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. 2008 Jun 19;22(10):1145-51.
doi: 10.1097/QAD.0b013e32830184df.

Neurosyphilis in a clinical cohort of HIV-1-infected patients

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Neurosyphilis in a clinical cohort of HIV-1-infected patients

Khalil G Ghanem et al. AIDS. .

Abstract

Objectives: To describe the risk factors, clinical presentation, and long-term follow up of patients enrolled in a clinical cohort of HIV-infected patients who were diagnosed and treated for neurosyphilis.

Methods: Comprehensive demographic, clinical, and therapeutic data were collected prospectively on all patients between 1990 and 2006. Patients were diagnosed with neurosyphilis if they had positive syphilis serologies and any of the following: (a) one or more cerebrospinal fluid abnormalities on lumbar puncture [white blood cells >10/microl; protein >50 mg/dl; reactive venereal diseases research laboratory], (b) an otherwise unexplained neurological finding.

Results: Of 231 newly diagnosed syphilis cases, 41 neurosyphilis cases met entry criteria (median age 38.6 years, 79.1% male). Risk factors for neurosyphilis included a CD4 cell count of less than 350 cells/ml at the time of syphilis diagnosis (odds ratio: 2.87; 95% confidence interval: 1.18-7.02), a rapid plasma regain titer >1: 128 (2.83; 1.11-7.26), and male sex (2.46; 1.06-5.70). Use of any highly active antiretroviral therapy before syphilis infection reduced the odds of neurosyphilis by 65% (0.35; 0.14-0.91). Sixty-three percent of cases presented with early neurosyphilis and the median time to neurosyphilis diagnosis was 9 months. Symptomatic patients had more cerebrospinal fluid abnormalities on initial lumbar puncture than asymptomatic patients (P = 0.01). Follow-up lumbar puncture within 12 months revealed that only 38% had resolution of all cerebrospinal fluid abnormalities. At 1 year, 38% had persistence of their major symptom despite adequate treatment for neurosyphilis. Twelve of 41 (29%) patients were retreated for syphilis.

Conclusion: Early neurosyphilis was common in this cohort. Highly active antiretroviral therapy to reverse immunosuppression may help mitigate neurological complications of syphilis.

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Figures

Fig. 1
Fig. 1. Range of initial RPR titers comparing symptomatic and asymptomatic neurosyphilis patients
RPR, rapid plasma regain.
Fig. 2
Fig. 2. Panel (a) summarizes the time at which neurosyphilis diagnosis was made following the initial diagnosis of syphilis; 63% of cases were diagnosed within the first year after syphilis diagnosis; the mean CD4 cell count at the time of syphilis diagnosis for each time frame is listed below
Panel (b) focuses on the distribution of neurosyphilis cases that occurred within the first year, with cases further stratified by the presence or absence of neurological symptoms. sx, symptoms; mo, month; yr, year. * Mean CD4 cell count at the time of neurosyphilis diagnosis (P >0.05 for all comparisons).
Fig. 3
Fig. 3. Kaplan–Meier curves demonstrating the effects of (a) 1 month and (b) 3 months of cumulative macrolide use after therapy for neurosyphilis and (c) 6 months or more of HAART use after therapy for neurosyphilis on the risk of first serological failure
HAART, highly active antiretroviral therapy; m, month(s); P-values based on the nonparametric log-rank test.

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