Interstitial lung disease in patients with idiopathic inflammatory myopathy (IIM-ILD): Definitions, epidemiology, pathophysiology, clinical manifestations, complications, risk, and mortality factors (narrative review)
Interstitial lung disease refers to a group of disorders generally characterized by progressive scarring of lung tissue due to a wide variety of causes and associated with a plethora of symptoms. Patients with this diagnosis can be asymptomatic or present severe symptoms that could lead to death. It...
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| Published in | Revista Colombiana de Reumatología (English Edition) Vol. 31; no. 3; pp. 399 - 411 |
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| Main Authors | , , , |
| Format | Journal Article |
| Language | English |
| Published |
Elsevier España, S.L.U
01.07.2024
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| Online Access | Get full text |
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| Abstract | Interstitial lung disease refers to a group of disorders generally characterized by progressive scarring of lung tissue due to a wide variety of causes and associated with a plethora of symptoms. Patients with this diagnosis can be asymptomatic or present severe symptoms that could lead to death. Its signs and symptoms are the same in patients with concomitant connective tissue disease and those without. Genetics and immunity play essential roles in patients with interstitial lung disease and idiopathic inflammatory myopathy. Alterations in genes and excessive production of specific cytokines can lead to the development of interstitial lung disease. Interstitial lung disease can have several complications, including chronic respiratory distress and infections, and can worsen the prognosis of patients with idiopathic inflammatory myopathy. Here, we present a narrative review describing the epidemiology, pathophysiology, clinical manifestations, risk factors, and complications of the population with interstitial lung disease and idiopathic inflammatory myopathy.
La enfermedad pulmonar intersticial se refiere a un grupo de trastornos generalmente caracterizados por cicatrización progresiva del tejido pulmonar, debidos a una amplia variedad de causas y asociados con múltiples síntomas. Los pacientes con este diagnóstico pueden estar asintomáticos o presentar síntomas severos que podrían conducir a la muerte. Los signos y los síntomas de esta enfermedad son iguales en pacientes que tienen una enfermedad del tejido conectivo concomitante y en aquellos que no la tienen. La genética y la inmunidad desempeñan papeles esenciales en pacientes con enfermedad pulmonar intersticial y miopatía idiopática inflamatoria. Las alteraciones en los genes y la producción excesiva de citoquinas específicas pueden conducir al desarrollo de la enfermedad. A su vez, la enfermedad pulmonar intersticial puede tener varias complicaciones, como dificultad respiratoria crónica e infecciones, y puede empeorar el pronóstico de los pacientes con miopatía idiopática inflamatoria. Presentamos una revisión narrativa que describe la epidemiología, la fisiopatología, las manifestaciones clínicas, los factores de riesgo y las complicaciones de la población con enfermedad pulmonar intersticial y miopatía idiopática inflamatoria. |
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| AbstractList | Interstitial lung disease refers to a group of disorders generally characterized by progressive scarring of lung tissue due to a wide variety of causes and associated with a plethora of symptoms. Patients with this diagnosis can be asymptomatic or present severe symptoms that could lead to death. Its signs and symptoms are the same in patients with concomitant connective tissue disease and those without. Genetics and immunity play essential roles in patients with interstitial lung disease and idiopathic inflammatory myopathy. Alterations in genes and excessive production of specific cytokines can lead to the development of interstitial lung disease. Interstitial lung disease can have several complications, including chronic respiratory distress and infections, and can worsen the prognosis of patients with idiopathic inflammatory myopathy. Here, we present a narrative review describing the epidemiology, pathophysiology, clinical manifestations, risk factors, and complications of the population with interstitial lung disease and idiopathic inflammatory myopathy.
La enfermedad pulmonar intersticial se refiere a un grupo de trastornos generalmente caracterizados por cicatrización progresiva del tejido pulmonar, debidos a una amplia variedad de causas y asociados con múltiples síntomas. Los pacientes con este diagnóstico pueden estar asintomáticos o presentar síntomas severos que podrían conducir a la muerte. Los signos y los síntomas de esta enfermedad son iguales en pacientes que tienen una enfermedad del tejido conectivo concomitante y en aquellos que no la tienen. La genética y la inmunidad desempeñan papeles esenciales en pacientes con enfermedad pulmonar intersticial y miopatía idiopática inflamatoria. Las alteraciones en los genes y la producción excesiva de citoquinas específicas pueden conducir al desarrollo de la enfermedad. A su vez, la enfermedad pulmonar intersticial puede tener varias complicaciones, como dificultad respiratoria crónica e infecciones, y puede empeorar el pronóstico de los pacientes con miopatía idiopática inflamatoria. Presentamos una revisión narrativa que describe la epidemiología, la fisiopatología, las manifestaciones clínicas, los factores de riesgo y las complicaciones de la población con enfermedad pulmonar intersticial y miopatía idiopática inflamatoria. |
| Author | Hormaza-Jaramillo, Andrés Fernandez-Trujillo, Liliana Vargas-Potes, Carlos Julio Delgado-Mora, Tatiana |
| Author_xml | – sequence: 1 givenname: Andrés surname: Hormaza-Jaramillo fullname: Hormaza-Jaramillo, Andrés email: andres.hormaza@fvl.org.co organization: Department of Internal Medicine, Rheumatology Service, Fundación Valle del Lili, Cali, Colombia – sequence: 2 givenname: Liliana surname: Fernandez-Trujillo fullname: Fernandez-Trujillo, Liliana organization: Department of Internal Medicine, Faculty of Health Sciences, Universidad Icesi, Cali, Colombia – sequence: 3 givenname: Tatiana surname: Delgado-Mora fullname: Delgado-Mora, Tatiana organization: Clinical Research Center, Fundación Valle del Lili, Cali, Colombia – sequence: 4 givenname: Carlos Julio surname: Vargas-Potes fullname: Vargas-Potes, Carlos Julio organization: Department of Internal Medicine, Faculty of Health Sciences, Universidad Icesi, Cali, Colombia |
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| Copyright | 2023 Asociación Colombiana de Reumatología |
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| Keywords | Clinical manifestations Epidemiología Enfermedad pulmonar intersticial Autoantibodies Autoanticuerpos Mortality Idiopathic inflammatory myopathy Mortalidad Interstitial lung disease Epidemiology Miopatía idiopática inflamatoria Manifestaciones clínicas |
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| SubjectTerms | Autoantibodies Autoanticuerpos Clinical manifestations Enfermedad pulmonar intersticial Epidemiology Epidemiología Idiopathic inflammatory myopathy Interstitial lung disease Manifestaciones clínicas Miopatía idiopática inflamatoria Mortalidad Mortality |
| Title | Interstitial lung disease in patients with idiopathic inflammatory myopathy (IIM-ILD): Definitions, epidemiology, pathophysiology, clinical manifestations, complications, risk, and mortality factors (narrative review) |
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