Accelerated Aging, HIV Infection, Antiretroviral Therapies (EP 45)
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ClinicalTrials.gov Identifier: NCT01038999 |
Recruitment Status
:
Completed
First Posted
: December 24, 2009
Last Update Posted
: December 27, 2012
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Condition or disease | Intervention/treatment |
---|---|
HIV Infection Aging Accelerated Antiretroviral Therapies | Biological: Peripheral blood biological tests |
Protease inhibitors block viral protease, as well as various other cell enzymes : ZMPSTE24 cliping off prelamin A into mature lamin A ; at least one of the Golgi proteases involved in the release of SREBP, controlling the transcription of lipid metabolism regulating genes ; mitochondrial proteases involved in the importation and further maturation of nuclear genome encoded proteins ; proteasome regulating the transcription of several genes through NF-B ; P450 cytochromes. Nucleosides inhibitors of the viral reverse transcriptase exhibit nuclear and mitochondrial DNA toxicity, disrupt lipid and protein glycosylation and inhibit telomerase. Therefore antiretroviral therapies target several pathways involved in accelerated or normal aging. Their combined effects are added to viral infection direct symptoms or to cell abnormalities induced by viral proteins.
Our multicentric (the 3 CISIH from Marseille, Nice and Montpellier) 3 year- long study will analyse 50 HIV1-infected naive patients (A group), apparied to 50 age- and sex-matched seronegative control subjects (recruited by CIC-UPCET of Marseille) and 100 HIV1-infected patients in first line of antiretroviral therapy for at least 12 months (B group). Patients of group A and B will be recruited in the 3 clinical unit. The HIV1- infected patients will be evaluated four times, at baseline, then every 12 months during 3 years. In case of initiation or changing of antiretroviral therapy, patients will be evaluated once more. Control subjects will be only evaluated at baseline.
Peripheral blood biological tests will be the following [Laboratory designation] : i/ viral load measurement, PBMC isolation, DNA extraction, proviral DNA measurement, cell and DNA storage [Virology, Timone CHU, Marseille]; ii/ assays of CD4, CD8, glycemia, insulinemia, HOMA, total-, LDL- and HDL-cholesterol, triglycerides [Biochemistry labs from the 3 CHU] ; iii/ antiretroviral drug assay (mass spectrometry) [Pharmacokinetics, Timone CHU, Marseille]; iv/ detection (western blotting, immunocytochemistry combined to image analysis of nuclear abnormalities) of PBMC nuclear, cytosolic and mitochondrial targets of antiretroviral drugs : A and B lamins, NF-B + I-B and proteasome activity assay, CD36 (glycosylation), mitochondrial Hsp70, ROS mitochondrial production, mitochondrial inner membrane potential, cytochrome C oxidase subunits 2 and 4 [Cell Biology, Timone CHU, Marseille] ; v/ genotyping the antiretroviral targets : lamin A (ZMPSTE24) and B (Rce1) processing proteases, Golgi SREBP-releasing proteases (MBTPS1 and S2), mitochondrial deoxynucleoside transporters (SLC25A4 to A6), mitochondrial proteases (MPPA, paraplegin) involved in processing of nuclear encoded proteins during their mitochondrial import ; quantitative PCR measurement of telomere length [Molecular Genetics, Timone CHU, Marseille]. Marseille's CIC-UPCET collaborated to the protocol design, will recruit control subjects and will be responsible for statistical treatment of data.
Study Type : | Observational |
Estimated Enrollment : | 200 participants |
Observational Model: | Case Control |
Time Perspective: | Prospective |
Official Title: | Accelerated Aging, HIV Infection, Antiretroviral Therapies |
Study Start Date : | April 2009 |
Actual Primary Completion Date : | April 2010 |
Actual Study Completion Date : | March 2012 |

