Acute onset of diabetes and rapid cognitive decline in a patient with mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes syndrome.
Nam Quang TranChien Cong PhanTran Bao VuongThang Viet TranPhat Tung MaPublished in: Endocrinology, diabetes & metabolism case reports (2023)
Diabetes is a common endocrine manifestation of mitochondrial diseases, presenting with a type 1- or type 2-like phenotype depending on the level of insulinopenia. Metformin should be avoided in patients with mitochondrial diseases to prevent metformin-induced lactic acidosis. Mitochondrial diabetes can manifest before or after the onset of MELAS syndrome. In patients with MELAS syndrome, diabetes can initially manifest with a life-threatening severe hyperglycemic crisis and can cause rapid cognitive decline. Diabetes screening tests (e.g. hemoglobin A1c, oral glucose tolerance test, or random blood glucose level measurement) should be performed either systematically or in the presence of symptoms, particularly after triggering events. Genetic testing and counseling should be provided to patients and their families for the purpose of better understanding the inheritance, progression, and possible outcomes of the disease.
Keyphrases
- cognitive decline
- glycemic control
- type diabetes
- blood glucose
- cardiovascular disease
- mild cognitive impairment
- oxidative stress
- case report
- end stage renal disease
- insulin resistance
- blood pressure
- gene expression
- weight loss
- chronic kidney disease
- newly diagnosed
- adipose tissue
- ejection fraction
- metabolic syndrome
- mitochondrial dna
- loop mediated isothermal amplification
- men who have sex with men
- hiv testing
- dna methylation
- red blood cell
- high glucose
- sleep quality
- genome wide
- patient reported