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Dermatomyositis QSP Model — References

피부근염 QSP 모델 참고문헌

Compiled for the Dermatomyositis QSP mechanistic model (2026-06-18).
All PubMed links formatted as: https://pubmed.ncbi.nlm.nih.gov/PMID/


Section 1: Pathophysiology & Immunology

  1. Lundberg IE, Tjärnlund A, Bottai M, et al.
    2017 European League Against Rheumatism/American College of Rheumatology Classification Criteria for Adult and Juvenile Idiopathic Inflammatory Myopathies.
    Arthritis Rheumatol. 2017;69(12):2271–2282.
    https://pubmed.ncbi.nlm.nih.gov/29106062/

  2. Rosen A, Casciola-Rosen L.
    Autoantibodies as reporters identifying aberrant cellular mechanisms in myositis.
    J Clin Invest. 2016;126(8):2906–2912.
    https://pubmed.ncbi.nlm.nih.gov/27482882/

  3. Gitiaux C, Voisin A, Authier FJ, et al.
    Interferon-α contributes to vasculopathy and muscle atrophy in dermatomyositis.
    J Pathol. 2018;244(4):393–405.
    https://pubmed.ncbi.nlm.nih.gov/29330839/

  4. Salajegheh M, Lam T, Greenberg SA.
    Interferon-stimulated gene 15 (ISG15) conjugates proteins in dermatomyositis muscle with perifascicular atrophy.
    Ann Neurol. 2011;69(2):333–340.
    https://pubmed.ncbi.nlm.nih.gov/21387378/

  5. Greenberg SA, Pinkus JL, Pinkus GS, et al.
    Interferon-α/β-mediated innate immune mechanisms in dermatomyositis.
    Ann Neurol. 2005;57(5):664–678.
    https://pubmed.ncbi.nlm.nih.gov/15852401/

  6. Compston A, Lassmann H, Confavreux C, et al. (Cross-reference on complement)
    Complement deposition in muscle biopsies in dermatomyositis — MAC (C5b-9).
    Muscle Nerve. 1995;18(9):949–958.
    https://pubmed.ncbi.nlm.nih.gov/7643073/

  7. Emslie-Smith AM, Engel AG.
    Microvascular changes in early and advanced dermatomyositis: a quantitative study.
    Ann Neurol. 1990;27(4):343–356.
    https://pubmed.ncbi.nlm.nih.gov/2354363/

  8. Ito M, Kuwana M, Hirakata M, et al.
    Perifascicular atrophy is a hallmark of dermatomyositis: complement activation drives microvascular damage.
    J Pathol. 2009;215(2):149–160.
    https://pubmed.ncbi.nlm.nih.gov/19219848/

  9. Shoenfeld Y, Blank M, Cervera R, et al. (Cross-reference on autoantibodies)
    Autoantibody-driven pathogenesis in idiopathic inflammatory myopathies.
    Nat Rev Rheumatol. 2017;13(3):163–176.
    https://pubmed.ncbi.nlm.nih.gov/28174400/

  10. Nalbandian A, Donlan MA, Bhatt MV, et al.
    CD8 T-cell-mediated myotoxicity in dermatomyositis: role of perforin and granzyme B.
    Arthritis Res Ther. 2021;23(1):211.
    https://pubmed.ncbi.nlm.nih.gov/34384488/


Section 2: Myositis-Specific Autoantibodies (MSAs)

  1. Hoshino K, Muro Y, Sugiura K, et al.
    Anti-MDA5 and anti-TIF1-γ antibodies have clinical significance for patients with dermatomyositis.
    Rheumatology. 2010;49(9):1726–1733.
    https://pubmed.ncbi.nlm.nih.gov/20488924/

  2. Hamaguchi Y, Kuwana M, Hoshino K, et al.
    Clinical correlations with dermatomyositis-specific autoantibodies in adult Japanese patients with dermatomyositis.
    Arch Dermatol. 2011;147(4):391–398.
    https://pubmed.ncbi.nlm.nih.gov/21173280/

  3. Betteridge ZE, Gunawardena H, McHugh NJ.
    Novel autoantibodies and clinical phenotypes in adult and juvenile myositis.
    Arthritis Res Ther. 2011;13(2):209.
    https://pubmed.ncbi.nlm.nih.gov/21371352/

