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Published on: May 2, 2025
Decreased circulating CD34+ cells are associated with progression of diabetic nephropathy
1Department of Atherosclerosis and Diabetes, National Cardiovascular Centre, Suita, Osaka, Japan. makinoh@hsp.ncvc.go.jp
Insights
Decreased circulating CD34+ cells are linked to worsening diabetic nephropathy. Low CD34+ cell counts predict disease progression, highlighting their role in microvascular complications.
Area of Science:
- Nephrology
- Hematology
- Endocrinology
Background:
- Circulating CD34+ cells are vital for vascular health and neovascularization.
- Reduced CD34+ cell counts are associated with cardiovascular disease.
- The role of CD34+ cells in diabetic nephropathy remains unclear.
Purpose of the Study:
- To investigate the association between circulating CD34+ cells and diabetic nephropathy.
- To determine if CD34+ cell numbers predict the progression of kidney disease in diabetic patients.
Main Methods:
- Measured circulating CD34+ cell counts in 85 Type 2 diabetic patients (aged 40-70).
- Assessed patients with normoalbuminuria and microalbuminuria.
- Correlated CD34+ cell numbers with urinary albumin excretion rate (UAER).
Main Results:
- A significant inverse correlation was found between CD34+ cell numbers and log UAER (r = -0.289, P = 0.008).
- Patients in the lowest quartile of CD34+ cells showed a significant UAER increase over 12 months.
- Patients in the highest quartile of CD34+ cells exhibited stable UAER levels.
Conclusions:
- Diminished circulating CD34+ cells are implicated in the progression of diabetic nephropathy.
- CD34+ cell counts may serve as a predictive biomarker for diabetic nephropathy.
- This finding underscores the role of progenitor cells in microvascular complications of diabetes.
Aims:
Circulating progenitor cells such as CD34+ cells play a key role in maintenance of vascular endothelial function and neovascularization, and a decrease in the number of CD34+ cells is associated with cardiovascular disease. However, the contribution of circulating progenitor cells to microvascular disease, such as diabetic nephropathy, is unclear. This study was therefore designed to clarify the association between diabetic nephropathy and circulating CD34+ cells.
Methods:
We measured circulating CD34+ cell numbers in 85 Type 2 diabetic patients aged 40-70 years with normo- and microalbuminuria and determined the association with urinary albumin excretion rate (UAER).
Results:
The number of circulating CD34+ cells significantly correlated with log UAER (r = -0.289, P = 0.008). Furthermore, in patients with low numbers of CD34+ cells (0.68 > cells/microl, lowest quartile of CD34+ cell number) UAER increased significantly after 12 months compared with baseline [from 34.3 +/- 7.0 to 53.6 +/- 10.8 mg/g creatinine (gCr), P < 0.05], whereas in patients with a high number of CD34+ cells (1.0 < cells/microl, highest quartile of CD34+ cell number) UAER did not change (from 16.7 +/- 4.8 to 20.1 +/- 3.0 mg/gCr).
Conclusions:
These results suggest that a decreased number of circulating CD34+ cells is involved in the progression of diabetic nephropathy and may be a predictor of the disease.
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