Multiplex Ligation-Dependent Probe Amplification Accurately Detects Turner Syndrome in Girls with Short Stature

We aimed at evaluating a standard multiplex ligation-dependent probe amplification (MLPA) probe set for the detection of aneuploidy to diagnose Turner syndrome (TS). We first fixed an MLPA ratio cutoff able to detect all cases of TS in a pilot TS group. We then tested this value on a second group of...

Full description

Saved in:
Bibliographic Details
Published inHormone research in paediatrics Vol. 86; no. 5; p. 330
Main Authors Grandone, Anna, Del Vecchio Blanco, Francesca, Torella, Annalaura, Caruso, Manuela, De Luca, Filippo, Di Mase, Raffaella, Messina, Maria Francesca, Salerno, Maria Carolina, Sallemi, Alessia, Perone, Lucia, Marzuillo, Pierluigi, Miraglia Del Giudice, Emanuele, Nigro, Vincenzo, Perrone, Laura
Format Journal Article
LanguageEnglish
Published Switzerland 01.01.2016
Subjects
Online AccessGet more information

Cover

Loading…
Abstract We aimed at evaluating a standard multiplex ligation-dependent probe amplification (MLPA) probe set for the detection of aneuploidy to diagnose Turner syndrome (TS). We first fixed an MLPA ratio cutoff able to detect all cases of TS in a pilot TS group. We then tested this value on a second group of TS patients and a short-stature population to measure specificity and sensitivity. 15 TS patients with X mosaicism or X structural abnormalities (Pilot TS Group), 45 TS karyotype-assessed patients (TS Group), and 74 prepubertal female patients with apparent idiopathic short stature (Short-Stature Group) were enrolled. All subjects underwent MLPA and karyotype analysis. In the TS and Short-Stature Groups, MLPA testing was performed in blind. The choice of an MLPA threshold ratio of 0.76 for at least 1 probe allowed us to detect all TS cases, including mosaicisms. Sensitivity and specificity were 100% (CI 95%, 0.92-1) and 88.89% (CI 95%, 0.79-0.94), respectively. The positive predictive value was 88.5%, and the negative predictive value was 100%. MLPA detected the presence of Y chromosome material in 2 patients. MLPA is an accurate and inexpensive tool to screen for TS in girls with short stature. A customized MLPA kit may be useful for the screening of an even larger population.
AbstractList We aimed at evaluating a standard multiplex ligation-dependent probe amplification (MLPA) probe set for the detection of aneuploidy to diagnose Turner syndrome (TS). We first fixed an MLPA ratio cutoff able to detect all cases of TS in a pilot TS group. We then tested this value on a second group of TS patients and a short-stature population to measure specificity and sensitivity. 15 TS patients with X mosaicism or X structural abnormalities (Pilot TS Group), 45 TS karyotype-assessed patients (TS Group), and 74 prepubertal female patients with apparent idiopathic short stature (Short-Stature Group) were enrolled. All subjects underwent MLPA and karyotype analysis. In the TS and Short-Stature Groups, MLPA testing was performed in blind. The choice of an MLPA threshold ratio of 0.76 for at least 1 probe allowed us to detect all TS cases, including mosaicisms. Sensitivity and specificity were 100% (CI 95%, 0.92-1) and 88.89% (CI 95%, 0.79-0.94), respectively. The positive predictive value was 88.5%, and the negative predictive value was 100%. MLPA detected the presence of Y chromosome material in 2 patients. MLPA is an accurate and inexpensive tool to screen for TS in girls with short stature. A customized MLPA kit may be useful for the screening of an even larger population.
