Fatigue in inflammatory rheumatic diseases: current knowledge and areas for future research.


Journal

Nature reviews. Rheumatology
ISSN: 1759-4804
Titre abrégé: Nat Rev Rheumatol
Pays: United States
ID NLM: 101500080

Informations de publication

Date de publication:
11 2021
Historique:
accepted: 27 08 2021
pubmed: 3 10 2021
medline: 16 11 2021
entrez: 2 10 2021
Statut: ppublish

Résumé

Fatigue is a complex phenomenon and an important health concern for many people with chronic inflammatory rheumatic diseases, such as rheumatoid arthritis, psoriatic arthritis, primary Sjögren syndrome and systemic lupus erythematosus. Although some clinical trials have shown the benefits of cognitive behavioural therapy in fatigue management, the effect of this approach is relatively modest, and no curative treatment has been identified. The pathogenesis of fatigue remains unclear. Despite many challenges and limitations, a growing body of research points to roles for the immune system, the central and autonomic nervous systems and the neuroendocrine system in the induction and maintenance of fatigue in chronic diseases. New insights indicate that sleep, genetic susceptibility, metabolic disturbances and other biological and physiological mechanisms contribute to fatigue. Furthermore, understanding of the relationships between psychosocial factors and fatigue is increasing. However, the interrelationships between these diverse mechanisms and fatigue remain poorly defined. In this Review, we outline various biological, physiological and psychosocial determinants of fatigue in inflammatory rheumatic diseases, and propose mechanistic and conceptual models of fatigue to summarize current understanding, stimulate debate and develop further research ideas.

Identifiants

pubmed: 34599320
doi: 10.1038/s41584-021-00692-1
pii: 10.1038/s41584-021-00692-1
doi:

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

651-664

Subventions

Organisme : Medical Research Council
ID : G0800629
Pays : United Kingdom
Organisme : Medical Research Council
ID : MR/J002720/1
Pays : United Kingdom

Informations de copyright

© 2021. Springer Nature Limited.

