The prevalence of comorbid and concomitant diseases in psoriatic arthritis patients, data from Russian register
https://doi.org/10.47360/1995-4484-2021-275-281
Abstract
Psoriatic arthritis (PsA) is a heterogeneous inflammatory arthritis associated with psoriasis (Ps); it belongs to the group of spondyloarthritis and is accompanied by damage to both the spine and peripheral joints, as well as the development of enteritis and dactylitis.
In addition to skin and joint damage, PsA has numerous comorbid conditions that are pathogenetically related to the underlying disease, such as inflammatory bowel disease (IBD) and autoimmune eye disease, as well as cardiovascular diseases, obesity and metabolic syndrome, diabetes, osteoporosis, malignancies, mental disorders, and various concomitant diseases. We present data of the prevalence of these pathological conditions among the cohort of PsA patients included in the Russian register.
Objective – to study the prevalence of comorbid and concomitant diseases in PsA patients.
Materials and methods. The Russian multicenter, observational study with retrospective and prospective data collection of PsA patients included 614 patients with the established diagnosis psoriatic arthritis, corresponding to the CASPAR criteria, from 39 subjects of the Russian Federation, female/male – 331 (54%)/283 (46%). The average age was 45.2±0.52 years, duration of PsA – 5.7±0.27 years, Ps – 15.71±0.56. Duration of observation period: January 2016 – November 26, 2019. The diagnosis of comorbid and concomitant diseases was confirmed by medical specialists in accordance with the ICD-10 code. The analysis of the frequency and structure (%) of these diseases was carried out.
Results. The majority of PsA patients had limited Ps: the area of Ps skin lesion (BSA, Basic Surface Area) was less than 3% in 372 (61.5%) patients, BSA from 3% to 10% – in 185 (30.6%), BSA>10% – in 47 (7.8%). Comorbid and concomitant diseases were detected in 297 (48%) of 614 patients. 183 (61.6%) patients had 2 or more diseases in addition to Ps and PsA.
Diseases of the circulatory system were detected in 229 (77.1%) PsA patients with comorbid and concomitant diseases (arterial hypertension – in 194 (65.3%), coronary heart disease – in 22 (7.4%)). Diseases of the endocrine system, metabolic disorders were detected in 156 (52.5%) patients with PsA (diabetes mellitus in 44 (14.8%), hyperlipidemia in 44 (14.8%), metabolic syndrome in 36 (12.1%), obesity in 7 (2.4%), and others). Gastrointestinal diseases were observed in 62 (20.9%) patients. Diseases of the biliary system – in 33 (11.1%) patients. Diseases of the musculoskeletal system and connective tissue that are not associated with PsA – in 44 (14.8%). Diseases of the genitourinary system – in 23 (7.7%) patients. Respiratory diseases – in 17 (5.7%) patients. Infectious diseases – in 11 (3.7%). Eye diseases were detected – in 10 (3.4%) patients. Hematological diseases were diagnosed in 6 (2.0%) patients. Depression – in 4 (1.3%) patients.
Conclusions. Among 297 patients with PsA with comorbid and concomitant diseases, diseases of the circulatory system are the most common (in 77.1%), less often – diseases of the endocrine system, metabolic disorders (in 52.5%) and diseases of the digestive system (in 32%). Uveitis (2.7%), IBD (1.3%), and depression (1.3%) were rarely detected in our cohort. The majority of patients in the Russian registry had mild forms of Ps (61.5%), and severe Ps (BSA>10%) was observed only in 7.8%.
Thus, PsA is associated with a high prevalence of comorbid and concomitant diseases, especially cardiovascular. When choosing a treatment, these diseases should be taken into account. In connection with the new possibilities of therapy, it is necessary to evaluate the potential impact of therapy on patients with comorbid and concomitant diseases in real clinical practice.
