Abstract
Objective
To investigate the characteristics and prognosis of anti-NMDAR encephalitis with the prevalence of anti-thyroid antibodies (ATAbs).
Methods
The clinical data of anti-NMDAR encephalitis patients admitted to Xuanwu Hospital from January 2012 to August 2018 was prospectively analyzed, and the patients were followed up for 24 months.
Results
A total of 120 patients were enrolled, of which 34.2% (41/120) were positive for ATAbs. The antibodies were more frequent in patients with severe disease compared to the non-severe group (51.4% vs. 25.6%, P=0.008). In addition, prevalence of ATAbs correlated with a higher incidence of disturbed consciousness, autonomic dysfunction, central hypoventilation and mechanical ventilation. The ATAbs-positive patients were also more likely to receive intravenous gamma immunoglobulin and immunosuppressor compared to the ATAbs-negative cases (P=0.006; P=0.035). Although the presence of ATAbs was associated with longer hospital stays and worse prognosis at 6 months (P=0.006; P=0.038), it had no impact on long-term patient prognosis. Positive status of anti-thyroglobulin antibody was an independent risk factor for worse prognosis at 6 months [odds ratio (OR)= 3.907, 95% CI: 1.178-12.958, P=0.026].
Conclusion
ATAbs are prevalent in patients with anti-NMDAR encephalitis, especially in severe cases, and correlate with poor prognosis and impaired short-term neurological recovery.
Keywords: anti-N-methyl-D-aspartate receptor encephalitis, anti-thyroglobulin antibody, anti-thyroperoxidase antibody, critically ill, outcome
Introduction
Anti-thyroid antibodies (ATAbs), including anti-thyroglobulin antibody (anti-TgAb) and anti-thyroperoxidase antibody (anti-TPOAb), are pathological markers of autoimmune thyroid disease. ATAbs are frequently detected in central nervous system (CNS) autoimmune diseases such as neuromyelitis optica spectrum disorders (NMO-SD) (1, 2), multiple sclerosis (3) and autoimmune encephalitis (AE) (4, 5). However, the pathogenic role of ATAbs in CNS autoimmune disease remains unclear. It may be associated with increased susceptibility for CNS autoimmunity. Previous studies have reported that ATAbs are significantly elevated in AE; besides, patients with ATAbs are inclined to develop anti-neuronal immune responses and AE, indicating that CNS autoimmune disease and autoimmune thyroid disease may represent a pathogenic spectrum (4, 6). ATAbs have also been considered as initial diagnostic markers when clinically suspecting AE or autoimmune epilepsy (5, 7). In addition, ATAbs are also found to be associated with disease severity in NMO-SD (1, 2).
Anti-N-methyl-D-aspartate receptor (NMDAR) encephalitis is an AE characterized by the production of autoantibodies against antigenic nerve surfaces or synapses (8). Very few studies have reported the coexistence of ATAbs in anti-NMDAR encephalitis (6, 9–13), and their clinical and prognostic relevance in anti-NMDAR encephalitis has not been systematically evaluated. The aim of this study was to determine the correlation between ATAbs and various clinicopathological factors in a cohort of anti-NMDAR encephalitis patients.
Methods
Study Design and Participants
We prospectively recruited anti-NMDAR encephalitis patients from the Department of Neurology of Xuanwu Hospital, Capital Medical University between January 2012 and August 2018 based on the following inclusion criteria (1): age ≥14 years old (2), acute or subacute onset symptoms of encephalitis (< 3 months) (3), presence of abnormal behavior or cognitive dysfunction, speech dysfunction, seizures, movement disorders, decreased level of consciousness, autonomic dysfunction or central hypoventilation, or a combination of the above symptoms (4), positive anti-GluN1 NMDAR antibodies in the cerebrospinal fluid (CSF) and/or serum positivity, and (5) absence of viral encephalitis, brain tumors, metabolic diseases, drug poisoning, et al. The exclusion criteria were as follows (1): non-compliance with the treatment (2), presence of other autoimmune antibodies or neurological paraneoplastic antibodies (3), not the first onset of anti-NMDAR encephalitis (4), history of thyroid diseases (5), prior prescription, such as thyroid hormones, antithyroid drugs, β-blockers, etc. (6), without thyroid function test (7), lost to the 6-month follow-up. The patients were divided into the severe and non-severe disease groups based on whether they were admitted to the neurological intensive care unit (NCU). Patients with severe disease who were admitted to the NCU met at least one of the following criteria: respiratory failure requiring mechanical ventilation, impaired consciousness (GCS ≤ 12), or status epilepticus.