Références

Dures, E. et al. Patients’ perspectives on the psychological impact of inflammatory arthritis and meeting the associated support needs: open-ended responses in a multi-centre survey. Musculoskeletal Care 15, 175–185 (2017).
pubmed: 27605495 doi: 10.1002/msc.1159
Overman, C. L., Kool, M. B., Da Silva, J. A. P. & Geenen, R. The prevalence of severe fatigue in rheumatic diseases: an international study. Clin. Rheumatol. 35, 409–415 (2016).
pubmed: 26272057 doi: 10.1007/s10067-015-3035-6
Dures, E. et al. “They didn’t tell us, they made us work it out ourselves”: patient perspectives of a cognitive-behavioral program for rheumatoid arthritis fatigue. Arthritis Care Res. 64, 494–501 (2012).
doi: 10.1002/acr.21562
Dures, E. et al. Patient preferences for psychological support in inflammatory arthritis: a multicentre survey. Ann. Rheum. Dis. 75, 142–147 (2016).
pubmed: 25261572 doi: 10.1136/annrheumdis-2014-205636
Swain, M. G. Fatigue in chronic disease. Clin. Sci. 99, 1–8 (2000).
doi: 10.1042/CS19990372
Druce, K. L. & Basu, N. Predictors of fatigue in rheumatoid arthritis. Rheumatology 58 (Suppl. 5), v29–v34 (2019).
pubmed: 31435677 pmcid: 6827266 doi: 10.1093/rheumatology/kez346
Meijer, J. M. et al. Health-related quality of life, employment and disability in patients with Sjögren’s syndrome. Rheumatology 48, 1077–1082 (2009).
pubmed: 19553376 doi: 10.1093/rheumatology/kep141
Westhoff, G., Dörner, T. & Zink, A. Fatigue and depression predict physician visits and work disability in women with primary Sjögren’s syndrome: results from a cohort study. Rheumatology 51, 262–269 (2012).
pubmed: 21705778 doi: 10.1093/rheumatology/ker208
McCormick, N., Marra, C. A., Sadatsafavi, M., Kopec, J. A. & Aviña-Zubieta, J. A. Excess productivity costs of systemic lupus erythematosus, systemic sclerosis, and Sjögren’s Syndrome: a general population-based study. Arthritis Care Res. 71, 142–154 (2019).
doi: 10.1002/acr.23573
Basu, N. et al. Markers for work disability in anti-neutrophil cytoplasmic antibody-associated vasculitis. Rheumatology 53, 953–956 (2014).
pubmed: 24489015 doi: 10.1093/rheumatology/ket483
Borrell-Carrió, F., Suchman, A. L. & Epstein, R. M. The biopsychosocial model 25 years later: principles, practice, and scientific inquiry. Ann. Fam. Med. 2, 576–582 (2004).
pubmed: 15576544 pmcid: 1466742 doi: 10.1370/afm.245
Ng, W.-F. & Bowman, S. J. Primary Sjögren’s syndrome: too dry and too tired. Rheumatology 49, 844–853 (2010).
pubmed: 20147445 doi: 10.1093/rheumatology/keq009
Ahn, G. E. & Ramsey-Goldman, R. Fatigue in systemic lupus erythematosus. Int. J. Clin. Rheumatol. 7, 217–227 (2012).
doi: 10.2217/ijr.12.4
Pope, J. E. Management of fatigue in rheumatoid arthritis. RMD Open 6, e001084 (2020).
pubmed: 32385141 pmcid: 7299512 doi: 10.1136/rmdopen-2019-001084
Korte, S. M. & Straub, R. H. Fatigue in inflammatory rheumatic disorders: pathophysiological mechanisms. Rheumatology 58 (Suppl. 5), v35–v50 (2019).
pubmed: 31682277 pmcid: 6827268 doi: 10.1093/rheumatology/kez413
Hackett, K. L. et al. Impaired functional status in primary Sjogren’s syndrome. Arthritis Care Res. 64, 1760–1764 (2012).
doi: 10.1002/acr.21738
Hewlett, S. et al. Patients’ perceptions of fatigue in rheumatoid arthritis: overwhelming, uncontrollable, ignored. Arthritis Rheum. 53, 697–702 (2005).
pubmed: 16208668 doi: 10.1002/art.21450
Primdahl, J. et al. The experience of people with rheumatoid arthritis living with fatigue: a qualitative metasynthesis. BMJ Open 9, e024338 (2019).
pubmed: 30898808 pmcid: 6475175 doi: 10.1136/bmjopen-2018-024338
Jones, D. E. J., Gray, J. C. & Newton, J. Perceived fatigue is comparable between different disease groups. QJM 102, 617–624 (2009).
pubmed: 19633030 doi: 10.1093/qjmed/hcp091
Jaime-Lara, R. B., Koons, B. C., Matura, L. A., Hodgson, N. A. & Riegel, B. A qualitative metasynthesis of the experience of fatigue across five chronic conditions. J. Pain. Symptom. Manag. 59, 1320–1343 (2020).
doi: 10.1016/j.jpainsymman.2019.12.358
Norheim, K. B., Jonsson, G. & Omdal, R. Biological mechanisms of chronic fatigue. Rheumatology 50, 1009–1018 (2011).
pubmed: 21285230 doi: 10.1093/rheumatology/keq454
Bower, J. E. Cancer-related fatigue — mechanisms, risk factors, and treatments. Nat. Rev. Clin. Oncol. 11, 597–609 (2014).
pubmed: 25113839 pmcid: 4664449 doi: 10.1038/nrclinonc.2014.127
Jhamb, M., Weisbord, S. D., Steel, J. L. & Unruh, M. Fatigue in patients receiving maintenance dialysis: a review of definitions, measures, and contributing factors. Am. J. Kidney Dis. 52, 353–365 (2008).
pubmed: 18572290 pmcid: 2582327 doi: 10.1053/j.ajkd.2008.05.005
James, K. et al. A transcriptional signature of fatigue derived from patients with primary Sjögren’s syndrome. PLoS ONE 10, e0143970 (2015).
pubmed: 26694930 pmcid: 4687914 doi: 10.1371/journal.pone.0143970
Da Costa, D. et al. Dimensions of fatigue in systemic lupus erythematosus: relationship to disease status and behavioral and psychosocial factors. J. Rheumatol. 33, 1282–1288 (2006).
pubmed: 16758508
Bruce, I. N., Mak, V. C., Hallett, D. C., Gladman, D. D. & Urowitz, M. B. Factors associated with fatigue in patients with systemic lupus erythematosus. Ann. Rheum. Dis. 58, 379–381 (1999).
pubmed: 10340963 pmcid: 1752900 doi: 10.1136/ard.58.6.379
Tench, C., McCurdie, I., White, P. & d’Cruz, D. The prevalence and associations of fatigue in systemic lupus erythematosus. Rheumatology 39, 1249–1254 (2000).
