Nutritional Assessment in Patients with Early-Onset Autosomal Dominant Alzheimer's Disease Due to PSEN1- E280A Genetic Variant: A Cross-Sectional Study
ABSTRACT: Background: Weight loss and malnutrition are frequent findings in late-onset and sporadic presentations of Alzheimer's Disease (AD). However, less is known about nutritional status in Early-Onset Autosomal Dominant AD (EO-ADAD). Objective: To analyze the association between nutritiona...
- Autores:
-
Gómez Vega, Manuela
García Cifuentes, Elkin Román
Vélez Hernández, Juan Esteban
Aguillón Niño, David Fernando
Vásquez Botero, Daniel
Jaramillo Jiménez, Alberto
Gómez Henck, Clara
Tobón Quintero, Carlos Andrés
Lopera Restrepo, Francisco Javier
Deossa Restrepo, Gloria Cecilia
- Tipo de recurso:
- Article of investigation
- Fecha de publicación:
- 2021
- Institución:
- Universidad de Antioquia
- Repositorio:
- Repositorio UdeA
- Idioma:
- eng
- OAI Identifier:
- oai:bibliotecadigital.udea.edu.co:10495/42316
- Acceso en línea:
- https://hdl.handle.net/10495/42316
- Palabra clave:
- Autosomal Dominant Alzheimer’s Disease
Mini Nutritional Assessment
malnutrition
- Rights
- openAccess
- License
- http://creativecommons.org/licenses/by/2.5/co/
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|
| dc.title.spa.fl_str_mv |
Nutritional Assessment in Patients with Early-Onset Autosomal Dominant Alzheimer's Disease Due to PSEN1- E280A Genetic Variant: A Cross-Sectional Study |
| title |
Nutritional Assessment in Patients with Early-Onset Autosomal Dominant Alzheimer's Disease Due to PSEN1- E280A Genetic Variant: A Cross-Sectional Study |
| spellingShingle |
Nutritional Assessment in Patients with Early-Onset Autosomal Dominant Alzheimer's Disease Due to PSEN1- E280A Genetic Variant: A Cross-Sectional Study Autosomal Dominant Alzheimer’s Disease Mini Nutritional Assessment malnutrition |
| title_short |
Nutritional Assessment in Patients with Early-Onset Autosomal Dominant Alzheimer's Disease Due to PSEN1- E280A Genetic Variant: A Cross-Sectional Study |
| title_full |
Nutritional Assessment in Patients with Early-Onset Autosomal Dominant Alzheimer's Disease Due to PSEN1- E280A Genetic Variant: A Cross-Sectional Study |
| title_fullStr |
Nutritional Assessment in Patients with Early-Onset Autosomal Dominant Alzheimer's Disease Due to PSEN1- E280A Genetic Variant: A Cross-Sectional Study |
| title_full_unstemmed |
Nutritional Assessment in Patients with Early-Onset Autosomal Dominant Alzheimer's Disease Due to PSEN1- E280A Genetic Variant: A Cross-Sectional Study |
| title_sort |
Nutritional Assessment in Patients with Early-Onset Autosomal Dominant Alzheimer's Disease Due to PSEN1- E280A Genetic Variant: A Cross-Sectional Study |
| dc.creator.fl_str_mv |
Gómez Vega, Manuela García Cifuentes, Elkin Román Vélez Hernández, Juan Esteban Aguillón Niño, David Fernando Vásquez Botero, Daniel Jaramillo Jiménez, Alberto Gómez Henck, Clara Tobón Quintero, Carlos Andrés Lopera Restrepo, Francisco Javier Deossa Restrepo, Gloria Cecilia |
| dc.contributor.author.none.fl_str_mv |
Gómez Vega, Manuela García Cifuentes, Elkin Román Vélez Hernández, Juan Esteban Aguillón Niño, David Fernando Vásquez Botero, Daniel Jaramillo Jiménez, Alberto Gómez Henck, Clara Tobón Quintero, Carlos Andrés Lopera Restrepo, Francisco Javier Deossa Restrepo, Gloria Cecilia |
| dc.contributor.researchgroup.spa.fl_str_mv |
Grupo de Neurociencias de Antioquia Grupo Neuropsicología y Conducta Socioantropología de la Alimentación |
| dc.subject.proposal.spa.fl_str_mv |
Autosomal Dominant Alzheimer’s Disease Mini Nutritional Assessment malnutrition |
| topic |
Autosomal Dominant Alzheimer’s Disease Mini Nutritional Assessment malnutrition |
| description |