Data Collection
Data regarding age of onset, sex, prodromal symptoms, clinical characteristics, CSF findings, brain magnetic resonance imaging (MRI) and electroencephalography (EEG) findings, treatment details and follow-up data were retrieved. The anti-NMDAR Encephalitis One-Year Functional Status (NEOS) score, including NCU admission, delayed treatment for more than 4 weeks, no improvement in clinical outcomes within 4 weeks, abnormal MRI, and white blood cell count of more than 20 cells/μL in CSF, was considered as a prognostic tool (14). Anti-GluN1 NMDA antibodies in the serum and CSF were measured using indirect immunofluorescence test (IIFT) kits (EUROIMMUN AG, Lübeck, Germany). Thyroid function was measured at 6 AM the day after admission using standardized radioimmunoassay kits. A patient was considered ATAbs-positive if the levels were >4 IU/ml for anti-TgAb or > 9 IU/ml for anti-TPOAb.
Outcomes
All the patients were followed up by outpatient clinic visit or phone contact by resident doctors who are not aware of the study design at 6, 12 and 24 months after discharge. The modified Rankin Scale (mRS) was used to evaluate treatment effects and prognosis. Relapse was defined as the deterioration of previous symptoms or the appearance of new symptoms two months after stabilization (15). Favorable and unfavorable outcomes were defined as mRS scores of 0-2 and 3-6 respectively.
Statistical analysis
Statistical analyses were performed using SPSS 20.0 (IBM Corporation, Armonk, NY, USA). Data are presented as mean ± SD, medians with the interquartile range (IQR) or counts (percentages), and compared by Student’s t test, Mann–Whitney U test, Pearson chi-square test or Fisher exact test as appropriate. Variables with P < 0.1 in the univariate analysis were included in multivariate logistic regression. A back-ward selection procedure was used for the screening of independent risk factors predicting the unfavorable outcomes at 6 months. P values < 0.05 were considered statistically significant.
Results
Patient Characteristics
One hundred and twenty patients (67 males and 53 females, mean age 29.3 ± 13.4 years) diagnosed with anti-NMDAR encephalitis were enrolled (Supplemental Figure 1). The overall prevalence of ATAbs was 34.2%. As shown in Figure 1, the patients with severe disease had a significantly higher proportion of those positive for one or both ATAbs compared to that in the non-severe group.
Figure 1.
Prevalence of ATA positivity in Anti-NMDAR encephalitis patients. ATAbs, Anti-thyroid antibodies; anti-TgAb, anti-thyroglobulin antibody; anti-TPOAb, anti-thyroperoxidase antibody.
Demographic, Clinical Characteristics, and Prognosis of Patients With or Without ATAbs
Furthermore, patients with ATAbs had higher incidence of disturbed consciousness (63.4% vs. 36.7%, P=0.005), autonomic dysfunction (48.8% vs. 17.7%, P<0.001), central hypoventilation (34.1% vs. 15.2%, P=0.010), mechanical ventilation (34.1% vs. 15.2%, P=0.017) and NCU admission (46.3% vs. 22.8%, P=0.008) (Table 1). As shown in Table 2, patients with ATAbs had lower FT3 levels (P=0.012) and while the EEG features (epileptic discharges, slow activity, and others), MRI lesions, CSF findings (pressure of lumbar puncture, white blood cells and protein levels), and the serum and CSF antibody titers were similar between the ATAbs-positive and ATAbs-negative patients. The ATAbs-positive patients were also more likely to receive intravenous immunoglobulins (IVIG) and immunosuppressor treatment (P=0.006, P=0.035), and have longer hospital stays and worse neurological outcomes at 6 months (P=0.006, P=0.038) (Table 1 and Supplementary Figure 2). There was no significant difference in the relapse and functional outcomes at 12 and 24 months in both groups (Table 1).
Table 1.
