Evidence map›Paper›PMID 40690123›Full record

Observational studyClinical rheumatology2025

Nailfold videocapillaroscopy in juvenile dermatomyositis: detailed correlations between microvascular abnormalities with clinical and laboratory parameters from an observational retrospective single-center study.

Pietro Francesco Bica, Elvis Hysa, Rosanna Campitiello, Alberto Sulli, Carmen Pizzorni, Emanuele Gotelli, Sabrina Paolino, Ana Rebollo Gimenez, Clara Malattia, Marco Gattorno and 3 more

Abstract readObservational Study
PubMed Publisher
In one paragraph

Observational study in Clinical rheumatology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors.

Pietro Francesco BicaLaboratory of Experimental Rheumatology and Academic Division of Clinical Rheumatology, Department of Internal Medicine and Specialties (DIMI), University of Genova, Viale Benedetto XV, n°6, 16132, Genova, Italy.
Elvis HysaLaboratory of Experimental Rheumatology and Academic Division of Clinical Rheumatology, Department of Internal Medicine and Specialties (DIMI), University of Genova, Viale Benedetto XV, n°6, 16132, Genova, Italy.ORCID http://orcid.org/0000-0002-6970-0983
Rosanna CampitielloLaboratory of Experimental Rheumatology and Academic Division of Clinical Rheumatology, Department of Internal Medicine and Specialties (DIMI), University of Genova, Viale Benedetto XV, n°6, 16132, Genova, Italy.ORCID http://orcid.org/0009-0009-1093-1611
Alberto SulliLaboratory of Experimental Rheumatology and Academic Division of Clinical Rheumatology, Department of Internal Medicine and Specialties (DIMI), University of Genova, Viale Benedetto XV, n°6, 16132, Genova, Italy.ORCID http://orcid.org/0000-0003-3674-4880
Carmen PizzorniLaboratory of Experimental Rheumatology and Academic Division of Clinical Rheumatology, Department of Internal Medicine and Specialties (DIMI), University of Genova, Viale Benedetto XV, n°6, 16132, Genova, Italy.ORCID http://orcid.org/0000-0001-5125-0200
Emanuele GotelliLaboratory of Experimental Rheumatology and Academic Division of Clinical Rheumatology, Department of Internal Medicine and Specialties (DIMI), University of Genova, Viale Benedetto XV, n°6, 16132, Genova, Italy.ORCID http://orcid.org/0000-0002-4732-0306
Sabrina PaolinoLaboratory of Experimental Rheumatology and Academic Division of Clinical Rheumatology, Department of Internal Medicine and Specialties (DIMI), University of Genova, Viale Benedetto XV, n°6, 16132, Genova, Italy.
Ana Rebollo GimenezDINOGMI, University of Genoa, Genova, Italy.ORCID http://orcid.org/0000-0002-3973-3442
Clara MalattiaDINOGMI, University of Genoa, Genova, Italy.
Marco GattornoDepartment of Rheumatology and Autoinflammatory diseases, IRCCS Istituto Giannina Gaslini, Genova, Italy.ORCID http://orcid.org/0000-0003-0704-1916
Silvia RosinaDepartment of Rheumatology and Autoinflammatory diseases, IRCCS Istituto Giannina Gaslini, Genova, Italy.ORCID http://orcid.org/0000-0002-3667-6155
Vanessa SmithDepartment of Internal Medicine, University of Ghent, Ghent University Hospital, Ghent, Belgium.ORCID http://orcid.org/0000-0001-6271-7945
Maurizio CutoloLaboratory of Experimental Rheumatology and Academic Division of Clinical Rheumatology, Department of Internal Medicine and Specialties (DIMI), University of Genova, Viale Benedetto XV, n°6, 16132, Genova, Italy. mcutolo@unige.it.ORCID http://orcid.org/0000-0002-5396-0932

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionJuvenile dermatomyositis (jDM) is a systemic autoimmune disease mainly affecting the skeletal muscle and skin. The aim of our study was to investigate the possible correlations between nailfold videocapillaroscopy (NVC) findings with clinical and laboratory parameters in patients with jDM.

methodsTwenty-eight jDM patients (mean age 7.1 ± 3 years, mean disease duration 3.1 ± 3 years), evaluated between 2019 and 2023, classified according to Bohan and Peter criteria, were age- and sex-matched with healthy controls. Clinical, laboratory, and NVC parameters were collected at first visit and after 1 year again in a subgroup of patients (n = 9).

resultsPositivity for myositis-specific autoantibodies (MSA) was associated with a lower mean capillary density (p = 0.02) in jDM patients. Additionally, the presence of giant capillaries was significantly more frequent in MSA-positive patients (p = 0.04). The skin component of the disease activity score (VAS and DAS skin score) showed a significant inverse correlation with capillary density (r = -0.53, p = 0.007) and was significantly higher in patients with giant capillaries (median 5.5 vs 1, p = 0.005). Periungual telangiectasias and Gottron's papules were significantly associated with a reduction of the mean capillary count and with the presence of giant capillaries (all p-values < 0.05). Interestingly, no significant changes in NVC parameters were reported after 1 year of receiving immunosuppressive treatment.

conclusionsCapillary loss and the presence of giant capillaries at NVC analysis were significantly associated with clinical and laboratory markers of skin disease activity in jDM. These findings suggest that NVC may serve as a promising non-invasive tool to support disease assessment, although further prospective studies are needed to confirm its role in clinical practice. Key Points • Nailfold videocapillaroscopy (NVC) abnormalities, particularly capillary loss and giant capillaries, correlate significantly with skin disease activity in juvenile dermatomyositis (jDM). • Myositis-specific antibodies (MSA), especially anti-TIF1γ, are associated with more severe microvascular damage, suggesting their potential role in patient stratification. • NVC parameters remained stable over 1 year of immunosuppressive treatment, highlighting the need for longer-term studies to evaluate microvascular change progressions in jDM. • NVC may represent a promising non-invasive biomarker to support the clinical assessment and follow-up of patients with jDM, but further validation in larger prospective studies is warranted.

Indexed as

CapillariesDermatomyositisMicroscopic AngioscopyNailsAdolescentAutoantibodiesChildChild, PreschoolFemaleHumansMaleRetrospective StudiesSkinAutoantibodiesCapillary morphologyJuvenile dermatomyositisMicrovascular abnormalitiesMicrovascular damageNailfold videocapillaroscopyPediatric rheumatology

Identifiers

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.