Clinical analysis of chronic active EBV infection with coronary artery dilatation and a matched case–control study
Abstract Objective To investigate the clinical characteristics, treatment, prognosis and risk factors for chronic active Epstein–Barr Virus infection (CAEBV) associated with coronary artery dilatation (CAD) in children. Methods Children with CAEBV associated with CAD hospitalized at Beijing Children...
Main Authors: | , , , , , , , , , |
---|---|
Format: | Article |
Language: | English |
Published: |
BMC
2021-01-01
|
Series: | Orphanet Journal of Rare Diseases |
Subjects: | |
Online Access: | https://doi.org/10.1186/s13023-021-01689-5 |
id |
doaj-fff8bdddeb9648f0a28e03203bf12cd1 |
---|---|
record_format |
Article |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Ang Wei Honghao Ma Liping Zhang Zhigang Li Yitong Guan Qing Zhang Dong Wang Hongyun Lian Rui Zhang Tianyou Wang |
spellingShingle |
Ang Wei Honghao Ma Liping Zhang Zhigang Li Yitong Guan Qing Zhang Dong Wang Hongyun Lian Rui Zhang Tianyou Wang Clinical analysis of chronic active EBV infection with coronary artery dilatation and a matched case–control study Orphanet Journal of Rare Diseases Epstein–Barr virus Coronary artery Clinical characteristics Pathogenesis |
author_facet |
Ang Wei Honghao Ma Liping Zhang Zhigang Li Yitong Guan Qing Zhang Dong Wang Hongyun Lian Rui Zhang Tianyou Wang |
author_sort |
Ang Wei |
title |
Clinical analysis of chronic active EBV infection with coronary artery dilatation and a matched case–control study |
title_short |
Clinical analysis of chronic active EBV infection with coronary artery dilatation and a matched case–control study |
title_full |
Clinical analysis of chronic active EBV infection with coronary artery dilatation and a matched case–control study |
title_fullStr |
Clinical analysis of chronic active EBV infection with coronary artery dilatation and a matched case–control study |
title_full_unstemmed |
Clinical analysis of chronic active EBV infection with coronary artery dilatation and a matched case–control study |
title_sort |
clinical analysis of chronic active ebv infection with coronary artery dilatation and a matched case–control study |
publisher |
BMC |
series |
Orphanet Journal of Rare Diseases |
issn |
1750-1172 |
publishDate |
2021-01-01 |
description |
Abstract Objective To investigate the clinical characteristics, treatment, prognosis and risk factors for chronic active Epstein–Barr Virus infection (CAEBV) associated with coronary artery dilatation (CAD) in children. Methods Children with CAEBV associated with CAD hospitalized at Beijing Children’s Hospital, Capital Medical University from March 2016 to December 2019 were analyzed. Children with CAEBV without CAD were selected as the control group and matched by sex, age, treatment and admission time. The clinical manifestations, laboratory and ultrasound examinations, treatment and prognosis of the children were collected in both groups. Results There were 10 children with CAEBV combined with CAD, including 6 males and 4 females, accounting for 8.9% (10/112) of CAEBV patients in the same period, with an onset age of 6.05 (2.8–14.3) years. The median follow-up time was 20 (6–48) months. All the patients had high copies of EBV-DNA in whole blood [1.18 × 107 (1.90 × 105–3.96 × 107) copies/mL] and plasma [1.81 × 104 (1.54 × 103–1.76 × 106) copies/mL], and all biopsy samples (bone marrow, lymph nodes or liver) were all positive for Epstein–Barr virus-encoded small RNA. Among the 10 children, 8 had bilateral CAD, and 2 patients had unilateral CAD. After diagnosis, 7 children were treated with L-DEP chemotherapy in our hospital. After chemotherapy, four patients underwent allogeneic hematopoietic stem cell transplantation (HSCT). The others were waiting for HSCT. At the time of the last patients follow up record, the CAD had returned to normal in 3 patients, and the time from the diagnosis of CAD to recovery was 21 (18–68) days. LDH, serum ferritin, TNF-α and IL-10 levels were statistically significantly different between the two groups (P = 0.009, 0.008, 0.026 and 0.030). There were no significant differences in survival rate between the two groups (P = 0.416). Conclusion The incidence of CAEBV with CAD was low. CAEBV with CAD did not influence the prognosis. Patients who had high LDH, serum ferritin, TNF-α, and IL-10 levels early in their illness were more likely to develop CAD. |
