Cargando…

Survival analysis of spinal muscular atrophy type I

PURPOSE: The life expectancy of patients with spinal muscular atrophy (SMA) type I is generally considered to be less than 2 years. Recently, with the introduction of proactive treatments, a longer survival and an improved survival rate have been reported. In this study, we analyzed the natural cour...

Descripción completa

Detalles Bibliográficos
Autores principales: Park, Hyun Bin, Lee, Soon Min, Lee, Jin Sung, Park, Min Soo, Park, Kook In, Namgung, Ran, Lee, Chul
Formato: Texto
Lenguaje:English
Publicado: The Korean Pediatric Society 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3012277/
https://www.ncbi.nlm.nih.gov/pubmed/21218019
http://dx.doi.org/10.3345/kjp.2010.53.11.965
_version_ 1782195115371003904
author Park, Hyun Bin
Lee, Soon Min
Lee, Jin Sung
Park, Min Soo
Park, Kook In
Namgung, Ran
Lee, Chul
author_facet Park, Hyun Bin
Lee, Soon Min
Lee, Jin Sung
Park, Min Soo
Park, Kook In
Namgung, Ran
Lee, Chul
author_sort Park, Hyun Bin
collection PubMed
description PURPOSE: The life expectancy of patients with spinal muscular atrophy (SMA) type I is generally considered to be less than 2 years. Recently, with the introduction of proactive treatments, a longer survival and an improved survival rate have been reported. In this study, we analyzed the natural courses and survival statistics of SMA type I patients and compared the clinical characteristics of the patients based on their survival periods. METHODS: We reviewed the medical records of 14 pediatric patients diagnosed with SMA type I during a 9-year period. We examined the demographic and clinical characteristics of these patients, calculated their survival probabilities, and plotted survival curves as on the censoring date, January 1, 2010. We also compared the characteristics of the patients who died before the age of 24 months (early-death, ED group) and those who survived for 24 months or longer (long-survival, LS group). RESULTS: The mean survival time was 22.8±2.0 months. The survival probabilities at 6 months, 12 months, 18 months, 24 months, and 30 months were 92.9%, 92.9%, 76.0%, 76.0%, and 65.1%, respectively. Birth weight was the only factor that showed a statistically significant difference between the ED and LS groups (P=0.048). CONCLUSION: In this study, the survival probabilities at 2 years were far greater than expected. Because of the limited number of patients and information in this study, the contribution of improved supportive care on longer survival could not be clarified; this may be elucidated in larger cohort studies.
format Text
id pubmed-3012277
institution National Center for Biotechnology Information
language English
publishDate 2010
publisher The Korean Pediatric Society
record_format MEDLINE/PubMed
spelling pubmed-30122772011-01-07 Survival analysis of spinal muscular atrophy type I Park, Hyun Bin Lee, Soon Min Lee, Jin Sung Park, Min Soo Park, Kook In Namgung, Ran Lee, Chul Korean J Pediatr Original Article PURPOSE: The life expectancy of patients with spinal muscular atrophy (SMA) type I is generally considered to be less than 2 years. Recently, with the introduction of proactive treatments, a longer survival and an improved survival rate have been reported. In this study, we analyzed the natural courses and survival statistics of SMA type I patients and compared the clinical characteristics of the patients based on their survival periods. METHODS: We reviewed the medical records of 14 pediatric patients diagnosed with SMA type I during a 9-year period. We examined the demographic and clinical characteristics of these patients, calculated their survival probabilities, and plotted survival curves as on the censoring date, January 1, 2010. We also compared the characteristics of the patients who died before the age of 24 months (early-death, ED group) and those who survived for 24 months or longer (long-survival, LS group). RESULTS: The mean survival time was 22.8±2.0 months. The survival probabilities at 6 months, 12 months, 18 months, 24 months, and 30 months were 92.9%, 92.9%, 76.0%, 76.0%, and 65.1%, respectively. Birth weight was the only factor that showed a statistically significant difference between the ED and LS groups (P=0.048). CONCLUSION: In this study, the survival probabilities at 2 years were far greater than expected. Because of the limited number of patients and information in this study, the contribution of improved supportive care on longer survival could not be clarified; this may be elucidated in larger cohort studies. The Korean Pediatric Society 2010-11 2010-11-30 /pmc/articles/PMC3012277/ /pubmed/21218019 http://dx.doi.org/10.3345/kjp.2010.53.11.965 Text en Copyright © 2010 by The Korean Pediatric Society http://creativecommons.org/licenses/by-nc/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Park, Hyun Bin
Lee, Soon Min
Lee, Jin Sung
Park, Min Soo
Park, Kook In
Namgung, Ran
Lee, Chul
Survival analysis of spinal muscular atrophy type I
title Survival analysis of spinal muscular atrophy type I
title_full Survival analysis of spinal muscular atrophy type I
title_fullStr Survival analysis of spinal muscular atrophy type I
title_full_unstemmed Survival analysis of spinal muscular atrophy type I
title_short Survival analysis of spinal muscular atrophy type I
title_sort survival analysis of spinal muscular atrophy type i
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3012277/
https://www.ncbi.nlm.nih.gov/pubmed/21218019
http://dx.doi.org/10.3345/kjp.2010.53.11.965
work_keys_str_mv AT parkhyunbin survivalanalysisofspinalmuscularatrophytypei
AT leesoonmin survivalanalysisofspinalmuscularatrophytypei
AT leejinsung survivalanalysisofspinalmuscularatrophytypei
AT parkminsoo survivalanalysisofspinalmuscularatrophytypei
AT parkkookin survivalanalysisofspinalmuscularatrophytypei
AT namgungran survivalanalysisofspinalmuscularatrophytypei
AT leechul survivalanalysisofspinalmuscularatrophytypei