Disease-modifying antirheumatic drugs improve cardiovascular autonomic neuropathy in psoriatic arthritis

被引:3
|
作者
Syngle, Ashit [2 ,3 ]
Verma, Inderjeet [1 ]
Krishan, Pawan [1 ]
Syngle, Vijaita [4 ]
机构
[1] Punjabi Univ, Dept Pharmaceut Sci & Drug Res, Patiala 147002, Punjab, India
[2] Cardio Rheuma & Healing Touch City Clin, Chandigarh, India
[3] Fortis Multispecial Hosp, Mohali, Punjab, India
[4] Healing Touch City Clin, Chandigarh, India
关键词
cardiovascular autonomic neuropathy; disease-modifying antirheumatic drugs; inflammation; psoriatic arthritis; HEART-RATE-VARIABILITY; RHEUMATOID-ARTHRITIS; SYSTEMIC-LUPUS; INFLAMMATORY MARKERS; VAGUS NERVE; DYSFUNCTION; ACTIVATION; MECHANISM;
D O I
10.1177/1759720X16635887
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Cardiovascular autonomic neuropathy (CAN) is a significant risk predictor for sudden cardiac death in autoimmune rheumatic diseases. As yet, there is no therapeutic treatment of CAN in psoriatic arthritis (PsA). Even now, the impact of the most commonly employed disease-modifying antirheumatic drug (DMARD) therapy on CAN in PsA is not known. Hence, we investigated the impact of DMARDs on CAN in PsA. Methods: In this prospective, cross-sectional study, 20 patients of PsA and 20 age- and sex-matched healthy controls were recruited. CAN was diagnosed by applying the five cardiovascular reflex tests according to Ewing. Parasympathetic dysfunction was established by performing three tests: heart-rate response to deep breathing, standing, and Valsalva tests. Sympathetic dysfunction was examined by applying two tests: blood pressure response to standing, and handgrip tests. Disease severity was assessed by the 28-joint-count disease activity score (DAS-28) and the disease activity score in psoriatic arthritis (DAPSA). Results: Cardiovascular reflex tests were impaired significantly among the PsA patients compared with well-matched healthy subjects (p < 0.05). Parasympathetic dysfunction was more prominent than sympathetic dysfunction. After 12 weeks treatment, parasympathetic dysfunction (heart rate response to deep breath and standing) significantly (p < 0.05) improved in patients with PsA, while there was no significant improvement in sympathetic function. Conclusion: These study results suggests parasympathetic autonomic dysfunction is more prominent than sympathetic dysfunction in PsA. Synthetic DMARDs improved parasympathetic dysfunction in PsA.
引用
收藏
页码:42 / 48
页数:7
相关论文
共 50 条
  • [31] Systematic review of disease-modifying antirheumatic drugs for juvenile idiopathic arthritis
    Alex R Kemper
    Heather A Van Mater
    Remy R Coeytaux
    John W Williams
    Gillian D Sanders
    BMC Pediatrics, 12
  • [32] Putting new disease-modifying antirheumatic drugs into perspective
    Saseen, Joseph J.
    PHARMACOTHERAPY, 2007, 27 (12): : 1609 - 1610
  • [33] Life-table analysis of cyclosporin A treatment in psoriatic arthritis: Comparison with other disease-modifying antirheumatic drugs
    Spadaro, A
    Taccari, E
    Mohtadi, B
    Riccieri, V
    Sensi, F
    Zoppini, A
    CLINICAL AND EXPERIMENTAL RHEUMATOLOGY, 1997, 15 (06) : 609 - 614
  • [34] Influence of disease-modifying antirheumatic drugs on oxidative and nitrosative stress in patients with rheumatoid arthritis
    Costa, Neide Tomimura
    Veiga Iriyoda, Tatiana Mayumi
    Alfieri, Daniela Frizon
    Colado Simao, Andrea Name
    Dichi, Isaias
    INFLAMMOPHARMACOLOGY, 2018, 26 (05) : 1151 - 1164
  • [35] Risk of Venous Thromboembolism in Patients with Rheumatoid Arthritis: Initiating Disease-Modifying Antirheumatic Drugs
    Kim, Seoyoung C.
    Solomon, Daniel H.
    Liu, Jun
    Franklin, Jessica M.
    Glynn, Robert J.
    Schneeweiss, Sebastian
    AMERICAN JOURNAL OF MEDICINE, 2015, 128 (05) : 539.e7 - 539.e17
  • [36] Use of Disease-modifying Antirheumatic Drugs After Cancer Diagnosis in Rheumatoid Arthritis Patients
    Joo, Young Bin
    Jung, Seung Min
    Park, Yune-Jung
    Kim, Ki-Jo
    Park, Kyung-Su
    JOURNAL OF RHEUMATIC DISEASES, 2022, 29 (03): : 162 - 170
  • [37] Network Meta-Analysis of Tofacitinib, Biologic Disease-Modifying Antirheumatic Drugs, and Apremilast for the Treatment of Psoriatic Arthritis
    Gladman, Dafna D.
    Orbai, Ana-Maria
    Gomez-Reino, Juan
    Chang-Douglass, Stacey
    Leoncini, Emanuele
    Burton, Hannah E.
    Kanik, Keith S.
    Belen Romero, Ana
    Cappelleri, Joseph C.
    Hsu, Ming-Ann
    CURRENT THERAPEUTIC RESEARCH-CLINICAL AND EXPERIMENTAL, 2020, 93
  • [38] Influence of disease-modifying antirheumatic drugs on oxidative and nitrosative stress in patients with rheumatoid arthritis
    Neide Tomimura Costa
    Tatiana Mayumi Veiga Iriyoda
    Daniela Frizon Alfieri
    Andréa Name Colado Simão
    Isaias Dichi
    Inflammopharmacology, 2018, 26 : 1151 - 1164
  • [39] High Prevalence of Metabolic Syndrome in Patients With Psoriatic Arthritis From Northeastern Brazil Association With Traditional Cardiovascular Risk Factors and Biologic Disease-Modifying Antirheumatic Drugs
    Adeodato Ramos, Lysiane Maria
    Poti Gomes, Kirla Wagner
    de Saboia Mont'Alverne, Andrea Rocha
    Braga, Marcio Vale
    Costa Vasconcelos, Antonio Helder
    Maia Rodrigues, Carlos Ewerton
    JCR-JOURNAL OF CLINICAL RHEUMATOLOGY, 2021, 27 : S186 - S192
  • [40] Comparative Effectiveness of Nonbiologic versus Biologic Disease-modifying Antirheumatic Drugs for Rheumatoid Arthritis
    DeWitt, Esi Morgan
    Li, Yanhong
    Curtis, Jeffrey R.
    Glick, Henry A.
    Greenberg, Jeffrey D.
    Anstrom, Kevin J.
    Kremer, Joel M.
    Reed, George
    Schulman, Kevin A.
    Reed, Shelby D.
    JOURNAL OF RHEUMATOLOGY, 2013, 40 (02) : 127 - 136