Author Sallemi, Alessia
De Luca, Filippo
Nigro, Vincenzo
Marzuillo, Pierluigi
Caruso, Manuela
Salerno, Maria Carolina
Torella, Annalaura
Grandone, Anna
Di Mase, Raffaella
Messina, Maria Francesca
Del Vecchio Blanco, Francesca
Miraglia Del Giudice, Emanuele
Perone, Lucia
Perrone, Laura
Author_xml – sequence: 1
  givenname: Anna
  surname: Grandone
  fullname: Grandone, Anna
  organization: Dipartimento della Donna, del Bambino, di Chirurgia Generale e Specialistica, Seconda Università degli Studi di Napoli, Naples, Italy
– sequence: 2
  givenname: Francesca
  surname: Del Vecchio Blanco
  fullname: Del Vecchio Blanco, Francesca
– sequence: 3
  givenname: Annalaura
  surname: Torella
  fullname: Torella, Annalaura
– sequence: 4
  givenname: Manuela
  surname: Caruso
  fullname: Caruso, Manuela
– sequence: 5
  givenname: Filippo
  surname: De Luca
  fullname: De Luca, Filippo
– sequence: 6
  givenname: Raffaella
  surname: Di Mase
  fullname: Di Mase, Raffaella
– sequence: 7
  givenname: Maria Francesca
  surname: Messina
  fullname: Messina, Maria Francesca
– sequence: 8
  givenname: Maria Carolina
  surname: Salerno
  fullname: Salerno, Maria Carolina
– sequence: 9
  givenname: Alessia
  surname: Sallemi
  fullname: Sallemi, Alessia
– sequence: 10
  givenname: Lucia
  surname: Perone
  fullname: Perone, Lucia
– sequence: 11
  givenname: Pierluigi
  surname: Marzuillo
  fullname: Marzuillo, Pierluigi
– sequence: 12
  givenname: Emanuele
  surname: Miraglia Del Giudice
  fullname: Miraglia Del Giudice, Emanuele
– sequence: 13
  givenname: Vincenzo
  surname: Nigro
  fullname: Nigro, Vincenzo
– sequence: 14
  givenname: Laura
  surname: Perrone
  fullname: Perrone, Laura
BackLink https://www.ncbi.nlm.nih.gov/pubmed/27784012$$D View this record in MEDLINE/PubMed
BookMark eNo1j8tOwzAURC0EoqV0wQ8g_0DA146dZFm1tCAFgdSyrhz7hholTuQ4gv49FY_VLM7oaOaKnPvOIyE3wO4AZHHPGEsl51CckSkoJRKeczUh82H4OCEm8qyA7JJMeJblKQM-Jd3z2ETXN_hFS_euo-t8ssIevUUf6WvoKqSLtm9c7cwPpQtjxqAjNke6wogmDnQ3Bo-Bbo_ehq5F6jzduNAM9NPFA90euhDpNuo4BrwmF7VuBpz_5Yy8rR92y8ekfNk8LRdlYkQKMbHstE4WqbEcK7Bo67QwUhkJWnORc1ZLq5TJjbAghAElK-A1porb_NTP-Izc_nr7sWrR7vvgWh2O-__n_Bso3FvO
CitedBy_id crossref_primary_10_23736_S2724_6507_20_03285_X
crossref_primary_10_1159_000499915
crossref_primary_10_13070_mm_en_8_2673
ContentType Journal Article
Copyright 2016 S. Karger AG, Basel.
Copyright_xml – notice: 2016 S. Karger AG, Basel.
DBID CGR
CUY
CVF
ECM
EIF
NPM
DOI 10.1159/000452219
DatabaseName Medline
MEDLINE
MEDLINE (Ovid)
MEDLINE
MEDLINE
PubMed
DatabaseTitle MEDLINE
Medline Complete
MEDLINE with Full Text
PubMed
MEDLINE (Ovid)
DatabaseTitleList MEDLINE
Database_xml – sequence: 1
  dbid: NPM
  name: PubMed
  url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed
  sourceTypes: Index Database
– sequence: 2
  dbid: EIF
  name: MEDLINE
  url: https://proxy.k.utb.cz/login?url=https://www.webofscience.com/wos/medline/basic-search
  sourceTypes: Index Database
DeliveryMethod no_fulltext_linktorsrc
Discipline Anatomy & Physiology
EISSN 1663-2826
ExternalDocumentID 27784012
Genre Clinical Trial
Multicenter Study
Journal Article
GroupedDBID ---
0R~
0~5
0~B
30W
327
3O.
3V.
4.4
53G
7RV
7X7
88E
8AO
8FI
8FJ
AAYIC
