Behavior of Scoliosis During Growth in Children with Osteogenesis Imperfecta

Background Spinal deformities are common in patients with osteogenesis imperfecta, a heritable disorder that causes bone fragility. The purpose of this study was to describe the behavior of spinal curvature during growth in patients with osteogenesis imperfecta and establish its relationship to dise...

Full description

Saved in:
Bibliographic Details
Published in:Journal of bone and joint surgery. American volume Vol. 96; no. 3; pp. 237 - 243
Main Authors: Anissipour, Alireza K., DO, Kostiuk, Theodore, DO, Hammerberg, Kim W., MD, Caudill, Angela, MPT, Krzak, Joseph J., PT, Smith, Peter A., MD, Tarima, Sergey, PhD, Zhao, Heather Shi, MS
Format: Journal Article
Language:English
Published: 2014
Subjects:
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Abstract Background Spinal deformities are common in patients with osteogenesis imperfecta, a heritable disorder that causes bone fragility. The purpose of this study was to describe the behavior of spinal curvature during growth in patients with osteogenesis imperfecta and establish its relationship to disease severity and medical treatment with bisphosphonates. Methods The medical records and radiographs of 316 patients with osteogenesis imperfecta were retrospectively reviewed. The severity of osteogenesis imperfecta was classified with the modified Sillence classification. Serial curve measurements were recorded throughout the follow-up period for each patient with scoliosis. Regression analysis was used to determine the effect of disease severity (Sillence type), patient age, and bisphosphonate treatment on the progression of scoliosis as measured with the Cobb method. Results Of the 316 patients with osteogenesis imperfecta, 157 had associated scoliosis, a prevalence of 50%. Scoliosis prevalence (68%) and mean progression rate (6° per year) were the highest in the group of patients with the most severe osteogenesis imperfecta (modified Sillence type III). A group with intermediate osteogenesis imperfecta severity, modified Sillence type IV, demonstrated intermediate scoliosis values (54%, 4° per year). The patient group with the mildest form of osteogenesis imperfecta, modified Sillence type I, had the lowest scoliosis prevalence (39%) and rate of progression (1° per year). Early treatment—before the patient reached the age of six years—of type-III osteogenesis imperfecta with bisphosphonate therapy decreased the curve progression rate by 3.8° per year, which was a significant decrease. Bisphosphonate treatment had no demonstrated beneficial effect on curve behavior in patients with other types of osteogenesis imperfecta or in patients of older age. Conclusions The prevalence of scoliosis in association with osteogenesis imperfecta is high. Progression rates of scoliosis in children with osteogenesis imperfecta are variable, depending on the Sillence type of osteogenesis imperfecta. High rates of scoliosis progression in type-III and type-IV osteogenesis imperfecta contrast with a benign course in type I. Bisphosphonate therapy initiated before the patient reaches the age of six years can modulate curve progression in type-III osteogenesis imperfecta. Level of Evidence Prognostic Level III . See Instructions for Authors for a complete description of levels of evidence.
AbstractList Background Spinal deformities are common in patients with osteogenesis imperfecta, a heritable disorder that causes bone fragility. The purpose of this study was to describe the behavior of spinal curvature during growth in patients with osteogenesis imperfecta and establish its relationship to disease severity and medical treatment with bisphosphonates. Methods The medical records and radiographs of 316 patients with osteogenesis imperfecta were retrospectively reviewed. The severity of osteogenesis imperfecta was classified with the modified Sillence classification. Serial curve measurements were recorded throughout the follow-up period for each patient with scoliosis. Regression analysis was used to determine the effect of disease severity (Sillence type), patient age, and bisphosphonate treatment on the progression of scoliosis as measured with the Cobb method. Results Of the 316 patients with osteogenesis imperfecta, 157 had associated scoliosis, a prevalence of 50%. Scoliosis prevalence (68%) and mean progression rate (6° per year) were the highest in the group of patients with the most severe osteogenesis imperfecta (modified Sillence type III). A group with intermediate osteogenesis imperfecta severity, modified Sillence type IV, demonstrated intermediate scoliosis values (54%, 4° per year). The patient group with the mildest form of osteogenesis imperfecta, modified Sillence type I, had the lowest scoliosis prevalence (39%) and rate of progression (1° per year). Early treatment—before the patient reached the age of six years—of type-III osteogenesis imperfecta with bisphosphonate therapy decreased the curve progression rate by 3.8° per year, which was a significant decrease. Bisphosphonate treatment had no demonstrated beneficial effect on curve behavior in patients with other types of osteogenesis imperfecta or in patients of older age. Conclusions The prevalence of scoliosis in association with osteogenesis imperfecta is high. Progression rates of scoliosis in children with osteogenesis imperfecta are variable, depending on the Sillence type of osteogenesis imperfecta. High rates of scoliosis progression in type-III and type-IV osteogenesis imperfecta contrast with a benign course in type I. Bisphosphonate therapy initiated before the patient reaches the age of six years can modulate curve progression in type-III osteogenesis imperfecta. Level of Evidence Prognostic Level III . See Instructions for Authors for a complete description of levels of evidence.
