Blood Viral Load in Symptomatic Congenital Cytomegalovirus Infection.


Journal

The Journal of infectious diseases
ISSN: 1537-6613
Titre abrégé: J Infect Dis
Pays: United States
ID NLM: 0413675

Informations de publication

Date de publication:
16 04 2019
Historique:
received: 05 09 2018
accepted: 03 12 2018
pubmed: 12 12 2018
medline: 10 1 2020
entrez: 12 12 2018
Statut: ppublish

Résumé

Viral loads (VLs) frequently are followed during treatment of symptomatic congenital cytomegalovirus disease, but their predictive value is unclear. Post hoc analysis of 2 antiviral studies was performed. Seventy-three subjects were treated for 6 weeks and 47 subjects were treated for 6 months. Whole blood VL was determined by real-time polymerase chain reaction before and during therapy. Higher baseline VL was associated with central nervous system involvement (3.82 log, range 1-5.65 vs 3.32 log, range 1-5.36; P = .001), thrombocytopenia (3.68 log, range 1-5.65 vs 3.43 log, range 1-5.36; P = .03), and transaminitis at presentation (3.73 log, range 1-5.60 vs 3.39 log, range 1-5.65; P = .009), but with overlap in the amount of virus detected between groups. In subjects treated for 6 months, lower VL at presentation correlated with better hearing outcomes at 12 months, but VL breakpoints predictive of hearing loss were not identified. Sustained viral suppression during 6 months of therapy correlated with better hearing outcomes at 6, 12, and 24 months (P = .01, P = .0007, P = .04), but a majority without viral suppression still had improved hearing. In infants with symptomatic congenital cytomegalovirus disease, higher whole blood VL before initiation of antiviral therapy has no clinically meaningful predictive value for long-term outcomes.

Sections du résumé

BACKGROUND
Viral loads (VLs) frequently are followed during treatment of symptomatic congenital cytomegalovirus disease, but their predictive value is unclear.
METHODS
Post hoc analysis of 2 antiviral studies was performed. Seventy-three subjects were treated for 6 weeks and 47 subjects were treated for 6 months. Whole blood VL was determined by real-time polymerase chain reaction before and during therapy.
RESULTS
Higher baseline VL was associated with central nervous system involvement (3.82 log, range 1-5.65 vs 3.32 log, range 1-5.36; P = .001), thrombocytopenia (3.68 log, range 1-5.65 vs 3.43 log, range 1-5.36; P = .03), and transaminitis at presentation (3.73 log, range 1-5.60 vs 3.39 log, range 1-5.65; P = .009), but with overlap in the amount of virus detected between groups. In subjects treated for 6 months, lower VL at presentation correlated with better hearing outcomes at 12 months, but VL breakpoints predictive of hearing loss were not identified. Sustained viral suppression during 6 months of therapy correlated with better hearing outcomes at 6, 12, and 24 months (P = .01, P = .0007, P = .04), but a majority without viral suppression still had improved hearing.
CONCLUSIONS
In infants with symptomatic congenital cytomegalovirus disease, higher whole blood VL before initiation of antiviral therapy has no clinically meaningful predictive value for long-term outcomes.

Identifiants

pubmed: 30535363
pii: 5232568
doi: 10.1093/infdis/jiy695
pmc: PMC6467187
doi:

Substances chimiques

Antiviral Agents 0
DNA, Viral 0
Valganciclovir GCU97FKN3R
Ganciclovir P9G3CKZ4P5

Types de publication

Clinical Trial, Phase I Clinical Trial, Phase II Clinical Trial, Phase III Journal Article Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

1398-1406

Subventions

Organisme : NIAID NIH HHS
ID : K08 AI108691
Pays : United States
Organisme : NIAID NIH HHS
ID : N01AI30025
Pays : United States

Informations de copyright

© The Author(s) 2018. Published by Oxford University Press for the Infectious Diseases Society of America. All rights reserved. For permissions, e-mail: journals.permissions@oup.com.

