Introduction
CNS tuberculosis (CNS TB), the most severe form of tuberculosis, is a leading cause of neurological infections in the world, especially in TB endemic areas like south Asia [1, 2]. CNS TB has remained to be a diagnostic challenge in medicine since 17th century when it was first described by Willis [3].
Despite advances in microbiological isolation, only one in three patients diagnosed as CNS TB have definite CNS TB [4]. With advent of newer MR imaging modalities, presence of radiological features like basal exudates, meningeal enhancement, tuberculoma, infarcts and tuberculoma has helped physicians in dealing with cases where microbiological evidence is lacking [5].
In 80–90% of healthy children and adults, there is an area of T1 hyperintensity in the posterior pituitary on T1 weighted mid sagittal MRI images described as the ‘Bright Spot’ [6, 7]. This is thought to result from the T1-shortening effect of stored vasopressin in the posterior lobe of the pituitary [8]. An enlarged pituitary bright spot is seen in certain physiological conditions such as newborn, pregnancy or lactation but is usually anterior in position [9]. The loss of normal posterior pituitary bright spot (PPBS) was previously described in primary diabetes insipidus and in water intoxication [10, 11]. Andronikou et al had found that there was absence of PPBS in 55% of children with TB meningitis [12]. However, its absence in adults with CNS tuberculosis hasn’t been studied so far.
Hence, we planned a case-control study to look at increase in prevalence of the radiological feature of absence of PPBS in MR imaging and its association with CNS TB in adults.
Methods
We conducted a retrospective case-control study using medical records of patients treated between January 2014 to April 2019 at a tertiary care hospital in South India. The need for informed consent was waived and this study was approved by the Institutional Research Board and Ethics Committee of the Institution (IRB Min.No.12031).
All patients with TB involving the brain (CNS TB) as diagnosed by treating physician were included during this time period as cases. Two controls were recruited for each case. From electronic medical records, patients who had MRI brain under the same unit in the same time period, and whose MRI was reported as normal were identified. Using computer generated random numbers 200 controls were selected.
The MRI images of both cases and controls were presented in a random sequence, after removing patient identifiers, to a blinded consultant radiologist to report the radiological feature of absence of PPBS.
The PPBS was identified on sagittal T1-weighted images (Fig 1). The image slice on which the PPBS was the largest was selected for measurements. PPBS was identified to be present (normal) if it measured between 1.2 and 8.5 mm in the long axis and between 0.4 and 4.4 mm in the short axis in patients who do not have any pituitary abnormality [8].
[Figure omitted. See PDF.]
(A) Presence of PPBS and(B) Absence of PPBS.
Three common clinical score for CNS TB were used for grading of cases–modified MRC score, Thwaites diagnostic index score and Lancet consensus score [13–15].
Summary data was presented as mean (standard deviation, SD) or median with interquartile range for continuous variables and categorical variables as numbers and percentages. The characteristics of cases of CNS TB or control (normal MRI brain) were compared using a t-test for continuous data and categorical data was compared using Chi-square/Fisher’s exact test as appropriate. Adjusted analysis with important factors associated with cases and controls were explored using logistic regression analysis and expressed as Odds Ratio (OR) with 95% Confidence Intervals (CI). Statistical significance was defined as P<0.05. The data was entered using Epidata v3.1 and analyses were performed using SPSS version 25.
Results
One-hundred cases and 200 controls were recruited as shown in Fig 2.
[Figure omitted. See PDF.]
Among cases fever (95%) and headache (84%) were the most common clinical symptoms while neck stiffness (69%) was the common clinical sign. (Table 1) cases (47%) compared to controls (8.5%) CSF examination was safe to perform in 93/100 cases among whom 15 /93 (16.13%) were positive for tuberculosis on mycobacterial growth indicator tube (MGIT). Seventy percent were MRC stage 2 or 3 and 16% had a definitive diagnosis on Lancet consensus score.
[Figure omitted. See PDF.]
Compared to the controls, cases had higher mean age at presentation (37.92 ±15.62 vs. 32.48 ± 6.98), more males (60% vs. 42%), more diabetics (17% vs. 5.5%) and higher proportion with past history of tuberculosis (16% vs. 3%) (Table 2).
[Figure omitted. See PDF.]
PPBS was absent in 47% (n = 47) of the cases when compared to 8.5% (n = 17) of the controls which was statistically significant (Adjusted OR 7.90(95%CI-4.04–15.44). The specificity of “absence of PPBS” in CNS TB is 91.5% (95%CI- 86.7–95), sensitivity is 47% (95%CI- 36.9–57.2) and positive predictive value is 73.4% (95%CI- 62.6–82) and positive likelihood ratio is 5.53 (95%CI- 3.35–9.12).