Demographic, clinical characteristics and prognosis of anti-NMDAR encephalitis patients with or without ATAbs.
| Total (n = 120) | ATAbs negative (n = 79) | ATAbs positive (n = 41) | P value | |
|---|---|---|---|---|
| Age at onset, y, mean ± SD | 29.3 ± 13.4 | 28.8 ± 12.6 | 30.3 ± 14.9 | 0.516 |
| Female, n (%) | 53 (44.2) | 32 (40.5) | 21 (51.2) | 0.262 |
| Ovarian teratoma, n (%) | 8 (6.7) | 3 (3.8) | 5 (12.2) | 0.080 |
| Prodromal symptoms, n (%) | 63 (52.5) | 41 (51.9) | 22 (53.7) | 0.855 |
| Clinical manifestations, n (%) | ||||
| Mental behavior disorder | 87 (72.5) | 55 (69.6) | 32 (78.0) | 0.327 |
| Epileptic seizure | 78 (65.0) | 51 (64.6) | 27 (65.9) | 0.888 |
| Involuntary movement | 56 (46.7) | 34 (43.0) | 22 (53.7) | 0.269 |
| Disturbance of consciousness | 55 (45.8) | 29 (36.7) | 26 (63.4) | 0.005 |
| Cognitive impairment | 37 (30.8) | 20 (25.3) | 17 (41.5) | 0.069 |
| Autonomic dysfunction | 34 (28.3) | 14 (17.7) | 20 (48.8) | <0.001 |
| Language impairment | 27 (22.5) | 14 (17.7) | 13 (31.7) | 0.082 |
| Central hypoventilation | 25 (20.8) | 11 (13.9) | 14 (34.1) | 0.010 |
| Mechanical ventilation, n (%) | 26 (21.7) | 12 (15.2) | 14 (34.1) | 0.017 |
| NCU admission, n (%) | 37 (30.8) | 18 (22.8) | 19 (46.3) | 0.008 |
| NEOS score, median (IQR) | 2 (2,4) | 2 (2,3) | 3 (2,4) | 0.190 |
| Immunotherapy, n (%) | ||||
| Steroids | 102 (85.0) | 66 (83.5) | 36 (87.8) | 0.535 |
| IVIG | 70 (58.3) | 39 (49.4) | 31 (75.6) | 0.006 |
| Plasma exchange | 22 (18.3) | 11 (13.9) | 11 (26.8) | 0.083 |
| Immunosuppressor | 25 (20.8) | 12 (15.2) | 13 (31.7) | 0.035 |
| Outcome | ||||
| Length of NCU length of stay, n=37, days, median (IQR) | 39.0 (23.0-73.0) | 37.0 (17.0,70.0) | 45.0 (24.0,82.0) | 0.362 |
| Hospital length of stay, days, median (IQR) | 18.0 (13.0-37.5) | 12.0 (12.0,27.0) | 21.0 (15.0,58.5) | 0.006 |
| Relapse, n (%) | 14 (11.7) | 11 (13.9) | 3 (7.3) | 0.285 |
| mRS>2 after 6 months, n (%) | 18 (15.0) | 8 (10.1) | 10 (24.4) | 0.038 |
| mRS>2 after 12 months, n=101, n (%) | 20 (19.8) | 13 (19.7) | 7 (20.0) | 0.971 |
| mRS>2 after 24 months, n=96, n (%) | 9 (9.4) | 5 (8.2) | 4 (11.4) | 0.601 |
ATAbs, Anti-thyroid antibodies; SD, standard deviation; IVIG, intravenous immunoglobins; mRS, modified Ranking scale; NCU, neurological intensive care unit; NEOS, the anti-NMDAR Encephalitis One-Year Functional Status.
Table 2.
Auxiliary features of anti-NMDAR encephalitis patients with or without ATAbs.