ABBTS
ABJNI
ABPAZ
ABUWG
ABWCG
ACGFS
ACPRK
ACPSR
ADBBV
AENEX
AEYAO
AFJJK
AFKRA
AFRAH
AHFRZ
AHMBA
ALDHI
ALIPV
ALMA_UNASSIGNED_HOLDINGS
AZPMC
AZQEC
BENPR
BKEYQ
BKNYI
BPHCQ
BVXVI
CAG
CCPQU
CGR
COF
CUY
CVF
CYUIP
DU5
E0A
EBS
ECM
EIF
EJD
EMOBN
EX3
F5P
FB.
FYUFA
HMCUK
HZ~
IY7
K9-
KUZGX
M0R
M1P
NAPCQ
NPM
O1H
O9-
OVD
PQQKQ
PROAC
PSQYO
RKO
RXVBD
SV3
TEORI
UJ6
UKHRP
WOW
ID FETCH-LOGICAL-c341t-d0012594cd2eb1dedf49c56c51aa23820f5d66c8c3d133c165b12fe462d8b1d72
IngestDate Wed Feb 19 02:17:05 EST 2025
IsDoiOpenAccess false
IsOpenAccess true
IsPeerReviewed true
IsScholarly true
Issue 5
Language English
License 2016 S. Karger AG, Basel.
LinkModel OpenURL
MergedId FETCHMERGED-LOGICAL-c341t-d0012594cd2eb1dedf49c56c51aa23820f5d66c8c3d133c165b12fe462d8b1d72
OpenAccessLink https://karger.com/hrp/article-pdf/86/5/330/3895652/000452219.pdf
PMID 27784012
ParticipantIDs pubmed_primary_27784012
PublicationCentury 2000
PublicationDate 2016-01-01
PublicationDateYYYYMMDD 2016-01-01
PublicationDate_xml – month: 01
  year: 2016
  text: 2016-01-01
  day: 01
PublicationDecade 2010
PublicationPlace Switzerland
PublicationPlace_xml – name: Switzerland
PublicationTitle Hormone research in paediatrics
PublicationTitleAlternate Horm Res Paediatr
PublicationYear 2016
SSID ssj0000387917
Score 2.1151497
Snippet We aimed at evaluating a standard multiplex ligation-dependent probe amplification (MLPA) probe set for the detection of aneuploidy to diagnose Turner syndrome...
SourceID pubmed
SourceType Index Database
StartPage 330
SubjectTerms Child
Child, Preschool
Chromosomes, Human, X - genetics
Female
Growth Disorders - diagnosis
Growth Disorders - genetics
Humans
Mosaicism
Multiplex Polymerase Chain Reaction - methods
Pilot Projects
Turner Syndrome - diagnosis
Turner Syndrome - genetics
Title Multiplex Ligation-Dependent Probe Amplification Accurately Detects Turner Syndrome in Girls with Short Stature
URI https://www.ncbi.nlm.nih.gov/pubmed/27784012
Volume 86
hasFullText
inHoldings 1
isFullTextHit
isPrint
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV1Jb9QwFLamcOGCCmUpm3xAXEaBZrNnjoVCR0jl0inqrXK80JHSZDQkUssv4mfyeclCCwi4RFGcRJHfl-fvPb-FkJeKxSZNDIvAXXmUCZFFcxFLnGUq5Vxx5pLCjj6xxUn28TQ_nUy-j6KW2qZ4Lb_9Mq_kf6SKa5CrzZL9B8n2L8UFnEO-OELCOP6VjI9CNOAlTOsvboqjg9DUtrEpAIXNGgHLNMExZ3tDtLY2RHkFRdO4QA7f6n56HCoXWP_H4WpThqy343PQc8dIQ-WRjsguwHXryvZcGfwma9H1_eiJ-iGWQlUHr2lV9WvAgS6nnyHX81U9fVsCeXXHoqG3huihZb2x0Vnd06VoN0Nkkdi0X2ufb1S1uhRjB0Y8dmBor3TBeiKYfmyslUOB7NV439up2NTv49xU_fncx0raGvFeDY8gsL5wGEg4h0XrA7f_PHqtCnc3tEW2YI_YBqvBK-RW_HTGYfaGwlX4kDf9Z9hi0-HRa4aLIzDLbXI3WB5038PoHpno6j7Z2a9EU19c0VfUxQK7TZYdUvfIojeRRR2y6E_IogOyaEAW9ciiHbLoqqIOWdQiizpk0YCsB-Tkw_vlu0UUWnNEErSniZSlyfk8kyrBYq-0Mtlc5kzmsRAggcmeyRVjciZTFaepjFlexInRGUvUDPfz5CG5VQF9jwkVUlsSqyVMgyw1ooAFwbEuaMX3TMbMLnnkp-1s7euvnHUT-uS3I0_JnQFpz8htgx9ePwd7bIoXTnQ_AI0udKc
linkProvider National Library of Medicine
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=Multiplex+Ligation-Dependent+Probe+Amplification+Accurately+Detects+Turner+Syndrome+in+Girls+with+Short+Stature&rft.jtitle=Hormone+research+in+paediatrics&rft.au=Grandone%2C+Anna&rft.au=Del+Vecchio+Blanco%2C+Francesca&rft.au=Torella%2C+Annalaura&rft.au=Caruso%2C+Manuela&rft.date=2016-01-01&rft.eissn=1663-2826&rft.volume=86&rft.issue=5&rft.spage=330&rft_id=info:doi/10.1159%2F000452219&rft_id=info%3Apmid%2F27784012&rft_id=info%3Apmid%2F27784012&rft.externalDocID=27784012