The “absence of PPBS” was compared with other characteristic radiological features of CNS TB like basal exudates/meningeal enhancement (BM), arachnoiditis (A), endarteritis (E), tuberculoma (T) and hydrocephalus (H). The absence of PPBS (47%) was the second most common feature after basal exudates and meningeal enhancement (60%) and seen more commonly than hydrocephalus (32%), tuberculoma (24%), endarteritis (22%) and arachnoiditis (8%) (Fig 3).
[Figure omitted. See PDF.]
(BM)Basal exudates or Meningeal enhancement,(A)Arachnoiditis, (E)Endarteritis,(T) Tuberculoma,(H) Hydrocephalus and absence of posterior pituitary bright spot(PPBS).
Adding of “absence of PPBS” as an additional radiological feature in diagnosis of CNS TB increased the sensitivity from 77% to 84% (Tables 3 and 4).
[Figure omitted. See PDF.]
[Figure omitted. See PDF.]
Discussion
This is the first study, to our knowledge, assessing prevalence of the radiological feature of absence of PPBS in adults with CNS TB and the added diagnostic value of this feature. Most were MRC grade 2 or 3 at presentation and only 16.1% of them had definite microbiological evidence of TBM.
In our study, the odds of not having PPBS in TBM were 7.90. As a diagnostic test, absence of PPBS had a 91.5% specificity and positive likelihood ratio of 5.53. Adding of absence of PPBS as an additional radiological feature in diagnosis of CNS TB increased the diagnostic yield from 77% to 84%, hence highlighting its importance as an additional diagnostic aid.
The pathophysiological basis for absence of PPBS in CNS TB remains to be investigated. The inflammatory response and granulation tissue formation in CNS TB is commonly concentrated around the basal cisterns [16]. CNS TB associated endarteritis and vascular thrombosis could result in destruction of parts of pituitary gland and disruption of the hypothalamic-hypophysial pathways which lie in close anatomical proximity [12]. As a result of these, there could be a decreased storage of vasopressin in posterior pituitary thereby causing absence of PPBS.
In comparison to other radiological features, absence of PPBS is a relatively simple radiological sign which can be easily picked up by a clinician without much radiological background knowledge or training especially in areas where radiology reporting is delayed.
(Fig 1).
Limitations
Though the finding of absence of PPBS was significantly higher in our TBM cases, its robustness in aiding diagnosis will need further prospective studies with controls with non tubercular CNS infections.
Conclusion
Among adults with suspected CNS tuberculosis this is the first study to show the odds of absence of PPBS was 7.90 in favour of a diagnosis of TB. Absence of PPBS can be a relatively simple radiological aid in diagnosis of adults with suspected CNS tuberculosis.
Supporting information
S1 Data. Minimal data sheet.
https://doi.org/10.1371/journal.pone.0275460.s001
(XLSX)
Citation: G. SG, Mannam P, Kumar V, George T, K. M, Prakash TV, et al. (2022) Absence of posterior pituitary bright spot in adults with CNS tuberculosis: A case-control study. PLoS ONE 17(10): e0275460. https://doi.org/10.1371/journal.pone.0275460
About the Authors:
Smitesh G. G.
Contributed equally to this work with: Smitesh G. G., Pavithra Mannam, Vignesh Kumar, Tina George, Thambu David Sudarsanam
Roles: Conceptualization, Data curation, Formal analysis, Investigation, Methodology, Writing – original draft, Writing – review & editing
Affiliation: Department of General Medicine, Christian Medical College Vellore, Vellore, Tamil Nadu, India
Pavithra Mannam
Contributed equally to this work with: Smitesh G. G., Pavithra Mannam, Vignesh Kumar, Tina George, Thambu David Sudarsanam
Roles: Conceptualization, Data curation, Methodology, Resources, Writing – original draft, Writing – review & editing
Affiliation: Department of Radiology, Christian Medical College Vellore, Vellore, Tamil Nadu, India
Vignesh Kumar
Contributed equally to this work with: Smitesh G. G., Pavithra Mannam, Vignesh Kumar, Tina George, Thambu David Sudarsanam
Roles: Conceptualization, Formal analysis, Methodology, Writing – review & editing
Affiliation: Department of General Medicine, Christian Medical College Vellore, Vellore, Tamil Nadu, India
https://orcid.org/0000-0001-9117-1996
Tina George
Contributed equally to this work with: Smitesh G. G., Pavithra Mannam, Vignesh Kumar, Tina George, Thambu David Sudarsanam
Roles: Conceptualization, Data curation, Investigation, Methodology, Project administration, Resources, Supervision, Visualization, Writing – original draft, Writing – review & editing
E-mail: [email protected]
Affiliation: Department of General Medicine, Christian Medical College Vellore, Vellore, Tamil Nadu, India
https://orcid.org/0000-0001-5978-7395
Murugabharathy K.
