Are serum autoantibodies associated with brain changes in systemic lupus erythematosus? MRI data from the Leiden NP-SLE cohort

Abstract

Objective

The effect of serum autoantibodies on the brain of systemic lupus erythematosus (SLE) patients remains unclear. We investigated whether serum autoantibodies, individually and assessed in groups, are associated with specific brain-MRI abnormalities or whether these structural changes are associated with other SLE-related or traditional cardiovascular disease risk factors.

Methods

All patients underwent brain 3Tesla-MRI. White matter hyperintensities (WMHs), ischemic lesions, inflammatory-like lesions and cerebral atrophy were scored. Serum autoantibodies analyzed included lupus anticoagulant (LAC), anticardiolipine (aCL) IgG and IgM (first 3 also grouped into antiphospholipid autoantibodies (aPL)), anti-dsDNA, anti-SSA, anti-SSB, anti-RNP, and anti-Sm (the latter 5 grouped into SLE-related autoantibodies). Associations were assessed using logistic regression analysis adjusted for potential confounders. Furthermore, a sensitivity analysis including anti-Beta2 glycoprotein-1 antibodies (anti-β2GP1) in the aPL group was performed and the potential modification role of the neuropsychiatric clinical status in the model was assessed.

Results

325 patients (mean age 42 years (SD 14), 89% female) were included. The following MRI-brain abnormalities were found: WMHs (71%), lacunar infarcts (21%), gliosis (11%), micro-hemorrhages (5%), large hemorrhages (2%), inflammatory-like lesions (6%) and atrophy (14%). No associations were found between individual or total SLE-related autoantibodies and inflammatory-like lesions. A higher number of positive aPL was associated with lacunar infarcts (OR 1.37 (95%CI 1.02–1.99) and gliosis (OR 2.15 (1.37–3.37)). LAC was associated with lacunar infarcts in white matter (OR 3.38 (1.32–8.68)) and atrophy (OR 2.49 (1.01–6.15)), and aCL IgG with gliosis (OR 2.71 (1.05–7.02)). Among other variables, SLE patients with hypertension presented a higher chance for WMHs (OR 5.61 (2.52–12.48)) and lacunar infarcts in WM (OR 2.52 (1.10–5.74)) and basal ganglia (OR 8.34 (2.19–31.70)), while cumulative SLE-damage was correlated with lacunar infarcts in WM (OR 1.43 (1.07–1.90)), basal ganglia (OR 1.72 (1.18–2.51)) and cerebellum (OR 1.79 (1.33–2.41)). These associations were confirmed in the sensitivity analysis.

Conclusions

Brain abnormalities in SLE represent different underlying pathogenic mechanisms. aPL are associated with ischemic brain changes in SLE, while the presence of SLE-related serum autoantibodies is not related to inflammatory-like lesions. Hypertension and cumulative SLE-damage associate with ischemic MRI-brain changes in SLE, suggesting the importance of accelerated atherosclerosis in this process.

Keywords

Systemic lupus erythematosus antibodies neuropsychiatric systemic lupus erythematosus NP-SLE magnetic resonance imaging cardiovascular risk pathogenesis

Introduction

Nervous system involvement in systemic lupus erythematosus (SLE) leads to a heterogeneous group of neuropsychiatric (NP) manifestations. The two main underlying pathophysiologic processes in the brain resulting in NP-SLE are thought to be inflammation and ischemia.^1,2 The mechanisms that ultimately result in these pathophysiological changes and how they are related to each other remain poorly understood.

Over the past decade type I interferon (IFN) was postulated to play a central role in SLE pathogenesis by promoting feedback loops, progressively disrupting peripheral immune tolerance and driving disease activity.³ Recent discoveries implicate IFN-alpha together with the classical complement cascade as major pathways used by microglia for synaptic pruning in mice. Chronic peripheral inflammation in SLE may play a role in the aberrant activation of microglia and subsequently stimulate synapse loss, tagging inappropriate synaptic connections between neurons and subsequently leading to cerebral dysfunction.^4,5 The elevation of IFN-alpha activity has been related to autoantibody accumulation.⁶ Moreover, several studies have described that autoantibody-containing immune-complexes may drive type I IFN activation.^7–9 Autoantibodies may also exert a direct effect upon neurons. The disruption of the blood brain barrier (BBB) integrity may permit the influx of neuropathic antibodies, which may target synapses for engulfment by microglia.¹⁰ Previous studies suggested that anti-dsDNA antibodies cross-react with N-methyl-D-aspartate (NMDA) receptors, and injecting these antibodies into mice causes hippocampal neuronal loss and cognitive impairment only when the BBB has been disrupted.^11,12

Autoantibodies have also been associated with an ischemic pathogenic process. Antiphospholipid antibodies (aPL), especially lupus anticoagulant (LA), have been related to intracranial thrombosis.¹³ The complement cascade in close relation to aPL also plays a role in microvascular injury and NP-SLE pathogenesis.^14–16 Furthermore, accelerated atherosclerosis and traditional cardiovascular disease (CVD) risk factors have been involved in the ischemic process in SLE.¹⁷