topic |
Epstein–Barr virus Coronary artery Clinical characteristics Pathogenesis |
url |
https://doi.org/10.1186/s13023-021-01689-5 |
work_keys_str_mv |
AT angwei clinicalanalysisofchronicactiveebvinfectionwithcoronaryarterydilatationandamatchedcasecontrolstudy AT honghaoma clinicalanalysisofchronicactiveebvinfectionwithcoronaryarterydilatationandamatchedcasecontrolstudy AT lipingzhang clinicalanalysisofchronicactiveebvinfectionwithcoronaryarterydilatationandamatchedcasecontrolstudy AT zhigangli clinicalanalysisofchronicactiveebvinfectionwithcoronaryarterydilatationandamatchedcasecontrolstudy AT yitongguan clinicalanalysisofchronicactiveebvinfectionwithcoronaryarterydilatationandamatchedcasecontrolstudy AT qingzhang clinicalanalysisofchronicactiveebvinfectionwithcoronaryarterydilatationandamatchedcasecontrolstudy AT dongwang clinicalanalysisofchronicactiveebvinfectionwithcoronaryarterydilatationandamatchedcasecontrolstudy AT hongyunlian clinicalanalysisofchronicactiveebvinfectionwithcoronaryarterydilatationandamatchedcasecontrolstudy AT ruizhang clinicalanalysisofchronicactiveebvinfectionwithcoronaryarterydilatationandamatchedcasecontrolstudy AT tianyouwang clinicalanalysisofchronicactiveebvinfectionwithcoronaryarterydilatationandamatchedcasecontrolstudy |
_version_ |
1724317354594140160 |
spelling |
doaj-fff8bdddeb9648f0a28e03203bf12cd12021-01-31T12:17:07ZengBMCOrphanet Journal of Rare Diseases1750-11722021-01-011611910.1186/s13023-021-01689-5Clinical analysis of chronic active EBV infection with coronary artery dilatation and a matched case–control studyAng Wei0Honghao Ma1Liping Zhang2Zhigang Li3Yitong Guan4Qing Zhang5Dong Wang6Hongyun Lian7Rui Zhang8Tianyou Wang9Beijing Key Laboratory of Pediatric Hematology Oncology; National Key Discipline of Pediatrics (Capital Medical University); Key Laboratory of Major Diseases in Children, Ministry of Education; Hematology Oncology Center, Beijing Children’s Hospital, Capital Medical University, National Center for Children’s HealthBeijing Key Laboratory of Pediatric Hematology Oncology; National Key Discipline of Pediatrics (Capital Medical University); Key Laboratory of Major Diseases in Children, Ministry of Education; Hematology Oncology Center, Beijing Children’s Hospital, Capital Medical University, National Center for Children’s HealthBeijing Key Laboratory of Pediatric Hematology Oncology; National Key Discipline of Pediatrics (Capital Medical University); Key Laboratory of Major Diseases in Children, Ministry of Education; Hematology Oncology Center, Beijing Children’s Hospital, Capital Medical University, National Center for Children’s HealthHematology and Oncology Laboratory, Beijing Pediatric Research Institute, Beijing Children’s Hospital Affiliated with Capital Medical University; National Center for Children’s Health; Beijing Key Laboratory of Pediatric Hematology Oncology, Key Laboratory of Major Diseases in Children; Ministry of Education, National Key Discipline of PediatricsBeijing Key Laboratory of Pediatric Hematology Oncology; National Key Discipline of Pediatrics (Capital Medical University); Key Laboratory of Major Diseases in Children, Ministry of Education; Hematology Oncology Center, Beijing Children’s Hospital, Capital Medical University, National Center