Response to multiple glucose-lowering agents in a sib-pair with a novel HNF1α (MODY3) variant.
Clara S H TanSu Fen AngSu Chi LimPublished in: European journal of human genetics : EJHG (2019)
Maturity-onset diabetes of the young (MODY) is a genetically and clinically heterogeneous group of disorders characterised by early onset, lean, non-autoimmunity mediated, non-insulin-dependent diabetes often with autosomal-dominant inheritance and specific pharmaco-genetic response. We describe two siblings with HNF1A-MODY (MODY3) due to a novel germline variant p.(His126Asp) which segregates with diabetes in the family. However, contrary to anticipated therapeutic response, blood glucose in this sib-pair did not respond to sulphonylureas (both low and high dose), dipeptidyl peptidase-4 inhibitors (DPP-4 inhibitors), and glucagon-like peptide-1 receptor agonists (GLP-1RA), also known as incretin mimetics. The unexpected limited pharmaco-therapeutic response could potentially be unique to this specific variant and/or progressive pancreatic β-cell failure associated with long-standing disease duration, higher BMI and glucose-toxicity. Therefore, we report a novel-variant MODY3 sib-pair with atypical pharmaco-therapeutic response i.e. resistant to multiple anti-diabetes agents namely sulphonylurea, DPP-4 inhibitors and GLP-1RA treatment.
Keyphrases
- glycemic control
- blood glucose
- type diabetes
- early onset
- cardiovascular disease
- high dose
- rheumatoid arthritis
- late onset
- low dose
- body mass index
- stem cells
- disease activity
- gene expression
- metabolic syndrome
- insulin resistance
- bone marrow
- blood pressure
- mitochondrial dna
- ankylosing spondylitis
- physical activity
- stem cell transplantation
- nuclear factor
- mesenchymal stem cells
- copy number
- weight gain
- dna damage
- skeletal muscle