Insulin‐like growth factor binding Protein‐4: A novel indicator of pulmonary arterial hypertension severity and survival

Author:

Torres Guillermo1ORCID,Yang Jun1ORCID,Griffiths Megan2,Brandal Stephanie1,Damico Rachel3,Vaidya Dhananjay45,Simpson Catherine E.3ORCID,Pauciulo Michael W.6,Nichols William C.6,Ivy David D.7,Austin Eric D.8,Hassoun Paul M.3,Everett Allen D.1

Affiliation:

1. Division of Pediatric Cardiology, Department of Pediatrics Johns Hopkins University Baltimore Maryland USA

2. Division of Pediatric Cardiology, Department of Pediatrics University of Texas Southwestern Medical Center Dallas Texas USA

3. Division of Pulmonary and Critical Care Medicine, Department of Medicine Johns Hopkins University Baltimore Maryland USA

4. Department of Epidemiology Johns Hopkins Bloomberg School of Public Health Baltimore Maryland USA

5. Division of General Internal Medicine Johns Hopkins School of Medicine Baltimore Maryland USA

6. Division of Human Genetics, Department of Pediatrics Cincinnati Children's Hospital Medical Center, University of Cincinnati College of Medicine Cincinnati Ohio USA

7. Department of Pediatric Cardiology Children's Hospital Colorado Denver Colorado USA

8. Division of Allergy, Immunology, and Pulmonary Medicine, Department of Pediatrics Vanderbilt University Medical Center Nashville Tennessee USA

Abstract

AbstractProteomic analysis of patients with pulmonary arterial hypertension (PAH) has demonstrated significant abnormalities in the insulin‐like growth factor axis (IGF). This study proposed to establish associations between a specific binding protein, insulin‐like growth factor binding protein 4 (IGFBP4), and PAH severity as well as survival across varying study cohorts. In all cohorts studied, serum IGFBP4 levels were significantly elevated in PAH compared to controls (p < 0.0001). IGFBP4 concentration was also highest in the connective tissue‐associated PAH (CTD‐PAH) and idiopathic PAH subtypes (876 and 784 ng/mL, median, respectively). After adjustment for age and sex, IGFBP4 was significantly associated with worse PAH severity as defined by a decreased 6‐min walk distance (6MWD), New York heart association functional class (NYHA‐FC), REVEAL 2.0 score and higher right atrial pressures. In longitudinal analysis provided by one of the study cohorts, IGFBP4 was prospectively significantly associated with a shorter 6MWD, worse NYHA‐FC classification, and decreased survival. Cox multivariable analysis demonstrated higher serum IGFBP4 as an independent predictor of survival in the overall PAHB cohort. Therefore, this study established that higher circulating IGFBP4 levels were significantly associated with worse PAH severity, decreased survival and disease progression. Dysregulation of IGF metabolism/growth axis may play a significant role in PAH cardio‐pulmonary pathobiology.

Funder

National Heart, Lung, and Blood Institute

Publisher

Wiley

Subject

Pulmonary and Respiratory Medicine

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