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Prevalence of morbidities across the lifespan for adults with spinal muscular atrophy: a retrospective cohort study
BACKGROUND: Recently approved treatments for spinal muscular atrophy (SMA) may shift clinical care priorities to secondary complications associated with SMA-related aging. To date, there is little knowledge about the natural history of morbidities across the adult lifespan for SMA. The objective of...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10472659/ https://www.ncbi.nlm.nih.gov/pubmed/37653507 http://dx.doi.org/10.1186/s13023-023-02872-6 |
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author | G. Whitney, Daniel E. Neil Knierbein, Erin K. Daunter, Alecia |
author_facet | G. Whitney, Daniel E. Neil Knierbein, Erin K. Daunter, Alecia |
author_sort | G. Whitney, Daniel |
collection | PubMed |
description | BACKGROUND: Recently approved treatments for spinal muscular atrophy (SMA) may shift clinical care priorities to secondary complications associated with SMA-related aging. To date, there is little knowledge about the natural history of morbidities across the adult lifespan for SMA. The objective of this study was to identify the prevalence and odds ratio (OR) of various morbidities among adults with vs. without SMA prior to SMA-related treatment. METHODS: This was a retrospective cohort study that accessed Medicare fee-for-service and commercial claims data from 01/01/2008-12/22/2016. Data from adults ≥ 18 years old with SMA and without SMA matched (1:200 case:control) on demographics, region, and study entry year were included. The prevalence of 30 morbidities across physiologic systems (e.g., cardiovascular, metabolic, musculoskeletal, urinary) and mental health disorders was examined. Age- and sex-adjusted OR was estimated using logistic regression for each morbidity and effect modification by age and sex was tested. RESULTS: There were 2,427 adults with SMA (mean [SD] age, 59.7 [17.4] years; 49.0% female) and 484,528 matched adults without SMA. Adults with vs. without SMA had a higher prevalence and adjusted OR of all 30 morbidities, ranging from OR = 1.61 (95% CI = 1.45–1.80) for hypothyroidism to OR = 7.80 (95% CI = 7.10–8.57) for fluid/electrolyte disorders. There was effect modification by age for 24 morbidities. The OR was highest for the youngest age group (18–40 years; OR range, 2.38 to 117.7; all P < 0.05) and declined with older age groups, but still remained significantly elevated in the oldest age group (≥ 75 years; OR range, 1.30 to 5.96; all P < 0.05). CONCLUSIONS: The limitations of this study are that evidence of morbidities were limited to diagnostic claims and information on SMA type and symptoms or onset were not available. In conclusion, adults with SMA had a higher and earlier prevalence of a variety of morbidities across physiological systems and mental health disorders. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13023-023-02872-6. |
format | Online Article Text |
id | pubmed-10472659 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-104726592023-09-02 Prevalence of morbidities across the lifespan for adults with spinal muscular atrophy: a retrospective cohort study G. Whitney, Daniel E. Neil Knierbein, Erin K. Daunter, Alecia Orphanet J Rare Dis Research BACKGROUND: Recently approved treatments for spinal muscular atrophy (SMA) may shift clinical care priorities to secondary complications associated with SMA-related aging. To date, there is little knowledge about the natural history of morbidities across the adult lifespan for SMA. The objective of this study was to identify the prevalence and odds ratio (OR) of various morbidities among adults with vs. without SMA prior to SMA-related treatment. METHODS: This was a retrospective cohort study that accessed Medicare fee-for-service and commercial claims data from 01/01/2008-12/22/2016. Data from adults ≥ 18 years old with SMA and without SMA matched (1:200 case:control) on demographics, region, and study entry year were included. The prevalence of 30 morbidities across physiologic systems (e.g., cardiovascular, metabolic, musculoskeletal, urinary) and mental health disorders was examined. Age- and sex-adjusted OR was estimated using logistic regression for each morbidity and effect modification by age and sex was tested. RESULTS: There were 2,427 adults with SMA (mean [SD] age, 59.7 [17.4] years; 49.0% female) and 484,528 matched adults without SMA. Adults with vs. without SMA had a higher prevalence and adjusted OR of all 30 morbidities, ranging from OR = 1.61 (95% CI = 1.45–1.80) for hypothyroidism to OR = 7.80 (95% CI = 7.10–8.57) for fluid/electrolyte disorders. There was effect modification by age for 24 morbidities. The OR was highest for the youngest age group (18–40 years; OR range, 2.38 to 117.7; all P < 0.05) and declined with older age groups, but still remained significantly elevated in the oldest age group (≥ 75 years; OR range, 1.30 to 5.96; all P < 0.05). CONCLUSIONS: The limitations of this study are that evidence of morbidities were limited to diagnostic claims and information on SMA type and symptoms or onset were not available. In conclusion, adults with SMA had a higher and earlier prevalence of a variety of morbidities across physiological systems and mental health disorders. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13023-023-02872-6. BioMed Central 2023-08-31 /pmc/articles/PMC10472659/ /pubmed/37653507 http://dx.doi.org/10.1186/s13023-023-02872-6 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research G. Whitney, Daniel E. Neil Knierbein, Erin K. Daunter, Alecia Prevalence of morbidities across the lifespan for adults with spinal muscular atrophy: a retrospective cohort study |
title | Prevalence of morbidities across the lifespan for adults with spinal muscular atrophy: a retrospective cohort study |
title_full | Prevalence of morbidities across the lifespan for adults with spinal muscular atrophy: a retrospective cohort study |
title_fullStr | Prevalence of morbidities across the lifespan for adults with spinal muscular atrophy: a retrospective cohort study |
title_full_unstemmed | Prevalence of morbidities across the lifespan for adults with spinal muscular atrophy: a retrospective cohort study |
title_short | Prevalence of morbidities across the lifespan for adults with spinal muscular atrophy: a retrospective cohort study |
title_sort | prevalence of morbidities across the lifespan for adults with spinal muscular atrophy: a retrospective cohort study |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10472659/ https://www.ncbi.nlm.nih.gov/pubmed/37653507 http://dx.doi.org/10.1186/s13023-023-02872-6 |
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