| Total (n = 120) | ATAbs negative (n = 79) | ATAbs positive (n = 41) | P value | |
|---|---|---|---|---|
| Thyroid function | ||||
| TSH, uIU/ml, median (IQR) | 1.60 (0.94,2.57) | 1.59 (0.91,2.48) | 1.84 (1.16,2.91) | 0.180 |
| TT3, ng/ml, median (IQR) | 0.83 (0.64,1.01) | 0.87 (0.68,1.02) | 0.79 (0.62,0.93) | 0.051 |
| TT4, ug/dl, median (IQR) | 7.5 (6.1,9.0) | 7.8 (6.1,9.1) | 7.2 (6.1,8.3) | 0.238 |
| FT3, pg/ml, median (IQR) | 2.7 (2.2,3.1) | 2.8 (2.4,3.3) | 2.58 (2.0,2.9) | 0.012 |
| FT4, ng/dl, median (IQR) | 1.14 (0.98,1.27) | 1.16 (0.98,1.28) | 1.12 (0.93,1.23) | 0.464 |
| Anti-TgAb, IU/ml, median (IQR) | 0.4 (0.02,14.1) | 0.1 (0-0.4) | 46.2 (12.4,77.0) | <0.001 |
| Anti-TPOAb, IU/ml, median (IQR) | 1.5 (0.5,24.3) | 0.7 (0.3,1.5) | 48.5 (22.7,82.6) | <0.001 |
| EEG, n=94, n (%) | ||||
| Normal | 9 (9.6) | 7 (11.3) | 2 (6.3) | 0.431 |
| Slow activity | 50 (53.2) | 35 (56.5) | 15 (46.9) | 0.378 |
| Epileptic discharges | 22 (23.4) | 12 (19.4) | 10 (31.3) | 0.197 |
| others | 13 (13.8) | 8 (12.9) | 5 (15.6) | 0.717 |
| Cranial MRI, n, (%) | ||||
| Normal | 45 (37.5) | 30 (38.0) | 15 (36.6) | 0.881 |
| Limbic lobe | 43 (35.8) | 26 (32.9) | 17 (41.5) | 0.354 |
| Temporal lobe | 31 (25.8) | 18 (22.8) | 13 (31.7) | 0.290 |
| Frontal lobe | 27 (22.5) | 17 (21.5) | 10 (24.4) | 0.721 |
| Insular lobe | 15 (12.5) | 7 (8.9) | 8 (19.5) | 0.094 |
| Parietal lobe | 14 (11.7) | 9 (11.4) | 5 (12.2) | 0.897 |
| Occipital lobe | 10 (8.3) | 5 (6.3) | 5 (12.2) | 0.270 |
| Brainstem | 9 (7.5) | 5 (6.3) | 4 (9.8) | 0.499 |
| Basal ganglia | 7 (5.8) | 3 (3.8) | 4 (9.8) | 0.187 |
| Diencephalon | 4 (3.3) | 2 (2.5) | 2 (4.9) | 0.605 |
| CSF analysis | ||||
| Opening pressure, mmH2O, median (IQR) | 180 (140,229) | 180 (135,220) | 190 (140,240) | 0.740 |
| WBC, ×106/L, median (IQR) | 19.0 (6.0,35.0) | 19.0 (5.0,35.0) | 19.5 (7.3,38.5) | 0.611 |
| Protein, mg/dl, median (IQR) | 32.0 (21.0,44.5) | 31.0 (21.0,45.0) | 34.0 (19.3,44.8) | 0.411 |
| CSF NMDAR antibody titers, n (%) | ||||
| + | 14 (11.7) | 8 (10.1) | 6 (14.2) | 0.466 |
| ++ | 65 (54.2) | 42 (53.2) | 23 (56.1) | 0.760 |
| +++ | 41 (34.2) | 29 (36.7) | 12 (29.3) | 0.415 |
| Serum NMDAR antibody titers, n (%) | ||||
| - | 64 (53.3) | 43 (54.4) | 21 (51.2) | 0.738 |
| + | 18 (15.0) | 11 (13.9) | 7 (17.1) | 0.647 |
| ++ | 32 (26.7) | 22 (27.8) | 10 (24.4) | 0.685 |
| +++ | 6 (5.0) | 3 (3.8) | 3 (7.3) | 0.410 |
ATAbs, Anti-thyroid antibodies; anti-TgAb, anti-thyroglobulin antibody; anti-TPOAb, anti-thyroperoxidase antibody; CSF, cerebral spinal fluid; EEG, electroencephalography; IQR, interquartile range; FT3, free triiodothyronine; FT4, free thyroxine; MRI, magnetic resonance imaging; TT3, triiodothyronine; TT4, total thyroxine; TSH, thyroid stimulating hormone.
