Searched over 200M research papers
10 papers analyzed
These studies suggest that chronic kidney disease (CKD) is prevalent globally, with significant risks and outcomes varying by stage, particularly highlighting the importance of early detection, intervention, and the role of specific treatments in managing progression and cardiovascular complications.
20 papers analyzed
Chronic Kidney Disease (CKD) is a significant global health issue, affecting approximately 11-13% of the population worldwide. The prevalence of CKD varies by stage, with Stage 3 being the most common. Specifically, the global prevalence by stage is as follows: Stage 1 (3.5%), Stage 2 (3.9%), Stage 3 (7.6%), Stage 4 (0.4%), and Stage 5 (0.1%). This distribution highlights the importance of early detection and intervention to prevent progression to more severe stages.
In LMICs in Asia, the prevalence of CKD stages 3-5 is comparable to global figures, with an average prevalence of 11.2%. However, there is significant variation among subregions, with prevalence rates ranging from 8.6% in East Asia to 13.5% in South Asia. The economic classification of countries also influences CKD prevalence, with lower-middle-income countries experiencing higher rates (13.8%) compared to upper-middle-income countries (9.8%). This data underscores the need for targeted public health strategies in these regions.
Screening and monitoring for CKD stages 1 to 3 can potentially lead to earlier interventions and improved clinical outcomes. Treatments such as angiotensin-converting enzyme inhibitors and angiotensin II-receptor blockers have shown efficacy in reducing the progression to end-stage renal disease, particularly in patients with diabetes and albuminuria. However, the role of routine screening and monitoring in improving outcomes remains uncertain.
The correlation between CKD stages and kidney histology is not always straightforward. Studies have shown that patients with the same estimated glomerular filtration rate (eGFR) can exhibit varying degrees of histological damage. For instance, some patients classified as CKD stage 3 may have mild or no histological lesions, while others in stage 1 may have moderate to severe lesions. This variability suggests that current CKD classification based on eGFR alone may not fully capture the extent of kidney damage.
CKD is a known predictor of cardiovascular disease (CVD). In early CKD stages (1 and 2), the presence of proteinuria significantly increases the risk of major adverse cardiovascular events (MACE), heart failure, and all-cause mortality. Interestingly, stage 2 CKD without proteinuria has a comparable prognosis to normal renal function, indicating that proteinuria is a critical factor in cardiovascular risk stratification.
Patients with advanced CKD (stage 5) face a high risk of cardiovascular complications, including coronary artery disease, heart failure, and sudden cardiac death. These complications are the leading causes of death in patients with kidney failure. Both traditional and non-traditional risk factors contribute to the progression of cardiovascular disease in CKD patients.
Risk factors for CKD include low nephron number at birth, aging, and kidney injuries from diseases such as obesity and type 2 diabetes. Management focuses on early detection, treatment of underlying causes, and addressing secondary processes like hypertension and metabolic acidosis. Effective management can slow CKD progression and improve patient outcomes.
Stage 2 CKD may represent a tipping point in disease progression, with significant changes in plasma protein profiles related to inflammation, lipoprotein metabolism, and tissue regeneration. Identifying and targeting these molecular changes could provide opportunities for early therapeutic interventions.
In the U.S., the lifetime risk of developing CKD stage 3a+ is high, with an overall risk of 59.1%. Women have a higher risk of CKD but a lower risk of end-stage renal disease (ESRD) compared to men. The risk of CKD increases with age, emphasizing the need for primary prevention and effective therapies to reduce CKD-related morbidity and mortality.
Urinary albumin excretion (UAE) is a crucial factor in assessing cardiovascular and renal outcomes in CKD stages 1-3. Higher UAE levels are associated with increased cardiovascular events and faster decline in eGFR. Therefore, monitoring UAE can improve risk stratification and guide treatment decisions in early CKD stages.
Understanding the stages of CKD and their associated risks is essential for effective management and intervention. Early detection, targeted treatment, and monitoring of key indicators like proteinuria and UAE can significantly improve patient outcomes and reduce the burden of CKD on global health systems.
Most relevant research papers on this topic