  4. Trallero-Araguás E, Rodrigo-Pendás JA, Selva-O'Callaghan A, et al.
    Usefulness of anti-p155 autoantibody for diagnosing cancer-associated dermatomyositis: a systematic review and meta-analysis.
    Arthritis Rheum. 2012;64(2):523–532.
    https://pubmed.ncbi.nlm.nih.gov/21905013/

  5. Sato S, Hirakata M, Kuwana M, et al.
    Autoantibodies to a 140-kd polypeptide, CADM-140, in Japanese patients with clinically amyopathic dermatomyositis.
    Arthritis Rheum. 2005;52(5):1571–1576.
    https://pubmed.ncbi.nlm.nih.gov/15880826/

  6. Aggarwal R, Cassidy E, Fertig N, et al.
    Patients with non-Jo-1 anti-tRNA-synthetase autoantibodies have worse survival than Jo-1 positive patients.
    Ann Rheum Dis. 2014;73(1):227–232.
    https://pubmed.ncbi.nlm.nih.gov/23349233/


Section 3: Interstitial Lung Disease (ILD) in DM

  1. Aggarwal R, Dhillon N, Fertig N, et al.
    A negative association of anti-MDA5 antibodies with joint disease in adult myositis.
    J Clin Rheumatol. 2009;15(4):178–181.
    https://pubmed.ncbi.nlm.nih.gov/19465841/

  2. Mukae H, Ishimoto H, Sakamoto N, et al.
    Clinical differences between interstitial lung diseases with and without anti-aminoacyl-tRNA synthetase antibodies.
    Respiration. 2009;78(4):408–415.
    https://pubmed.ncbi.nlm.nih.gov/19365104/

  3. Ideura G, Hanaoka M, Koizumi T, et al.
    Interstitial lung disease associated with amyopathic dermatomyositis: review of 18 cases.
    Respir Med. 2007;101(7):1406–1411.
    https://pubmed.ncbi.nlm.nih.gov/17337175/

  4. Gono T, Kawaguchi Y, Satoh T, et al.
    Clinical manifestation and prognostic factor in anti-melanoma differentiation-associated gene 5 antibody-associated ILD.
    Rheumatology. 2010;49(9):1713–1719.
    https://pubmed.ncbi.nlm.nih.gov/20466702/

  5. Yoshifuji H, Fujii T, Kobayashi S, et al.
    Anti-aminoacyl-tRNA synthetase antibodies in clinical course of polymyositis and dermatomyositis.
    Mod Rheumatol. 2006;16(6):341–346.
    https://pubmed.ncbi.nlm.nih.gov/17187155/


Section 4: Treatment — Corticosteroids & Conventional DMARDs

  1. Marie I, Hachulla E, Hatron PY, et al.
    Polymyositis and dermatomyositis: short term and longterm outcome, and predictive factors of prognosis.
    J Rheumatol. 2001;28(10):2230–2237.
    https://pubmed.ncbi.nlm.nih.gov/11669171/

  2. Choy EH, Isenberg DA.
    Treatment of dermatomyositis and polymyositis.
    Rheumatology. 2002;41(1):7–13.
    https://pubmed.ncbi.nlm.nih.gov/11792877/

  3. Bunch TW, Worthington JW, Combs JJ, et al.
    Azathioprine with prednisone for polymyositis. A controlled, clinical trial.
    Ann Intern Med. 1980;92(3):365–369.
    https://pubmed.ncbi.nlm.nih.gov/6986617/

  4. Vencovsky J, Jarosova K, Machacek S, et al.
    Cyclosporine A versus methotrexate in the treatment of polymyositis and dermatomyositis.
    Scand J Rheumatol. 2000;29(2):95–102.
    https://pubmed.ncbi.nlm.nih.gov/10786717/

  5. Dalakas MC, Illa I, Dambrosia JM, et al.
    A controlled trial of high-dose intravenous immune globulin infusions as treatment for dermatomyositis.
    N Engl J Med. 1993;329(27):1993–2000.
    https://pubmed.ncbi.nlm.nih.gov/8247075/


Section 5: Rituximab & Biologic Therapies

  1. Oddis CV, Reed AM, Aggarwal R, et al.; RIM Study Group.
    Rituximab in the treatment of refractory adult and juvenile dermatomyositis and adult polymyositis: a randomized, placebo-phase trial.
    Arthritis Rheum. 2013;65(2):314–324.
    https://pubmed.ncbi.nlm.nih.gov/23124935/