ABSTRACT: Background: Weight loss and malnutrition are frequent findings in late-onset and sporadic presentations of Alzheimer's Disease (AD). However, less is known about nutritional status in Early-Onset Autosomal Dominant AD (EO-ADAD). Objective: To analyze the association between nutritional status and other clinical and sociodemographic characteristics in individuals with a genetic form of EO-ADAD. Design settings and participants: Cross-sectional study with 75 non-institutionalized participants from a cohort of Autosomal Dominant AD (13 with mild cognitive impairment and 61 with dementia, ages from 38 to 67 years) underwent a structured clinical assessment with emphasis on nutritional status. Measurements: Primary outcome was nutritional status and it was measured using the Mini Nutritional Assessment (MNA). Patients were categorized according to MNA total score, as undernourished (MNA ≤23.5) and well-nourished (MNA ≥ 24). Sociodemographic and clinical variables identified as potential predictors or confounders of nutritional status were also collected. Results: Undernourishment by MNA was present in 57.3% of the sample. Forty-two percent of participants had abnormal BMI values considered lower than 18.5 or higher than 24.9 kg/m2. Total BMI values were similar in well and undernourished patients (median 24.2 IQR 3.59 and median 23.9 IQR 4.42, respectively, p=0.476). When comparing well and undernourished groups, we found statistically significant differences for variables: severity of dementia (p=0.034), frailty (p=0.001), multimorbidity (p=0.035) and, polymedication (p=0.045). Neither adjusted logistic regression nor the Poisson regression showed that any clinical or sociodemographic variables explained undernourishment. Conclusions: Undernourishment was a frequent finding in our sample of EO-ADAD, especially in later stages of the disease. Patients with polymedication, multimorbidity, frailty and severe dementia show differences in their nutritional status with a tendency to be more frequently undernourished. Further studies with larger sample sizes are needed to establish this association. |
| publishDate |
2021 |
| dc.date.issued.none.fl_str_mv |
2021 |
| dc.date.accessioned.none.fl_str_mv |
2024-09-20T22:24:13Z |
| dc.date.available.none.fl_str_mv |
2024-09-20T22:24:13Z |
| dc.type.spa.fl_str_mv |
Artículo de investigación |
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http://purl.org/coar/resource_type/c_2df8fbb1 |
| dc.type.redcol.spa.fl_str_mv |
https://purl.org/redcol/resource_type/ART |
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http://purl.org/coar/version/c_970fb48d4fbd8a85 |
| dc.type.driver.spa.fl_str_mv |
info:eu-repo/semantics/article |
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info:eu-repo/semantics/publishedVersion |
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http://purl.org/coar/resource_type/c_2df8fbb1 |
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publishedVersion |
| dc.identifier.citation.spa.fl_str_mv |
Gómez-Vega M, Garcia-Cifuentes E, Aguillon D, Velez JE, Jaramillo-Jimenez A, Vasquez D, Gómez-Henck C, Andrés Tobon C, Deossa Restrepo GC, Lopera F. Nutritional Assessment in Patients with Early-Onset Autosomal Dominant Alzheimer's Disease Due to PSEN1- E280A Genetic Variant: A Cross-Sectional Study. JAR Life. 2021 Jun 6;10:32-38. doi: 10.14283/jarlife.2021.6. PMID: 36923517; PMCID: PMC10002882. |
| dc.identifier.uri.none.fl_str_mv |
https://hdl.handle.net/10495/42316 |
| dc.identifier.doi.none.fl_str_mv |
10.14283/jarlife.2021.6 |
| dc.identifier.eissn.none.fl_str_mv |
2534-773X |
| identifier_str_mv |
Gómez-Vega M, Garcia-Cifuentes E, Aguillon D, Velez JE, Jaramillo-Jimenez A, Vasquez D, Gómez-Henck C, Andrés Tobon C, Deossa Restrepo GC, Lopera F. Nutritional Assessment in Patients with Early-Onset Autosomal Dominant Alzheimer's Disease Due to PSEN1- E280A Genetic Variant: A Cross-Sectional Study. JAR Life. 2021 Jun 6;10:32-38. doi: 10.14283/jarlife.2021.6. PMID: 36923517; PMCID: PMC10002882. 10.14283/jarlife.2021.6 2534-773X |
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https://hdl.handle.net/10495/42316 |
| dc.language.iso.spa.fl_str_mv |
eng |
| language |
eng |
| dc.relation.ispartofjournalabbrev.spa.fl_str_mv |