for Children’s HealthHematology and Oncology Laboratory, Beijing Pediatric Research Institute, Beijing Children’s Hospital Affiliated with Capital Medical University; National Center for Children’s Health; Beijing Key Laboratory of Pediatric Hematology Oncology, Key Laboratory of Major Diseases in Children; Ministry of Education, National Key Discipline of PediatricsBeijing Key Laboratory of Pediatric Hematology Oncology; National Key Discipline of Pediatrics (Capital Medical University); Key Laboratory of Major Diseases in Children, Ministry of Education; Hematology Oncology Center, Beijing Children’s Hospital, Capital Medical University, National Center for Children’s HealthBeijing Key Laboratory of Pediatric Hematology Oncology; National Key Discipline of Pediatrics (Capital Medical University); Key Laboratory of Major Diseases in Children, Ministry of Education; Hematology Oncology Center, Beijing Children’s Hospital, Capital Medical University, National Center for Children’s HealthBeijing Key Laboratory of Pediatric Hematology Oncology; National Key Discipline of Pediatrics (Capital Medical University); Key Laboratory of Major Diseases in Children, Ministry of Education; Hematology Oncology Center, Beijing Children’s Hospital, Capital Medical University, National Center for Children’s HealthBeijing Key Laboratory of Pediatric Hematology Oncology; National Key Discipline of Pediatrics (Capital Medical University); Key Laboratory of Major Diseases in Children, Ministry of Education; Hematology Oncology Center, Beijing Children’s Hospital, Capital Medical University, National Center for Children’s HealthAbstract Objective To investigate the clinical characteristics, treatment, prognosis and risk factors for chronic active Epstein–Barr Virus infection (CAEBV) associated with coronary artery dilatation (CAD) in children. Methods Children with CAEBV associated with CAD hospitalized at Beijing Children’s Hospital, Capital Medical University from March 2016 to December 2019 were analyzed. Children with CAEBV without CAD were selected as the control group and matched by sex, age, treatment and admission time. The clinical manifestations, laboratory and ultrasound examinations, treatment and prognosis of the children were collected in both groups. Results There were 10 children with CAEBV combined with CAD, including 6 males and 4 females, accounting for 8.9% (10/112) of CAEBV patients in the same period, with an onset age of 6.05 (2.8–14.3) years. The median follow-up time was 20 (6–48) months. All the patients had high copies of EBV-DNA in whole blood [1.18 × 107 (1.90 × 105–3.96 × 107) copies/mL] and plasma [1.81 × 104 (1.54 × 103–1.76 × 106) copies/mL], and all biopsy samples (bone marrow, lymph nodes or liver) were all positive for Epstein–Barr virus-encoded small RNA. Among the 10 children, 8 had bilateral CAD, and 2 patients had unilateral CAD. After diagnosis, 7 children were treated with L-DEP chemotherapy in our hospital. After chemotherapy, four patients underwent allogeneic hematopoietic stem cell transplantation (HSCT). The others were waiting for HSCT. At the time of the last patients follow up record, the CAD had returned to normal in 3 patients, and the time from the diagnosis of CAD to recovery was 21 (18–68) days. LDH, serum ferritin, TNF-α and IL-10 levels were statistically significantly different between the two groups (P = 0.009, 0.008, 0.026 and 0.030). There were no significant differences in survival rate between the two groups (P = 0.416). Conclusion The incidence of CAEBV with CAD was low. CAEBV with CAD did not influence the prognosis. Patients who had high LDH, serum ferritin, TNF-α, and IL-10 levels early in their illness were more likely to develop CAD.https://doi.org/10.1186/s13023-021-01689-5Epstein–Barr virusCoronary arteryClinical characteristicsPathogenesis |