Even 
        Low-level, Short-term Detectable Viral Load Raises the Risk of Virological 
        Treatment Failure and Death
        
        
          
           
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                  | SUMMARY: 
                    People with HIV who have 
                    persistent episodes of low-level viremia are more likely to 
                    experience sustained virological rebound and have a higher 
                    risk of death than individuals who maintain consistently undetectable 
                    viral load (< 50 copies/mL) or experience only transient 
                    "blips," according to a poster presented at the 
                    17th Conference on Retroviruses & Opportunistic Infections 
                    (CROI 2010) last month in San Francisco. 
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        By 
          Liz Highleyman
          
          Mark Hull and colleagues with the Canadian Observational Cohort Collaboration 
          evaluated the effect of ongoing viremia (detectable virus in the blood) 
          on risk of virological rebound and mortality among HIV positive people 
          on combination antiretroviral 
          therapy (ART).
          
          The analysis included 1674 HIV patients; most (84%) were men and the 
          median age was 41 years. All participants had 2 consecutive plasma viral 
          load measurements < 400 copies/mL at least 30 days apart, followed 
          by at least 6 subsequent measurements over 24 months (the classification 
          period), which the researchers used to categorize them into 4 groups:
        
           
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            Fully 
              suppressed: maintained plasma viral load < 50 copies/mL throughout 
              the classification period; | 
          
           
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            Transient 
              viremia: achieved plasma viral load < 50 copies/mL and remained 
              below this level for more than 75% of the classification period, 
              but had infrequent low-level viremia (50-1000 copies/mL) less than 
              25% of the time. | 
          
           
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            Short-term 
              persisting viremia: maintained plasma viral load < 50 copies/mL 
              for 25%-75% of the classification period, with the remainder spent 
              with > 50 copies/mL. | 
          
           
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            Long-term 
              persisting viremia: maintained plasma viral load < 50 copies/mL 
              for only 25% or less of the classification period but had detectable 
              viremia most of the time. | 
          
        
        After 
          the initial classification period, participants were followed to determine 
          time to virological rebound, defined as 2 consecutive plasma viral load 
          measurements > 1000 copies/mL, and time to death. From the time of 
          initial viral suppression, the median follow-up time for virological 
          rebound (1674 patients) was 36 months and the median follow-up time 
          for mortality outcomes (1430 patients) was 51 months.
          
          Results
        
           
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            Compared 
              with the fully suppressed group, the transient viremia group had 
              a similar risk of sustained virological rebound (hazard ratio [HR] 
              1.12, where 1.0 indicates equal risk). | 
          
           
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            The 
              short-term persisting viremia group was about 6 times more likely 
              to experience virological rebound than the fully suppressed group 
              (HR 6.05). | 
          
           
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            The 
              long-term persisting viremia group had more than a 20-fold higher 
              risk than the fully suppressed group (HR 20.46). | 
          
           
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            People 
              in the short-term persisting viremia group who mostly had low-level 
              viral load (majority of measurements < 200 copies/mL) were still 
              more likely to experience virological rebound (HR 4.95) and death 
              (HR 4.25) than people in the transient viremia group with the same 
              viral load levels. | 
          
        
        "Those 
          patients experiencing persisting viremia (short-term and long-term) 
          were more likely to experience subsequent viral rebound," the investigators 
          concluded. "Patients with only short-term low-level viremia remained 
          at higher risk of virological rebound and increased mortality compared 
          to those with full suppression or only transient low-level viremia."
          
          Given these findings, they advised, "Sustained virological suppression 
          remains an important target for ART therapy."
          
          Montreal Chest Institute, McGill University Health Ctr, Quebec, Canada; 
          University of Toronto, Ontario, Canada; British Columbia Ctr for Excellence 
          in HIV/AIDS, Vancouver, BC, Canada; Clin Med l'Actuel, Montreal, Quebec, 
          Canada.
        3/26/10
        Reference
          M 
          Hull, M Loutfy, W Zhang, and others (Canadian Observational Cohort Collaboration). 
          Persistent Low-level Viremia Is Associated with Increased Risk of Virologic 
          Failure and Mortality. 17th Conference on Retroviruses & Opportunistic 
          Infections (CROI 2010). San Francisco. February 16-19, 2010. Abstract 
          504.