Despite the fact that imaging abnormalities are not specific for NP-SLE, magnetic resonance imaging (MRI) remains the neuroimaging technique of choice due to its superior soft tissue resolution. In a paired neuroimaging-autopsy study, Sibbit and coworkers observed that brain lesions in NP-SLE detected by MRI represent underlying cerebrovascular and parenchymal brain injury on histopathology.¹⁸ Cerebral abnormalities that have been described in SLE on MRI are diverse; the most commonly reported is small vessel disease, especially white matter hyperintensities (WMHs) and lacunar infarcts, but also large vessel disease, inflammatory-like lesions (i.e. multifocal grey matter lesions) and brain atrophy are described.^19–23 Although a fair number of studies on MRI abnormalities in SLE and NP-SLE have been published, only a few have tried to unravel the mechanisms leading to these changes. It has been proposed that focal lesions in SLE represent neuronal injury from various etiologies, ischemia and inflammation being the most important.¹⁸ Luyendijk and coworkers described several distinct brain-MRI patterns in NP-SLE patients that were suggestive of different underlying pathogenic mechanisms.²⁴ The understanding of the pathogenic mechanisms leading to MRI abnormalities in SLE may be important to develop a rational prevention and treatment approach and in categorization of patients in further research.^23,24

Based on this knowledge, our primary hypothesis was that the total number of SLE-related autoantibodies is associated with inflammatory-like lesions and the number of aPL autoantibodies with ischemic changes as seen on brain MRI. As a secondary objective, we analyzed if MRI abnormalities were directly related to individual autoantibodies or otherwise with other SLE-related or CVD risk factors. Overall, we aim to investigate whether the underlying immune abnormalities in SLE are associated with pathophysiological changes as seen on brain MRI.

Methods

Study population

Between September 2007 and February 2016, a total of 325 SLE patients were seen in the Leiden NP-SLE clinic and included in the present study. All patients fulfilled the American College of Rheumatology 1982 revised criteria for SLE.^25,26 Our hospital is a tertiary referral centre serving as a national referral centre for NP-SLE in the Netherlands. Patients are sent by a referral rheumatologist or other medical specialist to our center when SLE patients present NP manifestations. Therefore, all patients included in this study presented NP manifestations at time of the MRI. They were admitted for a 1-day period to the Leiden University Medical Center. All patients underwent standardized multidisciplinary medical examination and extensive neuropsychological testing, serologic assessment and brain MRI. Evaluations included in the multidisciplinary assessment have been reported in detail before.²⁷ The attribution process of NP events to SLE and one of its underlying pathogenic mechanisms (ischemic or inflammatory) or to other etiologies was decided after multidisciplinary consensus and confirmed after re-assessment of patients at follow up as described elsewhere.²⁸ This study was approved by the local medical ethics committee and all patients provided written informed consent.

MRI protocol and scoring

All subjects underwent a 3 Tesla MRI in the same scanner according to a standardized protocol (Achieva; Philips Healthcare). The scanning protocol included high-resolution T1-weighted, T2-weighted and fluid-attenuated inversion recovery (FLAIR) sequences, followed by a T1-weighted sequence obtained after intravenous administration of gadolinium contrast agent. Scan parameters are shown in Supplementary Table 1. All MRI examinations were visually inspected by an experienced neuroradiologist (SK) who was blinded to clinical information. Areas of abnormalities were identified and their locations were documented. Deep WMHs were rated according to the visual Fazekas rating scale (ranging 0–3) on FLAIR images.²⁹ For analysis, we dichotomized this variable into low (Fazekas score < 2) and high presence of WMHs (Fazekas score ≥ 2). The presence or absence of lacunar infarcts, large vessel infarcts, dural sinus thrombosis, cerebral micro-bleeds (CMBs), large hemorrhages, gliosis and inflammatory-like changes was also assessed. Lacunar infarcts were defined as ovoid areas of T2 hyperintense signal, with a hyperintense rim on FLAIR, measuring less than 20mm. These were distinguished from WMHs on the basis of central low signal on FLAIR. Lacunar infarcts were assessed in the WM, basal ganglia, thalamus, brainstem, and cerebellum. Large vessel infarcts were defined as areas of T2/FLAIR hyperintensity involving the cortex and underlying WM confined to the distribution of a vascular territory. If these areas were restricted in diffusion, then the infarct was labeled acute. CMBs were defined as small (2–5mm), homogeneous and round areas of susceptibility artefacts on gradient echo images.³⁰ Gliosis was defined as a focal area of volume loss accompanied by T2 and FLAIR hyperintensity. If the area of gliosis was accompanied by hemosiderosis, it was deemed to have been the result of a previous hemorrhage. Presence of dural venous sinus thrombosis was suggested by the loss of normal flow voids in a dural venous sinus and absence of contrast enhancement within it and was confirmed by a MR venogram showing a loss of the corresponding normal flow signal. Lesions showing post-contrast enhancement following intravenous gadolinium injection, cortical hyperintensity and/or swelling on FLAIR or gyral restricted diffusion were thought to be inflammatory-type lesions according to Luyendijk et al.²⁴ Cerebral atrophy was assessed using the Pasquier scale, a four-point rating scale to assess cerebral atrophy ranging from 0 (absent) to 3 (severe cortical atrophy) and computed into low (Pasquier scale < 2) and high (Pasquier scale ≥ 2).³¹ See Supplementary Figures 1–3 in additional supporting material.

