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. Author manuscript; available in PMC: 2024 Jan 1.
Published in final edited form as: Lancet Neurol. 2023 Jan;22(1):28–29. doi: 10.1016/S1474-4422(22)00475-6

The African Dementia Consortium

Rufus O Akinyemi 1, Mayowa O Owolabi 1, Njideka Okubadejo 1, Adesola Ogunniyi 1, Raj N Kalaria 1, on behalf of the African Dementia Consortium
PMCID: PMC10022738  NIHMSID: NIHMS1877751  PMID: 36517165

In low-income and middle-income countries, particularly those in Africa, communicable diseases are still of concern. Accordingly, many clinicians and biomedical researchers have balked at the idea of exploring ageing-related disorders in sub-Saharan Africa. However, longevity is also a characteristic of African populations.1

Around 70% of all cases of dementia worldwide are due to Alzheimer’s disease, but the distribution of dementia subtypes in Africa remains unclear.2 Furthermore, little is known about the genetic and epigenetic architecture of dementia phenotypes among indigenous Africans. The APOE ε4 allele, which is robustly associated with Alzheimer’s disease in most populations, might have more nuanced links to Alzheimer’s disease in people with African ancestry.3 The pathology of Alzheimer’s disease is also intriguing, as African populations tend not to share risk factors with people living in high-income countries.4 Africa harbours the greatest genetic diversity of any continent (low linkage disequilibrium and short haplotype blocks). Thus, increasing the representation of indigenous Africans in genomic research could bring novel insights into the biology of brain health and cognition, facilitate translational genomics, and improve understanding of dementia phenotypes and protective and risk factors.2 Furthermore, fine mapping of new loci and variants identified in African populations could help to pinpoint causal genetic variants.

Our African Dementia Consortium brings together dementia researchers in a multidisciplinary framework to generate clinical and socioeconomic datasets. We believe that the Consortium will improve the characterisation of dementia phenotypes in Africans. The Consortium will focus on several research areas, including epidemiological studies on prevalence, incidence, and risk factors;4 genetic and epigenetic studies; detection of unique biomarkers; clinical trials; capacity building and networking among dementia researchers living or working in Africa; translational research; implementation science for the translation of research evidence to practice and policy; determinants of brain health; and ethical, legal, sociological, and anthropological issues in brain health. For our future research, the Consortium will build on the biobanking of brain samples, CSF, and blood that is already in place.5

Our Consortium includes more than 100 researchers, and more scientists are expected to join. It is coordinated from the Neuroscience and Ageing Research Unit of the Institute for Advanced Medical Research and Training, College of Medicine, University of Ibadan (Ibadan, Nigeria). Researchers from Nigeria, Ghana, Benin, Cameroon, Kenya, Uganda, Tanzania, Mozambique, and Ethiopia are already part of the Consortium. They are recipients of a grant award from the US National Institute of Aging.

The Recruitment and Retention for Alzheimer’s Disease Diversity Cohorts in the Alzheimer’s Disease Sequencing Project (READD-ADSP) study, which is led by Margaret Pericak-Vance and her team at the University of Miami (Coral Gables, FL, USA), will explore the genetics of Alzheimer’s disease and other dementias in minority ethnic groups and in resource-limited countries, including the aforementioned countries in sub-Saharan Africa. This study aims to recruit 5000 Africans (2500 participants with Alzheimer’s disease and 2500 controls). Our African Dementia Consortium will discuss the implementation of READD-ADSP in sub-Saharan Africa at a forthcoming quadrennial symposium on brain ageing and dementia in low-income and middle-income countries, which is to be held in Nairobi, Kenya, on Dec 6–9, 2022.

Footnotes

We declare no competing interests.

For more on READD-ADSP see https://www.readd-adsp.org/

For more on this symposium see https://conferences.ncl.ac.uk/advascular/

References

  • 1.Kalaria RN. Dementia comes of age in the developing world. Lancet 2003; 361: 888–89. [DOI] [PubMed] [Google Scholar]
  • 2.Akinyemi RO, Yaria J, Ojagbemi A, et al. Dementia in Africa: current evidence, knowledge gaps, and future directions. Alzheimers Dement 2022; 18: 790–809. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 3.Rajabli F, Beecham GW, Hendrie HC, et al. A locus at 19q13.31 significantly reduces the ApoE ε4 risk for Alzheimer’s disease in African ancestry. PLoS Genet 2022; 18: e1009977. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 4.Kalaria RN, Maestre GE, Arizaga R, et al. Alzheimer’s disease and vascular dementia in developing countries: prevalence, management, and risk factors. Lancet Neurol 2008; 7: 812–26. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 5.Akinyemi RO, Salami A, Akinyemi J, et al. Brain banking in low and middle-income countries: raison d’etre for the Ibadan Brain Ageing, Dementia And Neurodegeneration (IBADAN) Brain Bank Project. Brain Res Bull 2019; 145: 136–41. [DOI] [PMC free article] [PubMed] [Google Scholar]

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