pubmed: 11085805 doi: 10.1093/rheumatology/39.11.1249
Azizoddin, D. R. et al. Fatigue in systemic lupus: the role of disease activity and its correlates. Lupus 28, 163–173 (2019).
pubmed: 30580659 doi: 10.1177/0961203318817826
Hewlett, S., Dures, E. & Almeida, C. Measures of fatigue: Bristol Rheumatoid Arthritis Fatigue Multi-Dimensional Questionnaire (BRAF MDQ), Bristol Rheumatoid Arthritis Fatigue Numerical Rating Scales (BRAF NRS) for severity, effect, and coping, Chalder Fatigue Questionnaire (CFQ), Checklist Individual Strength (CIS20R and CIS8R), Fatigue Severity Scale (FSS), Functional Assessment Chronic Illness Therapy (Fatigue) (FACIT-F), Multi-Dimensional Assessment of Fatigue (MAF), Multi-Dimensional Fatigue Inventory (MFI), Pediatric Quality Of Life (PedsQL) Multi-Dimensional Fatigue Scale, Profile of Fatigue (ProF), Short Form 36 Vitality Subscale (SF-36 VT), and Visual Analog Scales (VAS). Arthritis Care Res. 63 (Suppl. 11), S263–S286 (2011).
doi: 10.1002/acr.20579
Santos, E. J. F., Duarte, C., da Silva, J. A. P. & Ferreira, R. J. O. The impact of fatigue in rheumatoid arthritis and the challenges of its assessment. Rheumatology 58 (Suppl. 5), v3–v9 (2019).
pubmed: 31435662 pmcid: 6827262 doi: 10.1093/rheumatology/kez351
Geenen, R. & Dures, E. A biopsychosocial network model of fatigue in rheumatoid arthritis: a systematic review. Rheumatology 58 (Suppl. 5), v10–v21 (2019).
pubmed: 31682275 pmcid: 6827269 doi: 10.1093/rheumatology/kez403
Dantzer, R., O’Connor, J. C., Freund, G. G., Johnson, R. W. & Kelley, K. W. From inflammation to sickness and depression: when the immune system subjugates the brain. Nat. Rev. Neurosci. 9, 46–56 (2008).
pubmed: 18073775 pmcid: 2919277 doi: 10.1038/nrn2297
Lopes, P. C., Block, P. & König, B. Infection-induced behavioural changes reduce connectivity and the potential for disease spread in wild mice contact networks. Sci. Rep. 6, 31790 (2016).
pubmed: 27548906 pmcid: 4993150 doi: 10.1038/srep31790
Muskardin, T. L. W. & Niewold, T. B. Type I interferon in rheumatic diseases. Nat. Rev. Rheumatol. 14, 214–228 (2018).
pubmed: 29559718 pmcid: 6625751 doi: 10.1038/nrrheum.2018.31
Howard Tripp, N. et al. Fatigue in primary Sjögren’s syndrome is associated with lower levels of proinflammatory cytokines. RMD Open 2, e000282 (2016).
pubmed: 27493792 pmcid: 4964201 doi: 10.1136/rmdopen-2016-000282
Umare, V. et al. Effect of proinflammatory cytokines (IL-6, TNF-α, and IL-1β) on clinical manifestations in Indian SLE patients. Mediators Inflamm. 2014, 385297 (2014).
pubmed: 25548434 pmcid: 4273527 doi: 10.1155/2014/385297
Druce, K. L., Bhattacharya, Y., Jones, G. T., Macfarlane, G. J. & Basu, N. Most patients who reach disease remission following anti-TNF therapy continue to report fatigue: results from the British Society for Rheumatology Biologics Register for Rheumatoid Arthritis. Rheumatology 55, 1786–1790 (2016).
pubmed: 27330158 doi: 10.1093/rheumatology/kew241
Tarn, J. R. et al. Symptom-based stratification of patients with primary Sjögren’s syndrome: multi-dimensional characterisation of international observational cohorts and reanalyses of randomised clinical trials. Lancet Rheumatol. 1, e85–e94 (2019).
pmcid: 7134527 doi: 10.1016/S2665-9913(19)30042-6
Lendrem, D. et al. Do the EULAR Sjögren’s syndrome outcome measures correlate with health status in primary Sjögren’s syndrome? Rheumatology 54, 655–659 (2015).
pubmed: 25240612 doi: 10.1093/rheumatology/keu361
Devauchelle-Pensec, V. et al. Improvement of Sjögren’s syndrome after two infusions of rituximab (anti-CD20). Arthritis Care Res. 57, 310–317 (2007).
doi: 10.1002/art.22536
Dass, S. et al. Reduction of fatigue in Sjögren syndrome with rituximab: results of a randomised, double-blind, placebo-controlled pilot study. Ann. Rheum. Dis. 67, 1541–1544 (2008).
pubmed: 18276741 doi: 10.1136/ard.2007.083865
Carubbi, F. et al. Efficacy and safety of rituximab treatment in early primary Sjögren’s syndrome: a prospective, multi-center, follow-up study. Arthritis Res. Ther. 15, R172 (2013).
pubmed: 24286296 pmcid: 3979092 doi: 10.1186/ar4359
St Clair, E. W. et al. Rituximab therapy for primary Sjögren’s Syndrome: an open-label clinical trial and mechanistic analysis. Arthritis Rheum. 65, 1097–1106 (2013).
doi: 10.1002/art.37850
Devauchelle-Pensec, V. et al. Treatment of primary Sjögren syndrome with rituximab: a randomized trial. Ann. Intern. Med. 160, 233–242 (2014).
pubmed: 24727841 doi: 10.7326/M13-1085
Bowman, S. J. et al. Randomized controlled trial of rituximab and cost-effectiveness analysis in treating fatigue and oral dryness in primary Sjögren’s Syndrome. Arthritis Rheumatol. 69, 1440–1450 (2017).
pubmed: 28296257 doi: 10.1002/art.40093
Posada, J. et al. Improvement of severe fatigue following nuclease therapy in patients with primary Sjögren’s syndrome: a randomized clinical trial. Arthritis Rheumatol. 73, 143–150 (2021).
pubmed: 32798283 doi: 10.1002/art.41489
Davies, K. et al. Fatigue in primary Sjögren’s syndrome (pSS) is associated with lower levels of proinflammatory cytokines: a validation study. Rheumatol. Int. 39, 1867–1873 (2019).
pubmed: 31250166 pmcid: 6791914 doi: 10.1007/s00296-019-04354-0
Almeida, C. et al. Biologic interventions for fatigue in rheumatoid arthritis. Cochrane Database Syst. Rev. 2016, CD008334 (2016).
pmcid: 7175833
