Neuropsychiatric symptoms in Systemic Lupus Erythematosus : mixed methods analysis of patient-derived attributional evidence in the international INSPIRE project
© The Author(s) 2024. Published by Oxford University Press on behalf of the British Society for Rheumatology..
OBJECTIVE: Attribution of neuropsychiatric symptoms in systemic lupus erythematosus (SLE) relies heavily on clinician assessment. Limited clinic time, variable knowledge, and symptom under-reporting contributes to discordance between clinician assessments and patient symptoms. We obtained attributional data directly from patients and clinicians in order to estimate and compare potential levels of direct attribution to SLE of multiple neuropsychiatric symptoms using different patient-derived measures.
METHODS: Quantitative and qualitative data analysed included: prevalence and frequency of neuropsychiatric symptoms, response to corticosteroids, and concurrence of neuropsychiatric symptoms with non-neuropsychiatric SLE disease activity. SLE patients were also compared with controls and inflammatory arthritis (IA) patients to explore attributability of neuropsychiatric symptoms to the direct disease effects on the brain/nervous system.
RESULTS: We recruited 2,817 participants, including 400 clinicians. SLE patients (n = 609) reported significantly higher prevalences of neuropsychiatric symptoms than controls (n = 463) and IA patients (n = 489). SLE and IA patients' quantitative data demonstrated multiple neuropsychiatric symptoms relapsing/remitting with other disease symptoms such as joint pain. Over 45% of SLE patients reported resolution/improvement of fatigue, positive sensory symptoms, severe headache, and cognitive dysfunction with corticosteroids. Evidence of direct attributability in SLE was highest for hallucinations and severe headache. SLE patients had greater reported improvement from corticosteroids (p= 0.008), and greater relapsing-remitting with disease activity (p< 0.001) in the comparisons with IA patients for severe headache. Clinician and patients reported insufficient time to discuss patient-reported attributional evidence. Symptoms viewed as indirectly related/non-attributable were often less prioritised for discussion and treatment.
CONCLUSION: We found evidence indicating varying levels of direct attributability of both common and previously unexplored neuropsychiatric symptoms in SLE patients, with hallucinations and severe headache assessed as the most directly attributable. There may also be-currently under-estimated-direct effects on the nervous system in IA and other systemic rheumatological diseases.
| Medienart: |
E-Artikel |
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| Erscheinungsjahr: |
2024 |
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| Erschienen: |
2024 |
| Enthalten in: |
Zur Gesamtaufnahme - year:2024 |
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| Enthalten in: |
Rheumatology (Oxford, England) - (2024) vom: 22. März |
| Sprache: |
Englisch |
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| Beteiligte Personen: |
Sloan, Melanie [VerfasserIn] |
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| Links: |
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| Anmerkungen: |
Date Revised 22.03.2024 published: Print-Electronic Citation Status Publisher |
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| doi: |
10.1093/rheumatology/keae194 |
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| Förderinstitution / Projekttitel: |
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| PPN (Katalog-ID): |
NLM370076664 |
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| 100 | 1 | |a Sloan, Melanie |e verfasserin |4 aut | |
| 245 | 1 | 0 | |a Neuropsychiatric symptoms in Systemic Lupus Erythematosus |b mixed methods analysis of patient-derived attributional evidence in the international INSPIRE project |
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| 500 | |a Date Revised 22.03.2024 | ||
| 500 | |a published: Print-Electronic | ||
| 500 | |a Citation Status Publisher | ||
