Mitochondrial heteroplasmy-phenotype correlation and response to glucose lowering therapy in subjects with m.3243A>G mutations

β-cell dysfunction and insulin resistance contribute to mitochondrial diabetes development. 65 % of subjects required insulin to improve glycaemic control. Early insulin initiation may be necessary to improve glycaemic control in the long term.

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Publication Details

Journal
Diabetes & Metabolism
Published
2025-06-18
DOI
https://doi.org/10.1016/j.diabet.2025.101678
Citations
3
Primary Topic
Mitochondrial Function and Pathology
Type
article
Field-Weighted Citation Impact
2.42

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article

Mitochondrial heteroplasmy-phenotype correlation and response to glucose lowering therapy in subjects with m.3243A>G mutations

Claire Gavin, Marie Burke, C J McCarrick, Jurcău Ioana et al.
3 citations
Diabetes & Metabolism
Mitochondrial Function and Pathology
2.42
article

Mitochondrial heteroplasmy-phenotype correlation and response to glucose lowering therapy in subjects with m.3243A>G mutations

Claire Gavin, Marie Burke, C J McCarrick, Jurcău Ioana, James J. O’Byrne, Charles E. Mangan, Nicholas Ng, Maria M. Byrne, Begoña Sánchez-Lechuga, R O’Byrne
article en
3 citations

Abstract

β-cell dysfunction and insulin resistance contribute to mitochondrial diabetes development. 65 % of subjects required insulin to improve glycaemic control. Early insulin initiation may be necessary to improve glycaemic control in the long term.

Diabetes & MetabolismVol. 51(5)
University College Dublin (IE), Trinity College Dublin (IE), Mater Misericordiae University Hospital (IE), Mater Private Hospital (AU)
Sanofi, Health Research Board, Novo Nordisk
Zero hunger
Openalex Percentile: Top 11%
Mitochondrial Function and Pathology
2.42
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Mitochondrial heteroplasmy-phenotype correlation and response to glucose lowering therapy in subjects with m.3243A>G mutations — Claire Gavin, Marie Burke, et al. · Diabetes & Metabolism (2025) | TGRS Research Map | TGRS