About the Authors
Yu. L. KorsakovaRussian Federation
115522, Moscow, Kashirskoye Highway, 34A
T. V. Korotaeva
Russian Federation
115522, Moscow, Kashirskoye Highway, 34A
E. Yu. Loginova
Russian Federation
115522, Moscow, Kashirskoye Highway, 34A
E. E. Gubar
Russian Federation
115522, Moscow, Kashirskoye Highway, 34A
E. A. Vasilenko
Russian Federation
191015, Saint-Petersburg, Kirochnaya str., 41
A. A. Vasilenko
Russian Federation
173008, Veliky Novgorod, Pavla Levitta str., 14
N. A. Kuznetsova
Russian Federation
620102, Yekaterinburg, Volgogradskaya str., 189
I. M. Patrikeeva
Russian Federation
625023, Tyumen, Kotovskogo str., 55
E. L. Nasonov
Russian Federation
115522, Moscow, Kashirskoye Highway, 34A;
119991, Moscow, Trubetskaya str., 8, building 2
References
1. Haddad A, Zisman D. Comorbidities in patients with psoriatic arthritis. Rambam Maimonides Med J. 2017;8(1):e0004. doi: 10.5041/RMMJ.10279
2. Taylor W, Gladman D, Helliwell P, Marchesoni A, Mease P, Mielants H, et al. Classification criteria for psoriatic arthritis: Development of new criteria from a large international study. Arthritis Rheum. 2006;54:2665-2673. doi: 10.1002/art.21972
3. Alinaghi F, Calov M, Kristensen LE, Gladman DD, Coates LC, Jullien D, et al. Prevalence of psoriatic arthritis in patients with psoriasis: A systematic review and meta-analysis of observational and clinical studies. J Am Acad Dermatol. 2019;80:251-265. doi: 10.1016/j.jaad.2018.06.027
4. Batkaeva NV, Korotaeva TV, Batkaev EA. Prevalence of psoriatic arthritis and comorbidities in patients with severe psoriasis: Data of a retrospective analysis of a hospital cohort. Modern Rheumatology Journal. 2017;11(1):19-22 (In Russ.). doi: 10.14412/1996-7012-2017-1-19-22
5. Kraemer HC. Statistical issues in assessing comorbidity. Stat Med. 1995;14:721-723. doi: 10.1002/sim.4780140803
6. van den Akker M, Buntinx F, Knottnerus JA. Comorbidity or multimorbidity: What’s in a name? A review of the literature. Eur J Gen Pract. 1996;2(2):65-70. doi: 10.3109/13814789609162146
7. Ogdie A, Yu Y, Haynes K, Love TJ, Maliha S, Jiang Y, et al. Risk of major cardiovascular events in patients with psoriatic arthritis, psoriasis and rheumatoid arthritis: A population-based cohort study. Ann Rheum Dis. 2015;74(2):326-332. doi: 10.1136/annrheumdis-2014-205675
8. Husni ME, Mease PJ. Managing comorbid disease in patients with psoriatic arthritis. Curr Rheumatol Rep. 2010;12(4):281-287. doi: 10.1007/s11926-010-0112-3
9. Gudu T, Peltea A, Abobului M, Balanescu A, Berghea F, Bojinca V, et al. Prevalence of comorbidities in psoriatic arthritis: a cross-sectional study. Ann Rheum Dis. 2017;76(Suppl 2):1460.2-1460. doi: 10.1136/annrheumdis-2017-eular.5838
10. Gladman DD, Coates LC, Jadon DR, Tillett W, Mease PJ, Vis M. The benefits and challenges of setting up a longitudinal psoriatic arthritis database. J Rheumatol Suppl. 2018;94:26-29. doi: 10.3899/jrheum.180132
11. Baillet A, Gossec L, Carmona L, Wit Md, van Eijk-Hustings Y, Bertheussen H, et al. Points to consider for reporting, screening for and preventing selected comorbidities in chronic inflammatory rheumatic diseases in daily practice: a EULAR initiative. Ann Rheum Dis. 2016;75(6):965-973. doi: 10.1136/annrheumdis-2016-209233
