ArticleNeuropsychiatric disease and treatment2017
Mitochondrial multiorgan disorder syndrome score generated from definite mitochondrial disorders.
Article in Neuropsychiatric disease and treatment, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.
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11 citing papers in PubMed, 22 citations in OpenAlex.
- Mitochondrial DNA Deletions and Plasma GDF-15 Protein Levels Are Linked to Hormonal Dysregulation and Multi-Organ Involvement in Female Reproductive Endocrine Disorders.Life (Basel, Switzerland) · 2025Article
- The Novel Role of PGC1α in Bone Metabolism.International journal of molecular sciences · 2021Review
- Genetic ataxias: update on classification and diagnostic approaches.Current neurology and neuroscience reports · 2021Review
- MELAS in a Walk-in Customer.Journal of neurosciences in rural practice · 2019Article
- Liability of sepsis is hardly determined by the COXI variant m.6459T>C.Journal of cellular and molecular medicine · 2019Article
- MELAS Missed for Years: Stroke-Like Lesions Are No Indication for Brain Biopsy.Case reports in neurological medicine · 2019Article
- Aortic root ectasia as a phenotypic feature of a mitochondrial disorder.Clinical case reports · 2018Article
- Polymegathism as a biomarker of mitochondrial disorders.Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie · 2018Article
- Biomarkers for Detecting Mitochondrial Disorders.Journal of clinical medicine · 2018Review
- Early identification of LHON carriers may improve outcome.Romanian journal of ophthalmologyArticle
- Malingering and Factitious Disorder (Münchausen-syndrome) can be Mitochondrial.Indian journal of psychological medicineArticle
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Authors and funding
2 authors at 2 institutions in 2 countries.
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No grant is acknowledged in the PubMed record.
Abstract
objectivesMitochondrial disorders (MIDs) frequently present as mitochondrial multiorgan disorder syndrome (MIMODS) at onset or evolve into MIMODS during the course. This study aimed to find which organs and/or tissues are most frequently affected by MIMODS, which are the most frequent abnormalities within an affected organ, whether there are typical MIMODS patterns, and to generate an MIMODS score to assess the diagnostic probability for an MID.
methodsThis is a retrospective evaluation of clinical, biochemical, and genetic investigations of adult patients with definite MIDs. A total of 36 definite MID patients, 19 men and 17 women, aged 29-82 years were included in this study. The diagnosis was based on genetic testing (n=21), on biochemical investigations (n=17), or on both (n=2).
resultsThe number of organs most frequently affected was 4 ranging from 1 to 9. MIMODS was diagnosed in 97% of patients. The organs most frequently affected were the muscle (97%), central nervous system (CNS; 72%), endocrine glands (69%), heart (58%), intestines (55%), and peripheral nerves (50%). The most frequent CNS abnormalities were leukoencephalopathy, prolonged visually evoked potentials, and atrophy. The most frequent endocrine abnormalities included thyroid dysfunction, short stature, and diabetes. The most frequent cardiac abnormalities included arrhythmias, systolic dysfunction, and hypertrophic cardiomyopathy. The most frequent MIMODS patterns were encephalomyopathy, encephalo-myo-endocrinopathy, and encepalo-myo-endocrino-cardiopathy. The mean ± 2SD MIMODS score was 35.97±27.6 (range =11-71). An MIMODS score >10 was regarded as indicative of an MID.
conclusionAdult MIDs manifest as MIMODS in the vast majority of the cases. The organs most frequently affected in MIMODS are muscles, CNS, endocrine glands, and heart. An MIMODS score >10 suggests an MID.
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