Blood Viral Load in Symptomatic Congenital Cytomegalovirus Infection

Author:

Marsico Concetta1ORCID,Aban Immaculada2,Kuo Huichien2,James Scott H3,Sanchez Pablo J4,Ahmed Amina5,Arav-Boger Ravit6,Michaels Marian G7,Ashouri Negar8,Englund Janet A9,Estrada Benjamin10,Jacobs Richard F11,Romero José R11,Sood Sunil K12,Whitworth Suzanne13,Jester Penelope M3,Whitley Richard J3,Kimberlin David W3,

Affiliation:

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

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

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

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

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

6. Medical College of Wisconsin, Milwaukee

7. Department of Pediatrics, Children’s Hospital of Pittsburgh of UPMC, Pennsylvania

8. Infectious Diseases, CHOC Children’s Hospital, Orange, California

9. University of Washington/Seattle Children’s Hospital

10. University of South Alabama, Mobile

11. University of Arkansas, Little Rock

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

13. Cook Children’s Medical Center, Fort Worth, Texas

Abstract

Abstract 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.

Funder

National Institute of Allergy and Infectious Diseases

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Immunology and Allergy

Reference37 articles.

1. Review and meta-analysis of the epidemiology of congenital cytomegalovirus (CMV) infection;Kenneson;Rev Med Virol,2007

2. New estimates of the prevalence of neurological and sensory sequelae and mortality associated with congenital cytomegalovirus infection;Dollard;Rev Med Virol,2007

3. The “silent” global burden of congenital cytomegalovirus;Manicklal;Clin Microbiol Rev,2013

4. Longitudinal investigation of hearing disorders in children with congenital cytomegalovirus;Dahle;J Am Acad Audiol,2000

5. Newborn hearing screening–a silent revolution;Morton;N Engl J Med,2006

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