Roles: Conceptualization, Data curation, Methodology, Writing – original draft, Writing – review & editing
¶‡ MK, TVP and BY also contributed equally to this work.
Affiliation: Department of General Medicine, Christian Medical College Vellore, Vellore, Tamil Nadu, India
Turaka Vijay Prakash
Roles: Conceptualization, Methodology, Project administration, Writing – review & editing
¶‡ MK, TVP and BY also contributed equally to this work.
Affiliation: Department of General Medicine, Royal Adelaide hospital, Adelaide, Australia
Bijesh Yadav
Roles: Conceptualization, Formal analysis, Writing – review & editing
¶‡ MK, TVP and BY also contributed equally to this work.
Affiliation: Department of Biostatistics, Christian Medical College Vellore, Vellore, Tamil Nadu, India
Thambu David Sudarsanam
Contributed equally to this work with: Smitesh G. G., Pavithra Mannam, Vignesh Kumar, Tina George, Thambu David Sudarsanam
Roles: Conceptualization, Formal analysis, Investigation, Methodology, Project administration, Resources, Writing – original draft, Writing – review & editing
Affiliation: Department of General Medicine, Christian Medical College Vellore, Vellore, Tamil Nadu, India
1. Zunt JR, Kassebaum NJ, Blake N, Glennie L, Wright C, Nichols E, et al. Global, regional, and national burden of meningitis, 1990–2016: a systematic analysis for the Global Burden of Disease Study 2016. The Lancet Neurology. 2018 Dec;17(12):1061–82. pmid:30507391
2. Borade PV, Haralkar SJ, Bennishirur WA, Mulje SM. Study of morbidity and mortality pattern of cases of meningitis admitted in tertiary health care centre in India. International Journal of Recent Trends in Science and Technology. 2014;10(2):213–7.
3. Ruhräh J. The History of Tuberculous Meningitis. Med Library Hist J. 1904 Jul;2(3):160–5. pmid:18340843
4. Jha SK, Garg RK, Jain A, Malhotra HS, Verma R, Sharma PK. Definite (microbiologically confirmed) tuberculous meningitis: predictors and prognostic impact. Infection. 2015 Dec;43(6):639–45. pmid:25724799
5. Garg RK, Malhotra HS, Jain A. Neuroimaging in tuberculous meningitis. Neurology India. 2016 Mar 1;64(2):219. pmid:26954796
6. Brooks BS, el Gammal T, Allison JD, Hoffman WH. Frequency and variation of the posterior pituitary bright signal on MR images. AJNR Am J Neuroradiol. 1989 Sep-Oct;10(5):943–8. pmid:2505538; PMCID: PMC8335287.
7. Krishna Kiran S, Anston Vernon Braggs. Posterior pituitary bright spot–a study in coastal Karnataka. International Journal of Contemporary Medicine Surgery and Radiology. 2020;5(1):A92–A94.
8. Côté M., Salzman K. L., Sorour M., & Couldwell W. T. (2014). Normal dimensions of the posterior pituitary bright spot on magnetic resonance imaging, Journal of Neurosurgery JNS, 120(2), 357–362. pmid:24329024
9. Bonneville F, Cattin F, Marsot-Dupuch K, Dormont D, Bonneville J-F, Chiras J. T1 Signal Hyperintensity in the Sellar Region: Spectrum of Findings. RadioGraphics. 2006 Jan;26(1):93–113. pmid:16418246
10. Ozata M, Tayfun C, Kurtaran K, Yetkin İ, Beyhan Z, Çorakcı A, et al. Magnetic resonance imaging of posterior pituitary for evaluation of the neurohypophyseal function in idiopathic and autosomal dominant neurohypophyseal diabetes insipidus. Eur Radiol. 1997 Aug 1;7(7):1098–102. pmid:9265683
11. Neville KA, Pereira JK, Andrews PI, Walker JL. Transient reduction in the posterior pituitary bright signal preceding water intoxication in a malnourished child. J Pediatr Endocrinol Metab. 2004 Sep;17(9):1245–9. pmid:15506686
12. Andronikou S, van Toorn R, Boerhout E. MR imaging of the posterior hypophysis in children with tuberculous meningitis. Eur Radiol. 2009 Sep 1;19(9):2249–54. pmid:19399504
13. Marais BJ, Heemskerk AD, Marais SS, van Crevel R, Rohlwink U, Caws M, et al Tuberculous Meningitis International Research Consortium. Standardized Methods for Enhanced Quality and Comparability of Tuberculous Meningitis Studies. Clin Infect Dis. 2017 Feb 15;64(4):501–509. pmid:28172588; PMCID: PMC5399942.
