- 1.
Aletaha, D.; Neogi, T.; Silman, A.J.; et al. Rheumatoid arthritis classification criteria: An American College of Rheumatology/European League Against Rheumatism collaborative initiative. Arthritis Rheum. 2010, 62, 2569–2581.
- 2.
Smolen, J.S.; Aletaha, D.; McInnes, I.B. Rheumatoid arthritis. Lancet 2016, 388, 2023–2038.
- 3.
Moosavian, S.P.; Paknahad, Z.; Habibagahi, Z.; et al. The effects of garlic (Allium sativum) supplementation on inflammatory biomarkers, fatigue, and clinical symptoms in patients with active rheumatoid arthritis: A randomized, double‐blind, placebo‐controlled trial. Phytother. Res. 2020, 34, 2953–2962.
- 4.
Wang, Z.; Zhao, F.; Wei, P.; et al. Phytochemistry, health benefits, and food applications of sea buckthorn (Hippophae rhamnoides L.): A comprehensive review. Front. Nutr. 2022, 9, 1036295.
- 5.
Trelle, S.; Reichenbach, S.; Wandel, S.; et al. Cardiovascular safety of non-steroidal anti- inflammatory drugs: Network meta-analysis. Br. Med. J. 2011, 342, c7086.
- 6.
Gabriel, S.E.; Jaakkimainen, L.; Bombardier, C. Risk for serious gastrointestinal complications related to use of NSAIDs. A meta-analysis. Ann. Intern. Med. 1991, 115, 787.
- 7.
Huerta, C.; Castellsague, J.; Varas-Lorenzo, C.; et al. NSAIDs and risk of ARF in the general population. Am. J. Kidney Dis. 2005, 45, 531.
- 8.
Murray, M.D.; Brater, D.C. Renal toxicity of the NSAIDs. Ann. Rev. Pharmacol. Toxicol. 1993, 33, 435.
- 9.
Edwards, J.E.; McQuay, H.J.; Moore, R.A. Efficacy and safety of valdecoxib for treatment of osteoarthritis and rheumatoid arthritis: Systematic review of randomised controlled trials. Pain 2004, 111, 286–296.
- 10.
Scheiman, J.M.; Hindley, C.E. Strategies to optimize treatment with NSAIDs in patients at risk for gastrointestinal and cardiovascular adverse events. Clin. Ther. 2010, 32, 667–677.
- 11.
Krug, H.; Broadwell, L.K.; Berry, M.; et al. Tolerability and efficacy of nabumetone and naproxen in the treatment of rheumatoid arthritis. Clin. Ther. 2000, 22, 40–52.
- 12.
Del Rincón, I.; Battafarano, D.F.; Restrepo, J.F.; et al. Glucocorticoid dose thresholds associated with all‐cause and cardiovascular mortality in rheumatoid arthritis. Arthritis Rheumatol. 2014, 66, 264–272.
- 13.
Van Staa, T.P.; Laan, R.F.; Barton, I.P.; et al. Bone density threshold and other predictors of vertebral fracture in patients receiving oral glucocorticoid therapy. Arthritis Rheumatol. 2003, 48, 3224–3229.
- 14.
Caramaschi, P.; Biasi, D.; Dal Forno, I.; et al. Osteonecrosis in systemic lupus erythematosus: An early, frequent, and not always symptomatic complication. Autoimmune Dis. 2012, 725249.
- 15.
Wilson, J.C.; Sarsour, K.; Gale, S.; et al. THU0172 Risk for Serious Adverse Events Associated with Oral Corticosteroid Therapy in Patients with Rheumatoid Arthritis: A Uk Population Based Study 2016. Ann. Rheum. Dis. 2016, 75, 246–247.
- 16.
Juge, P.A.; Lee, J.S.; Lau, J.; et al. Methotrexate and rheumatoid arthritis associated interstitial lung disease. Eur. Respir. J. 2021, 57, 2000337.
- 17.
Gilani, S.T.A.; Khan, D.A.; Khan, F.A.; et al. Adverse effects of low dose methotrexate in rheumatoid arthritis patients. J. Coll. Physicians Surg. Pak. 2012, 22, 101–104.
- 18.
Shin, K.; Baek, H.J.; Kang, Y.M.; et al. Efficacy and safety of add‐on tacrolimus versus leflunomide in rheumatoid arthritis patients with inadequate response to methotrexate. Int. J. Rheum. Dis. 2019, 22, 1115–1122.
