Mitochondrial toxicity in HIV type-1-exposed pregnancies in the era of highly active antiretroviral therapy

Author:

Gingelmaier Andrea1,Grubert Thomas A2,Kost Bernd P1,Setzer Bernhard3,Lebrecht Dirk3,Mylonas Ioannis1,Mueller-Hoecker Josef4,Jeschke Udo1,Hiedl Stephan5,Friese Klaus1,Walker Ulrich A36

Affiliation:

1. Department of Obstetrics and Gynaecology, Ludwig Maximilians University of Munich, Munich, Germany

2. Medical Practice of Obstetrics and Gynaecology, Ravensburg, Germany

3. Department of Rheumatology and Clinical Immunology, Albert Ludwigs University of Freiburg, Freiburg, Germany

4. Department of Pathology, Ludwig Maximilians University of Munich, Munich, Germany

5. Department of Paediatrics, Ludwig Maximilians University of Munich, Munich, Germany

6. Department of Rheumatology, Basel University, Basel, Switzerland

Abstract

Background The aim of this study was to determine the effects of HIV type-1 (HIV-1) infection and antiretroviral therapy (ART) on placental mitochondria. Methods HIV-1-infected pregnant women and HIV-1 -uninfected controls were enrolled prospectively. Placental mitochondrial DNA (mtDNA) copy numbers were determined by quantitative PCR, subunits II and IV of cytochrome c oxidase (COX) were quantified by western blot and mitochondrial ultrastructure was evaluated by electron microscopy. Venous blood lactate was measured in newborns. Results In total, 45 HIV-1-infected pregnant women on ART and 32 controls were included. Mean ±sd mtDNA copy numbers were significantly reduced in ART and HIV-1-exposed placentas (240 ±118 copies/ cell) in comparison with controls (686 ±842 copies/cell; P<0.001). The mean COX II/IV ratio was 48% lower in the investigational group compared with controls ( P<0.001). There was no evidence of severe ultrastructural damage within mitochondria of HIV-1-infected ART-exposed placentas. Although lactate levels between newborns did not differ, they were negatively correlated with placental mtDNA levels. There was no clear association between mitochondrial parameters and a particular nucleoside reverse transcriptase inhibitor (NRTI), the number of NRTIs or time of NRTI exposure. Conclusions Placental tissue of HIV-1-infected ART-exposed pregnancies shows evidence of mtDNA depletion with secondary respiratory chain compromise. The clinical effects of this finding warrant further investigation.

Publisher

SAGE Publications

Subject

Infectious Diseases,Pharmacology (medical),Pharmacology

Reference26 articles.

1. Mother-to-Child Transmission of HIV Infection in the Era of Highly Active Antiretroviral Therapy

2. Perinatal HIV Guidelines Working Group. Public Health Service Task Force recommendations for use of antiretroviral drugs in pregnant HIV-infected women for maternal health and interventions to reduce perinatal HIV transmission in the United States. (Updated 8 July 2008. Accessed 10 August 2008.) Available from http://aidsinfo.nih.gov/contentfiles/PerinatalGL_PDA.pdf.

3. Maternal-Fetal Transfer and Amniotic Fluid Accumulation of Nucleoside Analogue Reverse Transcriptase Inhibitors in Human Immunodeficiency Virus-Infected Pregnant Women

4. Persistent mitochondrial dysfunction and perinatal exposure to antiretroviral nucleoside analogues

5. Nucleoside Exposure in the Children of HIV-Infected Women Receiving Antiretroviral Drugs: Absence of Clear Evidence for Mitochondrial Disease in Children Who Died Before 5 Years of Age in Five United States Cohorts

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