Pollard, L. C., Choy, E. H., Gonzalez, J., Khoshaba, B. & Scott, D. L. Fatigue in rheumatoid arthritis reflects pain, not disease activity. Rheumatology 45, 885–889 (2006).
pubmed: 16449363 doi: 10.1093/rheumatology/kel021
Navarra, S. V. et al. Efficacy and safety of belimumab in patients with active systemic lupus erythematosus: a randomised, placebo-controlled, phase 3 trial. Lancet 377, 721–731 (2011).
pubmed: 21296403 doi: 10.1016/S0140-6736(10)61354-2
Furie, R. et al. A phase III, randomized, placebo-controlled study of belimumab, a monoclonal antibody that inhibits B lymphocyte stimulator, in patients with systemic lupus erythematosus. Arthritis Rheum. 63, 3918–3930 (2011).
pubmed: 22127708 pmcid: 5007058 doi: 10.1002/art.30613
Bangert, E., Wakani, L., Merchant, M., Strand, V. & Touma, Z. Impact of belimumab on patient-reported outcomes in systemic lupus erythematosus: review of clinical studies. Patient Relat. Outcome Meas. 10, 1–7 (2019).
pubmed: 30666173 pmcid: 6330963 doi: 10.2147/PROM.S134326
Strand, V. et al. Long-term impact of belimumab on health-related quality of life and fatigue in patients with systemic lupus erythematosus: six years of treatment. Arthritis Care Res. 71, 829–838 (2019).
doi: 10.1002/acr.23788
Russell, A. et al. Persistent fatigue induced by interferon-alpha: a novel, inflammation-based, proxy model of chronic fatigue syndrome. Psychoneuroendocrinology 100, 276–285 (2019).
pubmed: 30567628 pmcid: 6350004 doi: 10.1016/j.psyneuen.2018.11.032
Sharpe, M. & Wilks, D. Fatigue. BMJ 325, 480 (2002).
pubmed: 12202331 pmcid: 1124000 doi: 10.1136/bmj.325.7362.480
Taylor, J. L., Amann, M., Duchateau, J., Meeusen, R. & Rice, C. L. Neural contributions to muscle fatigue: from the brain to the muscle and back again. Med. Sci. Sports Exerc. 48, 2294–2306 (2016).
pubmed: 27003703 pmcid: 5033663 doi: 10.1249/MSS.0000000000000923
Quan, N. & Banks, W. A. Brain-immune communication pathways. Brain Behav. Immun. 21, 727–735 (2007).
pubmed: 17604598 doi: 10.1016/j.bbi.2007.05.005
Stetler, R. A. et al. Heat shock proteins: cellular and molecular mechanisms in the central nervous system. Prog. Neurobiol. 92, 184–211 (2010).
pubmed: 20685377 pmcid: 2939168 doi: 10.1016/j.pneurobio.2010.05.002
Elenkov, I. J., Kovács, K., Duda, E., Stark, E. & Vizi, E. Z. Presynaptic inhibitory effect of TNF-alpha on the release of noradrenaline in isolated median eminence. Neuroimmunology 41, 117–120 (1992).
doi: 10.1016/0165-5728(92)90203-W
Yamashita, M. & Yamamoto, T. Tryptophan circuit in fatigue: from blood to brain and cognition. Brain Res. 1675, 116–126 (2017).
pubmed: 28893581 doi: 10.1016/j.brainres.2017.09.002
Åkesson, K. et al. Kynurenine pathway is altered in patients with SLE and associated with severe fatigue. Lupus Sci. Med. 5, e000254 (2018).
pubmed: 29868176 pmcid: 5976103 doi: 10.1136/lupus-2017-000254
Schröcksnadel, K., Wirleitner, B., Winkler, C. & Fuchs, D. Monitoring tryptophan metabolism in chronic immune activation. Clin. Chim. Acta 364, 82–90 (2006).
pubmed: 16139256 doi: 10.1016/j.cca.2005.06.013
Karageorgas, T. et al. Fatigue in primary Sjögren’s syndrome: clinical, laboratory, psychometric, and biologic associations. Arthritis Care Res. 68, 123–131 (2016).
doi: 10.1002/acr.22720
Strasser, B. et al. Effects of exhaustive aerobic exercise on tryptophan-kynurenine metabolism in trained athletes. PLoS ONE 11, e0153617 (2016).
pubmed: 27124720 pmcid: 4849644 doi: 10.1371/journal.pone.0153617
Malhotra, R. et al. Tryptophan and kynurenine levels and its association with sleep, nonphysical fatigue, and depression in chronic hemodialysis patients. J. Ren. Nutr. 27, 260–266 (2017).
pubmed: 28366444 doi: 10.1053/j.jrn.2017.01.024
Larssen, E. et al. Fatigue in primary Sjögren’s syndrome: a proteomic pilot study of cerebrospinal fluid. SAGE Open Med. 7, 2050312119850390 (2019).
pubmed: 31205695 pmcid: 6537061 doi: 10.1177/2050312119850390
Harboe, E. et al. Fatigue in primary Sjögren’s syndrome — a link to sickness behaviour in animals? Brain Behav. Immun. 23, 1104–1108 (2009).
pubmed: 19560535 doi: 10.1016/j.bbi.2009.06.151
Bårdsen, K. et al. Interleukin-1-related activity and hypocretin-1 in cerebrospinal fluid contribute to fatigue in primary Sjögren’s syndrome. J. Neuroinflammation 16, 102 (2019).
pubmed: 31101054 pmcid: 6525358 doi: 10.1186/s12974-019-1502-8
Schrepf, A. et al. A multi-modal MRI study of the central response to inflammation in rheumatoid arthritis. Nat. Commun. 9, 2243 (2018).
pubmed: 29884867 pmcid: 5993749 doi: 10.1038/s41467-018-04648-0
Basu, N. et al. Neural correlates of fatigue in granulomatosis with polyangiitis: a functional magnetic resonance imaging study. Rheumatology 53, 2080–2087 (2014).
pubmed: 24929635 doi: 10.1093/rheumatology/keu243
Kraynak, T. E., Marsland, A. L., Wager, T. D. & Gianaros, P. J. Functional neuroanatomy of peripheral inflammatory physiology: a meta-analysis of human neuroimaging studies. Neurosci. Biobehav. Rev. 94, 76–92 (2018).
pubmed: 30067939 pmcid: 6363360 doi: 10.1016/j.neubiorev.2018.07.013
Goñi, M., Basu, N., Murray, A. D. & Waiter, G. D. Neural indicators of fatigue in chronic diseases: a systematic review of MRI studies. Diagnostics 8, 42 (2018).
pmcid: 6163988 doi: 10.3390/diagnostics8030042
Kutlubaev, M. A., Duncan, F. H. & Mead, G. E. Biological correlates of post-stroke fatigue: a systematic review. Acta Neurol. Scand. 125, 219–227 (2012).
pubmed: 22070461 doi: 10.1111/j.1600-0404.2011.01618.x
