3'-Deoxy-3'-[18F]Fluorothymidine Positron Emission Tomography Depicts Heterogeneous Proliferation Pathology in Idiopathic Pulmonary Arterial Hypertension Patient Lung

Circ Cardiovasc Imaging. 2018 Aug;11(8):e007402. doi: 10.1161/CIRCIMAGING.117.007402.

Abstract

Background: Pulmonary vascular cell hyperproliferation is characteristic of pulmonary vascular remodeling in pulmonary arterial hypertension. A noninvasive imaging biomarker is needed to track the pathology and assess the response to novel treatments targeted at resolving the structural changes. Here, we evaluated the application of radioligand 3'-deoxy-3'-[18F]-fluorothymidine (18FLT) using positron emission tomography.

Methods and results: We performed dynamic 18FLT positron emission tomography in 8 patients with idiopathic pulmonary arterial hypertension (IPAH) and applied in-depth kinetic analysis with a reversible 2-compartment 4k model. Our results show significantly increased lung 18FLT phosphorylation (k3) in patients with IPAH compared with nonpulmonary arterial hypertension controls (0.086±0.034 versus 0.054±0.009 min-1; P<0.05). There was heterogeneity in the lung 18FLT signal both between patients with IPAH and within the lungs of each patient, compatible with histopathologic reports of lungs from patients with IPAH. Consistent with 18FLT positron emission tomographic data, TK1 (thymidine kinase 1) expression was evident in the remodeled vessels in IPAH patient lung. In addition, hyperproliferative pulmonary vascular fibroblasts isolated from patients with IPAH exhibited upregulated expression of TK1 and the thymidine transporter, ENT1 (equilibrative nucleoside transporter 1). In the monocrotaline and SuHx (Sugen hypoxia) rat pulmonary arterial hypertension models, increased lung 18FLT uptake was strongly associated with peripheral pulmonary vascular muscularization and the proliferation marker, Ki-67 score, together with prominent TK1 expression in remodeled vessels. Importantly, lung 18FLT uptake was attenuated by 2 antiproliferative treatments: dichloroacetate and the tyrosine kinase inhibitor, imatinib.

Conclusions: Dynamic 18FLT positron emission tomography imaging can be used to report hyperproliferation in pulmonary hypertension and merits further study to evaluate response to treatment in patients with IPAH.

Keywords: positron emission tomography; pulmonary hypertension; thymidine kinase 1; vascular remodeling.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Animals
  • Case-Control Studies
  • Cell Proliferation*
  • Cells, Cultured
  • Dideoxynucleosides / administration & dosage*
  • Dideoxynucleosides / pharmacokinetics
  • Disease Models, Animal
  • Equilibrative Nucleoside Transporter 1 / metabolism
  • Familial Primary Pulmonary Hypertension / diagnostic imaging*
  • Familial Primary Pulmonary Hypertension / metabolism
  • Familial Primary Pulmonary Hypertension / pathology
  • Familial Primary Pulmonary Hypertension / physiopathology
  • Female
  • Fibroblasts / metabolism
  • Fibroblasts / pathology
  • Humans
  • Ki-67 Antigen / metabolism
  • Lung / blood supply*
  • Male
  • Middle Aged
  • Models, Biological
  • Positron-Emission Tomography / methods*
  • Predictive Value of Tests
  • Pulmonary Artery / diagnostic imaging*
  • Pulmonary Artery / metabolism
  • Pulmonary Artery / pathology
  • Pulmonary Artery / physiopathology
  • Radiopharmaceuticals / administration & dosage*
  • Radiopharmaceuticals / pharmacokinetics
  • Rats, Sprague-Dawley
  • Thymidine Kinase / metabolism
  • Thymidine Phosphorylase / metabolism
  • Vascular Remodeling*

Substances

  • Dideoxynucleosides
  • Equilibrative Nucleoside Transporter 1
  • Ki-67 Antigen
  • Radiopharmaceuticals
  • SLC29A1 protein, human
  • TYMP protein, human
  • Thymidine Phosphorylase
  • Thymidine Kinase
  • thymidine kinase 1
  • alovudine