Functional Outcome at 6 Months
Univariate analysis indicated that the older (mean: 37.9 vs. 27.8 years, P=0.003), mechanical ventilation (44.4% vs. 17.6%, P=0.011), NCU admission (61.1% vs. 25.5%, P=0.003), higher levels of NEOS scores (median: 4 vs. 2, P<0.001), and Anti-TgAb (55.6% vs. 25.6%, P=0.014) were associated with unfavorable outcomes at 6 months. Patients with unfavorable outcomes at 6 months also presented fewer prodromal symptoms (P=0.069), more disturbed consciousness (P=0.054), higher titers of Anti-TgAb (P=0.062) and more frequency receiving plasma exchange (P=0.074). Multivariate logistic regression analysis demonstrated that age at onset >31 years [odds ratio (OR)= 3.545, 95% CI: 1.070-11.738, P=0.048], NEOS score 4-5 (OR=9.660; 95% CI: 2.906-32.105, P<0.001), and anti-TgAb (OR=3.907, 95% CI: 1.178-12.958, P=0.026) were independent factors for the prediction of unfavorable outcomes at 6 months (Table 3).
Table 3.
Univariate and multivariate logistic regression analyses of outcome at 6 months.
| Univariate analyses | Multivariate analyses | ||||
|---|---|---|---|---|---|
| Favorable outcome at 6 months (n = 102) | Unfavorable outcome at 6 months (n = 18) | P value | OR (95%CI) | P value | |
| Age at onset, y, mean ± SD | 27.8 ± 11.7 | 37.9 ± 18.8 | 0.003 | ||
| Age at onset >31 years, n (%)* | 35 (34.2) | 11 (61.1) | 0.031 | 3.545 (1.070-11.738) | 0.038 |
| Female, n (%) | 43 (42.2) | 10 (55.6) | 0.291 | ||
| Ovarian teratoma, n (%) | 6 (5.9) | 2 (11.1) | 0.412 | ||
| Prodromal symptoms, n (%) | 50 (49.0) | 13 (20.6) | 0.069 | – | – |
| Clinical manifestations, n (%) | |||||
| Mental behavior disorder | 75 (73.5) | 12 (66.7) | 0.548 | ||
| Epileptic seizure | 68 (66.7) | 10 (55.6) | 0.362 | ||
| Involuntary movement | 46 (45.1) | 10 (55.6) | 0.412 | ||
| Disturbance of consciousness | 43 (42.2) | 12 (66.7) | 0.054 | – | – |
| Cognitive impairment | 29 (28.4) | 8 (44.4) | 0.175 | ||
| Autonomic dysfunction | 26 (25.5) | 8 (44.4) | 0.100 | ||
| Language impairment | 21 (20.6) | 6 (33.3) | 0.233 | ||
| Central hypoventilation | 19 (18.6) | 6 (33.3) | 0.157 | ||
| Mechanical ventilation, n (%) | 18 (17.6) | 8 (44.4) | 0.011 | – | – |
| NCU admission, n (%) | 26 (25.5) | 11 (61.1) | 0.003 | ||
| NEOS score, median (IQR) | 2 (2,3) | 4 (3.5,4.3) | <0.001 | ||
| NEOS score 4-5, n (%) | 21 (20.6) | 13 (72.2) | <0.001 | 9.660 (2.906-32.105) | <0.001 |
| Electroencephalogram, n=94, n (%) | |||||
| Normal | 8 (7.8) | 1 (5.6) | 0.734 | ||
| Slow activity | 18 (17.6) | 4 (22.2) | 0.644 | ||
| Epileptic discharges | 42 (41.2) | 8 (44.4) | 0.795 | ||
| others | 10 (9.8) | 3 (16.7) | 0.388 | ||
| Cranial MRI, n, (%) | |||||
| Normal | 40 (39.2) | 6 (33.3) | 0.636 | ||
| Lesions in cerebral cortex | 43 (42.2) | 7 (38.9) | 0.795 | ||
| Lesions in white matter | 17 (16.7) | 5 (27.8) | 0.261 | ||
| CSF analysis | |||||
| Opening pressure, mmH2O, median (IQR) | 180 (140,225) | 210 (115,273) | 0.628 | ||
| WBC, ×106/L, median (IQR) | 15.0 (6.5,33.5) | 29.0 (3.5,47.3) | 0.228 | ||
| Protein, mg/dl, median (IQR) | 31.0 (21.0,43.0) | 38.0 (19.8,53.0) | 0.389 | ||
| CSF NMDAR antibody titers, n (%) | |||||