Mastorakos, G., Chrousos, G. P. & Weber, J. S. Recombinant interleukin-6 activates the hypothalamic-pituitary-adrenal axis in humans. J. Clin. Endocrinol. Metab. 77, 1690–1694 (1993).
pubmed: 8263159
Tsigos, C. et al. Dose effects of recombinant human interleukin-6 on pituitary hormone secretion and energy expenditure. Neuroendocrinology 66, 54–62 (1997).
pubmed: 9258919 doi: 10.1159/000127219
Johnson, E. O., Vlachoyiannopoulos, P. G., Skopouli, F. N., Tzioufas, A. G. & Moutsopoulos, H. M. Hypofunction of the stress axis in Sjögren’s syndrome. J. Rheumatol. 25, 1508–1514 (1998).
pubmed: 9712092
Crofford, L. J. et al. Circadian relationships between interleukin (IL)-6 and hypothalamic-pituitary-adrenal axis hormones: failure of IL-6 to cause sustained hypercortisolism in patients with early untreated rheumatoid arthritis. J. Clin. Endocrinol. Metab. 82, 1279–1283 (1997).
pubmed: 9100607 doi: 10.1210/jcem.82.4.3852
Straub, R. H., Paimela, L., Peltomaa, R., Schölmerich, J. & Leirisalo-Repo, M. Inadequately low serum levels of steroid hormones in relation to interleukin-6 and tumor necrosis factor in untreated patients with early rheumatoid arthritis and reactive arthritis. Arthritis Rheum. 46, 654–662 (2002).
pubmed: 11920401 doi: 10.1002/art.10177
Gutiérrez, M. A., Garcia, M. E., Rodriguez, J. A., Rivero, S. & Jacobelli, S. Hypothalamic-pituitary-adrenal axis function and prolactin secretion in systemic lupus erythematosus. Lupus 7, 404–408 (1998).
pubmed: 9736324 doi: 10.1191/096120398678920343
Evers, A. W. et al. Does stress affect the joints? Daily stressors, stress vulnerability, immune and HPA axis activity, and short-term disease and symptom fluctuations in rheumatoid arthritis. Ann. Rheum. Dis. 73, 1683–1688 (2014).
pubmed: 23838082 doi: 10.1136/annrheumdis-2012-203143
Jump, R. L. et al. Fatigue in systemic lupus erythematosus: contributions of disease activity, pain, depression, and perceived social support. J. Rheumatol. 32, 1699–1705 (2005).
pubmed: 16142863
Cutolo, M., Sulli, A., Pizzorni, C., Craviotto, C. & Straub, R. H. Hypothalamic-pituitary-adrenocortical and gonadal functions in rheumatoid arthritis. Ann. N. Y. Acad. Sci. 992, 107–117 (2003).
pubmed: 12794051 doi: 10.1111/j.1749-6632.2003.tb03142.x
Moulton, V. R. Sex hormones in acquired immunity and autoimmune disease. Front. Immunol. 9, 2279 (2018).
pubmed: 30337927 pmcid: 6180207 doi: 10.3389/fimmu.2018.02279
Johnson, E. O. & Moutsopoulos, H. M. Neuroendocrine manifestations in Sjögren’s syndrome. Relation to the neurobiology of stress. Ann. N. Y. Acad. Sci. 917, 797–808 (2000).
pubmed: 11268409 doi: 10.1111/j.1749-6632.2000.tb05445.x
Sundman, E. & Olofsson, P. S. Neural control of the immune system. Adv. Physiol. Educ. 38, 135–139 (2014).
pubmed: 25039084 pmcid: 4056170 doi: 10.1152/advan.00094.2013
Porges, S. W. The polyvagal theory: phylogenetic substrates of a social nervous system. Int. J. Psychophysiol. 42, 123–146 (2001).
pubmed: 11587772 doi: 10.1016/S0167-8760(01)00162-3
Brunetta, E. et al. Autonomic abnormalities in patients with primary Sjogren’s syndrome — preliminary results. Front. Physiol. 10, 1104 (2019).
pubmed: 31551801 pmcid: 6736624 doi: 10.3389/fphys.2019.01104
Newton, J. L. et al. Autonomic symptoms are common and are associated with overall symptom burden and disease activity in primary Sjögren’s syndrome. Ann. Rheum. Dis. 71, 1973–1979 (2012).
pubmed: 22562982 doi: 10.1136/annrheumdis-2011-201009
Koh, J. H. et al. Pain, xerostomia, and younger age are major determinants of fatigue in Korean patients with primary Sjögren’s syndrome: a cohort study. Scand. J. Rheumatol. 46, 49–55 (2017).
pubmed: 27098775 doi: 10.3109/03009742.2016.1153142
Mandl, T., Wollmer, P., Manthorpe, R. & Jacobsson, L. T. Autonomic and orthostatic dysfunction in primary Sjögren’s syndrome. J. Rheumatol. 34, 1869–1874 (2007).
pubmed: 17659755
Fox, R. I., Kang, H. I., Ando, D., Abrams, J. & Pisa, E. Cytokine mRNA expression in salivary gland biopsies of Sjögren’s syndrome. J. Immunol. 152, 5532–5539 (1994).
pubmed: 8189070 doi: 10.4049/jimmunol.152.11.5532
Barendregt, P. J. et al. Parasympathetic failure does not contribute to ocular dryness in primary Sjögren’s syndrome. Ann. Rheum. Dis. 58, 746–750 (1999).
pubmed: 10577960 pmcid: 1752817 doi: 10.1136/ard.58.12.746
Kovács, L. et al. Cardiovascular autonomic dysfunction in primary Sjögren’s syndrome. Rheumatology 43, 95–99 (2004).
pubmed: 12949253 doi: 10.1093/rheumatology/keg468
Barendregt, P. J., Tulen, J. H., van den Meiracker, A. H. & Markusse, H. M. Spectral analysis of heart rate and blood pressure variability in primary Sjögren’s syndrome. Ann. Rheum. Dis. 61, 232–236 (2002).
pubmed: 11830428 pmcid: 1754013 doi: 10.1136/ard.61.3.232
Niemelä, R. K., Hakala, M., Huikuri, H. V. & Airaksinen, K. E. Comprehensive study of autonomic function in a population with primary Sjögren’s syndrome. No evidence of autonomic involvement. J. Rheumatol. 30, 74–79 (2003).
pubmed: 12508393
Tumiati, B., Perazzoli, F., Negro, A., Pantaleoni, M. & Regolisti, G. Heart rate variability in patients with Sjögren’s syndrome. Clin. Rheumatol. 19, 477–480 (2000).
pubmed: 11147760 doi: 10.1007/PL00011180
Tarn, J., Legg, S., Mitchell, S., Simon, B. & Ng, W. F. The effects of noninvasive vagus nerve stimulation on fatigue and immune responses in patients with primary Sjögren’s syndrome. Neuromodulation 22, 580–585 (2019).
