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Assessment of Vascular Function in Patients With Chronic Kidney Disease
Published on: June 16, 2014
Chronic Kidney Disease: Decreasing Serum Klotho Levels Predict Adverse Renal and Vascular Outcomes
Abhijit Konnur1, Sishir Gang1, Umapati Hegde1
1Department of Nephrology, Muljibhai Patel Urological Hospital, Nadiad, India.
Insights
Soluble alpha Klotho (s.Klotho) deficiency is linked to faster kidney function decline and increased vascular damage in chronic kidney disease (CKD) patients. Severe s.Klotho deficiency significantly raises mortality risk and the need for renal replacement therapy (RRT).
Area of Science:
- Nephrology
- Biochemistry
- Cardiology
Background:
- Soluble alpha Klotho (s.Klotho) is an emerging prognostic marker for chronic kidney disease (CKD).
- CKD is associated with decreased glomerular filtration rate (GFR), bone, and vascular complications.
Purpose of the Study:
- To investigate the association between s.Klotho levels and CKD progression.
- To examine the relationship between s.Klotho and GFR decline, bone damage, and vascular disease in CKD patients.
Main Methods:
- 107 patients with CKD stages 2-4 were monitored over 12 months.
- Serum s.Klotho levels were measured using ELISA at 6 and 12 months.
- GFR, Ankle Brachial Pressure Index (ABPI), and carotid intimal medial thickness (CIMT) were assessed.
Main Results:
- GFR decline was significantly steeper in patients with lower s.Klotho levels (p < 0.0001).
- s.Klotho positively correlated with ABPI (r=0.536, p<0.001) and negatively with CIMT (r=-0.712, p<0.001).
- All five deaths occurred in patients with Grade 4 (severe) s.Klotho deficiency; event-free survival was lowest in this group.
Conclusions:
- s.Klotho levels significantly decrease with progressive kidney failure.
- Reduced s.Klotho is strongly associated with vascular disease markers in CKD.
- Severe s.Klotho deficiency is a significant predictor of mortality and need for RRT in CKD.
Abstract:
Background and Objectives: Soluble alpha Klotho (s.Klotho) is an emerging marker for chronic kidney disease (CKD) prognosis. The objective was to study the association between s.Klotho and CKD-related decrease in glomerular filtration rate (GFR), bone and vascular damage. Method: A total of 118 patients with CKD stage 2-4 were enrolled and 107 patients continued in the study. Clinical and laboratory parameters were recorded at time of enrollment and 12 months. A double sandwich ELISA for s.Klotho was recorded in controls (n = 25) and patients' serum samples at 6 months (n = 107) and 12 months (n = 102). Primary endpoints like 40% or more fall in GFR, a requirement for renal replacement therapy (RRT), and death with different grades of s.Klotho deficiency were studied. Results: Of the 107 patients (80 male and 27 female), mean s.Klotho was 3.46 ng/mL (02.3-04.2). The GFR fall was significantly different (p value < 0.0001) in the different grades of s.Klotho deficiency with Grade 4 s.Klotho deficiency (0.1-2.99 ng/mL) having the maximum fall of GFR at 9.2 mL/min/1.73 m2 (04.8-12.0) and minimum in Grade 2 (3-5.99 ng/mL) at 1.35 mL/min/1.73 m2 (03.0-02.75). The Ankle Brachial Pressure Index positively correlated with s.Klotho and the correlation coefficient was 0.536 (0.382-0.662) (p < 0.001). The carotid intimal medial thickness negatively correlated with s.Klotho and the correlation coefficient was -0.712 (95% CI: -0.797--0.601, p < 0.001). All five deaths had s.Klotho Grade 4 (severe) deficiency. The event-free survival rate was maximum (100%) in Grade 2 Klotho deficiency and lowest (55%) in Grade 4 s.Klotho deficiency. Conclusions: s.Klotho levels decreased significantly in patients with progressive kidney failure. s.Klotho levels significantly correlated with the presence of vascular disease. Death and need for RRT were significantly more in patients with severe s.Klotho deficiency.
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