4.6 Article

Diagnostic and Prognostic Value of Cerebrospinal Fluid Lactate and Glucose in HIV-Associated Tuberculosis Meningitis

Journal

MICROBIOLOGY SPECTRUM
Volume 10, Issue 4, Pages -

Publisher

AMER SOC MICROBIOLOGY
DOI: 10.1128/spectrum.01618-22

Keywords

cerebrospinal fluid; tuberculosis meningitis; chronic meningitis; CSF lactate; HIV

Categories

Funding

  1. National Institute of Neurologic Diseases and Stroke [R01NS086312]
  2. Fogarty International Center [K01TW010268, R25TW009345]
  3. National Institute of Allergy and Infectious Diseases [T32AI055433]
  4. United Kingdom Medical Research Council/DfID/Wellcome Trust Global Clinical Trials [M007413/1, 210772/Z/18/Z]
  5. National Institutes of Health
  6. National Institute of Neurologic Disorders and Stroke [K23NS110470]
  7. Wellcome PhD Fellowship [210772/Z/17/Z]
  8. NIHR Academic Clinical Lectureship [CL-2020-27-001]
  9. Infectious Diseases Institute
  10. Wellcome Trust [210772/Z/18/Z] Funding Source: Wellcome Trust

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This study evaluated the role of CSF lactate in diagnosing and predicting outcomes of TBM in HIV-positive individuals. High CSF lactate levels were found to be associated with the diagnosis of TBM, but not predictive of 2-week mortality. CSF lactate may be a useful tool in diagnosing TBM in the clinical setting.
The role of cerebrospinal fluid (CSF) lactate in tuberculosis meningitis (TBM) diagnosis and prognosis is unclear. The aim of this study was to evaluate the performance of CSF lactate alone and in combination with CSF glucose in predicting a diagnosis of TBM and 14-day survival. HIV-positive Ugandan adults were investigated for suspected meningitis. The baseline CSF tests included smear microscopy; Gram stain; cell count; protein; and point-of-care glucose, lactate, and cryptococcal antigen (CrAg) assays. Where CrAg was negative or there was suspicion of TBM, a CSF Xpert MTB/RIF Ultra (Xpert Ultra) test was performed. We recorded baseline demographic and clinical data and 2-week outcomes. Of 667 patients, 25% (n = 166) had TBM, and of these, 49 had definite, 47 probable, and 70 possible TBM. CSF lactate was higher in patients with definite TBM (8.0 mmol/L; interquartile ratio [IQR], 6.1 to 9.8 mmol/L) than in those with probable TBM (3.4 [IQR, 2.5 to 7.0] mmol/L), possible TBM (2.6 [IQR 2.1 to 3.8] mmol/L), and non-TBM disease (3.5 [IQR 2.5 to 5.0] mmol/L). A 2-fold increase in CSF lactate was associated with 8-fold increased odds of definite TBM (odds ratio, 8.3; 95% confidence interval [CI], 3.6 to 19.1; P < 0.01) and 2-fold increased odds of definite/probable TBM (odds ratio, 2.3; 95% CI, 1.4 to 3.7; P < 0.001). At a cut point of >5.5 mmol/L, CSF lactate could be used to diagnose definite TBM with a sensitivity of 87.7%, specificity of 80.7%, and a negative predictive value of 98.8%. CSF lactate was not predictive of 2-week mortality. IMPORTANCE Tuberculosis meningitis (TBM) is the most severe form of tuberculosis, and its fatality is largely due to delays in diagnosis. The role of CSF lactate has not been evaluated in patients with HIV presenting with signs and symptoms of meningitis. In this study, using a point-of-care handheld lactate machine in patients with HIV-associated meningitis, we showed that high baseline CSF lactate (>5.5 mmol) may be used to rapidly identify patients with TBM and shorten the time to initiate treatment with a similar performance to the Xpert Ultra assay for definite TBM. Elevated CSF lactate levels, however, were not associated with increased 2-week mortality in patients with HIV-associated TBM. Due to moderate specificity, other etiologies of meningitis should be investigated.

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