pubmed: 30328647 doi: 10.1111/ner.12879
Ingegnoli, F. et al. The link between autonomic nervous system and rheumatoid arthritis: from bench to bedside. Front. Med. 7, 589079 (2020).
doi: 10.3389/fmed.2020.589079
Bortoluzzi, A., Silvagni, E., Furini, F., Piga, M. & Govoni, M. Peripheral nervous system involvement in systemic lupus erythematosus: a review of the evidence. Clin. Exp. Rheumatol. 37, 146–155 (2019).
pubmed: 29846158
Stojanovich, L. Autonomic dysfunction in autoimmune rheumatic disease. Autoimmun. Rev. 8, 569–572 (2009).
pubmed: 19393212 doi: 10.1016/j.autrev.2009.01.018
Koopman, F. A. et al. Vagus nerve stimulation inhibits cytokine production and attenuates disease severity in rheumatoid arthritis. Proc. Natl Acad. Sci. USA 113, 8284–8289 (2016).
pubmed: 27382171 pmcid: 4961187 doi: 10.1073/pnas.1605635113
Genovese, M. C. et al. Safety and efficacy of neurostimulation with a miniaturised vagus nerve stimulation device in patients with multidrug-refractory rheumatoid arthritis: a two-stage multicentre, randomised pilot study. Lancet Rheumatol. 2, e527–e538 (2020).
doi: 10.1016/S2665-9913(20)30172-7
Thomas, K. S., Motivala, S., Olmstead, R. & Irwin, M. R. Sleep depth and fatigue: role of cellular inflammatory activation. Brain Behav. Immun. 25, 53–58 (2011).
pubmed: 20656013 doi: 10.1016/j.bbi.2010.07.245
Meerlo, P., Sgoifo, A. & Suchecki, D. Restricted and disrupted sleep: effects on autonomic function, neuroendocrine stress systems and stress responsivity. Sleep Med. Rev. 12, 197–210 (2008).
pubmed: 18222099 doi: 10.1016/j.smrv.2007.07.007
Lewis, I., Hackett, K. L., Ng, W.-F., Ellis, J. & Newton, J. L. A two-phase cohort study of the sleep phenotype within primary Sjögren’s syndrome and its clinical correlates. Clin. Exp. Rheumatol. 37 (Suppl. 118), 78–82 (2019).
pubmed: 31365332
Irwin, M. R. Sleep and inflammation: partners in sickness and in health. Nat. Rev. Immunol. 19, 702–715 (2019).
pubmed: 31289370 doi: 10.1038/s41577-019-0190-z
Guyon, A. et al. Adverse effects of two nights of sleep restriction on the hypothalamic-pituitary-adrenal axis in healthy men. J. Clin. Endocrinol. Metab. 99, 2861–2868 (2014).
pubmed: 24823456 pmcid: 4121029 doi: 10.1210/jc.2013-4254
Grabovac, I. et al. Sleep quality in patients with rheumatoid arthritis and associations with pain, disability, disease duration, and activity. J. Clin. Med. 7, 336 (2018).
pmcid: 6210607 doi: 10.3390/jcm7100336
Sariyildiz, M. A. et al. Sleep quality in rheumatoid arthritis: relationship between the disease severity, depression, functional status and the quality of life. J. Clin. Med. Res. 6, 44–52 (2014).
pubmed: 24400031
Palagini, L. et al. Sleep disorders and systemic lupus erythematosus. Lupus 23, 115–123 (2014).
pubmed: 24421291 doi: 10.1177/0961203313518623
Hackett, K. L. et al. An investigation into the prevalence of sleep disturbances in primary Sjögren’s syndrome: a systematic review of the literature. Rheumatology 56, 570–580 (2017).
pubmed: 28013207
Reinisch, T. & Hinz, H. In Encyclopedic Reference of Genomics and Proteomics in Molecular Medicine (eds Ganten, D. & Ruckpaul, K.) Vol. 9, 919 (Springer, 2006).
Hausladen, A., Privalle, C. T., Keng, T., DeAngelo, J. & Stamler, J. S. Nitrosative stress: activation of the transcription factor OxyR. Cell 86, 719–729 (1996).
pubmed: 8797819 doi: 10.1016/S0092-8674(00)80147-6
Avalos, I. et al. Oxidative stress in systemic lupus erythematosus: relationship to disease activity and symptoms. Lupus 16, 195–200 (2007).
pubmed: 17432105 doi: 10.1177/0961203306075802
Shah, D., Kiran, R., Wanchu, A. & Bhatnagar, A. Oxidative stress in systemic lupus erythematosus: relationship to Th1 cytokine and disease activity. Immunol. Lett. 129, 7–12 (2010).
pubmed: 20105444 doi: 10.1016/j.imlet.2010.01.005
Powers, S. K., Ji, L. L., Kavazis, A. N. & Jackson, M. J. Reactive oxygen species: impact on skeletal muscle. Compr. Physiol. 1, 941–969 (2011).
pubmed: 23737208 pmcid: 3893116 doi: 10.1002/cphy.c100054
Novelli, G. P., Bracciotti, G. & Falsini, S. Spin-trappers and vitamin E prolong endurance to muscle fatigue in mice. Free Radic. Biol. Med. 8, 9–13 (1990).
pubmed: 2323584 doi: 10.1016/0891-5849(90)90138-9
Shindoh, C., DiMarco, A., Thomas, A., Manubay, P. & Supinski, G. Effect of N-acetylcysteine on diaphragm fatigue. J. Appl. Physiol. 68, 2107–2113 (1990).
pubmed: 2361912 doi: 10.1152/jappl.1990.68.5.2107
Dassouki, T. et al. Objectively measured physical activity and its influence on physical capacity and clinical parameters in patients with primary Sjögren’s syndrome. Lupus 26, 690–697 (2017).
pubmed: 27798360 doi: 10.1177/0961203316674819
Miyamoto, S. T. et al. Supervised walking improves cardiorespiratory fitness, exercise tolerance, and fatigue in women with primary Sjogren’s syndrome: a randomized-controlled trial. Rheumatol. Int. 39, 227–238 (2019).
pubmed: 30604204 doi: 10.1007/s00296-018-4213-z
Ng, W. F. et al. Physical activity but not sedentary activity is reduced in primary Sjogren’s syndrome. Rheumatol. Int. 37, 623–631 (2017).
pubmed: 28013357 doi: 10.1007/s00296-016-3637-6
Wouters, E. J. M. et al. Physical activity and physical activity cognitions are potential factors maintaining fatigue in patients with primary Sjögren’s syndrome. Ann. Rheum. Dis. 71, 668–673 (2012).
pubmed: 22121127 doi: 10.1136/ard.2011.154245
Keyser, R. E. et al. Evidence for aerobic insufficiency in women with systemic lupus erythematosus. Arthritis Rheum. 49, 16–22 (2003).
