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LipoDDx: a mobile application for identification of rare lipodystrophy syndromes

BACKGROUND: Lipodystrophy syndromes are a group of disorders characterized by a loss of adipose tissue once other situations of nutritional deprivation or exacerbated catabolism have been ruled out. With the exception of the HIV-associated lipodystrophy, they have a very low prevalence, which togeth...

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Autores principales: Araújo-Vilar, David, Fernández-Pombo, Antía, Rodríguez-Carnero, Gemma, Martínez-Olmos, Miguel Ángel, Cantón, Ana, Villar-Taibo, Rocío, Hermida-Ameijeiras, Álvaro, Santamaría-Nieto, Alicia, Díaz-Ortega, Carmen, Martínez-Rey, Carmen, Antela, Antonio, Losada, Elena, Muy-Pérez, Andrés E., González-Méndez, Blanca, Sánchez-Iglesias, Sofía
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7118879/
https://www.ncbi.nlm.nih.gov/pubmed/32241282
http://dx.doi.org/10.1186/s13023-020-01364-1
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author Araújo-Vilar, David
Fernández-Pombo, Antía
Rodríguez-Carnero, Gemma
Martínez-Olmos, Miguel Ángel
Cantón, Ana
Villar-Taibo, Rocío
Hermida-Ameijeiras, Álvaro
Santamaría-Nieto, Alicia
Díaz-Ortega, Carmen
Martínez-Rey, Carmen
Antela, Antonio
Losada, Elena
Muy-Pérez, Andrés E.
González-Méndez, Blanca
Sánchez-Iglesias, Sofía
author_facet Araújo-Vilar, David
Fernández-Pombo, Antía
Rodríguez-Carnero, Gemma
Martínez-Olmos, Miguel Ángel
Cantón, Ana
Villar-Taibo, Rocío
Hermida-Ameijeiras, Álvaro
Santamaría-Nieto, Alicia
Díaz-Ortega, Carmen
Martínez-Rey, Carmen
Antela, Antonio
Losada, Elena
Muy-Pérez, Andrés E.
González-Méndez, Blanca
Sánchez-Iglesias, Sofía
author_sort Araújo-Vilar, David
collection PubMed
description BACKGROUND: Lipodystrophy syndromes are a group of disorders characterized by a loss of adipose tissue once other situations of nutritional deprivation or exacerbated catabolism have been ruled out. With the exception of the HIV-associated lipodystrophy, they have a very low prevalence, which together with their large phenotypic heterogeneity makes their identification difficult, even for endocrinologists and pediatricians. This leads to significant delays in diagnosis or even to misdiagnosis. Our group has developed an algorithm that identifies the more than 40 rare lipodystrophy subtypes described to date. This algorithm has been implemented in a free mobile application, LipoDDx®. Our aim was to establish the effectiveness of LipoDDx®. Forty clinical records of patients with a diagnosis of certainty of most lipodystrophy subtypes were analyzed, including subjects without lipodystrophy. The medical records, blinded for diagnosis, were evaluated by 13 physicians, 1 biochemist and 1 dentist. Each evaluator first gave his/her results based on his/her own criteria. Then, a second diagnosis was given using LipoDDx®. The results were analysed based on a score table according to the complexity of each case and the prevalence of the disease. RESULTS: LipoDDx® provides a user-friendly environment, based on usually dichotomous questions or choice of clinical signs from drop-down menus. The final result provided by this app for a particular case can be a low/high probability of suffering a particular lipodystrophy subtype. Without using LipoDDx® the success rate was 17 ± 20%, while with LipoDDx® the success rate was 79 ± 20% (p < 0.01). CONCLUSIONS: LipoDDx® is a free app that enables the identification of subtypes of rare lipodystrophies, which in this small cohort has around 80% effectiveness, which will be of help to doctors who are not experts in this field. However, it will be necessary to analyze more cases in order to obtain a more accurate efficiency value.
