The DOI matches its Crossref record; 22 of the 22 references it cites were found in a registry or an index.
Psychiatric disturbances in five patients with MELAS syndrome
Open accessAbstract
Cel: Zaburzenia mitochondrialne metabolizmu energetycznego (ZM) stanowią niejednorodną grupę chorób, które mogą ujawnić się w każdym wieku szerokim spektrum objawów klinicznych, w tym zaburzeń psychicznych. Metoda: Celem niniejszej pracy było scharakteryzowanie objawów psychicznych oraz diagnoza u pięciu pacjentów w wieku od 17 do 53 lat cierpiących na zespół MELAS. Wyniki: U czterech pacjentów cierpiących na zespół MELAS stwierdzono obecność mutacji 3243A>G mitochondrialnego DNA (mtDNA), a u jednego pacjenta mutację 12706T>C mtDNA. W rodzinach trzech pacjentów występowały przypadki zespołu MELAS. U jednego pacjenta jako pierwszy objaw zespołu MELAS zdiagnozowano depresję. Depresja poprzedzała również incydent podobny do udaru u jednego pacjenta. Czterech pacjentów cierpiało na zaburzenia funkcji poznawczych, stany splątania wystąpiły u trzech pacjentów. Jeden pacjent przejawiał objawy psychotyczne (podobne do schizofrenii). Wnioski: Zaburzenia mitochondrialne zasługują na uwagę jako część diagnozy różnicowej, szczególnie gdy istnieje podejrzenie wystąpienia objawów chorobowych w innych grupach organów lub występowały przypadki ZM w rodzinie.
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“Studies have shown that psychiatric illnesses are common in patients with mitochondrial diseases. 3 , 4 , 5 , 6”
From Psychiatric care for a person with MELAS syndrome: A case report (2021) · cites this paper as [4]
In the citing paper
“and these include SSRIs, 12 , 14 , 15 SNRIs, 3 MAOIs, 4 antipsychotics, 16 , 17 , 18 and sodium‐valproate 19 , 20 , 21 , 22”
From Psychiatric care for a person with MELAS syndrome: A case report (2021) · cites this paper as [4]
Citations
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Population prevalence of the MELAS A3243G mutation
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Psychiatric Comorbidity in 36 Adults with Mitochondrial Cytopathies
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Natural history of MELAS associated with mitochondrial DNA m.3243A>G genotype
Kaufmann, P., Engelstad, K., Wei, Y., Kulikova, R., Oskoui, M., Sproule, D. M., Battista, V., Koenigsberger, D. Y., Pascual, J. M., Shanske, S., et al. (2011) · Neurology · doi:10.1212/wnl.0b013e31823a0c7f · Cited by 179
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Biomarkers for major depressive and bipolar disorders using metabolomics: A systematic review
MacDonald, K., Krishnan, A., Cervenka, E., Hu, G., Guadagno, E., & Trakadis, Y. J. (2018) · American Journal of Medical Genetics Part B Neuropsychiatric Genetics · doi:10.1002/ajmg.b.32680 · Cited by 108
Mitochondrial metabolic stroke: Phenotype and genetics of stroke-like episodes
Finsterer, J. (2019) · Journal of the Neurological Sciences · doi:10.1016/j.jns.2019.03.021 · Cited by 62
Stroke-like episodes, peri-episodic seizures, and MELAS mutations
Finsterer, J., & Wakil, S. M. (2016) · European Journal of Paediatric Neurology · doi:10.1016/j.ejpn.2016.08.002 · Cited by 23
Frye, M. A., Ryu, E., Nassan, M. M., Jenkins, G. D., Andreazza, A. C., Evans, J. M., McElroy, S. L., Oglesbee, D., Highsmith, W. E., & Biernacka, J. M. (2016) · Journal of Psychiatric Research · doi:10.1016/j.jpsychires.2016.09.027 · Cited by 19
Cognitive functioning and mental health in mitochondrial disease: A systematic scoping review
Klein, I., van de Loo, K. F. E., Smeitink, J. A. M., Janssen, M. C. H., Kessels, R. P. C., van Karnebeek, C., van der Veer, E., Custers, J. A. E., & Verhaak, C. M. (2021) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2021.02.004 · Cited by 21
Cerebral Manifestations of Mitochondrial Disorders
Finsterer, J., & de Carvalho, E. H. T. (2017) · Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques · doi:10.1017/cjn.2017.211 · Cited by 9
Psychiatric care for a person with MELAS syndrome: A case report
Leong, D. Y., Chee, R. Y., & Lui, Y. S. (2021) · Clinical Case Reports · doi:10.1002/ccr3.4146 · Cited by 2
Gujrati, A., Datar, M. C., Makhija, A. M., & Shetty, J. V. (2025) · BMJ Case Reports · doi:10.1136/bcr-2024-264055 · Cited by 2
Case Report: Abnormal pupils caused by the mitochondrial MT-TL1 gene m.3243A>G mutation
Li, Y., Ding, Y., Jin, E., & Yin, H. (2025) · Frontiers in Pediatrics · doi:10.3389/fped.2025.1573886 · Cited by 1
Kolářová, H., & Ješina, P. (2022) · Neurologie pro praxi · doi:10.36290/neu.2021.049 · Cited by 1
Effect of Selective Serotonin-Noradrenaline Reuptake Inhibitors on Mitochondrial Functionn
Finsterer, J., & Zarrouk‐Mahjoub, S. (2017) · Avicenna Journal of Neuro Psych Physiology · doi:10.32598/ajnpp.4.4.129
Metadata
- Authors
- Magner, M., Honzik, T., Tesarova, M., Dvorakova, V., Hansikova, H., Raboch, J., & Zeman, J.
- Corresponding author
- Zeman, Jiri
- Venue
- Psychiatria Polska
- Published
- 2014-10-31
- Volume
- 48
- Issue
- 5
- Pages
- 1035-1045
- ISSN
- 0033-2674 (ISSN-L)
- 2391-5854
- OpenAlex
- W2331005652
- Cited by
- 11
- References
- 22
- Citations by year
- 2025: 2 · 2022: 1 · 2021: 2 · 2019: 1 · 2018: 1 · 2017: 2 · 2016: 2
- FWCI
- 0.55
- Type
- journal article
- Language
- pl
- Open access
- diamond
- doi.org
- Locations
- Psychiatria Polska (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Mitochondrial Function and Pathology
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Clinical Biochemistry › Metabolism and Genetic Disorders
- Health Sciences › Medicine › Clinical Neurology › Parkinson's Disease Mechanisms and Treatments
- Keywords
- MELAS, mitochondrial disease, psychiatric symptoms, depression, stroke-like episodes, confusional state, cognitive impairment, psychosis, schizophrenia-like symptoms, differential diagnosis, family history (medicine)
- MeSH terms
- Adolescent, Adult, Anxiety, Cognition Disorders, Depression, Female, Humans, Male, Mental Health, MELAS Syndrome, Young Adult
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