12. Kaine J, Song X, Kim G, Hur P, Palmer JB. Higher incidence rates of comorbidities in patients with psoriatic arthritis compared with the general population using US. Administrative Claims Data. J Manag Care Spec Pharm. 2019;25:122-132. doi: 10.18553/jmcp.2018.17421
13. Ballegaard C, Højgaard P, Dreyer L. Cordtz R, Jørgensen TS, Skougaard M, et al. Impact of comorbidities on tumor necrosis factor inhibitor therapy in psoriatic arthritis: A population-based cohort study. Arthritis Care Res (Hoboken). 2018;70(4):592-599. doi: 10.1002/acr.23333
14. Højgaard P, Glintborg B, Kristensen LE, Gudbjornsson B, Love TJ, Dreyer L. The influence of obesity on response to tumour necrosis factor-α inhibitors in psoriatic arthritis: Results from the DANBIO and ICEBIO registries. Rheumatology (Oxford). 2016;55(12):2191-2199. doi: 10.1093/rheumatology/kew326
15. Nissen CB, Hørslev-Petersen K, Primdahl J. Cardiovascular risk profiles in a hospital-based population of patients with psoriatic arthritis and ankylosing spondylitis: a cross-sectional study. Rheumatol Int. 2017;37(1):113-120. doi: 10.1007/s00296-016-3614-0
16. Hellgren K, Dreyer L, Arkema EV, Glintborg B, Jacobsson LT, Kristensen LE, et al. Cancer risk in patients with spondyloarthritis treated with TNF inhibitors: a collaborative study from the ARTIS and DANBIO register. Ann Rheum Dis. 2017;76(1):105-111. doi: 10.1136/annrheumdis-2016-209270
17. Labitigan M, Bahče-Altuntas A, Kremer JM, Reed G, Greenberg JD, Jordan N, et al. Higher rates and clustering of abnormal lipids, obesity, and diabetes mellitus in psoriatic arthritis compared with rheumatoid arthritis. Arthritis Care Res (Hoboken). 2014;66:600-607. doi: 10.1002/acr.22185
18. Johnsson H, McInnes IB, Sattar N. Cardiovascular and metabolic risks in psoriasis and psoriatic arthritis: pragmatic clinical management based on available evidence. Ann Rheum Dis. 2012;71:480-483. doi: 10.1136/annrheumdis-2011-200567
19. Coto-Segura P, Eiris-Salvado N, Gonzalez-Lara L, Queiro-Silva R, Martinez-Camblor P, Maldonado-Seral C, et al. Psoriasis, psoriatic arthritis and type 2 diabetes mellitus: A systematic review and meta-analysis. Br J Dermatol. 2013;169:783-793. doi: 10.1111/bjd.12473
20. Armstrong AW, Guérin A, Sundaram M, Wu EQ, Faust ES, Ionescu-Ittu R, et al. Psoriasis and risk of diabetes-associated micro-vascular and macrovascular complications. J Am Acad Dermatol. 2015;72:968–977.e2. doi: 10.1016/j.jaad.2015.02.1095
21. Haroon M, Gallagher P, Heffernan E, FitzGerald O. High prevalence of metabolic syndrome and of insulin resistance in psoriatic arthritis is associated with the severity of underlying disease. J Rheumatol. 2014;41:1357-1365. doi: 10.3899/jrheum.140021
22. Tam LS, Tomlinson B, Chu TT, Li M, Leung YY, Kwok LW, et al. Cardiovascular risk profile of patients with psoriatic arthritis compared to controls – the role of inflammation. Rheumatology (Oxford). 2008;47:718-723. doi: 10.1093/rheumatology/ken090