pubmed: 12579589 doi: 10.1002/art.10926
Metsios, G. S. et al. Cardiorespiratory fitness levels and their association with cardiovascular profile in patients with rheumatoid arthritis: a cross-sectional study. Rheumatology 54, 2215–2220 (2015).
pubmed: 26209790
Løppenthin, K. et al. Physical activity and the association with fatigue and sleep in Danish patients with rheumatoid arthritis. Rheumatol. Int. 35, 1655–1664 (2015).
pubmed: 25947325 doi: 10.1007/s00296-015-3274-5
Rongen-van Dartel, S. A. et al. Effect of aerobic exercise training on fatigue in rheumatoid arthritis: a meta-analysis. Arthritis Care Res. 67, 1054–1062 (2015).
doi: 10.1002/acr.22561
Cramp, F. The role of non-pharmacological interventions in the management of rheumatoid-arthritis-related fatigue. Rheumatology 58 (Suppl. 5), v22–v28 (2019).
pubmed: 31682276 pmcid: 6827265 doi: 10.1093/rheumatology/kez310
Cramp, F. et al. Non-pharmacological interventions for fatigue in rheumatoid arthritis. Cochrane Database Syst. Rev. 8, CD008322 (2013).
Robb-Nicholson, L. C. et al. Effects of aerobic conditioning in lupus fatigue: a pilot study. Rheumatology 28, 500–505 (1989).
doi: 10.1093/rheumatology/28.6.500
Tench, C., McCarthy, J., McCurdie, I., White, P. & D’Cruz, D. Fatigue in systemic lupus erythematosus: a randomized controlled trial of exercise. Rheumatology 42, 1050–1054 (2003).
pubmed: 12730519 doi: 10.1093/rheumatology/keg289
Andonian, B. J. & Huffman, K. M. Skeletal muscle disease in rheumatoid arthritis: the center of cardiometabolic comorbidities? Curr. Opin. Rheumatol. 32, 297–306 (2020).
pubmed: 32141950 doi: 10.1097/BOR.0000000000000697
An, H. J. et al. Sarcopenia in autoimmune and rheumatic diseases: a comprehensive review. Int. J. Mol. Sci. 21, 5678 (2020).
pmcid: 7461030 doi: 10.3390/ijms21165678
Lindvall, B., Bengtsson, A., Ernerudh, J. & Eriksson, P. Subclinical myositis is common in primary Sjögren’s syndrome and is not related to muscle pain. J. Rheumatol. 29, 717–725 (2002).
pubmed: 11950012
Baker, J. F. et al. Deficits in muscle mass, muscle density, and modified associations with fat in rheumatoid arthritis. Arthritis Care Res. 66, 1612–1618 (2014).
doi: 10.1002/acr.22328
Caimmi, C. et al. Malnutrition and sarcopenia in a large cohort of patients with systemic sclerosis. Clin. Rheumatol. 37, 987–997 (2018).
pubmed: 29196890 doi: 10.1007/s10067-017-3932-y
Tournadre, A., Pereira, B., Gossec, L., Soubrier, M. & Dougados, M. Impact of comorbidities on fatigue in rheumatoid arthritis patients: results from a nurse-led program for comorbidities management (COMEDRA). Joint Bone Spine 86, 55–60 (2019).
pubmed: 30025953 doi: 10.1016/j.jbspin.2018.06.010
Feldthusen, C., Grimby-Ekman, A., Forsblad-d’Elia, H., Jacobsson, L. & Mannerkorpi, K. Explanatory factors and predictors of fatigue in persons with rheumatoid arthritis: a longitudinal study. J. Rehabil. Med. 48, 469–476 (2016).
pubmed: 27097684 doi: 10.2340/16501977-2090
Katz, P. et al. Role of sleep disturbance, depression, obesity, and physical inactivity in fatigue in rheumatoid arthritis. Arthritis Care Res. 68, 81–90 (2016).
doi: 10.1002/acr.22577
Chaiamnuay, S. et al. The impact of increased body mass index on systemic lupus erythematosus: data from LUMINA, a multiethnic cohort (LUMINA XLVI) [corrected]. J. Clin. Rheumatol. 13, 128–133 (2007).
pubmed: 17551377 doi: 10.1097/RHU.0b013e3180645865
Oeser, A., Chung, C. P., Asanuma, Y., Avalos, I. & Stein, C. M. Obesity is an independent contributor to functional capacity and inflammation in systemic lupus erythematosus. Arthritis Rheum. 52, 3651–3659 (2005).
pubmed: 16258902 doi: 10.1002/art.21400
Pajoutan, M., Ghesmaty Sangachin, M. & Cavuoto, L. A. Central and peripheral fatigue development in the shoulder muscle with obesity during an isometric endurance task. BMC Musculoskelet. Disord. 18, 314 (2017).
pubmed: 28732481 pmcid: 5521062 doi: 10.1186/s12891-017-1676-0
Osborn, O. & Olefsky, J. M. The cellular and signaling networks linking the immune system and metabolism in disease. Nat. Med. 18, 363–374 (2012).
pubmed: 22395709 doi: 10.1038/nm.2627
Matcham, F., Rayner, L., Steer, S. & Hotopf, M. The prevalence of depression in rheumatoid arthritis: a systematic review and meta-analysis. Rheumatology 52, 2136–2148 (2013).
pubmed: 24003249 pmcid: 3828510 doi: 10.1093/rheumatology/ket169
Gold, S. M. et al. Comorbid depression in medical diseases. Nat. Rev. Dis. Prim. 6, 69 (2020).
pubmed: 32820163 doi: 10.1038/s41572-020-0200-2
Hackett, K. L. et al. Pain and depression are associated with both physical and mental fatigue independently of comorbidities and medications in primary Sjögren’s syndrome. RMD Open 5, e000885 (2019).
pubmed: 31168409 pmcid: 6525628 doi: 10.1136/rmdopen-2018-000885
Wilson, N., Lee, J. J. & Bei, B. Postpartum fatigue and depression: a systematic review and meta-analysis. J. Affect. Disord. 246, 224–233 (2019).
pubmed: 30584956 doi: 10.1016/j.jad.2018.12.032
World Health Organisation. ICD-10 classification of mental and behavioural disorders (WHO, 2016).
Nerurkar, L., Siebert, S., McInnes, I. B. & Cavanagh, J. Rheumatoid arthritis and depression: an inflammatory perspective. Lancet Psychiatry 6, 164–173 (2019).
pubmed: 30366684 doi: 10.1016/S2215-0366(18)30255-4
Bårdsen, K. et al. Heat shock proteins and chronic fatigue in primary Sjögren’s syndrome. Innate Immun. 22, 162–167 (2016).
