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  • Hikmat, O. (author)

The impact of gender, puberty, and pregnancy in patients with POLG disease

  • Article/chapterEnglish2020

Publisher, publication year, extent ...

  • 2020-09-18
  • Wiley,2020

Numbers

  • LIBRIS-ID:oai:gup.ub.gu.se/297049
  • https://gup.ub.gu.se/publication/297049URI
  • https://doi.org/10.1002/acn3.51199DOI
  • http://kipublications.ki.se/Default.aspx?queryparsed=id:144700224URI

Supplementary language notes

  • Language:English

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  • Subject category:ref swepub-contenttype
  • Subject category:art swepub-publicationtype

Notes

  • Objective To study the impact of gender, puberty, and pregnancy on the expression of POLG disease, one of the most common mitochondrial diseases known. Methods Clinical, laboratory, and genetic data were collected retrospectively from 155 patients with genetically confirmed POLG disease recruited from seven European countries. We used the available data to study the impact of gender, puberty, and pregnancy on disease onset and deterioration. Results We found that disease onset early in life was common in both sexes but there was also a second peak in females around the time of puberty. Further, pregnancy had a negative impact with 10 of 14 women (71%) experiencing disease onset or deterioration during pregnancy. Interpretation Gender clearly influences the expression of POLG disease. While onset very early in life was common in both males and females, puberty in females appeared associated both with disease onset and increased disease activity. Further, both disease onset and deterioration, including seizure aggravation and status epilepticus, appeared to be associated with pregnancy. Thus, whereas disease activity appears maximal early in life with no subsequent peaks in males, both menarche and pregnancy appear associated with disease onset or worsening in females. This suggests that hormonal changes may be a modulating factor.

Subject headings and genre

Added entries (persons, corporate bodies, meetings, titles ...)

  • Naess, K. (author)
  • Engvall, M.Karolinska Institutet (author)
  • Klingenberg, C. (author)
  • Rasmussen, M. (author)
  • Tallaksen, C. M. E. (author)
  • Samsonsen, C. (author)
  • Brodtkorb, E. (author)
  • Ostergaard, E. (author)
  • de Coo, R. (author)
  • Pias-Peleteiro, L. (author)
  • Isohanni, P. (author)
  • Uusimaa, J. (author)
  • Darin, Niklas,1964Gothenburg University,Göteborgs universitet,Institutionen för kliniska vetenskaper, Avdelningen för pediatrik,Institute of Clinical Sciences, Department of Pediatrics(Swepub:gu)xdarin (author)
  • Rahman, S. (author)
  • Bindoff, L. A. (author)
  • Karolinska InstitutetInstitutionen för kliniska vetenskaper, Avdelningen för pediatrik (creator_code:org_t)

Related titles

  • In:Annals of Clinical and Translational Neurology: Wiley7:10, s. 2019-20252328-9503

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