Group/Cohort | Intervention/treatment |
---|---|
A HIV1-infected naive patients |
Biological: Peripheral blood biological tests
A group and B group will be evaluated three times, at baseline, then every 12 months during 3 years. In case of initiation or changing of antiretroviral therapy, patients will be evaluated once more. Control subjects will be only evaluated at baseline.
|
B HIV1-infected patients
in 1st line of ARV therapy for at least 12 months
|
Biological: Peripheral blood biological tests
A group and B group will be evaluated three times, at baseline, then every 12 months during 3 years. In case of initiation or changing of antiretroviral therapy, patients will be evaluated once more. Control subjects will be only evaluated at baseline.
|
C= control Non infected HIV volunters |
Biological: Peripheral blood biological tests
A group and B group will be evaluated three times, at baseline, then every 12 months during 3 years. In case of initiation or changing of antiretroviral therapy, patients will be evaluated once more. Control subjects will be only evaluated at baseline.
|
- lamin A measurement by western blotting
- Peripheral blood biological tests (cellular, molecular genetic)

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Ages Eligible for Study: | 18 Years to 65 Years (Adult) |
Sexes Eligible for Study: | All |
Accepts Healthy Volunteers: | Yes |
Sampling Method: | Non-Probability Sample |
Inclusion Criteria:
Age ≥ 18 years and <65 years Able to give written consent Covered by French Social Security Non infected by HIV-2
- - A group HIV1-infected naive patients
- -B group infected patients in first line of antiretroviral therapy for at least 12 months
- -C group HIV seronegative Confirmed by a fast test of screening of the HIV at day one of study
Exclusion Criteria:
- Age < 18 years and > 65 years
- Not Able to give written consent
- Not Covered by French Social Security
- Infected by HIV-2
- treated by statin or biphosphonat amino
- concomitant treatment: diabetic or testosteron

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01038999
France | |
ANRS center from Marseille, Timone and Montpellier and Nice | |
country of French, France |
Principal Investigator: | Isabelle POIZOT-MARTIN | CHU Sainte Marguerite -Marseille | |
Principal Investigator: | Marie-Pierre DROGOUL | CHU Sainte Marguerite -Marseille | |
Principal Investigator: | Olivia FAUCHER | CHU Sainte Marguerite -Marseille | |
Principal Investigator: | Amélie MENARD | CHU Sainte Marguerite -Marseille | |
Principal Investigator: | Joëlle MICALLEF-ROLL | CHU Timone | |
Principal Investigator: | Jacques REYNES | CISIH CHRU Gui de Chauliac- Montpellier | |
Principal Investigator: | Pierre DELLAMONICA | CISIH CHU Nice | |
Principal Investigator: | Pierre CAU | INSERM UMR S910 MARSEILLE | |
Principal Investigator: | Catherine TAMALET | Laboratoire Virologie Marseille | |
Principal Investigator: | Bruno LACARELLE | Unité INSERM U911 Marseille | |
Principal Investigator: | Nicolas LEVY | Laboratoire Génétique Moléculaire Marseille | |
Principal Investigator: | Patrick ROLL | Laboratoire biologie cellulaire Marseille |
Additional Information:
Publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
Responsible Party: | Lucie Marchand/Project manager, French National Agency for Research on AIDS and Viral Hepatitis |
ClinicalTrials.gov Identifier: | NCT01038999 History of Changes |
Other Study ID Numbers: |
2008-A00905-50 |
First Posted: | December 24, 2009 Key Record Dates |
Last Update Posted: | December 27, 2012 |
Last Verified: | December 2012 |
Keywords provided by French National Institute for Health and Medical Research-French National Agency for Research on AIDS and Viral Hepatitis (Inserm-ANRS):
Complementary Therapies |
Additional relevant MeSH terms:
Infection Communicable Diseases HIV Infections Acquired Immunodeficiency Syndrome Lentivirus Infections Retroviridae Infections RNA Virus Infections |
Virus Diseases Sexually Transmitted Diseases, Viral Sexually Transmitted Diseases Immunologic Deficiency Syndromes Immune System Diseases Slow Virus Diseases |