pubmed: 26921255 doi: 10.1177/1753425916633236
Mondelli, V. & Vernon, A. C. From early adversities to immune activation in psychiatric disorders: the role of the sympathetic nervous system. Clin. Exp. Immunol. 197, 319–328 (2019).
pubmed: 31319436 pmcid: 6694015 doi: 10.1111/cei.13351
Rossi, S. et al. Neuroinflammation drives anxiety and depression in relapsing-remitting multiple sclerosis. Neurology 89, 1338–1347 (2017).
pubmed: 28842450 doi: 10.1212/WNL.0000000000004411
Omdal, R., Mellgren, S. I. & Norheim, K. B. Pain and fatigue in primary Sjögren’s syndrome. Rheumatology https://doi.org/10.1093/rheumatology/kez027 (2019).
doi: 10.1093/rheumatology/kez027 pubmed: 30815693
Nichilatti, L. P., Fernandes, J. M. & Marques, C. P. Physiopathology of pain in systemic erythematosus lupus. Lupus 29, 721–726 (2020).
pubmed: 32323601 doi: 10.1177/0961203320919872
Morgan, C., Bland, A. R., Maker, C., Dunnage, J. & Bruce, I. N. Individuals living with lupus: findings from the LUPUS UK Members Survey 2014. Lupus 27, 681–687 (2018).
pubmed: 29310537 pmcid: 5888773 doi: 10.1177/0961203317749746
Sanderson, T., Morris, M., Calnan, M., Richards, P. & Hewlett, S. Patient perspective of measuring treatment efficacy: the rheumatoid arthritis patient priorities for pharmacologic interventions outcomes. Arthritis Care Res. 62, 647–656 (2010).
doi: 10.1002/acr.20151
Bower, J. E. Behavioral symptoms in patients with breast cancer and survivors. J. Clin. Oncol. 26, 768–777 (2008).
pubmed: 18258985 doi: 10.1200/JCO.2007.14.3248
Treharne, G. J. et al. Predictors of fatigue over 1 year among people with rheumatoid arthritis. Psychol. Health Med. 13, 494–504 (2008).
pubmed: 18825587 doi: 10.1080/13548500701796931
Camacho, E. M., Verstappen, S. M., Chipping, J. & Symmons, D. P. Learned helplessness predicts functional disability, pain and fatigue in patients with recent-onset inflammatory polyarthritis. Rheumatology 52, 1233–1238 (2013).
pubmed: 23424265 pmcid: 3685331 doi: 10.1093/rheumatology/kes434
Jacobsen, P. B., Andrykowski, M. A. & Thors, C. L. Relationship of catastrophizing to fatigue among women receiving treatment for breast cancer. J. Consult. Clin. Psychol. 72, 355–361 (2004).
pubmed: 15065968 pmcid: 2562276 doi: 10.1037/0022-006X.72.2.355
Segal, B. M. et al. Pain in primary Sjögren syndrome: the role of catastrophizing and negative illness perceptions. Scand. J. Rheumatol. 43, 234–241 (2014).
pubmed: 24392761 doi: 10.3109/03009742.2013.846409
Hewlett, S. et al. Reducing arthritis fatigue impact: two-year randomised controlled trial of cognitive behavioural approaches by rheumatology teams (RAFT). Ann. Rheum. Dis. 78, 465–472 (2019).
pubmed: 30793700 doi: 10.1136/annrheumdis-2018-214469
Sanada, K. et al. Effects of mindfulness-based interventions on biomarkers and low-grade inflammation in patients with psychiatric disorders: a meta-analytic review. Int. J. Mol. Sci. 21, 2484 (2020).
pmcid: 7177919 doi: 10.3390/ijms21072484
Nadarajah, M. & Goh, H. T. Post-stroke fatigue: a review on prevalence, correlates, measurement, and management. Top. Stroke Rehabil. 22, 208–220 (2015).
pubmed: 25779764 doi: 10.1179/1074935714Z.0000000015
Sterling, P. Allostasis: a model of predictive regulation. Physiol. Behav. 106, 5–15 (2012).
pubmed: 21684297 doi: 10.1016/j.physbeh.2011.06.004
Smets, E. M., Garssen, B., Bonke, B. & De Haes, J. C. The Multidimensional Fatigue Inventory (MFI) psychometric qualities of an instrument to assess fatigue. J. Psychom. Res. 39, 315–325 (1995).
doi: 10.1016/0022-3999(94)00125-O
Chorus, A. M., Miedema, H. S., Boonen, A. & van der Linden, S. Quality of life and work in patients with rheumatoid arthritis and ankylosing spondylitis of working age. Ann. Rheum. Dis. 62, 1178–1184 (2003).
pubmed: 14644855 pmcid: 1754383 doi: 10.1136/ard.2002.004861
Barendregt, P. J. et al. Fatigue in primary Sjögren’s syndrome. Ann. Rheum. Dis. 57, 291–295 (1998).
pubmed: 9741313 pmcid: 1752605 doi: 10.1136/ard.57.5.291
Evers, A. W., Kraaimaat, F. W., Geenen, R., Jacobs, J. W. & Bijlsma, J. W. Stress-vulnerability factors as long-term predictors of disease activity in early rheumatoid arthritis. J. Psychosom. Res. 55, 293–302 (2003).
pubmed: 14507538 doi: 10.1016/S0022-3999(02)00632-3
Zautra, A. J., Fasman, R., Parish, B. P. & Davis, M. C. Daily fatigue in women with osteoarthritis, rheumatoid arthritis, and fibromyalgia. Pain 128, 128–135 (2007).
pubmed: 17055648 doi: 10.1016/j.pain.2006.09.004
Drewes, A. M. Pain and sleep disturbances with special reference to fibromyalgia and rheumatoid arthritis. Rheumatology 38, 1035–1038 (1999).
pubmed: 10556252 doi: 10.1093/rheumatology/38.11.1035

Auteurs

Kristen Davies (K)

Translational and Clinical Research Institute, Newcastle University and NIHR Newcastle Biomedical Research Centre, Newcastle upon Tyne, UK.
Newcastle upon Tyne Hospitals NHS Foundation Trust, Newcastle Upon Tyne, UK.

Emma Dures (E)

Academic Rheumatology, Bristol Royal Infirmary, Bristol, UK.
Faculty of Health and Applied Sciences, University of the West of England, Bristol, UK.

Wan-Fai Ng (WF)

Translational and Clinical Research Institute, Newcastle University and NIHR Newcastle Biomedical Research Centre, Newcastle upon Tyne, UK. wan-fai.ng@ncl.ac.uk.
Newcastle upon Tyne Hospitals NHS Foundation Trust, Newcastle Upon Tyne, UK. wan-fai.ng@ncl.ac.uk.

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