Type 1 Diabetes Mellitus (T1DM)
- Polyuria, polydipsia, polyphagia, lassitude, nausea, blurred vision
- Young lean patient; not obese; strikes children/young adults (any age)
- Weight loss despite normal/increased appetite (catabolic state)
- Severe nocturnal enuresis in children (2° polyuria)
- May present initially with DKA; onset sudden or stress-precipitated
- Islet autoantibodies — usually present (vs absent in T2DM)
- C-peptide — undetectable/low (absent endogenous insulin)
- FPG ≥7.0 mmol/L or random ≥11.1 mmol/L with symptoms
- HbA1c ≥6.5% — but NOT valid for suspected T1DM
- Venous pH/bicarbonate + ketones if DKA suspected
- Lifelong insulin — basal-bolus (MDI) or continuous SC infusion (CSII pump)
- Rapid-acting analogs (lispro/aspart/glulisine) — reduce hypoglycaemia risk
- Starting dose 0.2–1 U/kg/day (½ basal at bedtime + ½ bolus in 3 divided doses)
- CGM + sensor-augmented pump with low-glucose suspend — nocturnal hypoglycaemia
- Explosive onset in a young lean patient with ketoacidosis — diagnostic of T1DM
- Autoimmune β-cell destruction → absolute insulin deficiency
- Highest susceptibility: HLA-DR3-DQB1*0201 + HLA-DR4-DQB1*0302 heterozygote; monozygotic twin concordance >50%
physiology · background · low-yield
- Environmental triggers for β-cell autoimmunity — viruses (enterovirus, mumps, rubella, coxsackievirus B4), toxic chemicals, cow's milk in infancy, cytotoxins
- Acute presentation — acute fatty liver distends the hepatic capsule → RUQ pain (flood of FFAs); persistent pain → suspect pancreatitis
- Insulin injection-site absorption — abdomen fastest/preferred > upper arm intermediate > thigh slowest
- Split-mixed regimen — 2/3 intermediate-acting + 1/3 short-acting
- Twin concordance — dizygotic 5–6% vs monozygotic >50%