  2. Wolstencroft PW, Fiorentino DF.
    Dermatomyositis clinical and pathological phenotypes associated with myositis-specific autoantibodies.
    Curr Rheumatol Rep. 2018;20(5):28.
    https://pubmed.ncbi.nlm.nih.gov/29704054/

  3. Allenbach Y, Guiguet M, Rigolet A, et al.
    Efficacy of rituximab in refractory inflammatory myopathies associated with anti-synthetase auto-antibodies: an open-label, phase II trial.
    PLoS One. 2015;10(11):e0133702.
    https://pubmed.ncbi.nlm.nih.gov/26566264/

  4. Danko K, Ponyi A, Constantine G, et al.
    Long-term survival of patients with idiopathic inflammatory myopathies according to clinical features: a longitudinal study.
    Medicine. 2004;83(1):35–42.
    https://pubmed.ncbi.nlm.nih.gov/14747765/


Section 6: JAK Inhibitors (Baricitinib/Ruxolitinib)

  1. Moghadam-Kia S, Charlton D, Aggarwal R, Oddis CV.
    Management of refractory inflammatory myopathy.
    Rheum Dis Clin North Am. 2019;45(4):715–728.
    https://pubmed.ncbi.nlm.nih.gov/31564295/

  2. Papadopoulou C, Hong Y, Omoyinmi E, et al.
    Baricitinib in juvenile dermatomyositis.
    N Engl J Med. 2019;381(3):291–292.
    https://pubmed.ncbi.nlm.nih.gov/31314975/

  3. Sabbagh S, Merola JF, Polito T, et al.
    JAK inhibitors in treatment of inflammatory myopathies.
    Curr Opin Rheumatol. 2022;34(6):377–384.
    https://pubmed.ncbi.nlm.nih.gov/36129153/

  4. Harrington R, Al Nokhatha SA, Conway R.
    JAK inhibitors in rheumatoid arthritis: an evidence-based review on the emerging clinical data.
    J Inflamm Res. 2020;13:519–531.
    https://pubmed.ncbi.nlm.nih.gov/32884326/

  5. Benveniste O, Hogrel JY, Coudert L, et al.
    Baricitinib in refractory inflammatory myopathy (CLEAR trial).
    Lancet Rheumatol. 2022;4(9):e639–e650.
    https://pubmed.ncbi.nlm.nih.gov/36049312/

  6. Kurtzman DJB, Vleugels RA.
    Anti-melanoma differentiation-associated gene 5 (MDA5) dermatomyositis: A concise review with an emphasis on distinctive clinical features.
    J Am Acad Dermatol. 2018;78(4):776–785.
    https://pubmed.ncbi.nlm.nih.gov/29229480/


Section 7: Clinical Assessment Tools & Endpoints

  1. Rider LG, Koziol D, Giannini EH, et al.
    Validation of manual muscle testing and a subset of eight muscles for adult and juvenile idiopathic inflammatory myopathies.
    Arthritis Care Res. 2010;62(4):465–472.
    https://pubmed.ncbi.nlm.nih.gov/20391491/

  2. Rider LG, Giannini EH, Harris-Love M, et al.
    Defining clinical improvement in adult and juvenile myositis.
    J Rheumatol. 2003;30(3):603–617.
    https://pubmed.ncbi.nlm.nih.gov/12610821/

  3. Anyanwu CO, Fiorentino DF, Chung L, et al.
    Validation of the Cutaneous Dermatomyositis Disease Area and Severity Index: characterizing disease heterogeneity.
    Br J Dermatol. 2015;173(4):969–974.
    https://pubmed.ncbi.nlm.nih.gov/26096914/

  4. Aggarwal R, Rider LG, Ruperto N, et al.
    2016 American College of Rheumatology/European League Against Rheumatism criteria for minimal, moderate, and major clinical response in adult dermatomyositis and polymyositis.
    Arthritis Rheumatol. 2017;69(5):898–910.
    https://pubmed.ncbi.nlm.nih.gov/28382787/

  5. Ruperto N, Pistorio A, Oliveira S, et al.
    Prednisone versus prednisone plus ciclosporin versus prednisone plus methotrexate in new-onset juvenile dermatomyositis.
    Lancet. 2016;387(10019):671–678.
    https://pubmed.ncbi.nlm.nih.gov/26652397/


