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    <subfield code="2">doi</subfield>
    <subfield code="a">10.1016/j.medcli.2025.107283</subfield>
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    <subfield code="2">sideral</subfield>
    <subfield code="a">147976</subfield>
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    <subfield code="a">ART-2026-147976</subfield>
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    <subfield code="a">eng</subfield>
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  <datafield tag="100" ind1=" " ind2=" ">
    <subfield code="a">Pérez Abad, Laura</subfield>
    <subfield code="u">Universidad de Zaragoza</subfield>
  </datafield>
  <datafield tag="245" ind1=" " ind2=" ">
    <subfield code="a">Unlocking the potential of nailfold videocapillaroscopy in diagnosing and staging wild-type transthyretin amyloidosis: A preliminary approach</subfield>
  </datafield>
  <datafield tag="260" ind1=" " ind2=" ">
    <subfield code="c">2026</subfield>
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  <datafield tag="520" ind1="3" ind2=" ">
    <subfield code="a">Background. Wild-type transthyretin amyloidosis (ATTRwt) is a serious condition. At early stages, symptoms resemble those of heart failure with preserved ejection fraction (HFpEF). Our aim was to perform software-supported nailfold videocapillaroscopy (NVC) analysis to identify hallmarks useful for diagnosis and build machine learning (ML)-based models to assess severity.
Methods. Thirty-two ATTRwt patients underwent NVC. Nineteen initiated TTR-stabilizing therapy and had a new NVC 12 months afterwards. Forty-one capillary-related variables were analyzed. Thirty NVCs were randomly chosen to train models to discriminate between poorer or less poor prognosis according to N-terminal pro-B-type natriuretic peptide (NT-proBNP) or Cheng score (cut-offs: 2000 pg/mL and 4 points, respectively). The remaining 21 NVCs were used for validation purposes. A control population of 99 patients with heart failure with preserved ejection fraction (HFpEF) but without signs of amyloidosis was included.
Results. A profound disorganization in the nailfold capillary architecture was generally observed. The models achieved accuracies of 0.81 and 0.90, respectively, in predicting disease severity. An additional model designed to distinguish a profile suggestive of amyloidosis (vs. HFpEF controls) achieved an accuracy of 0.73.
Conclusions. NVC-based ML models may contribute to early diagnosis and staging of ATTRwt.</subfield>
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    <subfield code="a">Access copy available to the general public</subfield>
    <subfield code="f">Unrestricted</subfield>
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  <datafield tag="536" ind1=" " ind2=" ">
    <subfield code="9">info:eu-repo/grantAgreement/ES/IISAragón/GIIS-009</subfield>
    <subfield code="9">info:eu-repo/grantAgreement/ES/IISAragón/GIIS-084</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Aibar Arregui, Miguel Ángel</subfield>
    <subfield code="0">(orcid)0000-0002-1774-6488</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Aramburu Llorente, Jimena</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Ramón y Cajal Calvo, Juan</subfield>
    <subfield code="u">Universidad de Zaragoza</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Andrés Gracia, Alejandro</subfield>
    <subfield code="u">Universidad de Zaragoza</subfield>
    <subfield code="0">(orcid)0000-0003-3501-0121</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Revilla Martí, Pablo</subfield>
    <subfield code="u">Universidad de Zaragoza</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Atienza Ayala, Saida</subfield>
    <subfield code="0">(orcid)0000-0003-0715-2843</subfield>
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    <subfield code="a">Lahuerta Pueyo, Carmen</subfield>
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    <subfield code="a">Campos Sáenz de Santamaría, Amelia</subfield>
    <subfield code="u">Universidad de Zaragoza</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Ramos Ibañez, Eduardo</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Gracia Tello, Borja del Carmelo</subfield>
    <subfield code="u">Universidad de Zaragoza</subfield>
    <subfield code="0">(orcid)0000-0003-3248-2908</subfield>
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  <datafield tag="710" ind1="2" ind2=" ">
    <subfield code="1">1011</subfield>
    <subfield code="2">770</subfield>
    <subfield code="a">Universidad de Zaragoza</subfield>
    <subfield code="b">Dpto. Microb.Ped.Radio.Sal.Pú.</subfield>
    <subfield code="c">Área Radiol. y Medicina Física</subfield>
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    <subfield code="1">1007</subfield>
    <subfield code="2">610</subfield>
    <subfield code="a">Universidad de Zaragoza</subfield>
    <subfield code="b">Dpto. Medicina, Psiqu. y Derm.</subfield>
    <subfield code="c">Area Medicina</subfield>
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  <datafield tag="773" ind1=" " ind2=" ">
    <subfield code="g">166, 2 (2026), 107283 [8 pp.]</subfield>
    <subfield code="p">Med. clín.</subfield>
    <subfield code="t">Medicina clinica</subfield>
    <subfield code="x">0025-7753</subfield>
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