Low‐affinity insulin‐like growth factor binding protein 7 and its association with pulmonary arterial hypertension severity and survival

Author:

Torres Guillermo1ORCID,Lancaster Andrew C.2,Yang Jun1ORCID,Griffiths Megan3,Brandal Stephanie1,Damico Rachel4,Vaidya Dhananjay56,Simpson Catherine E.4ORCID,Martin Lisa J.7,Pauciulo Michael W.7,Nichols William C.7,Ivy David D.8,Austin Eric D.9,Hassoun Paul M.4,Everett Allen D.1

Affiliation:

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

2. School of Medicine Johns Hopkins University Baltimore Maryland USA

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

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

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

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

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

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

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

Abstract

AbstractInsulin‐like growth factor (IGF) binding proteins (IGFBPs) are a family of growth factor modifiers, some of which are known to be independently associated with pulmonary arterial hypertension (PAH) survival. IGF factor binding protein 7 (IGFBP7) is a unique low‐affinity IGFBP that, independent of IGF, stimulates prostacyclin production. This study proposed to establish associations between IGFBP7 and PAH severity and survival, using enrollment and longitudinal samples. Serum IGFBP7 levels were significantly elevated in patients with PAH compared to controls. After adjusting for age and sex, logarithmic increases in IGFBP7 were associated with a 20 m shorter six‐minute walk distance (6MWD; p < 0.001), a 2−3 mmHg higher mean right atrial pressure (p < 0.001 and 0.02), and a higher likelihood of a greater REVEAL 2.0 risk category placement (p < 0.001). Kaplan−Meier analysis demonstrated significantly decreased survival with IGFBP7 above the median and Cox multivariable analysis adjusted for age and sex, demonstrated higher serum IGFBP7 was an independent predictor of survival. Though the exact mechanism is still unknown, given IGFBP7's role as a prostacyclin stimulant, it has potential use as a therapeutic target for disease modulation.

Funder

National Heart, Lung, and Blood Institute

Publisher

Wiley

Subject

Pulmonary and Respiratory Medicine

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