Author Kostiuk, Theodore, DO
Tarima, Sergey, PhD
Krzak, Joseph J., PT
Anissipour, Alireza K., DO
Zhao, Heather Shi, MS
Caudill, Angela, MPT
Hammerberg, Kim W., MD
Smith, Peter A., MD
Author_xml – sequence: 1
  fullname: Anissipour, Alireza K., DO
– sequence: 2
  fullname: Kostiuk, Theodore, DO
– sequence: 3
  fullname: Hammerberg, Kim W., MD
– sequence: 4
  fullname: Caudill, Angela, MPT
– sequence: 5
  fullname: Krzak, Joseph J., PT
– sequence: 6
  fullname: Smith, Peter A., MD
– sequence: 7
  fullname: Tarima, Sergey, PhD
– sequence: 8
  fullname: Zhao, Heather Shi, MS
BookMark eNqljs2KwjAUhbNQmDozjyBkqYvqTYyKGxfjPwy4qPtQ6q29NSZDUhXf3ioyL-DqcA4fh6_FGtZZZKwtoCdAjPoJgBTxZDAcdoTqjhVIiGWDRf_zB2uFUAKAUjCO2O8PFumFnOcu50nmDLlAgc_PnuyBr7y7VgUny2cFmb1Hy69UD9tQoTugxQe7Of2hzzGr0i_WzFMT8PuVn2y6XOxm6xjrciH0OjNkKUvNEW8YSnf2tua00EFq0E_3h6NQT3E5ePvgDhoAVmY
ContentType Journal Article
Copyright The Journal of Bone and Joint Surgery, Inc.
Copyright_xml – notice: The Journal of Bone and Joint Surgery, Inc.
DOI 10.1016/S0021-9355(14)74020-2
DatabaseTitleList
DeliveryMethod fulltext_linktorsrc
EndPage 243
ExternalDocumentID 1_s2_0_S0021935514740202
GroupedDBID .55
.GJ
.XZ
07C
08G
08P
0R~
123
1CY
1KJ
29K
2WC
34G
36B
39C
3O-
3V.
4.4
53G
5RE
5RS
6NX
7RV
7X7
88E
88I
8AF
8F7
8FI
8FJ
8R4
8R5
AAAAV
AAAXR
AAEJM
AAFTM
AAGIX
AAHPQ
AAIQE
AAMOA
AAQKA
AASCR
AAWTL
AAXQO
ABASU
ABDIG
ABJNI
ABPMR
ABUWG
ABVCZ
ABXVJ
ACCJW
ACEWG
ACGFS
ACGOD
ACILI
ACIWK
ACNWC
ACPRK
ACRZS
ACXJB
ADGGA
ADHPY
ADNKB
AEETU
AFCHL
AFDTB
AFFNX
AFKRA
AFMFG
AFRAH
AFUWQ
AHMBA
AHOMT
AHQNM
AHVBC
AI.
