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

Edwin Nuwagira, Kathy Huppler Hullsiek, Samuel Jjunju, Morris Rutakingirwa, John Kasibante, Kiiza Kandole Tadeo, Enock Kagimu, Lillian Tugume, Kenneth Ssebambulidde, Abdu K Musubire, Ananta Bangdiwala, Conrad Muzoora, David B Meya, David R. Boulware, Nathan C Bahr, Fiona V. Creswell

Research output: Contribution to journalArticlepeer-review

2 Scopus citations

Abstract

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.

Original languageEnglish (US)
JournalMicrobiology Spectrum
Volume10
Issue number4
DOIs
StatePublished - Aug 2022

Bibliographical note

Funding Information:
We also thank the Infectious Diseases Institute for research support. This work was supported by the National Institute of Neurologic Diseases and Stroke (R01NS086312), the Fogarty International Center (K01TW010268 and R25TW009345), the National Institute of Allergy and Infectious Diseases (T32AI055433), United Kingdom Medical Research Council/DfID/Wellcome Trust Global Clinical Trials (M007413/1 and 210772/Z/18/Z). N.C.B. is supported by the National Institutes of Health and the National Institute of Neurologic Disorders and Stroke via K23NS110470. F.V.C. was supported by a Wellcome PhD Fellowship (210772/Z/17/Z) and an NIHR Academic Clinical Lectureship (CL-2020-27-001).

Funding Information:
We thank all study participants and their caretakers. We also thank the Infectious Diseases Institute for research support. This work was supported by the National Institute of Neurologic Diseases and Stroke (R01NS086312), the Fogarty International Center (K01TW010268 and R25TW009345), the National Institute of Allergy and Infectious Diseases (T32AI055433), United Kingdom Medical Research Council/DfID/Wellcome Trust Global Clinical Trials (M007413/1 and 210772/Z/18/Z). N.C.B. is supported by the National Institutes of Health and the National Institute of Neurologic Disorders and Stroke via K23NS110470. F.V.C. was supported by a Wellcome PhD Fellowship (210772/Z/17/Z) and an NIHR Academic Clinical Lectureship (CL-2020-27-001).

Publisher Copyright:
© 2022 Nuwagira et al.

Keywords

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

Fingerprint

Dive into the research topics of 'Diagnostic and Prognostic Value of Cerebrospinal Fluid Lactate and Glucose in HIV-Associated Tuberculosis Meningitis'. Together they form a unique fingerprint.

Cite this