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Revista Colombiana de Reumatología (English Edition) Nailfold capillaroscopy in mixed connective tissue disease, systemic sclerosis, ...
Journal Information
Vol. 32. Issue 3.
Pages 209-215 (July - September 2025)
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474
Vol. 32. Issue 3.
Pages 209-215 (July - September 2025)
Original Investigation
Nailfold capillaroscopy in mixed connective tissue disease, systemic sclerosis, and primary Raynaud phenomenon in a capillaroscopy service from Medellin, Colombia 2015–2020
Hallazgos capilaroscópicos en pacientes con enfermedad mixta del tejido conectivo, fenómeno de Raynaud primario y esclerosis sistémica en una institución en Medellín (Colombia), 2015−2020
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474
Adriana Margarita Trejos Tenorioa, Carlos Jaime Velásquez Francob,c,
Corresponding author
carjaivel@gmail.com

Corresponding author.
, Libia María Rodríguez Padillab,c, Miguel Antonio Mesa Navasb,d
a Departamento de Medicina Interna, Facultad de Medicina, Universidad Pontificia Bolivariana, Medellín, Colombia
b Grupo de Investigación UNIR, Escuela de Ciencias de la Salud, Universidad Pontificia Bolivariana, Medellín, Colombia
c Departamento de Reumatología, Clínica Universitaria Bolivariana, Medellín, Colombia
d Departamento de Reumatología, Clínica Rosario El Tesoro-Equipo de Investigación SURA, Medellín, Colombia
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Tables (3)
Table 1. Sociodemographic and serological characteristics of patients with mixed connective tissue disease, systemic sclerosis, and primary Raynaud's phenomenon in a capillaroscopy service in Medellín, Colombia.
Tables
Table 2. Clinical features of patients with mixed connective tissue disease in a capillaroscopy service in Medellín (Colombia).
Tables
Table 3. Capillaroscopic features in patients with mixed connective tissue disease, primary Raynaud's phenomenon, and systemic sclerosis in a capillaroscopy service in Medellín (Colombia).
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Abstract
Introduction

Nailfold capillaroscopy is a useful tool to evaluate microcirculation. In mixed connective tissue disease (MCTD), microvascular changes are not clearly defined. This study aims to compare the angiographic findings between patients with mixed connective tissue disease, systemic sclerosis, and primary Raynaud phenomenon (pRP) in a capillaroscopy reference centre.

Methods

A retrospective descriptive study with an exploratory analytical component was designed. Clinical and capillaroscopic characteristic information was obtained from medical records and capillaroscopic reports from an expert capillaroscopy service using an Optilia 200x videocapillaroscope. To compare qualitative variables, the Pearson or Fisher exact chi-square test was used in case of expected frequencies lower than five.

Results

One hundred and twenty capillaroscopy charts were reviewed. In the MCTD group, 42.5% of patients showed a normal pattern, 37.5% had a non-scleroderma pattern, and 20% exhibited a scleroderma pattern. Among pRP patients, 62.5% had a normal and 37.5% had a non-specific pattern; both groups preserved capillary density. In MCTS, compared to SS, there were fewer avascular areas (10% vs. 62.5% p < .001), megacapillaries (20% vs 100%, p < .001), and haemorrhages (37.5 vs. 92.5% p < .001). Bushy capillaries predominated in the MCTD (10%) compared to SS (5%) and pRP (0%) groups without significance difference (p = .122).

Conclusions

Compared to systemic sclerosis, mixed connective tissue disease presents greater capillary density and a greater frequency of arborescent capillaries.

Keywords:
Mixed connective tissue disease
Microscopic angioscopy
Raynaud phenomenon
Systemic sclerosis
Resumen
Introducción

La videocapilaroscopia de lecho ungular es una herramienta útil en el estudio de la microcirculación. En la enfermedad mixta del tejido conectivo los cambios microvasculares no están claramente definidos. El objetivo de este estudio fue comparar los hallazgos capilaroscópicos en pacientes con EMTC, esclerosis sistémica (ES) o fenómeno de Raynaud primario (FRp) en una institución, entre el 2015 y el 2020.

Materiales y métodos

Se diseñó un estudio descriptivo retrospectivo con un componente analítico exploratorio. La información de características clínicas y capilaroscópicas se obtuvo de las historias clínicas y los reportes capilaroscópicos realizados en un servicio de capilaroscopia experto utilizando un videocapilaroscopio Optilia 200×. Para la comparación entre los tres grupos de pacientes para variables cualitativas, se utilizó la prueba chi cuadrado de Pearson o Fisher exacto en caso de frecuencias esperadas menores a 5.

Resultados

Se incluyeron 120 pacientes; en EMTC, el 42,5% presentó un patrón normal; el 37,5%, no escleroderma; y el 20%, escleroderma. De los pacientes con FRp, el 62,5% tuvo un patrón normal y el 37,5% tuvo uno no específico; en ambos grupos la densidad capilar se preservó. En EMTC, comparado con ES, hubo menos áreas avasculares (10% vs. 62,5% p < 0,001), megacapilares (20% vs 100%, p < 0,001) y hemorragias (37,5 vs. 92,5%, p < 0,001). Los capilares arborescentes predominaron en EMTC (10%) con respecto a ES (5%) y FRp (0%), sin diferencia estadística (p = 0,122).

Conclusiones

En comparación con esclerosis sistémica, la enfermedad mixta del tejido conectivo presenta mayor densidad capilar y mayor frecuencia de capilares arborescentes.

Palabras clave:
Enfermedad mixta del tejido conectivo
Capilaroscopia
Fenómeno de raynaud
Esclerosis sistémica

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