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Journal of Clinical Microbiology, January 2005, p. 497-498, Vol. 43, No. 1
0095-1137/05/$08.00+0 doi:10.1128/JCM.43.1.497-498.2005
Copyright © 2005, American Society for Microbiology. All Rights Reserved.
Low Proportion of Recent Human Immunodeficiency Virus (HIV) Infections among Newly Diagnosed Cases of HIV Infection as Shown by the Presence of HIV-Specific Antibodies of Low Avidity
Elisabeth Puchhammer-Stöckl,1*
Brigitte Schmied,2
Armin Rieger,3
Mario Sarcletti,4
Maria Geit,5
Robert Zangerle,4 and
Hanns Hofmann1
Institute of Virology,1
Department of Dermatology, Medical University of Vienna,3
Otto Wagner Spital, Vienna,2
Department of Dermatology University of Innsbruck, Innsbruck,4
Department of Dermatology, Allgemeines Krankenhaus Linz, Linz, Austria5
Received 6 July 2004/
Returned for modification 18 September 2004/
Accepted 29 September 2004

ABSTRACT
The time between human immunodeficiency virus (HIV) infection
and diagnosis is mostly unknown. Two hundred five newly diagnosed
patients were investigated for the duration of their HIV infection
by avidity testing. Recent HIV infection was identified in 27.3%
of the cases. Early diagnosis was achieved significantly less
frequently in heterosexually infected persons than in other
patients.

TEXT
The diagnosis of a human immunodeficiency virus (HIV) infection
is often delayed for years after the infection event (
8). Knowing
the infection time point would, however, be important for epidemiological
surveillance, partner notification, or judging the likelihood
of eventually detecting transmitted drug-resistant HIV strains
(
3,
4,
6).
Recently, on the basis of the knowledge that antibody avidity increases with time after infection (2), Suligoi et al. have reported that discrimination between HIV infections detected within 6 months of seroconversion and older infections is possible when the avidity of the virus-specific antibodies identified is determined (9). Similar data have been shown for various other viral infections before (1, 5, 7).
The aim of the present study was to assess the proportion of recent HIV infections among those routinely diagnosed in a population in which information about HIV transmission, diagnostic facilities, and antiretroviral treatment is widely available. For this purpose, an avidity test was established as previously described (9). As controls for recent infection, we included 12 serum samples obtained from 12 patients either within 3 months after the infection event, as indicated by the patients and confirmed by a negative HIV antibody test result prior to this event, or within 3 months after laboratory-proven seroconversion. As controls for long-term infection, 23 serum samples from patients infected with HIV for more than 1 year were analyzed. The data obtained are shown in Fig. 1. The difference between the mean avidity index (AI) of the recent infection controls (0.4085 ± 0.03709) and that of the long-term infection controls (0.9664 ± 0.01749) was statistically highly significant (P < 0.0001, unpaired t test). From our data, an AI of 0.8, selected as the border between low and high avidity, allowed complete discrimination between long-term infection and infection or seroconversion within 3 months before diagnosis. A previous study showed that an AI of <0.8 also exhibits high sensitivity and specificity for recent infections diagnosed within 6 months of seroconversion (10). Thus, in the further analysis we have considered an AI of <0.8 as being significantly associated with infection within the last 6 months.
It was then assessed how frequently HIV infection is already
diagnosed in the Austrian population within the first months
after infection. Between January 2002 and October 2003, 794
new HIV infections were diagnosed in Austria. Each case was
serologically confirmed by enzyme-linked immunosorbent assay
and Western blotting with two independent serum samples. For
205 (25.8%) of the patients, the serum sample used for the first
diagnosis of HIV infection by antibody testing was still available.
These samples had been obtained at various Austrian hospitals
with the patients' informed consent. Samples were coded and
further analyzed for the HIV antibody AI to assess retrospectively
the interval between the infection event and the first diagnosis.
The results obtained from the patients are shown in Fig.
1.
In 56 (27.3%) of 205 patients, an AI of <0.8 was observed
at the time of the first diagnosis of HIV infection. Thus, it
was shown for the first time, to our knowledge, that even in
a population in which information about HIV infection is widely
distributed and to which diagnostic facilities are easily accessible,
only about a quarter of the infections are detected within about
6 months after the infection event.
It was further investigated whether there was a connection between the time an HIV infection was diagnosed and the patient's gender or age. The patient group included 63 women (30.7%) and 142 men (69.3%). In 13 (20.6%) of the 63 female patients and 43 (30.3%) of the 142 male patients, an AI of <0.8 was identified at the first diagnosis. Although the women, in general, less frequently received an early diagnosis of HIV infection, the difference was not significant (P > 0.176, Fisher's exact test). The ages of 193 of the patients were known, and they ranged between 16 and 69 years. The results obtained with respect to age and gender are presented in Table 1. No significant association among age, gender, and early diagnosis of HIV infection was observed.
Finally, the association between early diagnosis of HIV infection
and the route of transmission was also investigated. For 116
patients, the way they were infected was known; 48 were infected
by heterosexual transmission, 40 were infected by homosexual
transmission, and 28 were infected by intravenous drug abuse
(IDU). The AIs of the individual risk groups are shown in Fig.
1, and the frequency of early HIV diagnosis is presented in
Table
2. In the group of heterosexually infected persons, early
diagnosis of HIV infection was achieved less frequently than
in the other groups. The difference between early diagnosis
of heterosexually versus homosexually transmitted infections
was statistically significant (
P = 0.0175, Fisher's exact test),
as was the difference between these two groups when regarding
only the male patients (
P = 0.0465). These data indicate that
heterosexually infected persons are less frequently undergoing
early diagnosis of HIV infection. This may be due to different
factors. On the one hand, the awareness of the heterosexual
population of their infection risk is obviously especially low.
On the other hand, the present findings may also mean that physicians
confronted with the symptoms of acute HIV infection, which occur
in about half of the primary infections (
8), less frequently
initiate further HIV-specific testing of heterosexual persons.
This is probably due to the fact that HIV infections are still
associated with certain risk groups. Recently, differences in
achieving early diagnosis of HIV infection in nonwhite compared
to white persons were described (
11), also indicating that prejudgments
of physicians are an important factor influencing the likelihood
of achieving early diagnosis of HIV infection.
No significant differences were found in the detection of recent
infections in persons infected by IDU versus heterosexually
(
P = 0.155, Fisher's exact) or homosexually (
P = 0.612) infected
persons, respectively.
In conclusion, our data show that about 70% of HIV infections in general and even more than 80% of heterosexually acquired HIV infections were detected more than 6 months after infection, providing prolonged opportunities for further HIV transmission. These findings demonstrate that even in a population in which information about HIV is widely distributed, awareness of the personal infection risk is still very low and is especially low in heterosexually infected persons.

ACKNOWLEDGMENTS
We thank Kornelia Irger and Sandra Hackl for excellent technical
assistance.

FOOTNOTES
* Corresponding author. Mailing address: Institute of Virology, University of Vienna, Kinderspitalgasse 15, A-1095 Vienna, Austria. Phone: 0043 1 40490 79520. Fax: 0043 1 40490 9795. E-mail:
elisabeth.puchhammer{at}meduniwien.ac.at.


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Journal of Clinical Microbiology, January 2005, p. 497-498, Vol. 43, No. 1
0095-1137/05/$08.00+0 doi:10.1128/JCM.43.1.497-498.2005
Copyright © 2005, American Society for Microbiology. All Rights Reserved.
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