Academic Thesis

Basic information

Name Ousaka Daiki
Belonging department
Occupation name
researchmap researcher code B000342311
researchmap agency Okayama University of Science

Title

Intracoronary Cardiac Progenitor Cells in Single Ventricle Physiology The PERSEUS (Cardiac Progenitor Cell Infusion to Treat Univentricular Heart Disease) Randomized Phase 2 Trial

Bibliography Type

 

Author

Shuta Ishigami
Shinichi Ohtsuki
Takahiro Eitoku
Daiki Ousaka
Maiko Kondo
Yoshihiko Kurita
Kenta Hirai
Yosuke Fukushima
Kenji Baba
Takuya Goto
Naohiro Horio
Junko Kobayashi
Yosuke Kuroko
Yasuhiro Kotani
Sadahiko Arai
Tatsuo Iwasaki
Shuhei Sato
Shingo Kasahara
Shunji Sano
Hidemasa Oh

Summary

Rationale: Patients with single ventricle physiology are at high risk of mortality resulting from ventricular dysfunction. The preliminary results of the phase 1 trial showed that cardiosphere-derived cells (CDCs) may be effective against congenital heart failure.
Objective: To determine whether intracoronary delivery of autologous CDCs improves cardiac function in patients with single ventricle physiology.
Methods and Results: We conducted a phase 2 randomized controlled study to assign in a 1: 1 ratio 41 patients who had single ventricle physiology undergoing stage 2 or 3 palliation to receive intracoronary infusion of CDCs 4 to 9 weeks after surgery or staged reconstruction alone (study A). The primary outcome measure was to assess improvement in cardiac function at 3-month follow-up. Four months after palliation, controls had an alternative option to receive late CDC infusion on request (study B). Secondary outcomes included ventricular function, heart failure status, somatic growth, and health-related quality of life after a 12-month observation. At 3 months, the absolute changes in ventricular function were significantly greater in the CDC-treated group than in the controls (+ 6.4% [SD, 5.5] versus + 1.3% [SD, 3.7]; P= 0.003). In study B, a late CDC infusion in 17 controls increased the ventricular function at 3 months compared with that at baseline (38.8% [SD, 7.7] versus 34.8% [SD, 7.4]; P< 0.0001). At 1 year, overall CDC infusion was associated with improved ventricular function (41.4% [SD, 6.6] versus 35.0% [SD, 8.2]; P< 0.0001) and volumes (P< 0.001), somatic growth (P< 0.0001) with increased trophic factors production, such as insulin-like growth factor-1 and hepatocyte growth factor, and quality of life, along with a reduced heart failure status (P< 0.0001) and cardiac fibrosis (P= 0.014) relative to baseline.
Conclusions: Intracoronary infusion of CDCs after staged palliation favorably affected cardiac function by reverse remodeling in patients with single ventricle physiology. This impact may improve heart failure status, somatic growth, and quality of life in patients and reduce parenting stress for their families.

Magazine(name)

CIRCULATION RESEARCH

Publisher

LIPPINCOTT WILLIAMS & WILKINS

Volume

120

Number Of Pages

7

StartingPage

1162

EndingPage

+

Date of Issue

2017-03

Referee

Exist

Invited

Not exist

Language

English

Thesis Type

Research papers (academic journals)

ISSN

 

DOI

10.1161/CIRCRESAHA.116.310253

NAID

 

PMID

 

J-GLOBAL ID

 

arXiv ID

 

ORCID Put Code

 

DBLP ID