| + | 12 (11.8) | 2 (11.1) | 0.937 | ||
| ++ | 58 (56.9) | 7 (38.9) | 0.158 | ||
| +++ | 32 (31.4) | 9 (50.0) | 0.124 | ||
| Serum NMDAR antibody titers, n (%) | |||||
| - | 52 (51.0) | 12 (66.7) | 0.219 | ||
| + | 16 (15.7) | 2 (11.1) | 0.616 | ||
| ++ | 28 (27.5) | 4 (22.2) | 0.644 | ||
| +++ | 6 (5.9) | 0 | 0.291 | ||
| ATAbs | |||||
| Anti-TgAb + | 27 (25.6) | 10 (55.6) | 0.014 | 3.907 (1.178-12.958) | 0.026 |
| Anti-TgAb titers, IU/ml, median (IQR) | 0.2 (0-10.5) | 6.2 (0.2-56.7) | 0.062 | ||
| Anti-TPOAb + | 29 (28.4) | 7 (38.9) | 0.372 | ||
| Anti-TPOAb titers, IU/ml, median (IQR) | 1.4 (0.4-21.2) | 1.5 (0.6-40.6) | 0.513 | ||
| Anti-TgAb or Anti-TPOAb + | 31 (30.4) | 10 (55.6) | 0.038 | ||
| Anti-TgAb and Anti-TPOAb + | 25 (24.5) | 7 (38.9) | 0.203 | ||
| Immunotherapy, n (%) | |||||
| Steroids | 88 (86.3) | 14 (77.8) | 0.352 | ||
| IVIG | 58 (56.9) | 12 (66.7) | 0.437 | ||
| Plasma exchange | 16 (15.7) | 6 (33.3) | 0.074 | – | – |
| Immunosuppressor | 19 (18.6) | 6 (33.3) | 0.157 | ||
| Outcome | |||||
| Length of NCU length of stay, n=37, days, median (IQR) | 37.5 (21.0,73.0) | 44.0 (24.0,82.0) | 0.666 | ||
| Hospital length of stay, days, median (IQR) | 18.0 (13.0,29.0) | 32.5 (16.5,52.3) | 0.121 | ||
| Relapse, n (%) | 13 (12.7) | 1 (5.6) | 0.381 | ||
*The optimal cutoff value of age to predict unfavorable outcome was 31 with a sensitivity of 61.1% and a specificity of 69.6%. ATAbs, Anti-thyroid antibodies; CSF, cerebral spinal fluid; CI, confidence interval; EEG, electroencephalography; IQR, interquartile range; IVIG, intravenous immunoglobins; MRI, magnetic resonance imaging; NCU, neurological intensive care unit; NEOS, the anti-NMDAR Encephalitis One-Year Functional Status; OR, odds ratio.
Discussion
ATAbs are present in more than 10% of the healthy population (16), and the titer depends on age and sex. In the present study, the overall ATAbs positivity rate in patients with anti-NMDAR encephalitis was 37.1%, which is similar to that seen in other autoimmune diseases (17), but increased to 51.4% in the severe cases. Patients with ATAbs displayed higher rates of impaired consciousness, autonomic dysfunction, central hypoventilation and mechanical ventilation, all of which are typical features of severe anti-NMDAR encephalitis. Similar observations have been reported by Lin et al (9). In addition, the severity of NMO-SD is also associated with the presence of ATAbs (1). Elevated levels of ATAbs may lead to immune dysfunction in the brain by interacting with antibodies directed against neuronal surface antigens, which in can trigger a more aggressive autoimmune response against neurons. Therefore, it is reasonable to surmise that anti-NMDAR encephalitis patients with ATAbs may have a worse prognosis. The ATAbs-positive patients receiving aggressive immunotherapy show improved long-term prognosis. Interestingly, we identified anti-TgAb as an independent risk factor of poor short-term prognosis of anti-NMDAR encephalitis, although the positive rate of anti-TgAb in critically ill patients is lower than that of anti-TPOAb. The exact mechanisms remain to be unraveled.