| 520 | |a © The Author(s) 2024. Published by Oxford University Press on behalf of the British Society for Rheumatology. | ||
| 520 | |a OBJECTIVE: Attribution of neuropsychiatric symptoms in systemic lupus erythematosus (SLE) relies heavily on clinician assessment. Limited clinic time, variable knowledge, and symptom under-reporting contributes to discordance between clinician assessments and patient symptoms. We obtained attributional data directly from patients and clinicians in order to estimate and compare potential levels of direct attribution to SLE of multiple neuropsychiatric symptoms using different patient-derived measures | ||
| 520 | |a METHODS: Quantitative and qualitative data analysed included: prevalence and frequency of neuropsychiatric symptoms, response to corticosteroids, and concurrence of neuropsychiatric symptoms with non-neuropsychiatric SLE disease activity. SLE patients were also compared with controls and inflammatory arthritis (IA) patients to explore attributability of neuropsychiatric symptoms to the direct disease effects on the brain/nervous system | ||
| 520 | |a RESULTS: We recruited 2,817 participants, including 400 clinicians. SLE patients (n = 609) reported significantly higher prevalences of neuropsychiatric symptoms than controls (n = 463) and IA patients (n = 489). SLE and IA patients' quantitative data demonstrated multiple neuropsychiatric symptoms relapsing/remitting with other disease symptoms such as joint pain. Over 45% of SLE patients reported resolution/improvement of fatigue, positive sensory symptoms, severe headache, and cognitive dysfunction with corticosteroids. Evidence of direct attributability in SLE was highest for hallucinations and severe headache. SLE patients had greater reported improvement from corticosteroids (p= 0.008), and greater relapsing-remitting with disease activity (p< 0.001) in the comparisons with IA patients for severe headache. Clinician and patients reported insufficient time to discuss patient-reported attributional evidence. Symptoms viewed as indirectly related/non-attributable were often less prioritised for discussion and treatment | ||
| 520 | |a CONCLUSION: We found evidence indicating varying levels of direct attributability of both common and previously unexplored neuropsychiatric symptoms in SLE patients, with hallucinations and severe headache assessed as the most directly attributable. There may also be-currently under-estimated-direct effects on the nervous system in IA and other systemic rheumatological diseases | ||
| 650 | 4 | |a Journal Article | |
| 650 | 4 | |a CNS lupus | |
| 650 | 4 | |a NPSLE | |
| 650 | 4 | |a Neuropsychiatric lupus | |
| 650 | 4 | |a SLE | |
| 650 | 4 | |a attribution | |
| 650 | 4 | |a autoimmunity | |
| 650 | 4 | |a biopsychosocial | |
| 650 | 4 | |a diagnosis | |
| 650 | 4 | |a inflammatory arthritis | |
| 650 | 4 | |a mental health | |
| 650 | 4 | |a misattribution | |
| 650 | 4 | |a patient-clinician interactions | |
| 650 | 4 | |a rheumatology | |
| 700 | 1 | |a Pollak, Thomas A |e verfasserin |4 aut | |
| 700 | 1 | |a Massou, Efthalia |e verfasserin |4 aut | |
| 700 | 1 | |a Leschziner, Guy |e verfasserin |4 aut | |
| 700 | 1 | |a Andreoli, Laura |e verfasserin |4 aut | |
| 700 | 1 | |a Harwood, Rupert |e verfasserin |4 aut | |
| 700 | 1 | |a Bosley, Michael |e verfasserin |4 aut | |
| 700 | 1 | |a Pitkanen, Mervi |e verfasserin |4 aut | |
| 700 | 1 | |a Diment, Wendy |e verfasserin |4 aut | |
| 700 | 1 | |a Bortoluzzi, Alessandra |e verfasserin |4 aut | |
| 700 | 1 | |a Zandi, Michael S |e verfasserin |4 aut | |
| 700 | 1 | |a Ubhi, Mandeep |e verfasserin |4 aut | |
| 700 | 1 | |a Gordon, Caroline |e verfasserin |4 aut | |
| 700 | 1 | |a Jayne, David |e verfasserin |4 aut | |
| 700 | 1 | |a Naughton, Felix |e verfasserin |4 aut | |
| 700 | 1 | |a Barrere, Colette |e verfasserin |4 aut | |
| 700 | 1 | |a Wincup, Chris |e verfasserin |4 aut | |
| 700 | 1 | |a Brimicombe, James |e verfasserin |4 aut | |
| 700 | 1 | |a Bourgeois, James A |e verfasserin |4 aut | |
| 700 | 1 | |a D'Cruz, David |e verfasserin |4 aut | |
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