Autoantibodies

Blood samples of all patients were collected from each participant at 08:00 a.m. Determinations of serum anti-dsDNA, anti-Sm, anti-RNP, anti-SSA/Ro52, anti-SSB/La and aPL including anticardiolipin (aCL), anti-Beta2 glycoprotein 1 antibodies (anti-β2GP1) and LA were performed the same day of the blood extraction in the routine clinical laboratory. IgG anti-dsDNA antibodies were detected using the Crithidia luciliae indirect immune fluorescence technique (Immuno Concepts, Sacramento, CA, USA). IgG antibodies against SS-A/Ro-52, SS-B/La, Sm, RNP, and IgG and IgM aCL and anti-β2GP1 were determined using a Phadia 250 EliA fluorescence enzyme immunoassay (Thermo Fisher Scientific, Freiburg, Germany). LA was determined using STA-Rack and STA Evolution coagulation analyzers (Stago, Parsippany, NJ, USA).

Complement levels

Levels of C3 and C4 in serum were measured using laser nephelometry. Based on the normal limits for our laboratory, C3 < 0.9 g/l and C4 < 95 mg/l were defined as low.

SLE-related activity and damage

SLE disease activity was assessed with the Systemic Lupus Erythematosus Disease Activity Index 2000 (SLEDAI-2K).³² Permanent and irreversible damage due to SLE was calculated with the Systemic Lupus International Collaborating Clinics/American College of Rheumatology damage index (SDI).³³ All SLEDAI-2K and SDI values were calculated without NP variables. SDI was calculated without the diabetes variable.

Cardiovascular variables

At inclusion, data on age, gender, duration of SLE, medical history and CVD risk factors (smoking, hypertension, diabetes, dyslipidemia, body mass index (BMI)) were recorded, through interviewing the patient and by studying medical records. Furthermore, at this point glucose, triglycerides, total cholesterol, low-density and high-density lipoproteins cholesterol concentrations (LDLc and HDLc) were determined. Hypertension was defined as elevated blood pressure >140/90 mmHg or receiving antihypertensive therapy. Dyslipidemia was defined according to the National Cholesterol Education Program (total cholesterol > 5.2 mmol/L, triglycerides > 1.7 mmol/L, LDLc > 3.4 mmol/L and HDLc < 1 mmol/L for men and <1.3 mmol for women) or receiving dyslipidemia therapy.³⁴ Cigarette smoking was divided into current and ever smoking. Diabetes was defined as a fasting plasma glucose >7.0 mmol/liter or receiving current anti-diabetic therapy. BMI was used as a continuous variable.

Statistical analysis

Demographic and clinical parameters were described as mean and standard deviations (SD) or proportions, as appropriate. The relationship between autoantibodies and MRI abnormalities was investigated through means of logistic regression analyses through which the odds ratio (OR) and 95% confidence intervals (95% CI) were calculated. First, an analysis of interaction between each of the autoantibodies (in groups and individually) and the diagnosis (NP-SLE vs. SLE without NP-SLE) on the different outcomes was conducted. If interactions were statistically significant (p < 0.1), analyses were stratified in both subgroups. If differences in the relationships (between autoantibodies and MRI abnormalities) were considered clinically relevant, all analyses were further stratified for NP-SLE diagnosis. Subsequently, analyses were conducted with groups of autoantibodies including the number of positive aPL (LA, aCL IgG and IgM) ranging from 0–3 and the number of positive SLE-related antibodies (anti-dsDNA, anti-Sm, anti-RNP, anti-SSA/Ro52, anti-SSB/La) ranging from 0–5. Afterwards, all these antibodies were included individually in separate models. Univariable regression was followed by multivariable regression. Variables from the univariable analysis with p < 0.20 were included in the multivariable model. Some variables known from the literature as potential confounders were forced into the models to test whether they confounded the main relationships of interest. Significant variables or variables with a confounding effect on the relationship between autoantibodies and MRI abnormalities were kept in the final models. Because anti-β2GP1 (IgG and IgM) were not tested in all patients, a sensitivity analysis was performed including these autoantibodies in the model as covariates first added in the aPL group (LA, aCL IgG and IgM, anti-β2GP1 IgG and IgM) ranging 0–5 and later analyzed individually; p < 0.05 was used as the level of significance. Statistical analysis was performed using SPSS version 21.0 (IBM Corp., Armonk, MY, USA).

Results

In total, 325 participants underwent a brain MRI scan. Table 1 shows the clinical characteristics, autoantibody profile, CVD risk and SLE-related factors in the study population.

Table 1

Clinical characteristics of the 325 SLE included patients

	n (%) or mean (SD)
Age, years	42.1 (13.7)
Female	287 (88.3%)
Age at diagnosis SLE, years	33.9 (14.3)
Duration SLE, years	8.3 (8.9)
Antibodies
aCL IgG	63 (19.4%)
aCL IgM	31 (9.5%)
LA	99 (30.5%)
Anti- β2GP1 IgG^a	40 (14.4%)
Anti- β2GP1 IgM^a	12 (4.3%)
ANA	315 (96.9%)
ENA	181 (55.7%)
Anti-ds-DNA	160 (49.2%)
Anti-SSA/Ro52	134 (41.2%)
Anti-SSB/La	43 (13.2%)
Anti-RNP	62 (19.1%)
Anti-Sm	41 (12.6%)
SLE-related factors
SLEDAI-2K	5.1 (5.1)
SDI	1.2 (1.3)
C3 low	104 (32%)
C4 low	85 (26.2%)
Cardiovascular risk factors
Hypertension	130 (40%)
Smoking
Current smoker	86 (26.5%)
Ever smoker	160 (49.2%)
Never smoker	165 (50.8%)
BMI (kg/m²)	24 (21-28)
Dyslipidemia	186 (57.2%)
Diabetes mellitus	19 (5.8%)
Attribution of NP events
Non-NP-SLE	204 (62.8%)
Ischemic NP-SLE	43 (13.2%)
Inflammatory NP-SLE	78 (24%)