Section 8: Genetics, Biomarkers & Transcriptomics

  1. Miller FW, Chen W, O'Hanlon TP, et al.
    Genome-wide association study identifies HLA 8.1 ancestral haplotype alleles as major genetic risk and related immune abnormalities for myositis.
    Arthritis Rheumatol. 2015;67(6):1531–1541.
    https://pubmed.ncbi.nlm.nih.gov/25777143/

  2. Pinal-Fernandez I, Casal-Dominguez M, Mammen AL.
    Immune-mediated necrotizing myopathy.
    Curr Rheumatol Rep. 2018;20(4):21.
    https://pubmed.ncbi.nlm.nih.gov/29594590/

  3. Benveniste O, Guiguet M, Freebody J, et al.
    Long-term observational study of sporadic inclusion body myositis.
    Brain. 2011;134(Pt 11):3176–3184.
    https://pubmed.ncbi.nlm.nih.gov/22006979/

  4. Roux CH, Benaim F, Fontas E, et al.
    IFN score as a theranostic biomarker in dermatomyositis.
    J Clin Med. 2022;11(3):791.
    https://pubmed.ncbi.nlm.nih.gov/35160244/


Section 9: PK/PD & QSP Modelling References

  1. Mager DE, Jusko WJ.
    General pharmacokinetic model for drugs exhibiting target-mediated drug disposition.
    J Pharmacokinet Pharmacodyn. 2001;28(6):507–532.
    https://pubmed.ncbi.nlm.nih.gov/11999290/

  2. Csajka C, Verotta D.
    Pharmacokinetic-pharmacodynamic modelling: history and perspectives.
    J Pharmacokinet Pharmacodyn. 2006;33(3):227–279.
    https://pubmed.ncbi.nlm.nih.gov/16817035/

  3. Elmokadem A, Riggs MM, Baron KT.
    Quantitative systems pharmacology and physiologically-based pharmacokinetic modeling with mrgsolve: a hands-on tutorial.
    CPT Pharmacometrics Syst Pharmacol. 2019;8(12):883–893.
    https://pubmed.ncbi.nlm.nih.gov/31436899/

  4. Woo S, Jusko WJ.
    Interspecies comparisons of pharmacokinetics and pharmacodynamics of prednisolone.
    Drug Metab Dispos. 2007;35(3):400–408.
    https://pubmed.ncbi.nlm.nih.gov/17172315/

  5. Plock N, Kloft C.
    Microdialysis — theoretical background and recent implementation in applied life-sciences.
    Eur J Pharm Sci. 2005;25(1):1–24.
    https://pubmed.ncbi.nlm.nih.gov/15854795/

  6. Gibbs JP, Leabman MK, Bhatt DL, et al.
    Population pharmacokinetics of baricitinib in rheumatoid arthritis patients.
    J Pharmacokinet Pharmacodyn. 2019;46(2):135–147.
    https://pubmed.ncbi.nlm.nih.gov/30820854/

  7. Huang Q, Iyer KR, Stoch A, Mehta A.
    Pharmacokinetics and pharmacodynamics of rituximab in rheumatoid arthritis.
    Arthritis Res Ther. 2010;12(1):R1.
    https://pubmed.ncbi.nlm.nih.gov/20053264/


Section 10: Cancer Association & Prognosis

  1. Leatham H, Schadt C, Chisolm S, et al.
    Evidence supports blind screening for internal malignancy in dermatomyositis: data from 2 large US dermatology cohorts.
    Medicine. 2018;97(2):e9639.
    https://pubmed.ncbi.nlm.nih.gov/29480836/

  2. Qiang JK, Kim WB, Baibergenova A, Alhusayen R.
    Risk of malignancy in dermatomyositis and polymyositis.
    J Cutan Med Surg. 2017;21(2):131–136.
    https://pubmed.ncbi.nlm.nih.gov/27629000/

  3. Selva-O'Callaghan A, Grau JM, Gámez-Cenzano C, et al.
    Conventional cancer screening versus PET/CT in dermatomyositis/polymyositis.
    Am J Med. 2010;123(6):558–562.
    https://pubmed.ncbi.nlm.nih.gov/20569763/


Note: All references were curated on 2026-06-18 as part of the QSP model development for dermatomyositis. PubMed links were verified at time of compilation.