Références

Pediatr Infect Dis J. 2009 Jul;28(7):588-92
pubmed: 19478688
N Engl J Med. 2015 Mar 5;372(10):933-43
pubmed: 25738669
J Infect Dis. 2008 Mar 15;197(6):836-45
pubmed: 18279073
J Pediatr. 2003 Jul;143(1):16-25
pubmed: 12915819
Am J Otolaryngol. 1990 Sep-Oct;11(5):292-8
pubmed: 2176062
J Pediatr. 2005 Jun;146(6):817-23
pubmed: 15973325
J Infect Dis. 2015 Jul 1;212(1):67-71
pubmed: 25387583
J Clin Virol. 2015 Apr;65:41-5
pubmed: 25766986
Int J Pediatr Otorhinolaryngol. 2000 Oct 16;55(3):215-24
pubmed: 11035181
Microbes Infect. 2007 Feb;9(2):183-91
pubmed: 17208485
Rev Med Virol. 2007 Sep-Oct;17(5):355-63
pubmed: 17542052
Pediatrics. 2006 Jan;117(1):e76-83
pubmed: 16326692
Laryngoscope. 2004 Dec;114(12):2235-8
pubmed: 15564852
Bone Marrow Transplant. 1998 Mar;21(6):597-605
pubmed: 9543064
J Infect Dis. 2005 Jan 15;191(2):227-33
pubmed: 15609232
Clin Infect Dis. 2013 Dec;57 Suppl 4:S178-81
pubmed: 24257422
Laryngoscope. 2005 Feb;115(2):223-5
pubmed: 15689739
N Engl J Med. 2006 May 18;354(20):2151-64
pubmed: 16707752
J Am Acad Audiol. 2000 May;11(5):283-90
pubmed: 10821506
J Infect Dis. 1998 Sep;178(3):626-35
pubmed: 9728529
Lancet. 2000 Jun 10;355(9220):2032-6
pubmed: 10885354
Clin Microbiol Rev. 2009 Jan;22(1):99-126, Table of Contents
pubmed: 19136436
Clin Microbiol Rev. 2013 Jan;26(1):86-102
pubmed: 23297260
Acta Otolaryngol. 2016;136(2):132-5
pubmed: 26484748
Laryngoscope. 1993 Aug;103(8):904-9
pubmed: 8395628
Lancet. 2004 Jun 26;363(9427):2116-21
pubmed: 15220032
Rev Med Virol. 2007 Jul-Aug;17(4):253-76
pubmed: 17579921
Am J Otolaryngol. 1988 May-Jun;9(3):135-41
pubmed: 2845828
Clin Infect Dis. 2017 May 15;64(10):1335-1342
pubmed: 28158709
J Clin Virol. 2016 Sep;82:152-158
pubmed: 27500364

Auteurs

Concetta Marsico (C)

Neonatology Unit, Department of Medical and Surgical Sciences, University of Bologna, Italy.

Immaculada Aban (I)

Department of Biostatistics, Division of Infectious Diseases, University of Alabama at Birmingham.

Huichien Kuo (H)

Department of Biostatistics, Division of Infectious Diseases, University of Alabama at Birmingham.

Scott H James (SH)

Department of Pediatrics, Division of Infectious Diseases, University of Alabama at Birmingham.

Pablo J Sanchez (PJ)

Department of Pediatrics, Divisions of Pediatric Infectious Diseases and Neonatology, Nationwide Children's Hospital - Ohio State University College of Medicine, Columbus.

Amina Ahmed (A)

Department of Pediatrics, Carolinas Medical Center, Charlotte, North Carolina.

Ravit Arav-Boger (R)

Medical College of Wisconsin, Milwaukee.

Marian G Michaels (MG)

Department of Pediatrics, Children's Hospital of Pittsburgh of UPMC, Pennsylvania.

Negar Ashouri (N)

Infectious Diseases, CHOC Children's Hospital, Orange, California.

Janet A Englund (JA)

University of Washington/Seattle Children's Hospital.

Benjamin Estrada (B)

University of South Alabama, Mobile.

Richard F Jacobs (RF)

University of Arkansas, Little Rock.

José R Romero (JR)

University of Arkansas, Little Rock.

Sunil K Sood (SK)

Steven and Alexandra Cohen Children's Medical Center, New Hyde Park, New York.

Suzanne Whitworth (S)

Cook Children's Medical Center, Fort Worth, Texas.

Penelope M Jester (PM)

Department of Pediatrics, Division of Infectious Diseases, University of Alabama at Birmingham.

Richard J Whitley (RJ)

Department of Pediatrics, Division of Infectious Diseases, University of Alabama at Birmingham.

David W Kimberlin (DW)

Department of Pediatrics, Division of Infectious Diseases, University of Alabama at Birmingham.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH