Polymyositis and dermatomyositis biomarkers

Xu, Shiqi; Hu, Xiaowei; Wang, Jing; Xu, Qiangwei; Han, Ze‐Guang; Zhou, Haiyan; Gao, Mingyang

doi:10.1016/j.cca.2023.117443

Cited by 4 publications

(3 citation statements)

References 72 publications

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“…Recently, different methods and strategies have been reported and developed for the detection of YKL-40, including enzyme-linked immunosorbent assay (ELISA), electrochemical method, and optical assays. 6,7 Schmalenberg et al developed a magnetic bead fluorescent immunoassay for the rapid detection of the inflammation marker YKL-40. 8 The Chaocharoen group designed a label-free electrochemical immunosensor for the voltammetric detection of human chitinase-3-like protein 1 by matching the antibody-modified gold electrode.…”

Section: Introductionmentioning

confidence: 99%

Platinum nanozyme-mediated temperature sensor for sensitive photothermal immunoassay of YKL-40 under near-infrared light

Yu,

Ke,

Cai

et al. 2023

Sens. Diagn.

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Section: Introductionmentioning

confidence: 99%

Platinum nanozyme-mediated temperature sensor for sensitive photothermal immunoassay of YKL-40 under near-infrared light

Yu,

Ke,

Cai

et al. 2023

Sens. Diagn.

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“…Dermatomyositis can be associated with either myositis-associated or myositis-specific autoantibodies, which are associated with different clinical phenotypes. 2 , 3 The best known are ARS, anti-Mi-2, MDA5, TIF1-γ, and NXP-2/MORC-2 antibodies. 3 NXP-2/MORC-3 is found in the nucleus and in nuclear dots known as Promyelocytic Leukemia (PML) nuclear bodies.…”

mentioning

confidence: 99%

“… 2 , 3 The best known are ARS, anti-Mi-2, MDA5, TIF1-γ, and NXP-2/MORC-2 antibodies. 3 NXP-2/MORC-3 is found in the nucleus and in nuclear dots known as Promyelocytic Leukemia (PML) nuclear bodies. 4 A patient with NXP-2-associated dermatomyositis with severe dysphagia after an insect bite has not been reported.…”

mentioning

confidence: 99%

NXP-2 positive dermatomyositis with marked dysphagia following an insect bite

Bombardi,

Scorza,

Finsterer

et al. 2024

Clinics

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Interstitial lung disease and myositis

Gono,

Kuwana

2024

Current Opinion in Rheumatology

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Purpose of review In patients with myositis, interstitial lung disease (ILD) is one of the major causes of morbidity and mortality. Given the limited evidence, there is an urgent need to refine the treatment for myositis-ILD. This review aims to highlight recent updates on the management of myositis-associated ILD, focusing on screening, risk stratification, and treatment. Recent findings Asian race and/or residence, dermatomyositis, mechanic's hand, antisynthetase antibodies, and antimelanoma differentiation-associated gene 5 antibodies are risk factors for ILD development. Patients with such risk factors should be screened for ILD using high-resolution computed tomography. Various prediction models for mortality or rapidly progressive ILD (RP-ILD) in patients with myositis-ILD have been proposed, but validation of these models in multiple independent studies is required. Academic societies in Japan, the United Kingdom, and the United States have proposed tentative treatment algorithms for myositis-ILD on the basis of the presence or absence of RP-ILD. Summary Knowledge on myositis-ILD risk stratification, potentially useful for personalized management approaches in clinical practice, is accumulating. However, further global joint efforts are necessary to build a strong evidence base for consensus algorithms for myositis-ILD.

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Polymyositis and dermatomyositis biomarkers

Cited by 4 publications

References 72 publications

Platinum nanozyme-mediated temperature sensor for sensitive photothermal immunoassay of YKL-40 under near-infrared light

Platinum nanozyme-mediated temperature sensor for sensitive photothermal immunoassay of YKL-40 under near-infrared light

NXP-2 positive dermatomyositis with marked dysphagia following an insect bite

Interstitial lung disease and myositis

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