- 19.
Aletaha, D.; Stamm, T.; Kapral, T.; et al. Survival and effectiveness of leflunomide compared with methotrexate and sulfasalazine in rheumatoid arthritis: A matched observational study. Ann. Rheum. Dis. 2013, 62, 944–951.
- 20.
Jiang, M.; Zha, Q.; He, Y.; et al. Risk factors of gastrointestinal and hepatic adverse drug reactions in the treatment of rheumatoid arthritis with biomedical combination therapy and Chinese medicine. J. Ethnopharmacol. 2012, 141, 615–621.
- 21.
Chen, Z.; Li, X.P.; Li, Z.J.; et al. Reduced hepatotoxicity by total glucosides of paeony in combination treatment with leflunomide and methotrexate for patients with active rheumatoid arthritis. Int. Immunopharmacol. 2013, 15, 474–477.
- 22.
Hänninen, O.; Kaartinen, K.; Rauma, A.L.; et al. Antioxidants in vegan diet and rheumatic disorders. Toxicology 2000, 155, 45–53.
- 23.
Quinonez-Flores, C.M.; Gonzalez-Chavez, S.A.; Del Rio Najera, D.; et al. Oxidative stress relevance in the pathogenesis of the rheumatoid arthritis: A systematic review. Biomed. Res. Int. 2016, 097417.
- 24.
Fernández-Llanio Comella, N.; Fernández Matilla, M.; Castellano Cuesta, J.A. Have complementary therapies demonstrated effectiveness in rheumatoid arthritis? Reumatol. Clin. 2016, 12, 151–157.
- 25.
Efthimiou, P.; Kukar, M.; MacKenzie, C.R. Complementary and alternative medicine in rheumatoid arthritis: No longer the last resort! HSS J. 2010, 6, 108–111.
- 26.
Salaffi, F.; Ciapetti, A. Clinical disease activity assessments in rheumatoid arthritis. Int. J. Clin. Rheumatol. 2013, 8, 347–360.
- 27.
Duarte-García, A.; Leung, Y.Y.; Coates, L.C.; et al. Endorsement of the 66/68 joint count for the measurement of musculoskeletal disease activity: OMERACT 2018 psoriatic arthritis workshop report. J. Rheumatol. 2019, 46, 996–1005.
- 28.
Wells, G.; Becker, J.C.; Teng, J.; et al. Validation of the 28-joint Disease Activity Score (DAS28) and European League Against Rheumatism response criteria based on C-reactive protein against disease progression in patients with rheumatoid arthritis, and comparison with the DAS28 based on erythrocyte sedimentation rate. Ann. Rheum. Dis. 2009, 68, 954–960.
- 29.
Seror, R.; Tubach, F.; Baron, G.; et al. Measure of function in rheumatoid arthritis: Individualised or classical scales? Ann. Rheum. Dis. 2010, 69, 97–101.
- 30.
Felson, D.T.; LaValley, M.P. The ACR20 and defining a threshold for response in rheumatic diseases: Too much of a good thing. Arthritis Res. Ther. 2014, 16, 101–106.
- 31.
Goldbach-Mansky, R.; Wilson, M.; Fleischmann, R.; et al. Comparison of Tripterygium wilfordii Hook F versus sulfasalazine in the treatment of rheumatoid arthritis: A randomized trial. Ann. Intern. Med. 2009, 151, 229–240.
- 32.
Tao, X.; Younger, J.; Fan, F.Z.; et al. Benefit of an extract of Tripterygium wilfordii Hook F in patients with rheumatoid arthritis: A double-blind, placebo-controlled study. Arthritis Rheum. 2002, 46, 1735–1743.
- 33.
Molnar, V.; Matišić, V.; Kodvanj, I.; et al. Cytokines and chemokines involved in osteoarthritis pathogenesis. Int. J. Mol. Sci. 2021, 22, 9208.
- 34.
Ingegnoli, F.; Castelli, R.; Gualtierotti, R. Rheumatoid Factors: Clinical Applications. Dis. Markers 2013, 35, 727–734.
- 35.
Lv, Q.W.; Zhang, W.; Shi, Q.; et al. Comparison of Tripterygium wilfordii Hook F with methotrexate in the treatment of active rheumatoid arthritis (TRIFRA): A randomised, controlled clinical trial. Ann. Rheum. Dis. 2015, 74, 1078–1086.
- 36.
Cibere, J.; Deng, Z.; Lin, Y.; et al. A randomized double blind, placebo controlled trial of topical Tripterygium wilfordii in rheumatoid arthritis: Reanalysis using logistic regression analysis. J. Rheumatol. 2003, 30, 465–467.
- 37.
Piao, X.; Zhou, J.; Xue, L. Triptolide decreases rheumatoid arthritis fibroblast-like synoviocyte proliferation, invasion, inflammation and presents a therapeutic effect in collagen induced arthritis rats via inactivating lncRNA RP11-83J16. 1 mediated URI1 and β-catenin signaling. Int. Immunopharmacol. 2021, 99, 108010.
- 38.
Shan, Y.; Zhao, J.; Wei, K.; et al. A comprehensive review of Tripterygium wilfordii hook. f. in the treatment of rheumatic and autoimmune diseases: Bioactive compounds, mechanisms of action, and future directions. Front. Pharmacol. 2023, 14.
- 39.
Luo, J.; Jin, D.-E.; Yang, G.-Y.; et al. Total glucosides of paeony for rheumatoid arthritis: A protocol for a systematic review. BMJ Open 2016, 6, e010116.
- 40.
Feng, Z.-T.; Xu, J.; He, G.-C.; et al. A systematic review and meta-analysis of the clinical efficacy and safety of total glucosides of peony combined with methotrexate in rheumatoid arthritis. Clin. Rheumatol. 2018, 37, 35–42.
- 41.
Huang, Y.; Wang, H.; Chen, Z.; et al. Efficacy and safety of total glucosides of paeony combined with methotrexate and leflunomide for active rheumatoid arthritis: A meta-analysis. Drug Des. Devel. Ther. 2019, 13, 1969–1984.
- 42.
Zhang, L.; Wei, W. Anti-inflammatory and immunoregulatory effects of paeoniflorin and total glucosides of paeony. Pharmacol. Ther. 2020, 207, 107452.
- 43.
Čabarkapa, A.; Živković, L.; Borozan, S. Dry olive leaf extract in combination with methotrexate reduces cell damage in early rheumatoid arthritis patients—A pilot study. Phytother. Res. 2016, 30, 1615–1623.
- 44.
Nediani, C.; Ruzzolini, J.; Romani, A.; et al. Oleuropein, a bioactive compound from Olea europaea L., as a potential preventive and therapeutic agent in non-communicable diseases. Antioxidants 2019, 8, 578.
- 45.
Savairam, V.D.; Patil, N.A.; Borate, S.R.; et al. Allicin: A review of its important pharmacological activities. Pharmacol. Res. – Mod. Chin. Med. 2023, 8, 100283.
- 46.
Zugravu, G.S.; Pintilescu, C.; Cumpat, C.-M.; et al. Silymarin supplementation in active rheumatoid arthritis: Outcomes of a pilot randomized controlled clinical study. Medicina 2024, 60, 999.
- 47.
Wu, W.T.; Chen, Y.R., Lu, D.H.; et al. Silymarin modulates catabolic cytokine expression through Sirt1 and SOX9 in human articular chondrocytes. J. Orthop. Surg. Res. 2021, 16, 1–9.
- 48.
Gupta, O.P.; Sing, S.; Bani, S.; et al. Anti-inflammatory and anti-arthritic activities of silymarin acting through inhibition of 5-lipoxygenase. Phytomedicine 2000, 7, 21–24.
- 49.
Saber, M.S.; Fahim, H.I.; Ahmed, O.M.; et al. Assessment of the preventive effects of Silybum marianum (L.) Gaertn. seeds hydroethanolic extract and silymarin on complete Freund’s adjuvant induced arthritis in Wistar rats. Ann. Phytomed. 2020, 9, 172–182.
- 50.
Olas B. The beneficial health aspects of sea buckthorn (Elaeagnus rhamnoides (L.) A. Nelson) oil. J. Ethnopharmacol. 2018, 213, 183–190.
- 51.
Zielińska, A.; Nowak I. Abundance of active ingredients in sea-buckthorn oil. Lipids Health Dis. 2017, 16, 95.
- 52.
Solà Marsiñach, M.; Cuenca A.P. The impact of sea buckthorn oil fatty acids on human health. Lipids Health Dis. 2019, 18, 145.
- 53.
Zugravu, G.S.; Dimitriu, D.C.; Ciobanu, C.P.; et al. Benefits of sea buckthorn fruit oil as adjuvant therapy in rheumatoid arthritis. Farmacia 2024, 72, 554–564.