AIJEX
AINUH
AJIOK
AJJEV
AJNWD
AJNYG
AJZMW
AKULP
ALMA_UNASSIGNED_HOLDINGS
ALMTX
AMJPA
AMKUR
AMNEI
AOHHW
AZQEC
BENPR
BKEYQ
BOWHD
BPHCQ
BQLVK
BVXVI
C45
CCPQU
CS3
D-I
DIWNM
DUNZO
DWQXO
E3Z
EBS
EEVPB
EJD
ERAAH
EX3
F5P
FCALG
FEDTE
FYUFA
GNUQQ
GNXGY
GQDEL
H13
HCIFZ
HLJTE
HMCUK
HVGLF
H~9
IKREB
IKYAY
JG8
K-O
L7B
M1P
M2P
M5~
NAPCQ
O9-
OCB
OGEVE
OHH
OJAPA
OPUJH
OUVQU
OVD
OVDNE
OVIDH
OVLEI
OXXIT
PCD
PQQKQ
PROAC
PSQYO
PZZ
Q2X
RLZ
SJN
TEORI
TJB
TSPGW
UKHRP
VH1
VVN
W1K
WH7
WOQ
WOW
X7M
YCJ
YOC
YQJ
YRY
ZGI
ZXP
ZY1
ZZMQN
~H1
~ZZ
ID FETCH-elsevier_clinicalkeyesjournals_1_s2_0_S00219355147402023
ISSN 0021-9355
IngestDate Tue Oct 15 22:53:54 EDT 2024
IsPeerReviewed true
IsScholarly true
Issue 3
Language English
LinkModel OpenURL
MergedId FETCHMERGED-elsevier_clinicalkeyesjournals_1_s2_0_S00219355147402023
ParticipantIDs elsevier_clinicalkeyesjournals_1_s2_0_S0021935514740202
PublicationCentury 2000
PublicationDate 2014
PublicationDateYYYYMMDD 2014-01-01
PublicationDate_xml – year: 2014
  text: 2014
PublicationDecade 2010
PublicationTitle Journal of bone and joint surgery. American volume
PublicationYear 2014
SSID ssj0004407
Score 4.283063
Snippet Background Spinal deformities are common in patients with osteogenesis imperfecta, a heritable disorder that causes bone fragility. The purpose of this study...
SourceID elsevier
SourceType Publisher
StartPage 237
SubjectTerms Orthopedics
Title Behavior of Scoliosis During Growth in Children with Osteogenesis Imperfecta
URI https://www.clinicalkey.es/playcontent/1-s2.0-S0021935514740202
Volume 96
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
link http://sdu.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwtV1NS8NAEF1qe_Eiiorf7EFBKanJJmmbi1D7YaXWCi3oLSRNohFMpGkv_npnM5tssBS04CEhLLvbpe8xOzuZNyHk3FB9ixeSUyzVcRVjalmKqzfrCji_ZrMeTPWGzsXJ_XHj8aXZ6RrdUimr5ifb_hVpaAOsuXL2D2jnk0IDPAPmcAfU4f4r3EXBwzT4PwaUw5iXHOmgGvEODt3zNMbRLoq4qyPAOn7lZg_63oMnPeNZHs4Kz9WNI3zp8B6H0byaoLK6Jt_-oMmTEQYAN_yE8aioASP75VQHqVnqjHKLH4OxWWDe9psfeyL_V3bAGHuWjjYIP6rP6RTDPGe57Sw8UZ27xXN1U794-DQpRjZQS5prDDSFV34v2mn88q3go140ulg2RuzfDMs-LW0NGKUY51PzOljGBYPzFD9BM7kfZjkA3fZAUxJWU5V0EB-jGWnvH53xMGUnzFbtpa4bpMLABrIyqbR6ncmtFO0aqvieMK5Hysuu5SIvNeNKLLDgLRU8oMk22RIEoC3k3A4p-dEuecj4RuOA5nyjyDeKfKNhRDO-Uc43WuQblXzbIze97qTdV7Il2JlwF7YaPxH8T-xV_4K-T8oRkPOAUAt8JtfSXLPhewYLmKXCFZi656hTk3nBIWms-SNHa488JpucgBhaOyHl-Wzhn5KNxFucCdi-Af51fso
link.rule.ids 315,782,786,4028,27932,27933,27934
linkProvider Ovid
openUrl ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Behavior+of+Scoliosis+During+Growth+in+Children+with+Osteogenesis+Imperfecta&rft.jtitle=Journal+of+bone+and+joint+surgery.+American+volume&rft.au=Anissipour%2C+Alireza+K.%2C+DO&rft.au=Kostiuk%2C+Theodore%2C+DO&rft.au=Hammerberg%2C+Kim+W.%2C+MD&rft.au=Caudill%2C+Angela%2C+MPT&rft.date=2014&rft.issn=0021-9355&rft.volume=96&rft.issue=3&rft.spage=237&rft.epage=243&rft_id=info:doi/10.1016%2FS0021-9355%2814%2974020-2&rft.externalDBID=ECK1-s2.0-S0021935514740202&rft.externalDocID=1_s2_0_S0021935514740202
thumbnail_m http://sdu.summon.serialssolutions.com/2.0.0/image/custom?url=https%3A%2F%2Fcdn.clinicalkey.com%2Fck-thumbnails%2F00219355%2FS0021935514X7150X%2Fcov150h.gif