Myriam Calle Rubio

Dr. Myriam Calle Rubio

Complutense University of Madrid, Madrid, Spain
+1
orcid

Research Focus & Metrics

Academic Career Length

30Years (1997-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 June 2017 in Archivos de Bronconeumología
Verified
Journal Article
Closed access
MMMarc Miravitlles
Marc Miravitlles
JSJuan José Soler-Cataluña
Juan José Soler-Cataluña
MRMyriam Calle Rubio
Myriam Calle Rubio
JMJesús Molina
Jesús Molina
PAPere Almagro
Pere Almagro
JAJulio Ancochea
Julio Ancochea

1 January 2019 in The Lancet Respiratory Medicine
Verified
Journal Article
Closed access
WBWilliam W Busse
William W Busse
EBEugene R Bleecker
Eugene R Bleecker
JFJ Mark FitzGerald
J Mark FitzGerald
GFGary T Ferguson
Gary T Ferguson
PBPeter Barker
Peter Barker
LLLan Le
Lan Le

1 January 2016 in Chest
Verified
Journal Article
Closed access
Borja G CosíoBorja G Cosío
Borja G Cosío
JSJoan B Soriano
Joan B Soriano
Jose Luis Lopez-CamposJose Luis Lopez-Campos
Jose Luis Lopez-Campos
MRMyriam Calle Rubio
Myriam Calle Rubio
JSJuan José Soler-Cataluna
Juan José Soler-Cataluna
ADAlfredo de Diego Damia
Alfredo de Diego Damia

1 September 2013 in Archivos de Bronconeumología
Verified
Journal Article
Closed access
FGFrancisco Garcia-Rio
Francisco Garcia-Rio
MRMyriam Calle Rubio
Myriam Calle Rubio
FBFelip Burgos
Felip Burgos
PCPere Casan
Pere Casan
FCFélix del Campo
Félix del Campo
LMLuis Puente MAestu
Luis Puente MAestu

11 October 2012 in European Respiratory Journal
Verified
Journal Article
Open access
PDF file
MMMarc Miravitlles
Marc Miravitlles
JSJuan José Soler-Cataluña
Juan José Soler-Cataluña
MRMyriam Calle Rubio
Myriam Calle Rubio
JSJoan B Soriano
Joan B Soriano
The new Global Initiative for Chronic Obstructive Lung Disease update has moved the principles of treatment of stable chronic obstructive pulmonary disease (COPD) forward by including the concepts of symptoms and risks into the decision of therapy. However, no mention of the concept of clinical phenotypes is included. It is recognised that COPD is a very heterogeneous disease and not all patients respond to all drugs available for treatment. The identification of responders to therapies is crucial in chronic diseases to provide the most appropriate treatment and avoid unnecessary medications. The classically defined phenotypes of chronic bronchitis and emphysema, together with the newly described phenotypes of overlap COPD-asthma and frequent exacerbator, allow a simple classification of patients that share clinical characteristics and outcomes and, more importantly, similar responses to existing treatments.These clinical phenotypes can help clinicians identify patients that respond to specific pharmacological interventions. For example, frequent exacerbators are the only subjects with an indication for anti-inflammatory treatment in COPD. Among them, those with chronic bronchitis are the only candidates to receive phosphodiesterase-4 inhibitors. Patients with overlap COPD-asthma phenotype show an enhanced response to inhaled corticosteroids and infrequent exacerbators should only receive bronchodilators. These well-defined clinical phenotypes could potentially be incorporated into treatment guidelines.

22 November 2017 in European Respiratory Journal
Verified
Journal Article
Closed access
PDF file
CCCiro Casanova
Ciro Casanova
BCBartolome R. Celli
Bartolome R. Celli
JDJuan Pablo De-Torres
Juan Pablo De-Torres
CMCristina Martínez-Gonzalez
Cristina Martínez-Gonzalez
Borja G CosíoBorja G Cosío
Borja G Cosío
JMJose M. Marin
Jose M. Marin
The impact of blood eosinophilia in chronic obstructive pulmonary disease (COPD) remains controversial.To evaluate the prevalence and stability of a high level of blood eosinophils (≥300 cells·μL–1) and its relationship to outcomes, we determined blood eosinophils at baseline and over 2 years in 424 COPD patients (forced expiratory volume in 1 s (FEV1) 60% predicted) and 67 smokers without COPD from the CHAIN cohort, and in 308 COPD patients (FEV160% predicted) in the BODE cohort. We related eosinophil levels to exacerbations and survival using Cox hazard analysis.In COPD patients, 15.8% in the CHAIN cohort and 12.3% in the BODE cohort had persistently elevated blood eosinophils at all three visits. A significant proportion (43.8%) of patients had counts that oscillated above and below the cut-off points, while the rest had persistent eosinophil levels <300 cells·μL–1. A similar eosinophil blood pattern was observed in controls. Exacerbation rates did not differ in patients with and without eosinophilia. All-cause mortality was lower in patients with high eosinophils compared with those with values <300 cells·μL–1(15.8%versus33.7%; p=0.026).In patients with COPD, blood eosinophils ≥300 cells·μL–1persisting over 2 years was not a risk factor for COPD exacerbations. High eosinophil count was associated with better survival.