- 54.
Zugravu, G.S.; Pintilescu, C.; Cumpat, C.-M.; et al. Sea buckthorn fruit oil supplementation in active rheumatoid arthritis: A focus on composite disease activity indices and EULAR response. Med. Surg. J. – Rev. Med. Chir. Soc. Med. Nat., Iasi 2024, 128, 422–436.
- 55.
Santa-Maria, C.; López-Enríquez, S.; Montserrat-de la Paz, S.; et al. Up-date on anti-inflammatory molecular mechanisms induced by oleic acid. Nutrients 2023, 15, 224.
- 56.
Passos, M.E.P.; Alves, H.H.O.; Momesso, C.M.; et al. Differential effects of palmitoleic acid on human lymphocyte proliferation and function. Lipids Health Dis. 2016, 15, 217.
- 57.
Talbot, N.A.; Wheeler-Jones, C.P.; Cleasby, M.E. Palmitoleic acid prevents palmitic acid-induced macrophage activation and consequent p38 MAPK-mediated skeletal muscle insulin resistance. Mol. Cell. Endocrinol. 2014, 393, 129–142.
- 58.
Devaraj, S.; Jialal, I. α-Tocopherol decreases interleukin-1β release from activated human monocytes by inhibition of 5-lipoxygenase. Arterioscler. Thromb. Vasc. Biol. 1999, 19, 1125–1133.
- 59.
Bai, S.K.; Lee, S.J.; Na, H.J.; et al. β-Carotene inhibits inflammatory gene expression in lipopolysaccharide-stimulated macrophages by suppressing redox-based NF-κB activation. Exp. Mol. Med. 2005, 37, 323–334.
- 60.
Kawata, A.; Murakami, Y.; Suzuki, S.; et al. Anti-inflammatory activity of β-carotene, lycopene and tri-n-butylborane, a scavenger of reactive oxygen species. In Vivo 2018, 32, 255–264.
- 61.
Liao, P.C.; Lai, M.H.; Hsu, K.P.; et al. Identification of β-sitosterol as in vitro anti-inflammatory constituent in Moringa oleifera. J. Agric. Food Chem. 2018, 66, 10748–10759.
- 62.
Liu, R.; Hao, D.; Xu, W.; et al. β-Sitosterol modulates macrophage polarization and attenuates rheumatoid inflammation in mice. Pharm. Biol. 2019, 57, 161–168.
- 63.
Camillo, L.; Grossini, E.; Farruggio, S.; et al. Alpha-tocopherol protects human dermal fibroblasts by modulating nitric oxide release, mitochondrial function, redox status, and inflammation. Skin Pharmacol. Physiol. 2022, 35, 1–12.
- 64.
Ghavipour, M.; Sotoudeh, G.; Tavakoli, E.; et al. Pomegranate extract alleviates disease activity and some biomarkers of inflammation and oxidative stress in Rheumatoid Arthritis patients. Eur. J. Clin. Nutr. 2017, 71, 92–96.
- 65.
Golmei, P.; Kasna, S.; Roy, K.P.; et al. Review on pharmacological advancement of ellagic acid. J. Pharmacol. Pharmacother. 2024, 15, 93–104.
- 66.
Yeoh, N.; Burton, J.P.; Suppiah, P.; et al. The role of the microbiome in rheumatic diseases. Curr. Rheumatol. Rep. 2013, 15, 314.
- 67.
Thimóteo, N.S.B.; Iryioda, T.M.V.; Alfieri, D.F.; et al. Cranberry juice decreases disease activity in women with rheumatoid arthritis. Nutrition 2019, 60, 112–117.
- 68.
Mur, E.; Hartig, F.; Eibl, G.; et al. Randomized double blind trial of an extract from the pentacyclic alkaloid-chemotype of Uncaria tomentosa for the treatment of rheumatoid arthritis. J. Rheumatol. 2002, 29, 678–681.
- 69.
Willich, S.N.; Rossnagel, K.; Roll, S.; et al. Rose hip herbal remedy in patients with rheumatoid arthritis – a randomised controlled trial. Phytomedicine 2010, 17, 87–93.
- 70.
Winther, K.; Apel, K.; Thamsborg, G. A powder made from seeds and shells of a rose-hip subspecies (Rosa canina) reduces symptoms of knee and hip osteoarthritis: A randomized, double-blind, placebo-controlled clinical trial. Scand. J. Rheumatol. 2005, 34, 302–308.