β οΈ Metabolic Syndrome is defined by a cluster of risk factors including hypercholesterolaemia, hypertriglyceridaemia, impaired glucose tolerance/diabetes, hyperuricaemia, and hypertension. It markedly increases the risk of cardiovascular disease and stroke.
π About
- Also called Syndrome X or Insulin Resistance Syndrome.
- Core components: diabetes/insulin resistance, central obesity, hypertension, and dyslipidaemia.
- Prevalence: ~25β30% of adults in Western populations; rising globally due to obesity epidemic.
- Strongly linked to type 2 diabetes and premature coronary heart disease.
β οΈ Aetiology & Pathophysiology
- Underlying driver = insulin resistance, often secondary to visceral adiposity (central obesity).
- Additional mechanisms: atherogenic dyslipidaemia, endothelial dysfunction, low-grade chronic inflammation, genetic susceptibility, and sympathetic overactivity.
- Abnormal adipocytokines (TNF-Ξ±, IL-6, leptin, adiponectin) contribute to pro-inflammatory and pro-thrombotic state.
- Hypercoagulability (β fibrinogen, PAI-1) and chronic stress add to vascular risk.
π Diagnostic Criteria (IDF, 2005)
Diagnosis requires central obesity (waist circumference >94 cm for Europid men, >80 cm for Europid women) plus any 2 of:
- Raised triglycerides: >1.7 mmol/L (150 mg/dL) or on treatment.
- Reduced HDL: <1.03 mmol/L (40 mg/dL) in men, <1.29 mmol/L (50 mg/dL) in women, or on treatment.
- Raised blood pressure: β₯130/85 mmHg or treatment for hypertension.
- Raised fasting glucose: β₯5.6 mmol/L (100 mg/dL) or type 2 diabetes.
π§Ύ Risk Factors
- Obesity (especially central/visceral).
- Sedentary lifestyle and poor diet.
- Advancing age.
- Family history of diabetes and CVD.
- Ethnicity: South Asians and Afro-Caribbeans at higher risk.
π©Ί Clinical Features
- Often asymptomatic until complications arise.
- Central obesity, elevated BP, hyperglycaemia, abnormal lipids.
- Can present with features of diabetes (polyuria, polydipsia, fatigue).
- Increased risk of fatty liver disease, gout (due to hyperuricaemia), and PCOS in women.
π Differentials / Related Conditions
- Primary cardiovascular disease (e.g. MI, angina).
- Type 2 diabetes mellitus (progression risk is high).
- Polycystic ovarian syndrome (PCOS).
- Cushingβs syndrome and secondary causes of obesity/hypertension.
π Management
- Lifestyle: Cornerstone of therapy β diet (reduced refined carbs, lower saturated fat), weight loss, regular aerobic and resistance exercise, smoking cessation, reduced alcohol.
- Pharmacological:
- Statins for dyslipidaemia.
- Antihypertensives (ACE inhibitors/ARBs preferred in diabetics).
- Metformin for insulin resistance/type 2 diabetes.
- Allopurinol if significant hyperuricaemia/gout.
- Multifactorial approach: Simultaneous control of BP, glucose, and lipids gives the greatest CVD risk reduction.
- Monitoring: Regular review for CVD risk assessment, HbA1c, lipid profile, renal function.
π References
Clinical Exmaples
- βοΈ Case 1 β Age 49: Overweight man (BMI 32 kg/mΒ²) attended for an insurance medical. Bloods showed fasting glucose 6.4 mmol/L, triglycerides 2.5 mmol/L, HDL 0.9 mmol/L, and BP 148/92 mmHg. Waist circumference 108 cm.
Diagnosis: Metabolic syndrome (abdominal obesity, dyslipidaemia, hypertension, impaired glucose tolerance).
Management: Lifestyle modification with weight loss, aerobic exercise, and dietary counselling; started on statin and ACE inhibitor.
Teaching point: Central obesity drives insulin resistance β early intervention prevents type 2 diabetes and cardiovascular disease.
- π Case 2 β Age 57: Woman with polycystic ovary syndrome (PCOS) presented with increasing waist size and fatigue. Fasting glucose 7.2 mmol/L, triglycerides 3.0 mmol/L, HDL 0.8 mmol/L.
Diagnosis: Metabolic syndrome secondary to insulin resistance.
Management: Metformin initiated, along with structured exercise and low-glycaemic index diet.
Teaching point: In women, PCOS often coexists with metabolic syndrome β both improve with insulin-sensitising therapy and weight reduction.
- π©Ί Case 3 β Age 62: Retired lorry driver with long-standing hypertension and fatty liver found incidentally on ultrasound. BMI 34 kg/mΒ², fasting glucose 6.9 mmol/L, triglycerides 2.1 mmol/L, HDL 0.7 mmol/L.
Diagnosis: Metabolic syndrome with non-alcoholic fatty liver disease (NAFLD).
Management: Weight reduction, alcohol minimisation, statin therapy, and annual screening for diabetes.
Teaching point: NAFLD is now considered the hepatic manifestation of metabolic syndrome β improving insulin sensitivity can reverse early liver changes.