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1 In einer knapp 500 Teilnehmer umfassenden
Untergruppe der SMART Studie wurde ein ca. 5-fach erhöhtes
Risiko schwerwiegender klinischer Ereignisse bei verzögertem
Therapiebeginn und intermittierender Therapiegabe (CD4 < 250/µl)
im Vergleich zu einer kontinuierlich behandelten Gruppe mit einer mittleren
Ausgangs-CD4-Zellzahl von 447 CD4+ Zellen/µl
beobachtet. Dies betraf sowohl HIV- als auch nicht-HIV assoziierte
Ereignisse.
2 Ein
um 10 Jahre höheres Alter ist mit einem 1,3-fach höheren
Risiko einer AIDS-Erkrankung und einem 1,5-fach höheren
Sterberisiko assoziiert (Referenzgruppe 15 – 24
Jahre).
3 Bei
CD4+ T-Lymphozytenzahlen <50 Zellen/µl
haben Frauen in der Regel eine höhere, bei Zellzahlen > 350/µl
eine niedrigere Viruslast als Männer, ohne dass sich diese
Unterschiede in einer unterschiedlichen Krankheitsprogession niederschlagen.
4 In einer Untersuchung des Robert Koch-Instituts im Jahr 2006
wurde bei HIV-positiven Männern mit gleichgeschlechtlichen
Sexualkontakten, die keine antiretrovirale Therapie erhielten, weil
noch keine Therapieindikation gestellt worden war, eine nahezu doppelt
so hohe Inzidenz bakterieller sexuell übertragbarer Infektionen
(Chlamydien-Infektionen, Gonorrhö, Syphilis) festgestellt
wie bei Männern, die eine antiretrovirale Kombinationstherapie
erhielten (Ulrich M, Schmidt AJ, Hamouda O. Erste Ergebnisse der
KABaSTI-Studie des RKI. HIV and MORE 2006; 04: 35-37). Nach diesen
Daten führt die HAART in dieser Betroffenengruppe nicht
zur Zunahme, sondern eher zur Abnahme von Risikoverhalten.
5 In
der D:A:D Studie und der SMART-Studie hatten Patienten mit einer kardiovaskulären
Risikokonstellation (Framingham-Score > 20 %)
signifikant häufiger Myokardinfarkte, wenn sie mit Abacavir
behandelt wurden. Bei solchen Patienten sollte Abacavir am ehesten
als alternative Therapie eingesetzt werden.
Deutsche AIDS-Gesellschaft
Universitätsklinikum Bonn, Medizinische Klinik und Poliklinik I
Sigmund-Freud-Str. 1
53127 Bonn
Phone: +49/228/287-11208
Fax: +49/228/287-15034
Email: DAIG@ukb.uni-bonn.de