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spelling pubmed-71188792020-04-07 LipoDDx: a mobile application for identification of rare lipodystrophy syndromes Araújo-Vilar, David Fernández-Pombo, Antía Rodríguez-Carnero, Gemma Martínez-Olmos, Miguel Ángel Cantón, Ana Villar-Taibo, Rocío Hermida-Ameijeiras, Álvaro Santamaría-Nieto, Alicia Díaz-Ortega, Carmen Martínez-Rey, Carmen Antela, Antonio Losada, Elena Muy-Pérez, Andrés E. González-Méndez, Blanca Sánchez-Iglesias, Sofía Orphanet J Rare Dis Research BACKGROUND: Lipodystrophy syndromes are a group of disorders characterized by a loss of adipose tissue once other situations of nutritional deprivation or exacerbated catabolism have been ruled out. With the exception of the HIV-associated lipodystrophy, they have a very low prevalence, which together with their large phenotypic heterogeneity makes their identification difficult, even for endocrinologists and pediatricians. This leads to significant delays in diagnosis or even to misdiagnosis. Our group has developed an algorithm that identifies the more than 40 rare lipodystrophy subtypes described to date. This algorithm has been implemented in a free mobile application, LipoDDx®. Our aim was to establish the effectiveness of LipoDDx®. Forty clinical records of patients with a diagnosis of certainty of most lipodystrophy subtypes were analyzed, including subjects without lipodystrophy. The medical records, blinded for diagnosis, were evaluated by 13 physicians, 1 biochemist and 1 dentist. Each evaluator first gave his/her results based on his/her own criteria. Then, a second diagnosis was given using LipoDDx®. The results were analysed based on a score table according to the complexity of each case and the prevalence of the disease. RESULTS: LipoDDx® provides a user-friendly environment, based on usually dichotomous questions or choice of clinical signs from drop-down menus. The final result provided by this app for a particular case can be a low/high probability of suffering a particular lipodystrophy subtype. Without using LipoDDx® the success rate was 17 ± 20%, while with LipoDDx® the success rate was 79 ± 20% (p < 0.01). CONCLUSIONS: LipoDDx® is a free app that enables the identification of subtypes of rare lipodystrophies, which in this small cohort has around 80% effectiveness, which will be of help to doctors who are not experts in this field. However, it will be necessary to analyze more cases in order to obtain a more accurate efficiency value. BioMed Central 2020-04-02 /pmc/articles/PMC7118879/ /pubmed/32241282 http://dx.doi.org/10.1186/s13023-020-01364-1 Text en © The Author(s) 2020 Open AccessThis 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/. The Creative Commons Public Domain Dedication waiver (http://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
Araújo-Vilar, David
Fernández-Pombo, Antía
Rodríguez-Carnero, Gemma
Martínez-Olmos, Miguel Ángel
Cantón, Ana
Villar-Taibo, Rocío
Hermida-Ameijeiras, Álvaro
Santamaría-Nieto, Alicia
Díaz-Ortega, Carmen
Martínez-Rey, Carmen
Antela, Antonio
Losada, Elena
Muy-Pérez, Andrés E.
González-Méndez, Blanca
Sánchez-Iglesias, Sofía
LipoDDx: a mobile application for identification of rare lipodystrophy syndromes
title LipoDDx: a mobile application for identification of rare lipodystrophy syndromes
title_full LipoDDx: a mobile application for identification of rare lipodystrophy syndromes
title_fullStr LipoDDx: a mobile application for identification of rare lipodystrophy syndromes
title_full_unstemmed LipoDDx: a mobile application for identification of rare lipodystrophy syndromes
title_short LipoDDx: a mobile application for identification of rare lipodystrophy syndromes
title_sort lipoddx: a mobile application for identification of rare lipodystrophy syndromes
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7118879/
https://www.ncbi.nlm.nih.gov/pubmed/32241282
http://dx.doi.org/10.1186/s13023-020-01364-1
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