TY - JOUR
T1 - Diabetes mellitus associated with 3243 mitochondrial tRNA (Leu(UUR)) mutation
T2 - Clinical features and coenzyme Q10 treatment
AU - Suzuki, Y.
AU - Taniyama, M.
AU - Muramatsu, T.
AU - Atsumi, Y.
AU - Hosokawa, K.
AU - Asahina, T.
AU - Shimada, A.
AU - Murata, C.
AU - Matsuoka, K.
N1 - Copyright:
Copyright 2018 Elsevier B.V., All rights reserved.
PY - 1997
Y1 - 1997
N2 - Diabetes mellitus associated with mitochondrial tRNA mutation at position 3243(DM-Mt3243) is a new disease. Patients have a distinctly different picture from MELAS (mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes). During observations at the Saiseikai Central Hospital, the following findings were noted in DM-Mt3243 patients: DM-Mt3243 patients are diagnosed earlier with diabetes, compared to NIDDM (non-insulin dependent diabetes mellitus) controls without family history. DM-Mt3243 patients often need insulin more often than NIDDM controls without family history. Post-treatment neuropathy and insulin edema are often found in DM-Mt3243, and the two phenomena possibly have a similar pathophysiology related to mitochondrial dysfunction. Ambiguous psychiatric disorders of functional psychosis are observed frequently in DM-Mt3243. Mild headache is common in DM-Mt3243 cases. Ambiguous neuromuscular abnormaltiies such as sleep disturbance, paresthesia of the legs, edema of the legs, and palpitation may be symptoms associated with mitochondrial dysfunction in DM-Mt3243. Coenzyme a maybe effective in the relief of these neuromuscular symptoms.
AB - Diabetes mellitus associated with mitochondrial tRNA mutation at position 3243(DM-Mt3243) is a new disease. Patients have a distinctly different picture from MELAS (mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes). During observations at the Saiseikai Central Hospital, the following findings were noted in DM-Mt3243 patients: DM-Mt3243 patients are diagnosed earlier with diabetes, compared to NIDDM (non-insulin dependent diabetes mellitus) controls without family history. DM-Mt3243 patients often need insulin more often than NIDDM controls without family history. Post-treatment neuropathy and insulin edema are often found in DM-Mt3243, and the two phenomena possibly have a similar pathophysiology related to mitochondrial dysfunction. Ambiguous psychiatric disorders of functional psychosis are observed frequently in DM-Mt3243. Mild headache is common in DM-Mt3243 cases. Ambiguous neuromuscular abnormaltiies such as sleep disturbance, paresthesia of the legs, edema of the legs, and palpitation may be symptoms associated with mitochondrial dysfunction in DM-Mt3243. Coenzyme a maybe effective in the relief of these neuromuscular symptoms.
KW - ALDH2
KW - Coenzyme Q
KW - MELAS
KW - Mitochondrial DNA mutation at position 3243
KW - Mitochondrial diabetes mellitus
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U2 - 10.1016/S0098-2997(97)00041-1
DO - 10.1016/S0098-2997(97)00041-1
M3 - Article
C2 - 9266520
AN - SCOPUS:0030823104
SN - 0098-2997
VL - 18
SP - 181
EP - 188
JO - Molecular Aspects of Medicine
JF - Molecular Aspects of Medicine
IS - SUPPL.
ER -