The edition · Nephrology
Across 49 trials and 66,449 patients, early eGFR and albuminuria changes tracked each other equally on drug and placebo
What an early eGFR dip or albuminuria fall in one patient can and cannot tell you, music during haemodialysis, the complement signature inside IgA nephropathy deposits, and a heme–kallikrein pathway in childhood HUS.
The edition in brief
An individual patient meta-analysis of 49 randomised CKD trials and 66,449 participants found no trial-level link between a treatment's acute effect on GFR and its effect on albuminuria. Within individuals, a larger early GFR decline came with a slightly larger albuminuria fall — about 8% per standard deviation on treatment and 6.6% on control — so these early changes in one patient largely reflect natural variation and disease course rather than drug response. A Cochrane review of 27 trials and 1,584 people on haemodialysis found music-based interventions may reduce short-term fatigue, pain and depressive symptoms, with low to very low certainty and no long-term data. Laser microdissection and mass spectrometry of 22 IgA nephropathy biopsies showed deposits of dimeric IgA1 and IgA2 with IgG1, and complement mostly from the alternative and terminal pathways, consistent with the targets of new complement-directed drugs. In 34 children with E. coli HUS and in mice, heme released by haemolysis activated factor XII and the kallikrein–kinin system, an effect blocked by C1-inhibitor in experiments.
Music during haemodialysis may ease fatigue, pain and low mood in the short term
Consider offering music during haemodialysis as a low-cost addition to symptom care.
Inside IgA nephropathy deposits: dimeric IgA with IgG1, and alternative-pathway complement
IgA nephropathy deposits show alternative and terminal complement activity, matching the targets of new therapies.
In childhood HUS, heme from haemolysis activated the kallikrein–kinin system
Haemolysis may drive injury in HUS through the kallikrein–kinin system; no treatment change follows yet.
An early eGFR dip after starting a RAS blocker or SGLT2 inhibitor is expected
Expect and tolerate a modest early eGFR dip on RAS blockers and SGLT2 inhibitors; investigate larger falls.
Early eGFR and albuminuria changes in one patient reflect disease course as much as drug effect
Avoid reading early eGFR or albuminuria changes in one patient as proof of drug response; continue proven therapy.
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