JAR Life |
| dc.relation.citationendpage.spa.fl_str_mv |
38 |
| dc.relation.citationstartpage.spa.fl_str_mv |
32 |
| dc.relation.citationvolume.spa.fl_str_mv |
10 |
| dc.relation.ispartofjournal.spa.fl_str_mv |
JAR Life |
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http://creativecommons.org/licenses/by/2.5/co/ |
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https://creativecommons.org/licenses/by/4.0/ |
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info:eu-repo/semantics/openAccess |
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openAccess |
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7 páginas |
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SERDI |
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Auzeville-Tolosane, Francia |
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Universidad de Antioquia |
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Gómez Vega, ManuelaGarcía Cifuentes, Elkin RománVélez Hernández, Juan EstebanAguillón Niño, David FernandoVásquez Botero, DanielJaramillo Jiménez, AlbertoGómez Henck, ClaraTobón Quintero, Carlos AndrésLopera Restrepo, Francisco JavierDeossa Restrepo, Gloria CeciliaGrupo de Neurociencias de AntioquiaGrupo Neuropsicología y ConductaSocioantropología de la Alimentación2024-09-20T22:24:13Z2024-09-20T22:24:13Z2021Gómez-Vega M, Garcia-Cifuentes E, Aguillon D, Velez JE, Jaramillo-Jimenez A, Vasquez D, Gómez-Henck C, Andrés Tobon C, Deossa Restrepo GC, Lopera F. Nutritional Assessment in Patients with Early-Onset Autosomal Dominant Alzheimer's Disease Due to PSEN1- E280A Genetic Variant: A Cross-Sectional Study. JAR Life. 2021 Jun 6;10:32-38. doi: 10.14283/jarlife.2021.6. PMID: 36923517; PMCID: PMC10002882.https://hdl.handle.net/10495/4231610.14283/jarlife.2021.62534-773XABSTRACT: Background: Weight loss and malnutrition are frequent findings in late-onset and sporadic presentations of Alzheimer's Disease (AD). However, less is known about nutritional status in Early-Onset Autosomal Dominant AD (EO-ADAD). Objective: To analyze the association between nutritional status and other clinical and sociodemographic characteristics in individuals with a genetic form of EO-ADAD. Design settings and participants: Cross-sectional study with 75 non-institutionalized participants from a cohort of Autosomal Dominant AD (13 with mild cognitive impairment and 61 with dementia, ages from 38 to 67 years) underwent a structured clinical assessment with emphasis on nutritional status. Measurements: Primary outcome was nutritional status and it was measured using the Mini Nutritional Assessment (MNA). Patients were categorized according to MNA total score, as undernourished (MNA ≤23.5) and well-nourished (MNA ≥ 24). Sociodemographic and clinical variables identified as potential predictors or confounders of nutritional status were also collected. Results: Undernourishment by MNA was present in 57.3% of the sample. Forty-two percent of participants had abnormal BMI values considered lower than 18.5 or higher than 24.9 kg/m2. Total BMI values were similar in well and undernourished patients (median 24.2 IQR 3.59 and median 23.9 IQR 4.42, respectively, p=0.476). When comparing well and undernourished groups, we found statistically significant differences for variables: severity of dementia (p=0.034), frailty (p=0.001), multimorbidity (p=0.035) and, polymedication (p=0.045). Neither adjusted logistic regression nor the Poisson regression showed that any clinical or sociodemographic variables explained undernourishment. Conclusions: Undernourishment was a frequent finding in our sample of EO-ADAD, especially in later stages of the disease. Patients with polymedication, multimorbidity, frailty and severe dementia show differences in their nutritional status with a tendency to be more frequently undernourished. Further studies with larger sample sizes are needed to establish this association.Colombia. 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