Key Points
- Diabetic nephropathy is the most common cause of severe CKD in the UK
- Definition = persistent albuminuria (ACR>2.5) on ≥ 2 separate occasions separated by >3 months
- Typically coexists withretinopathy and neuropathy
Epidemiology
- 20% of all ESRF patients are diabetic
- Diabetes is the most common cause of ESRF
- 20% of DMII patients will develop ESRF
Pathophysiology
- Diabetic nephropathy describes kidney disease due to microvascular disease
- Result in intrinsic kidney damage followed by GFR deterioration (i.e. CKD)
- Exacerbated by hypertension which often coexists with diabetes
- Natural history of progression (Mnemonic – Elevated Glomerulus Means Nephropathy)
- Renal hyper-perfusion due to high BP which results in :
- Initial GFR elevation due to hyperglycaemia
- Albuminuria (ACR >2.5)
- Glomerular hypertrophy
- This stage is reversible with glycaemic control and HTN management – therefore screening is key
- Glomerular hyperfiltration follows on from the hyperperfusion
- Hyperglycaemia causes pathological changes via AGEs (Advanced Glycosylated End-products) that cause destruction in the glomerulus/tubules, leading to:
- Mesangial expansion
- GBM thickening
- Glomerulosclerosisdue to intraglomerular HTN
- Hyperglycaemia causes pathological changes via AGEs (Advanced Glycosylated End-products) that cause destruction in the glomerulus/tubules, leading to:
- Proteinuria indicates progression of disease (ACR >25mg)
- T
- GFR may be raised or normal
- Stage 4 – Nephropathy (i.e. CKD develops)
- GFR decreases (as creatinine rises)
- Increased proteinuria develops (ACR >300mg can develop)
Aetiology
- As with most conditions, risk factors are unmodifiable and modifiable
- Unmodifiable:
- Genetics
- Increasing age
- Increasing duration of diabetes (usually develops after ≥10 years with diabetes)
- Ethnicity
- Modifiable
- Tightly linked with cardiovascular disease – both cause and effects it
- Hypertension
- Hyperlipidaemia
- Low baseline albuminuria
- Smoking
- Presence of retinopathy/neuropathy
- Tightly linked with cardiovascular disease – both cause and effects it
Clinical features
- These generally stem from the complications of CKD, and so are the same for all CKD (for which I will do a separate set of notes)
Diagnosis and staging
As with all CKD, the two main factors to consider are:
- GFR – indicates the level of kidney damage
- Can remain high in isolated kidney damage
- If low, this indicates advanced disease (Nephropathy)
- Albuminuria/proteinuria – the amount of protein in the urine
- Urine dipstick gives a qualitative indication
- Urine ACR can also be assessed quantitatively using 2 tests:
- Urinalysis with first pass morning sample with specialised sticks
- 24hr test with albumin/creatinine can be used instead
- A higher ACR indicates more kidney damage:
- >2.5mg/mmol = albuminuria (>3.5 in males)
- >25mg/mmol = proteinuria
- >250mg/mmol = severe proteinuria
Management
Both prevention and management (of diagnosed nephropathy) have the same 3 main principles
- Treating hypertension is the mainstay- maintain a BP of <130/80mmHg in all diabetics
- ACE inhibitors are used in all diabetics for primary prevention (ARBs are used if ACEIs are not tolerated). These not only treat hypertension, but also reduce progression of albuminuria
- Glycaemic control
- Statins can help in patient
Referral criteria
- Patients are referred to a nephrologist if:
- Urine ACR >70
- Suspecting other differentials of CKD (e.g. glomerulonephritis, CCF, etc).
- These are indicated by sudden onset, rapid deterioration eGFR, and an absence of other diabetic complications (e.g. retinopathy)