aCL: anticardiolipin; β2GP1: Beta2 glycoprotein 1; BMI: body mass index; LA: lupus anticoagulant; NP: neuropsychiatric; SD: standard deviation; SDI: Systemic Lupus International Collaborating Clinics damage index; SLE: systemic lupus erythematosus; SLEDAI-2K: Systemic Lupus Erythematosus Disease Activity Index 2000.

Only 278 patients were assessed for B2GP IgG and IgM.

Brain MRI abnormalities in SLE

Brain abnormalities in all SLE patients included in our cohort are shown in Table 2. WMHs were the most frequent radiologic finding with at least one WMH observed in 229 SLE patients (70.5%). Of all 325 patients, 61 (18.8%) had a Fazekas score ≥2. A total of 118 lacunar infarcts in 68 SLE patients were found. Cerebral atrophy (Pasquier ≥ 2) was found in 44 (13.6%) patients. A description of brain-MRI abnormalities according to the attribution of NP-events into the different clinical subgroups (non-NP-SLE, ischemic and inflammatory NP-SLE) is given in Supplementary Table 2.

Table 2

Brain-MRI findings of the 325 SLE included patients

	n (%)
Normal MRI	83 (25.5)
Restricted diffusion	3 (0.9)
Gyral T2 hyperintensities	3 (0.9)
Gyral T1 hyperintensities	1 (0.3)
White matter lesions
Periventricular WMHs	166 (51.1)
Deep WMHs	204 (62.8)
Subcortical	196 (60.3)
Fazekas score
0	96 (29.5)
1	168 (51.7)
2	49 (15.1)
3	12 (3.7)
Basal ganglia	6 (1.8)
Thalamus	5 (1.5)
Brainstem	25 (7.7)
Cerebellum	6 (1.8)
Lacunar infarcts	68 (20.9)
White matter supratentorial	38 (11.7)
Basal ganglia	24 (7.4)
Thalamus	10 (3.1)
Brainstem	7 (2.2)
Cerebellum	39 (12)
Large vessel infarcts	14 (4.3)
Sinus thrombosis	8 (2.5)
Focal white matter lesions	6 (1.8)
Parenchymal enhancement^a	11 (3.4)
Leptomeningeal enhancement^a	2 (0.6)
Inflammatory-like lesions^a	19 (6)
Cerebral micro-bleeds	17 (5.2)
Large hemorrhages	7 (2.2)
Gliosis	34 (10.5)
Cerebrocalcinosis	1 (0.3)
Cerebral atrophy (Pasquier scale)
0	160 (49.2)
1	121 (37.2)
2	34 (10.5)
3	10 (3.1)

MRI: magnetic resonance imaging; SLE: systemic lupus erythematosus; WMHs: white matter hyperintensities.

In 10 patients gadolinium was not used due to previous contrast allergy or because the patient denied the use of contrast.

Relationship between groups of autoantibodies and SLE-associated MRI-brain lesions

The interaction between autoantibodies and NP-SLE status on MRI abnormalities was statistically significant in some cases (several not statistically significant), but not clinically relevant (i.e. difference in the ORs between the two groups was not substantial); therefore, we decided to run the analysis in the whole population. The relationship between groups of autoantibodies and SLE-associated MRI-brain lesions are shown in Table 3. No relationship was found between the total number of SLE-related autoantibodies and MRI-brain abnormalities. Univariable analysis showed an association between an increasing number of positive aPL antibodies and the presence of lacunar infarcts, CMBs, gliosis, and atrophy. After adjustment for potential confounders, a significant relationship was only found for the increasing number of positive aPL antibodies and the presence of lacunar infarcts (OR 1.37 (1.02–1.99); p < 0.05) and gliosis (OR 2.15 (1.37–3.37); p < 0.05). None of the groups of autoantibodies was related to WMHs or inflammatory-like lesions. The clinical NP-status did not confound any of the relationships of interest and was therefore not kept in the models (data not shown). In the sensitivity analysis, after the inclusion of anti-β2GP1 in the aPL antibodies group, only the relationship between the total number of aPL and gliosis (OR 1.56 (1.10–2.20); p < 0.001) remained significant after multivariable analysis (Supplementary Table 3).

