Home LiteratureArticle Details
PMID: 17202228 Published · ppublish English Journal Article

Co-occurrence of affective and schizophrenia spectrum disorders with PINK1 mutations.

Journal of neurology, neurosurgery, and psychiatry ·Vol. 78 ·No. 5 ·2007-05-00 ·Pages 532-5

Steinlechner S, Stahlberg J, Völkel B, Djarmati A, Hagenah J, Hiller A, Hedrich K, König I, Klein C, Lencer R

Abstract

To investigate a possible association of mutations in the PTEN-induced putative kinase 1 (PINK1) gene with psychiatric disorders in a large family with monogenic parkinsonism. 20 members of a family (4 homozygous, 11 heterozygous and 5 non-mutation carriers) were investigated for the presence of psychiatric disorders using the structured clinical interview for Diagnostic and Statistical Manual of Mental Disorders, 4th edition (DSM-IV); information on three additional heterozygous mutation carriers was obtained according to the family history research diagnostic criteria. We found predominantly affective and schizophrenia spectrum disorders in 11 (61%) of the 18 mutation carriers and in 1 (20%) of the 5 mutation-negative cases. First, affective and psychotic symptoms may be part of the phenotypic spectrum or even the sole manifestation of PINK1 mutations. Second, patients with familial movement disorders associated with psychiatric conditions may serve as a valuable study population to explore (genetic) causes of neuropsychiatric disease.

MeSH Terms
Adult Aged Female Humans Male Middle Aged Mood Disorders/genetics Mutation Parkinsonian Disorders/genetics,psychology Pedigree Protein Kinases/genetics Schizophrenia/genetics
Chemicals
Protein Kinases PTEN-induced putative kinase
Authors & Affiliations
10 authors, click to expand affiliations / ORCID
Steinlechner Susanne
Department of Psychiatry and Psychotherapy, University of Lübeck, Ratzeburger Allee 160, D-23538 Lübeck, Germany.
Stahlberg Jessica
Völkel Birgit
Djarmati Ana
Hagenah Johann
Hiller Anja
Hedrich Katja
König Inke
Klein Christine
Lencer Rebekka
References (15)
15 references, click to expand
  1. Does treatment with dopamine agonists affect utilization of exogenous levodopa in the parkinsonian striatum?
    J Neural Transm Suppl. 1995;45:57-60 PMID: 8748609
  2. The Roscommon Family Study. I. Methods, diagnosis of probands, and risk of schizophrenia in relatives.
    Arch Gen Psychiatry. 1993 Jul;50(7):527-40 PMID: 8317947
  3. Depression in Parkinson's disease. An update.
    Adv Neurol. 2001;86:373-83 PMID: 11553999
  4. Novel PINK1 mutations in early-onset parkinsonism.
    Ann Neurol. 2004 Sep;56(3):424-7 PMID: 15349870
  5. PINK1 mutations are associated with sporadic early-onset parkinsonism.
    Ann Neurol. 2004 Sep;56(3):336-41 PMID: 15349860
  6. Range of neuropsychiatric disturbances in patients with Parkinson's disease.
    J Neurol Neurosurg Psychiatry. 1999 Oct;67(4):492-6 PMID: 10486397
  7. Phenotypic features of myoclonus-dystonia in three kindreds.
    Neurology. 2002 Oct 22;59(8):1187-96 PMID: 12391346
  8. The genetics of Parkinson disease: Implications for neurological care.
    Nat Clin Pract Neurol. 2006 Mar;2(3):136-46 PMID: 16932540
  9. Homozygous PINK1 C-terminus mutation causing early-onset parkinsonism.
    Ann Neurol. 2004 Sep;56(3):427-31 PMID: 15349871
  10. Hallucinations in Parkinson's disease. prevalence, phenomenology and risk factors. Fenelon G* mahieux F, huon R, Ziegler M. Brain 2000;123:733-745
    Am J Ophthalmol. 2000 Aug;130(2):261-2 PMID: 11004314
  11. A heterozygous effect for PINK1 mutations in Parkinson's disease?
    Ann Neurol. 2006 Oct;60(4):414-9 PMID: 16969854
  12. Clinical spectrum of homozygous and heterozygous PINK1 mutations in a large German family with Parkinson disease: role of a single hit?
    Arch Neurol. 2006 Jun;63(6):833-8 PMID: 16769864
  13. Parkin disease: a phenotypic study of a large case series.
    Brain. 2003 Jun;126(Pt 6):1279-92 PMID: 12764051
  14. Expanded motor and psychiatric phenotype in autosomal dominant Segawa syndrome due to GTP cyclohydrolase deficiency.
    J Neurol Neurosurg Psychiatry. 2006 Jan;77(1):18-23 PMID: 16361586
  15. PINK1 protein in normal human brain and Parkinson's disease.
    Brain. 2006 Jul;129(Pt 7):1720-31 PMID: 16702191
Article Info
Journal
Journal of neurology, neurosurgery, and psychiatry
Abbr.
J Neurol Neurosurg Psychiatry
ISSN
1468-330X
Published
2007-05-00
Epub
2007-00-03
Pages
532-5
Language
English
Region
England
NLM ID
2985191R
PMCID
PMC2117826
Subset
IM
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: product@genelibs.com