Hashimoto’s encephalopathy (HE) has similar neurological and psychiatric symptoms as AEs, but can be distinguished from the latter on the basis of ATAbs (8). As the low specificity of ATAbs defining HE and their coexistence with other antibodies defining various AEs. It is possible that ATAbs may only be part of an episodic phenomenon triggered by anti-neuronal antibodies, which should be the treatment focus for patients exhibiting symptoms of immune-mediated encephalitis regardless of the presence of ATAbs. Since most ancillary tests for HE are non-specific, we also did not find specific features of anti-NMDAR encephalitis in the ATAbs-positive patients in the ancillary tests. Nevertheless, one study has reported that ATAbs-positive patients have more common limbic system lesions (9).
In conclusion, the prevalence of ATAbs is common in patients with anti-NMDAR encephalitis, especially in the severe cases. Presence of ATAbs is associated with worse short-term neurological recovery and may be need more aggressive immunotherapy.
Data Availability Statement
The original contributions presented in the study are included in the article/Supplementary Material. Further inquiries can be directed to the corresponding author.
Ethics Statement
The studies involving human participants were reviewed and approved by Ethics Committee of the Xuanwu Hospital. Written informed consent to participate in this study was provided by the participants’ legal guardian/next of kin.
Author Contributions
ZC carried out the patients enrollment, statistical analysis and drafted the manuscript. HH carried out the patients enrollment and verification of data. WC and LC carried out the verification of data and statistical analysis. YZ and YS conceived of the study, and participated in its design and coordination and helped to draft the manuscript. All authors contributed to the article and approved the submitted version.
Funding
This project was supported by the National Key Research and Development Program of China Research (2020YFC2005403) and by Beijing Municipal Administration of Hospitals Incubating Program (PX2020035).
Conflict of Interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Publisher’s Note
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.
Supplementary Material
The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fimmu.2021.725950/full#supplementary-material
Patient enrollment flow chart.
Relationship between ATAbs and prognosis at 6 months. ATAbs, Anti-thyroid antibodies; anti-TgAb, anti-thyroglobulin antibody; anti-TPOAb, anti-thyroperoxidase antibody.
References
- 1.Wang X, Yi H, Liu J, Li M, Mao ZF, Xu L, et al. Anti-Thyroid Antibodies and Thyroid Function in Neuromyelitis Optica Spectrum Disorders. J Neurol Sci (2016) 366:3–7. 10.1016/j.jns.2016.04.039 [DOI] [PubMed] [Google Scholar]
- 2.Li H, Dai Y, Wu AM, Sun X, Lin Y, Lv K, et al. Anti-Thyroid Antibodies and Cerebrospinal Fluid Findings in Neuromyelitis Optica Spectrum Disorders. J Neuroimmunol (2015) 281:38–43. 10.1016/j.jneuroim.2015.02.014 [DOI] [PubMed] [Google Scholar]
- 3.Munteis E, Cano JF, Flores JA, Martinez-Rodriguez JE, Miret M, Roquer J. Prevalence of Autoimmune Thyroid Disorders in a Spanish Multiple Sclerosis Cohort. Eur J Neurol (2007) 14(9):1048–52. 10.1111/j.1468-1331.2007.01882.x [DOI] [PubMed] [Google Scholar]
- 4.Tüzün E, Erdağ E, Durmus H, Brenner T, Türkoglu R, Kürtüncü M, et al. Autoantibodies to Neuronal Surface Antigens in Thyroid Antibody-Positive and -Negative Limbic Encephalitis. Neurol India (2011) 59(1):47–50. 10.4103/0028-3886.76857 [DOI] [PubMed] [Google Scholar]
- 5.Culler G, Bachman E, VanHaerents S. Paraclinical Serum Markers as Aids in the Diagnosis of Autoimmune Encephalitis. J Neuroimmunol (2020) 347:577324. 10.1016/j.jneuroim.2020.577324 [DOI] [PubMed] [Google Scholar]