14. Thwaites GE, Chau TTH, Stepniewska K, Phu NH, Chuong LV, Sinh DX, et al. Diagnosis of adult tuberculous meningitis by use of clinical and laboratory features. The Lancet. 2002;360(9342):1287–92. pmid:12414204
15. Marais S, Thwaites G, Schoeman JF, Török ME, Misra UK, Prasad K, et al. Tuberculous meningitis: a uniform case definition for use in clinical research. The Lancet infectious diseases. 2010;10(11):803–12.
16. Andronikou S, Smith B, Hatherhill M, Douis H, Wilmshurst J. Definitive neuroradiological diagnostic features of tuberculous meningitis in children. Pediatr Radiol. 2004 Nov;34(11):876–85. pmid:15378213
You have requested "on-the-fly" machine translation of selected content from our databases. This functionality is provided solely for your convenience and is in no way intended to replace human translation. Show full disclaimer
Neither ProQuest nor its licensors make any representations or warranties with respect to the translations. The translations are automatically generated "AS IS" and "AS AVAILABLE" and are not retained in our systems. PROQUEST AND ITS LICENSORS SPECIFICALLY DISCLAIM ANY AND ALL EXPRESS OR IMPLIED WARRANTIES, INCLUDING WITHOUT LIMITATION, ANY WARRANTIES FOR AVAILABILITY, ACCURACY, TIMELINESS, COMPLETENESS, NON-INFRINGMENT, MERCHANTABILITY OR FITNESS FOR A PARTICULAR PURPOSE. Your use of the translations is subject to all use restrictions contained in your Electronic Products License Agreement and by using the translation functionality you agree to forgo any and all claims against ProQuest or its licensors for your use of the translation functionality and any output derived there from. Hide full disclaimer
© 2022 G. et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.
Abstract
Introduction
Current diagnostic methods used in Central Nervous System Tuberculosis (CNS TB) are limited by the paucibacillary nature of this form of tuberculosis. Posterior pituitary bright spot (PPBS) refers to an area of T1 hyperintensity in the posterior pituitary in MR imaging of the brain. It is found in 80–90% of healthy children and adults. In children with CNS TB, nearly half have absence of PPBS. This finding has not been described in adults. Our study looked for absence of PPBS in MR imaging and its association with CNS tuberculosis.
Objective
To study prevalence of the absence of PPBS in patients with CNS tuberculosis when compared to a control group of normal patients.
Methods
This was a retrospective case-control study of 100 patients with CNS tuberculosis and 200 controls (matched in 1:2 ratio) of patients with normal MRI brain. The MRI images were presented to a blinded radiologist in a randomised sequence to report for absence of PPBS. The data was subsequently analysed to look for association of absence of PPBS with CNS tuberculosis.
Results
Absence of PPBS (cases (47%), controls (8.5%)) was significantly associated with CNS tuberculosis in (Odds ratio-7.90, 95%CI 4.04–15.44, P-value<0.0001). The specificity, sensitivity, positive predictive value and positive likelihood ratio are 91.5%, 47%, 73.4% and 5.53 respectively. Adding of absence of PPBS as an additional radiological feature in diagnosis of CNS TB increased the sensitivity from 77% to 84%.
Conclusion
Absence of PPBS is significantly associated with CNS tuberculosis and could be a relatively simple diagnostic aid in the diagnosis of CNS tuberculosis.
You have requested "on-the-fly" machine translation of selected content from our databases. This functionality is provided solely for your convenience and is in no way intended to replace human translation. Show full disclaimer
Neither ProQuest nor its licensors make any representations or warranties with respect to the translations. The translations are automatically generated "AS IS" and "AS AVAILABLE" and are not retained in our systems. PROQUEST AND ITS LICENSORS SPECIFICALLY DISCLAIM ANY AND ALL EXPRESS OR IMPLIED WARRANTIES, INCLUDING WITHOUT LIMITATION, ANY WARRANTIES FOR AVAILABILITY, ACCURACY, TIMELINESS, COMPLETENESS, NON-INFRINGMENT, MERCHANTABILITY OR FITNESS FOR A PARTICULAR PURPOSE. Your use of the translations is subject to all use restrictions contained in your Electronic Products License Agreement and by using the translation functionality you agree to forgo any and all claims against ProQuest or its licensors for your use of the translation functionality and any output derived there from. Hide full disclaimer
Details
