Bone tissue homeostasis and risk of fractures in Costello syndrome: A 4-year follow-up study

被引:6
作者
Leoni, Chiara [1 ]
Bisanti, Cristian [1 ]
Viscogliosi, Germana [1 ]
Onesimo, Roberta [1 ]
Massese, Miriam [1 ]
Giorgio, Valentina [1 ]
Corbo, Fabio [1 ]
Acampora, Anna [2 ]
Cipolla, Clelia [1 ]
Flex, Elisabetta [3 ]
Dell'Atti, Claudia [4 ]
Rigante, Donato [1 ,5 ]
Tartaglia, Marco [6 ]
Zampino, Giuseppe [1 ,5 ]
机构
[1] Fdn Policlin Univ A Gemelli IRCCS, Ctr Rare Dis & Birth Defects, Dept Woman & Child Hlth & Publ Hlth, Largo Gemelli 8, Rome, Italy
[2] Univ Cattolica Sacro Cuore, Univ Dept Life Sci & Publ Hlth, Sect Hyg, Rome, Italy
[3] Ist Super Sanita, Dept Oncol & Mol Med, Rome, Italy
[4] Fdn Policlin Univ A Gemelli IRCCS, Dipartimento Diagnost Immagini Radioterapia Oncol, Rome, Italy
[5] Univ Cattolica Sacro Cuore, Rome, Italy
[6] Osped Pediat Bambino Gesu, IRCCS, Genet & Rare Dis Res Div, Rome, Italy
关键词
bone metabolism biomarkers; bone mineral density; Costello syndrome; patient-centered care; personalized medicine; RASopathies; MINERAL DENSITY; PHENOTYPIC SPECTRUM; NEUROFIBROMATOSIS TYPE-1; NOONAN SYNDROME; CHILDREN; RAS; OSTEOPOROSIS; INDIVIDUALS; DIAGNOSIS; NF1;
D O I
10.1002/ajmg.a.62615
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Costello syndrome (CS) is a neurodevelopmental disorder with a distinctive musculoskeletal phenotype and reduced bone mineral density (BMD) caused by activating de novo mutations in the HRAS gene. Herein, we report the results of a prospective study evaluating the efficacy of a 4-year vitamin D supplementation on BMD and bone health. A cohort of 16 individuals ranging from pediatric to adult age with molecularly confirmed CS underwent dosages of bone metabolism biomarkers (serum/urine) and dual-energy X-ray absorptiometry (DXA) scans to assess bone and body composition parameters. Results were compared to age-matched control groups. At baseline evaluation, BMD was significantly reduced (p <= 0.05) compared to controls, as were the 25(OH)vitD levels. Following the 4-year time interval, despite vitamin D supplementation therapy at adequate dosages, no significant improvement in BMD was observed. The present data confirm that 25(OH)vitD and BMD parameters are reduced in CS, and vitamin D supplementation is not sufficient to restore proper BMD values. Based on this evidence, routine monitoring of bone homeostasis to prevent bone deterioration and possible fractures in adult patients with CS is highly recommended.
引用
收藏
页码:422 / 430
页数:9
相关论文
共 47 条
[1]   Germline mutations in HRAS proto-oncogene cause Costello syndrome [J].
Aoki, Y ;
Niihori, T ;
Kawame, H ;
Kurosawa, K ;
Filocamo, M ;
Kato, K ;
Suzuki, Y ;
Kure, S ;
Matsubara, Y .
NATURE GENETICS, 2005, 37 (10) :1038-1040
[2]   Recent advances in RASopathies [J].
Aoki, Yoko ;
Niihori, Tetsuya ;
Inoue, Shin-ichi ;
Matsubara, Yoichi .
JOURNAL OF HUMAN GENETICS, 2016, 61 (01) :33-39
[3]   Bone Densitometry in Children and Adolescents [J].
Bachrach, Laura K. ;
Gordon, Catherine M. .
PEDIATRICS, 2016, 138 (04)
[4]   Clinical Report-Bone Densitometry in Children and Adolescents [J].
Bachrach, Laura K. ;
Sills, Irene N. .
PEDIATRICS, 2011, 127 (01) :189-194
[5]   Constitutional Bone Impairment in Noonan Syndrome [J].
Baldassarre, Giuseppina ;
Mussa, Alessandro ;
Carli, Diana ;
Molinatto, Cristina ;
Ferrero, Giovanni Battista .
AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2017, 173 (03) :692-698
[6]   Phenotypic spectrum of Costello syndrome individuals harboring the rare HRAS mutation p.Gly13Asp [J].
Bertola, Debora ;
Buscarilli, Michelle ;
Stabley, Deborah L. ;
Baker, Laura ;
Doyle, Daniel ;
Bartholomew, Dennis W. ;
Sol-Church, Katia ;
Gripp, Karen W. .
AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2017, 173 (05) :1309-1318
[7]   Fracture Prediction and the Definition of Osteoporosis in Children and Adolescents: The ISCD 2013 Pediatric Official Positions [J].
Bishop, Nick ;
Arundel, Paul ;
Clark, Emma ;
Dimitri, Paul ;
Farr, Joshua ;
Jones, Graeme ;
Makitie, Outi ;
Munns, Craig F. ;
Shaw, Nick .
JOURNAL OF CLINICAL DENSITOMETRY, 2014, 17 (02) :275-280
[8]  
Camacho PM, 2020, ENDOCR PRACT, V26, P1, DOI 10.4158/GL-2020-0524SUPPL
[9]   Decreased bone mineralization in children with Noonan syndrome: Another consequence of dysregulated RAS MAPKinase pathway? [J].
Choudhry, Kiran S. ;
Grover, Monica ;
Tran, Alyssa A. ;
Smith, E. O'Brian ;
Ellis, Kenneth J. ;
Lee, Brendan H. .
MOLECULAR GENETICS AND METABOLISM, 2012, 106 (02) :237-240
[10]   Dystonia in Costello syndrome [J].
Dileone, M. ;
Zampino, G. ;
Profice, P. ;
Pilato, F. ;
Leoni, C. ;
Ranieri, F. ;
Capone, F. ;
Tartaglia, M. ;
Brown, P. ;
Di Lazzaro, V. .
PARKINSONISM & RELATED DISORDERS, 2012, 18 (06) :798-800