- 6.Xu CL, Liu L, Zhao WQ, Li JM, Wang RJ, Wang SH, et al. Anti-N-Methyl-D-Aspartate Receptor Encephalitis With Serum Anti-Thyroid Antibodies and IgM Antibodies Against Epstein-Barr Virus Viral Capsid Antigen: A Case Report and One Year Follow-Up. BMC Neurol (2011) 11:149. 10.1186/1471-2377-11-149 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 7.Linnoila J, Pittock SJ. Autoantibody-Associated Central Nervous System Neurologic Disorders. Semin Neurol (2016) 36(4):382–96. 10.1055/s-0036-1585453 [DOI] [PubMed] [Google Scholar]
- 8.Graus F, Titulaer MJ, Balu R, Benseler S, Bien CG, Cellucci T, et al. A Clinical Approach to Diagnosis of Autoimmune Encephalitis. Lancet Neurol (2016) 15(4):391–404. 10.1016/s1474-4422(15)00401-9 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 9.Lin Y, Tan S, Wang Y, Shen X, Shu Y, Shan Y, et al. Anti-Thyroid Antibodies and Thyroid Function in Anti-N-Methyl-D-Aspartate Receptor Encephalitis. Neurochem Int (2018) 113:107–11. 10.1016/j.neuint.2017.11.019 [DOI] [PubMed] [Google Scholar]
- 10.Matera E, Gabellone A, Petruzzelli MG, Marzulli L, Furente F, Margari L. Anti-N-Methyl-D-Aspartate Receptor Encephalitis With Serum Anti-Thyroid Antibodies: A Case Report and Literature Review. Am J Case Rep (2021) 22:e931104. 10.12659/ajcr.931104 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 11.Prüss H, Dalmau J, Harms L, Höltje M, Ahnert-Hilger G, Borowski K, et al. Retrospective Analysis of NMDA Receptor Antibodies in Encephalitis of Unknown Origin. Neurology (2010) 75(19):1735–9. 10.1212/WNL.0b013e3181fc2a06 [DOI] [PubMed] [Google Scholar]
- 12.Tojo K, Nitta K, Ishii W, Sekijima Y, Morita H, Takahashi Y, et al. A Young Man With Anti-NMDAR Encephalitis Following Guillain-Barré Syndrome. Case Rep Neurol (2011) 3(1):7–13. 10.1159/000323751 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 13.Florance NR, Davis RL, Lam C, Szperka C, Zhou L, Ahmad S, et al. Anti-N-Methyl-D-Aspartate Receptor (NMDAR) Encephalitis in Children and Adolescents. Ann Neurol (2009) 66(1):11–8. 10.1002/ana.21756 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 14.Balu R, McCracken L, Lancaster E, Graus F, Dalmau J, Titulaer MJ. A Score That Predicts 1-Year Functional Status in Patients With Anti-NMDA Receptor Encephalitis. Neurology (2019) 92(3):e244–52. 10.1212/wnl.0000000000006783 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 15.Xu X, Lu Q, Huang Y, Fan S, Zhou L, Yuan J, et al. Anti-NMDAR Encephalitis: A Single-Center, Longitudinal Study in China. Neurol Neuroimmunol Neuroinflamm (2019) 7(1):e633. 10.1212/nxi.0000000000000633 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 16.Hollowell JG, Staehling NW, Flanders WD, Hannon WH, Gunter EW, Spencer CA, et al. Serum TSH, T(4), and Thyroid Antibodies in the United States Population (1988 to 1994): National Health and Nutrition Examination Survey (NHANES III). J Clin Endocrinol Metab (2002) 87(2):489–99. 10.1210/jcem.87.2.8182 [DOI] [PubMed] [Google Scholar]
- 17.Wang Q, Shangguan J, Zhang Y, Pan Y, Yuan Y, Que W. The Prevalence of Thyroid Autoantibodies in Autoimmune Connective Tissue Diseases: A Systematic Review and Meta-Analysis. Expert Rev Clin Immunol (2020) 16(9):923–30. 10.1080/1744666x.2020.1811089 [DOI] [PubMed] [Google Scholar]
Associated Data
This section collects any data citations, data availability statements, or supplementary materials included in this article.
Supplementary Materials
Patient enrollment flow chart.
Relationship between ATAbs and prognosis at 6 months. ATAbs, Anti-thyroid antibodies; anti-TgAb, anti-thyroglobulin antibody; anti-TPOAb, anti-thyroperoxidase antibody.
Data Availability Statement
The original contributions presented in the study are included in the article/Supplementary Material. Further inquiries can be directed to the corresponding author.