Table 3

Relationship between groups of auto-antibodies and MRI-brain lesions in 325 SLE patients

	WMH	Ischemic changes^b			Inflammatory-like changes	Atrophy^c
	Fazekas^d	Lacunar infarcts	CMBs	Gliosis	Inflammatory-like changes	Atrophy^c
	OR (95% CI)	OR (95% CI)	OR (95% CI)	OR (95% CI)	OR (95% CI)	OR (95% CI)
Antiphospholipid antibodies (0–3)
Univariable	1.11 (0.79–1.54)	1.45 (1.07–1.97)*	1.62 (1.01–2.63)*	2.24 (1.52–3.29)**	1.39 (0.84–2.30)	1.51 (1.07–2.16)*
Multivariable^a	1.18 (0.79–1.76)	1.37 (1.02–1.99)*	1.46 (0.81–2.65)	2.15 (1.37–3.37)**	1.46 (0.82–2.61)	1.395 (0.92–2.13)
SLE related antibodies (0–5)
Univariable	0.81 (0.62–1.07)	0.82 (0.63–1.08)	0.77 (0.48–1.23)	0.76 (0.52–1.11)	1.01 (0.65–1.54)	0.766 (0.55–1.07)
Multivariable^a	0.84 (0.61–1.17)	0.91 (0.66–1.25)	0.74 (0.42–1.30)	0.88 (0.58–1.34)	1.07 (0.67–1.72)	0.795 (0.55–1.16)

CI: confidence interval; CMBs: cerebral micro-bleeds; MRI: magnetic resonance imaging; OR: odds ratio; SDI: Systemic Lupus International Collaborating Clinics damage index; SLE: systemic lupus erythematosus; SLEDAI-2K: Systemic Lupus Erythematosus Disease Activity Index 2000; WMH: white matter hyperintensities.

Antiphospholipid antibodies included lupus anticoagulant, anticardiolipin IgM and IgG; SLE related antibodies included anti-dsDNA, anti-SSA/Ro52, anti-SSB/La, anti-Sm and anti-RNP.

Multivariable analysis was adjusted for age, gender, hypertension, smoking (current or ever), BMI, dyslipidemia, diabetes mellitus, low C3, low C4, duration of SLE, SLEDAI-2K and SDI.

Lacunar infarcts load includes: white matter, basal ganglia, thalamus, brainstem and cerebellum infarcts. No associations were found for large vessel infarcts, large hemorrhages and sinus thrombosis.

Pasquier scale ≥ 2.

Reference Fazekas score ≤ 1.

*p < 0.05; **p < 0.001.

Relationship between individual autoantibodies, CVD risk factors, SLE-specific factors, and SLE-associated MRI-brain abnormalities

Associations between brain MRI abnormalities, individual autoantibodies, CVD risk factors and other SLE-related factors are shown in Table 4. Patients with hypertension had higher odds of a high Fazekas score (OR 5.61 (2.52–12.48); p < 0.001). SLE patients with hypertension (OR 2.52 (1.10–5.74); p < 0.05), positivity for LA (OR 3.38 (1.32–8.68); p < 0.05) and higher SDI score (OR 1.43 (1.07–1.90; p < 0.05) presented a higher chance for lacunar infarcts in WM. Hypertension (OR 8.34 (2.19–31.70); p < 0.05), male gender and higher SDI (OR 1.72 (1.18–2.51); p < 0.05) were associated with lacunar infarcts in basal ganglia. Furthermore, SDI was also associated with the presence of infarcts in the cerebellum (OR 1.79 (1.33–2.41); p < 0.05). aCL IgG was associated with gliosis (OR 2.71 (1.05–7.02); p < 0.05) and LA with cerebral atrophy (OR 2.49 (1.01–6.15); p < 0.05). Again, the clinical NP-status did not confound any of the relationships of interest and was therefore not kept in the models. All these significant relationships were confirmed in the sensitivity analysis. In the main analysis, anti-RNP antibodies were related to the presence of inflammatory-like lesions; however, this relationship was not confirmed in the sensitivity analysis. Other CVD risk factors were not associated with brain abnormalities (Supplementary Table 4).

Table 4

Relationship between individual auto-antibodies and MRI-brain lesions in 325 SLE patients

