Evaluation of cerebrospinal fluid ubiquitin C-terminal hydrolase-L1, glial fibrillary acidic protein, and neurofilament light protein as novel markers for the diagnosis of neurosyphilis among HIV-negative patients. (February 2023)
- Record Type:
- Journal Article
- Title:
- Evaluation of cerebrospinal fluid ubiquitin C-terminal hydrolase-L1, glial fibrillary acidic protein, and neurofilament light protein as novel markers for the diagnosis of neurosyphilis among HIV-negative patients. (February 2023)
- Main Title:
- Evaluation of cerebrospinal fluid ubiquitin C-terminal hydrolase-L1, glial fibrillary acidic protein, and neurofilament light protein as novel markers for the diagnosis of neurosyphilis among HIV-negative patients
- Authors:
- Chen, Rui
Lin, Li-Rong
Xiao, Yao
Ke, Wu-Jian
Yang, Tian-Ci - Abstract:
- HIGHLIGHTS: Sensitive, easy-to-perform diagnostic markers for early neurosyphilis (NS) are vital. Patients with NS gave higher cerebrospinal fluid ubiquitin C-terminal hydrolase L1 (CSF UCH-L1), glial fibrillary acidic protein (GFAP), and neurofilament light protein (NF-L) as indicators of neuronal damage. CSF UCH-L1, GFAP, and NF-L had high screening performance for patients with NS who are HIV-negative. CSF UCH-L1, GFAP, and NF-L were markers for NS, independent of rapid plasma reagin, white blood cells, and protein. ABSTRACT: Objectives: To evaluate the possibility of using cerebrospinal fluid (CSF) ubiquitin C-terminal hydrolase L1 (UCH-L1), glial fibrillary acidic protein (GFAP), and neurofilament light protein (NF-L) for the diagnosis of neurosyphilis (NS). Methods: A cross-sectional study of 576 subjects was conducted at Zhongshan Hospital from January 2021 to August 2022 to evaluate the diagnostic accuracy of CSF UCH-L1, GFAP, and NF-L for NS and analyze their correlations with CSF rapid plasma reagin (RPR), white blood cells (WBCs), and protein. Results: Patients with NS had higher CSF UCH-L1, GFAP, and NF-L levels than patients with syphilis/non-NS and nonsyphilis. Using a cut-off point of 652.25 pg/ml, 548.89 pg/ml, and 48.38 pg/ml, CSF UCH-L1, GFAP, and NF-L had a sensitivity of 85.11%, 76.60%, and 82.98%, with a specificity of 92.22%, 85.56%, and 91.11%, respectively, for NS diagnosis. Moreover, parallel and serial testing algorithms improved their sensitivityHIGHLIGHTS: Sensitive, easy-to-perform diagnostic markers for early neurosyphilis (NS) are vital. Patients with NS gave higher cerebrospinal fluid ubiquitin C-terminal hydrolase L1 (CSF UCH-L1), glial fibrillary acidic protein (GFAP), and neurofilament light protein (NF-L) as indicators of neuronal damage. CSF UCH-L1, GFAP, and NF-L had high screening performance for patients with NS who are HIV-negative. CSF UCH-L1, GFAP, and NF-L were markers for NS, independent of rapid plasma reagin, white blood cells, and protein. ABSTRACT: Objectives: To evaluate the possibility of using cerebrospinal fluid (CSF) ubiquitin C-terminal hydrolase L1 (UCH-L1), glial fibrillary acidic protein (GFAP), and neurofilament light protein (NF-L) for the diagnosis of neurosyphilis (NS). Methods: A cross-sectional study of 576 subjects was conducted at Zhongshan Hospital from January 2021 to August 2022 to evaluate the diagnostic accuracy of CSF UCH-L1, GFAP, and NF-L for NS and analyze their correlations with CSF rapid plasma reagin (RPR), white blood cells (WBCs), and protein. Results: Patients with NS had higher CSF UCH-L1, GFAP, and NF-L levels than patients with syphilis/non-NS and nonsyphilis. Using a cut-off point of 652.25 pg/ml, 548.89 pg/ml, and 48.38 pg/ml, CSF UCH-L1, GFAP, and NF-L had a sensitivity of 85.11%, 76.60%, and 82.98%, with a specificity of 92.22%, 85.56%, and 91.11%, respectively, for NS diagnosis. Moreover, parallel and serial testing algorithms improved their sensitivity and specificity to 93.62% and 98.89%, respectively. Interestingly, levels between patients with NS who are CSF RPR-positive and -negative did not differ and showed a weak or moderate correlation with WBC and CSF protein in patients with syphilis. Conclusion: CSF UCH-L1, GFAP, and NF-L can be used as novel markers for the diagnosis of NS, independent of CSF RPR, WBC, and proteins. … (more)
- Is Part Of:
- International journal of infectious diseases. Volume 127(2023)
- Journal:
- International journal of infectious diseases
- Issue:
- Volume 127(2023)
- Issue Display:
- Volume 127, Issue 2023 (2023)
- Year:
- 2023
- Volume:
- 127
- Issue:
- 2023
- Issue Sort Value:
- 2023-0127-2023-0000
- Page Start:
- 36
- Page End:
- 44
- Publication Date:
- 2023-02
- Subjects:
- Neurosyphilis -- UCH-L1 -- GFAP -- NF-L -- Diagnostic marker -- Neuronal damage
Communicable diseases -- Periodicals
Communicable Diseases -- Periodicals
Communicable diseases
Periodicals
Electronic journals
616.9 - Journal URLs:
- http://bibpurl.oclc.org/web/73769 ↗
http://www.journals.elsevier.com/international-journal-of-infectious-diseases/ ↗
http://www.sciencedirect.com/science/journal/12019712 ↗
http://www.clinicalkey.com/dura/browse/journalIssue/12019712 ↗
http://www.clinicalkey.com.au/dura/browse/journalIssue/12019712 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.ijid.2022.11.013 ↗
- Languages:
- English
- ISSNs:
- 1201-9712
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 4542.304750
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 25494.xml