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. Author manuscript; available in PMC: 2018 Jan 16.
Published in final edited form as: Nat Rev Nephrol. 2017 Nov 27;14(1):57–70. doi: 10.1038/nrneph.2017.155

Table 3.

Clinical trials and studies of dyslipidaemia treatments in patients with nephrotic syndrome

Treatment Action Outcomes Limitations Refs or trials
Conservative lifestyle changes (diet, weight, exercise) • ↓ Cholesterol
• ↓ Apolipoproteins (small reduction)
• ↓ Triglycerides
• ↓ Hyperlipidaemia
• ↓ Proteinuria
Implementation and patient compliance 121123
Statins • ↓ HMG CoA • ↓ LDL
• ↓ Cholesterol
• ↓ Triglycerides
• ↑ HDL
• Few adverse effects
• Improved cardiovascular outcome in CKD
Limited number of studies 125–131,139*,140*, NCT00004466* (REF. 157), NCT01845428 (REF. 158)
Bile acid sequestrants • ↓ Enterohepatic bile acid circulation • ↓ LDL • Gastrointestinal adverse effects
• Less effective than statins
133
Fibrates • ↑ Lipoprotein lipase activity • ↓ Triglycerides
• ↓ LDL
• ↓ Cholesterol
Meta-analysis found a lack of support for fibrate efficacy 112,134,135
LDL-apheresis • ↓ LDL
• ↓ Cholesterol
• ↓ Triglycerides
• ↑ Response to immunosuppressants
• Complete or partial remission of nephrotic syndrome
• Few adverse effects
Requires central venous access 141*,142–144, NCT02235857* (REF. 154)
• Anti PCSK9 antibodies
PCSK9 RNA interference
• Inactivation of PCSK9
• Degradation of PCSK9 mRNA
• ↑ Hepatic LDLR
• ↓ LDL Very expensive 44, NCT03004001 (REF. 149), NCT02314442 (REF. 146)
*

Studies or trials with paediatric patients.

Not in nephrotic syndrome setting. CKD, chronic kidney disease; HDL, high density lipoprotein; HMG CoA, 3 hydroxy 3 methyl glutaryl coenzyme A; LDL, low density lipoprotein; LDLR, LDL receptor; PCSK9, proprotein convertase subtilisin/kexin type 9.