23. Gottlieb AB, Dann F, Menter A. Psoriasis and the metabolic syndrome. J Drugs Dermatol. 2008;7:563-572.
24. Channual J, Wu JJ, Dann FJ. Effects of tumor necrosis factor-alpha blockade on metabolic syndrome components in psoriasis and psoriatic arthritis and additional lessons learned from rheumatoid arthritis. Dermatol Ther. 2009;22:61-73. doi: 10.1111/j.1529-8019.2008.01217.x
25. Sonnenberg GE, Krakower GR, Kissebah AH. A novel pathway to the manifestations of metabolic syndrome. Obes Res. 2004;12:180-186. doi: 10.1038/oby.2004.24
26. Das SK, Elbein SC. The search for type 2 diabetes susceptibility loci: the chromosome 1q story. Curr Diab Rep. 2007;7:154-164. doi: 10.1007/s11892-007-0025-3
27. Yoo H, Kim SJ, Kim Y, Lee H, Kim TY. Insulin-like growth factor-II regulates the 12-lipoxygenase gene expression and promotes cell proliferation in human keratinocytes via the extracellular regulatory kinase and phosphatidylinositol 3-kinase pathways. Int J Biochem Cell Biol. 2007;39:1248-1259. doi: 10.1016/j.biocel.2007.04.009
28. Wolf N, Quaranta M, Prescott NJ, Allen M, Smith R, Burden AD, et al. Psoriasis is associated with pleiotropic susceptibility loci identified in type II diabetes and Crohn disease. J Med Genet. 2008;45:114-116. doi: 10.1136/jmg.2007.053595
29. Pershadsingh HA. Peroxisome proliferator-activated receptor-gamma: Therapeutic target for diseases beyond diabetes: Quo vadis? Expert Opin Investig Drugs. 2004;13:215-228. doi: 10.1517/13543784.13.3.215
30. Mastrofrancesco A, Kovacs D, Sarra M, Bastonini E, Cardinali G, Aspite N, et al. Preclinical studies of a specific PPARγ modulator in the control of skin inflammation. J Invest Dermatol. 2014;134:1001-1011. doi: 10.1038/jid.2013.448
31. Fang L, Karakiulakis G, Roth M. Are patients with hypertension and diabetes mellitus at increased risk for COVID-19 infection? Lancet Respir Med. 2020;8(4):e21. doi: 10.1016/S2213-2600(20)30116-8
32. Huang C, Wang Y, Li X, Ren L, Zhao J, Hu Y, et al. Clinical features of patients infected with 2019 novel coronavirus in Wuhan, China. Lancet. 2020;395:497-506. doi: 10.1016/S0140-6736(20)30183-5
33. Yang X, Yu Y, Xu J, Shu H, Xia J, Liu H, et al. Clinical course and outcomes of critically ill patients with SARS-CoV-2 pneumonia in Wuhan, China: A single-centered, retrospective, observational study. Lancet Respir Med. 2020;8:475-481. doi: 10.1016/S2213-2600(20)30079-5
34. Guan W, Ni Z, Hu Y, Xie M, Shi Z, Tang Z, et al. Clinical characteristics of coronavirus disease 2019 in China. J Emerg Med. 2020;58(4):711-712. doi: 10.1016/j.jemermed.2020.04.004
35. Zhang JJ, Dong X, Cao YY, Yuan YD, Yang YB, Yan YQ, et al. Clinical characteristics of 140 patients infected with SARS-CoV-2 in Wuhan, China. Allergy. 2020;00:1-12. doi: 10.1111/all.14238
Review
For citations:
Korsakova Yu.L., Korotaeva T.V., Loginova E.Yu., Gubar E.E., Vasilenko E.A., Vasilenko A.A., Kuznetsova N.A., Patrikeeva I.M., Nasonov E.L. The prevalence of comorbid and concomitant diseases in psoriatic arthritis patients, data from Russian register. Rheumatology Science and Practice. 2021;59(3):275-281. (In Russ.) https://doi.org/10.47360/1995-4484-2021-275-281