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Sensitivity of the African neuropsychology battery memory subtests and learning slopes in discriminating APOE 4 and amyloid pathology in adult individuals in the Democratic Republic of Congo.
Ikanga, Jean; Patrick, Sarah D; Schwinne, Megan; Patel, Saranya Sundaram; Epenge, Emmanuel; Gikelekele, Guy; Tshengele, Nathan; Kavugho, Immaculee; Mampunza, Samuel; Yarasheski, Kevin E; Teunissen, Charlotte E; Stringer, Anthony; Levey, Allan; Rojas, Julio C; Chan, Brandon; Lario Lago, Argentina; Kramer, Joel H; Boxer, Adam L; Jeromin, Andreas; Alonso, Alvaro; Spencer, Robert J.
Afiliación
  • Ikanga J; Department of Rehabilitation Medicine, Emory University School of Medicine, Atlanta, GA, United States.
  • Patrick SD; Department of Psychiatry, School of Medicine, University of Kinshasa and Catholic University of Congo, Kinshasa, Democratic Republic of Congo.
  • Schwinne M; Veteran Affairs Ann Arbor Healthcare System, Ann Arbor, MI, United States.
  • Patel SS; Department of Biomedical Informatics, School of Medicine, Emory University, Atlanta, GA, United States.
  • Epenge E; Department of Rehabilitation Medicine, Emory University School of Medicine, Atlanta, GA, United States.
  • Gikelekele G; Department of Neurology, University of Kinshasa, Kinshasa, Democratic Republic of Congo.
  • Tshengele N; Department of Psychiatry, School of Medicine, University of Kinshasa and Catholic University of Congo, Kinshasa, Democratic Republic of Congo.
  • Kavugho I; Department of Psychiatry, School of Medicine, University of Kinshasa and Catholic University of Congo, Kinshasa, Democratic Republic of Congo.
  • Mampunza S; Memory Clinic of Kinshasa, Kinshasa, Democratic Republic of Congo.
  • Yarasheski KE; Department of Psychiatry, School of Medicine, University of Kinshasa and Catholic University of Congo, Kinshasa, Democratic Republic of Congo.
  • Teunissen CE; C2N Diagnostics, St. Louis, MO, United States.
  • Stringer A; Neurochemistry Laboratory, Department of Clinical Chemistry, Amsterdam Neuroscience, Neurodegeneration, Amsterdam University Medical Centers, Vrije Universiteit, Amsterdam, Netherlands.
  • Levey A; Department of Rehabilitation Medicine, Emory University School of Medicine, Atlanta, GA, United States.
  • Rojas JC; Department of Neurology, School of Medicine, Emory University, Atlanta, GA, United States.
  • Chan B; Department of Neurology, University of San Francisco, Memory and Aging Center, Weill Institute for Neurosciences, University of California San Francisco, San Francisco, CA, United States.
  • Lario Lago A; Department of Neurology, University of San Francisco, Memory and Aging Center, Weill Institute for Neurosciences, University of California San Francisco, San Francisco, CA, United States.
  • Kramer JH; Department of Neurology, University of San Francisco, Memory and Aging Center, Weill Institute for Neurosciences, University of California San Francisco, San Francisco, CA, United States.
  • Boxer AL; Department of Neurology, University of San Francisco, Memory and Aging Center, Weill Institute for Neurosciences, University of California San Francisco, San Francisco, CA, United States.
  • Jeromin A; Department of Neurology, University of San Francisco, Memory and Aging Center, Weill Institute for Neurosciences, University of California San Francisco, San Francisco, CA, United States.
  • Alonso A; ALZpath, Inc., Carlsbad, CA, United States.
  • Spencer RJ; Department of Epidemiology, Rollins School of Public Health, Emory University, Atlanta, GA, United States.
Front Neurol ; 15: 1320727, 2024.
Article en En | MEDLINE | ID: mdl-38601333
ABSTRACT

Background:

The current study examined the sensitivity of two memory subtests and their corresponding learning slope metrics derived from the African Neuropsychology Battery (ANB) to detect amyloid pathology and APOEε4 status in adults from Kinshasa, the Democratic Republic of the Congo.

Methods:

85 participants were classified for the presence of ß-amyloid pathology and based on allelic presence of APOEε4 using Simoa. All participants were screened using CSID and AQ, underwent verbal and visuospatial memory testing from ANB, and provided blood samples for plasma Aß42, Aß40, and APOE proteotype. Pearson correlation, linear and logistic regression were conducted to compare amyloid pathology and APOEε4 status with derived learning scores, including initial learning, raw learning score, learning over trials, and learning ratio.

Results:

Our sample included 35 amyloid positive and 44 amyloid negative individuals as well as 42 without and 39 with APOEε4. All ROC AUC ranges for the prediction of amyloid pathology based on learning scores were low, ranging between 0.56-0.70 (95% CI ranging from 0.44-0.82). The sensitivity of all the scores ranged between 54.3-88.6, with some learning metrics demonstrating good sensitivity. Regarding APOEε4 prediction, all AUC values ranged between 0.60-0.69, with all sensitivity measures ranging between 53.8-89.7. There were minimal differences in the AUC values across learning slope metrics, largely due to the lack of ceiling effects in this sample.

Discussion:

This study demonstrates that some ANB memory subtests and learning slope metrics can discriminate those that are normal from those with amyloid pathology and those with and without APOEε4, consistent with findings reported in Western populations.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Front Neurol Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Front Neurol Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos