Skip to main content

Advertisement

Log in

Lack of association between mtDNA haplogroups and Alzheimer’s disease in Tuscany

  • Original
  • Published:
Neurological Sciences Aims and scope Submit manuscript

Abstract

Mitochondrial DNA (mtDNA) haplogroup-specific polymorphisms were previously related to several neurodegenerative diseases, including Alzheimer’s disease (AD). However, the precise role of mtDNA haplogroups in the neurodegenerative cascade leading to AD is still unclear. In this work we have genotyped predefined European mtDNA haplogroups in 209 patients with AD and 191 matched controls. In order to minimise the risk of “genetic contamination”, which could lead to false associations between gene markers and disease, we were careful to enrol in the study only patients and controls of clear Tuscan origin (with at least three generations of Tuscanborn relatives). The frequency of the haplogroups did not differ between the two groups, and no correlation with gender, ApoE genotype, age of onset or disease status was observed. Further studies will be required to define the contribution of mtDNA haplogroups, if any, to the pathogenesis of AD. A correct population selection, in order to minimise the risk of genetic contamination, is essential in these studies.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  1. Hardy J, Selkoe DJ (2002) The amyloid hypothesis of Alzheimer’s disease: progress and problems on the road to therapeutics. Science 297:353–356

    Article  PubMed  CAS  Google Scholar 

  2. Davis DG, Schmitt FA, Wekstein DR, Markesbery WR (1999) Alzheimer neuropathologic alterations in aged cognitively normal subjects. J Neuropathol Exp Neurol 58:376–388

    Article  PubMed  CAS  Google Scholar 

  3. Swerdlow RH, Khan SM (2004) A “mitochondrial cascade hypothesis” for sporadic Alzheimer’s disease. Med Hypotheses 63:8–20

    Article  PubMed  CAS  Google Scholar 

  4. Beal MF (2005) Mitochondria take center stage in aging and neurodegeneration. Ann Neurol 58:495–505

    Article  PubMed  CAS  Google Scholar 

  5. Onyango I, Khan S, Miller B et al (2006) Mitochondrial genomic contribution to mitochondrial dysfunction in Alzheimer’s disease. J Alzheimers Dis 9:183–193

    PubMed  Google Scholar 

  6. Torroni A, Huoponen K, Francalacci P et al (1996) Classification of European mtDNAs from an analysis of three European populations. Genetics 144:1835–1850

    PubMed  CAS  Google Scholar 

  7. Hofmann S, Jaksch M, Bezold R et al (1997) Population genetics and disease susceptibility: characterization of central European haplogroups by mtDNA gene mutations, correlation with D loop variants and association with disease. Hum Mol Genet 6:1835–1846

    Article  PubMed  CAS  Google Scholar 

  8. Ghezzi D, Marelli C, Achilli A et al (2005) Mitochondrial DNA haplogroup K is associated with a lower risk of Parkinson’s disease in Italians. Eur J Hum Genet 13:748–752

    Article  PubMed  CAS  Google Scholar 

  9. Carrieri G, Bonafe M, De Luca M et al (2001) Mitochondrial DNA haplogroups and ApoE4 allele are non-independent variables in sporadic Alzheimer’s disease. Hum Genet 108:194–198

    Article  PubMed  CAS  Google Scholar 

  10. Van der Walt JM, Dementieva YA, Martin ER et al (2004) Analysis of European mitochondrial haplogroups with Alzheimer disease risk. Neurosci Lett 365:28–32

    Article  PubMed  CAS  Google Scholar 

  11. Chinnery PF, Taylor GA, Howell N et al (2000) Mitochondrial DNA haplogroups and susceptibility to AD and dementia with Lewy bodies. Neurology 55:302–304

    PubMed  CAS  Google Scholar 

  12. Elson JL, Herrnstadt C, Preston G et al (2006) Does the mitochondrial genome play a role in the etiology of Alzheimer’s disease? Hum Genet 119:241–254

    Article  PubMed  CAS  Google Scholar 

  13. Richards M, Macaulay V, Hickey E et al (2000) Tracing European founder lineages in the near Eastern mtDNA pool. Am J Hum Genet 67:1251–1276

    PubMed  CAS  Google Scholar 

  14. Simoni L, Calafell F, Pettener D et al (2000) Geographic patterns of mtDNA diversity in Europe. Am J Hum Genet 66:262–278

    Article  PubMed  CAS  Google Scholar 

  15. Barbujani G, Sokal RR (1991) Genetic population structure of Italy II. Physical and cultural barriers to gene flow. Am J Hum Genet 48:398–411

    PubMed  CAS  Google Scholar 

  16. McKhann G, Drachman D, Folstein M et al (1984) Clinical diagnosis of Alzheimer’s disease: report of the NINCDSADRDA Work Group under the auspices of Department of Health and Human Services Task Force on Alzheimer’s Disease. Neurology 34:939–944

    PubMed  CAS  Google Scholar 

  17. Sambrook J, Russel DW (2001) Molecular cloning: a laboratory manual. Cold Spring Harbor Laboratory Press, Cold Spring Harbor, NY, pp 6.4–6.11

    Google Scholar 

  18. Andrews RM, Kubacka I, Chinnery PF et al (1999) Reanalysis and revision of Cambridge reference sequence for human mitochondrial DNA. Nat Genet 23:147

    Article  PubMed  CAS  Google Scholar 

  19. Mitomap: a Human Mitochondrial Genome Database. Available at: http://www.mitomap.org

  20. Mancuso M, Conforti FL, Rocchi A et al (2004) Could mitochondrial haplogroups play a role in sporadic amyotrophic lateral sclerosis? Neurosci Lett 371:158–162

    Article  PubMed  CAS  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to M. Mancuso.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Mancuso, M., Nardini, M., Micheli, D. et al. Lack of association between mtDNA haplogroups and Alzheimer’s disease in Tuscany. Neurol Sci 28, 142–147 (2007). https://doi.org/10.1007/s10072-007-0807-z

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s10072-007-0807-z

Key words

Navigation