		Ischemic changes^a
	WMH	Lacunar infarcts				Large vessel infarcts	CMBs	Gliosis	Inflammatory-like changes	Atrophy^b
	Fazekas^c	White matter	Basal ganglia	Thalamus	Cerebellum
	OR (95% CI)	OR (95% CI)	OR (95% CI)	OR (95% CI)	OR (95% CI)	OR (95% CI)	OR (95% CI)	OR (95% CI)	OR (95% CI)	OR (95% CI)
aCL IgG	0.89 (0.31–2.61)	0.84 (0.32–2.52)	0.70 (0.15–3.14)	8.75 (1.24–62.09)*	1.34 (0.50–3.61)	2.20 (0.50–9.82)	1.11 (0.31–3.95)	2.71 (1.05–7.02)*	1.16 (0.34–4.00)	1.05 (0.40–2.72)
aCL IgM	0.54 (0.13–2.35)	0.38 (0.08–1.79)	1.02 (0.17–5.94)	5.46 (0.79–37.92)	0.94 (0.26–3.37)	5.31 (0.93–30.32)	0.61 (0.10–3.57)	2.01 (0.62–6.51)	1.72 (0.40–7.38)	0.91 (0.28–2.94)
LA	1.64 (0.64–4.22)	3.38 (1.32–8.68)*	0.68 (0.18–2.51)	1.24 (0.19–8.12)	1.87 (0.75–4.69)	1.04 (0.23–4.70)	2.03 (0.59–6.97)	1.98 (0.75–5.24)	1.62 (0.51–5.12)	2.49 (1.01–6.15)*
Anti-dsDNA	0.77 (0.37–1.63)	0.62 (0.27–1.44)	1.29 (0.45–3.68)	0.42 (0.08–2.20)	1.31 (0.57–2.99)	0.34 (0.08–1.37)	0.95 (0.29–3.13)	1.08 (0.45–2.62)	1.09 (0.37–3.22)	0.50 (0.23–1.11)
Anti-SSA/Ro52	1.09 (0.47–2.55)	0.91 (0.37–2.23)	2.50 (0.76–8.25)	0.12 (0.01–1.76)	1.14 (0.46–2.97)	0.35 (0.06–1.99)	1.59 (0.49–5.13)	0.41 (0.13–1.36)	0.985 (0.33–2.98)	0.97 (0.41–2.30)
Anti-SSB/La	1.37 (0.43–4.37)	0.70 (0.16–3.07)	0.85 (0.17–4.09)	4.48 (0.36–55.37)	2.10 (0.59–7.47)	6.00 (0.85–42.26)	3.68 (0.79–29.30)	3.57 (0.80–15.91)	0.00	0.87 (0.25–3.09)
Anti-RNP	0.53 (0.17–1.64)	0.73 (0.22–2.46)	1.42 (0.35–5.71)	0.49 (0.05–5.19)	0.43 (0.11–1.62)	0.21 (0.02–2.09)	0.95 (0.20–4.43)	0.11 (0.01–0.91)*	3.37 (1.01–10.56)*	1.52 (0.56–4.14)
Anti-Sm	1.07 (0.25–4.51)	0.98 (0.23–4.14)	0.44 (0.04–4.57)	4.38 (0.29–65.31)	0.68 (0.13–3.61)	6.25 (0.82–47.80)	0.37 (0.04–3.62)	2.08 (0.46–9.38)	1.06 (0.24–4.70)	0.46 (0.09–2.28)
C3 low	0.91 (0.34–2.39)	0.92 (0.35–2.47)	0.96 (0.26–3.64)	3.66 (0.55–24.51)	1.44 (0.54–3.86)	1.01 (0.21–4.92)	3.93 (0.93–13.62)	1.07 (0.39–2.94)	0.45 (0.13–1.58)	1.75 (0.69–4.39)
C4 low	1.11 (0.43–2.86)	1.00 (0.35–2.84)	3.42 (0.90–13.06)	0.51 (0.07–3.70)	0.59 (0.20–1.75)	0.29 (0.04–2.15)	1.01 (0.27–3.80)	1.60 (0.57–4.55)	1.19 (0.34–4.23)	0.98 (0.37–2.61)
Age	1.05 (1.01–1.08)*	1.02 (0.98–1.05)	1.01 (0.97–1.06)	1.03 (0.97–1.01)	1.03 (1.00–1.07)	1.02 (0.97–1.08)	1.06 (1.01–1.11)*	1.01 (0.98–1.05)	1.00 (0.95–1.04)	1.05 (1.01–1.08)*
Gender	0.59 (0.21–1.66)	1.57 (0.40–6.14)	0.24 (0.06–0.94)*	2.25 (0.17–30.62)	0.30 (0.10–0.88)*	0.27 (0.05–1.46)	1.08 (0.17–6.88)	0.65 (0.18–2.32)	2.67 (0.31–23.20)	0.63 (0.22–1.79)
Duration SLE	1.03 (0.99–1.07)	1.05 (1.01–1.10)*	1.03 (0.97–1.08)	0.93 (0.84–1.03)	1.02 (0.97–1.06)	0.91 (0.82–1.01)	1.04 (0.98–1.10)	1.00 (0.95–1.05)	1.01 (0.94–1.08)	1.04 (1.01–1.08)*
SLEDAI-2K	1.02 (0.93–1.11)	1.03 (0.94–1.12)	0.89 (0.77–1.03)	0.97 (0.81–1.17)	1.02 (0.94–1.11)	1.00 (0.87–1.15)	1.01 (0.90–1.14)	0.93 (0.84–1.03)	1.00 (0.91–1.11)	1.07 (0.99–1.16)
SDI	0.91 (0.68–1.22)	1.43 (1.07–1.90)*	1.72 (1.18–2.51)*	1.41 (0.73–2.71)	1.79 (1.33–2.41)*	2.07 (1.23–3.50)*	1.23 (0.83–1.82)	1.60 (1.17–2.18)*	1.46 (0.97–2.18)	1.23 (0.97–1.62)
Hypertension	5.61 (2.52–12.48)**	2.52 (1.10–5.74)*	8.34 (2.19–31.70)*	7.82 (1.06–57.77)*	1.98 (0.89–4.44)	0.98 (0.25–3.88)	1.47 (0.47–4.57)	1.77 (0.72–4.36)	0.79 (0.25–2.55)	1.92 (0.91–4.07)
Smoking
-Current	2.45 (0.89–6.74)	1.24 (0.45–3.39)	1.47 (0.39–5.52)	1.45 (0.17–12.49)	0.59 (0.20–1.72)	0.46 (0.10–2.13)	5.12 (0.90–29.13)	0.84 (0.26–2.75)	0.41 (0.09–1.95)	1.06 (0.39–2.88)
-Ever	0.52 (0.21–1.35)	2.22 (0.85–5.83)	2.21 (0.60–8.13)	0.69 (0.07–6.96)	1.64 (0.64–4.21)	4.78 (0.88–26.04)	0.25 (0.05–1.28)	1.06 (0.37–3.07)	1.37 (0.43–4.32)	1.04 (0.42–2.57)
BMI	0.99 (0.93–1.07)	0.99 (0.92–1.08)	1.02 (0.93–1.12)	1.07 (0.91–1.26)	1.01 (0.94–1.09)	1.04 (0.90–1.19)	0.98 (0.86–1.11)	1.01 (0.93–1.10)	0.89 (0.79–1.01)	1.05 (0.98–1.13)
Dyslipidemia	1.44 (0.71–2.93)	0.99 (0.45–2.20)	0.70 (0.25–1.92)	2.28 (0.45–11.69)	0.93 (0.42–2.08)	0.60 (0.16–2.22)	0.39 (0.12–1.26)	0.59 (0.25–1.42)	0.66 (0.21–2.10)	1.42 (0.67–3.01)
Diabetes	1.53 (0.37–6.29)	0.15 (0.01–1.62)	0.93 (0.13–6.68)	0.58 (0.03–10.67)	0.54 (0.10–2.90)	0.44 (0.02–9.30)	0.38 (0.03–5.87)	1.02 (0.17–6.20)	1.56 (0.15–16.67)	0.84 (0.21–3.46)

aCL: anticardiolipin; BMI: body mass index; C3: complement component 3; C4: complement component 4; CMBs: cerebral micro-bleeds; LA: lupus anticoagulant; MRI: magnetic resonance imaging; SLE: systemic lupus erythematosus; SLEDAI-2K: systemic lupus erythematosus disease activity index 2000; SDI: Systemic Lupus International Clinics damage index; WMH: white matter hyperintensities.

No association was found for lacunar infracts in the brainstem, large hemorrhages and sinus thrombosis.

Pasquier scale ≥ 2.

Reference Fazekas score ≤ 1.

*p < 0.05; **p < 0.001.

Discussion

In the present study, we have demonstrated the association of aPL, especially LA, cumulative SLE-organ damage and several CVD risk factors and the presence of ischemic changes in the brain of SLE patients. In contrast, SLE-related autoantibodies in serum, both total number and individual autoantibodies, were not associated with inflammatory-like lesions or other brain-MRI abnormalities.

Ischemic changes in the brains of SLE patients seem to be driven by aPL. Among all the serum autoantibodies analyzed, LA, but not aCL or anti-β2GP1, was associated with lacunar infarcts in the WM and with cerebral atrophy. Previous reports have also found that LA is a major risk factor for arterial thrombotic disease, especially for ischemic stroke in young women.^35,36 Furthermore, a higher prevalence of MRI abnormalities, mainly lacunar and large territorial infarctions, has been found in SLE patients with antiphospholipid syndrome;^21,37 LA has been suggested to play the most important role in this association.²⁰ The relation between LA and cerebral atrophy is more inconsistent. This relationship has been found using the Pasquier scale in a small study in SLE patients and another study including only NP-SLE patients without correction for other variables.^22,38 Other studies failed to demonstrate any significant association between LA and cerebral atrophy, even when quantitative MRI-methods were used.^37,39 aCL IgG was related to gliosis. We hypothesize that gliosis seen in the brain of SLE patients is driven by aCL IgG and may be part of an underlying ischemic process or due to an autoimmune-mediated glial activation.

Inflammatory-like lesions in the brain of SLE patients were not found to be related to the total number of SLE-related autoantibodies. There may be different possible explanations for these negative findings. We report a low prevalence of inflammatory-like lesions (5.8%). In the presence of a low frequency of brain-MRI inflammatory-like lesions, it is difficult to capture factors associated with it due to a lack of power. Despite this, it is difficult to interpret this frequency, as in the literature there are no other studies reporting the prevalence of inflammatory-like lesions. The MRI may have shown no abnormalities despite overt NP-SLE manifestations as it has been demonstrated with other quantitative MRI-techniques.^24,40 Moreover, the inflammatory-like lesions included are still a group of heterogeneous MRI changes that may reflect different pathophysiological changes. Another reason may be the autoantibodies selected for our analysis. In the future, other serum autoantibodies (i.e. anti-ribosomal P or anti-NMDA-receptor) and autoantibodies acquired from cerebrospinal fluid (CSF) may yield stronger associations when associated with quantitative MRI techniques.

Other mechanisms, such as SLE-related and CVD risk factors, showed a correlation with brain-MRI abnormalities in SLE. Cumulative SLE organ-damage measured with SDI was found to be associated with lacunar infarcts in WM, basal ganglia and cerebellum and with cerebral atrophy. Contrary to previous reports, SDI was not related to WMHs.⁴¹ The presence of brain MRI abnormalities in general has been previously related to higher disease severity scores and the need for more aggressive therapy.⁴² Our data suggest that both infarcts and cerebral atrophy are related to chronic SLE-related damage in other organs. Therefore, patients with these brain-MRI abnormalities may have a more severe disease but also more damage due to systemic accelerated atherosclerosis affecting the whole arterial tree, which points to the importance of thrombotic/ischemic nature in leading to SLE-related damage.⁴³ In the general population, the presence of atherosclerosis measured by carotid intima media thickness has been related to an increased risk for brain atrophy.⁴⁴ This accelerated atherogenesis in combination with other factors such as LA and duration of disease may lead to brain infarcts and increased brain atrophy in SLE. Early diagnosis, meticulous monitoring of SLE activity, and effective use of immunosuppressive therapy may help avoid SLE-related organ damage.

Among the CVD risk factors, hypertension was correlated with a higher Fazekas score and lacunar infarcts. A relationship between long-standing hypertension and the presence of WMHs has been also described in a prospective study in a healthy population.⁴⁵ Furthermore, the strongest risk factor for ischemic stroke in the general population is hypertension.⁴⁶ Wiseman et al. recently showed an association between Fazekas score and age and hypertension in SLE patients after unadjusted univariable association.⁴⁷ Our results confirm this association after correcting for multiple confounding factors and even when the influence of the clinical status (non-NP-SLE vs. NP-SLE) was taken into account. Contrary to a previous longitudinal SLE study,¹⁹ correlations between WMHs and aPL or SDI were not found. The different method used to assess WMHs in this previous study, semiautomatic volumetric measurements instead of Fazekas score, may explain these differences. Although hypertension and not antibodies such as aCL seem to play the most important role in the genesis of WMHs, we believe there may be other unknown SLE and non-SLE-related contributing factors leading to WMHs. Compromised BBB integrity has been recently suggested as a contributor to the pathogenesis of WMHs in the healthy population.⁴⁸ Future studies on SLE analyzing if adequate treatment of hypertension may prevent WMHs and atherosclerosis and the contribution of BBB permeability in the pathogenesis of WMHs are warranted.

Some limitations of this study should be taken into account. Due to the characteristics of our cohort and referral nuances, we were not able to measure ultrasound carotid atherosclerosis markers or calculate the cumulative dose of corticosteroids and its effect in the brain could not be investigated. Lumbar puncture is not routinely performed in the patients included in our cohort; therefore, we lack the results of CSF autoantibodies. Another limitation lies in the fact that MRIs were scored by one reader. The cross-sectional study design does not allow an interpretation of temporal or causal relationships. Another limitation may be the use of the visual Fazekas score and Pasquier scale for assessing WMHs and brain atrophy, respectively. Although these are widely used and accepted methods, the use of automated or semi-automated computer programs for quantifying lesion load and volume of WMHs and to assess measures of whole-brain atrophy may be more accurate.

Our study has important strengths. So far, most studies have focused on small groups of NP-SLE patients or on the difference between NP-SLE and SLE patients. On the contrary, we decided to include all SLE patients in the study and focus in the nature of the MRI abnormalities. We have looked into the potential modification role of the NP clinical status in the association between the investigated antibodies and the brain-MRI alterations, which was not confirmed. Furthermore, because MRI abnormalities were probably used to establish an NP-SLE diagnosis, these studies would not avoid a certain level of selection bias and circular reasoning. It is also important to consider that a proportion of patients have abnormal MRI patterns without overt clinical symptoms or a normal MRI while presenting severe NP-SLE.⁴² Thus, we are convinced that including all SLE patients in the study better captures the possible underlying pathophysiological mechanisms of these MRI abnormalities. Another strength of our study is that we assessed all patients with the same high field strength (3T) using a standardized MRI protocol. To date, most studies included MRI-scans performed using different field strengths or using lower field strength (0.5–1.5T).

In summary, there is no indication that the total number or the individual SLE-related autoantibodies are associated with inflammatory-like lesions on the brain-MRI but the total number of aPL, especially the positivity for LA, are associated with ischemic brain changes, mainly with lacunar infarcts and cerebral atrophy. Furthermore, cumulative SLE-organ damage and modifiable CVD risk factors, such as hypertension, contribute to these ischemic changes, pointing to the importance of systemic accelerated atherosclerosis in SLE. We suggest that future studies should focus on CSF and other serum autoantibodies and their relationship with MRI abnormalities. Moreover, the inclusion of quantitative MRI-techniques at this point may help to understand better the underlying pathophysiological processes at a microstructural level.

Supplemental Material

Supplemental material for Are serum autoantibodies associated with brain changes in systemic lupus erythematosus? MRI data from the Leiden NP-SLE cohort

Supplemental Material for Are serum autoantibodies associated with brain changes in systemic lupus erythematosus? MRI data from the Leiden NP-SLE cohort by C. Magro-Checa, S. Kumar, S. Ramiro, L.J. Beaart-van de Voorde, J. Eikenboom, I. Ronen, J de Bresser, M.A van Buchem, T.W. Huizinga and G.M. Steup-Beekman in Lupus

Footnotes

Acknowledgements

We thank all the referral doctors and all members of the Leiden NP-SLE clinic who collected data for this study. We would like to thank Hannelore JL Beaart for her help in the database preparation.

Declaration of conflicting interests

The authors declared no potential conflicts of interest with respect to the research, authorship, and/or publication of this article.

Funding

The authors disclosed receipt of the following financial support for the research, authorship, and/or publication of this article: This work was substantially supported by a project grant from the Dutch Arthritis Foundation (Reumafonds grant 05-1-303).

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