This national cohort demonstrated pronounced regional and etiologic heterogeneity in CKD and revealed stage- and albuminuria-dependent patterns of metabolic complications, supporting the use of KDIGO G-A staging and regional profiles to prioritise etiologic evaluation and tailor laboratory monitoring in low- and middle-income settings.
Key Findings
Results
Diabetic nephropathy and hypertensive nephrosclerosis were the most common causes of CKD in the THAI-CKD cohort.
Diabetic nephropathy accounted for 41% of cases.
Hypertensive nephrosclerosis accounted for 34% of cases.
The cohort included 3371 participants with a mean age of 69 ± 12 years, 55% male.
Participants had stages G3-G5 CKD from 41 hospitals across Thailand.
Results
Chronic kidney disease of unknown aetiology (CKDu) accounted for 22% of all cases overall and showed significant regional concentration.
CKDu was concentrated in the Central (33%) and Western (24%) regions.
CKDu was more prevalent in earlier CKD stages with lower albuminuria.
CKDu accounted for 22% of the total cohort of 3371 participants.
Regional associations remained significant after multivariable adjustment.
Results
CKD stage distribution in the cohort was predominantly G3b and G4.
G3a comprised 20% of participants.
G3b comprised 33% of participants.
G4 comprised 37% of participants.
G5 comprised 10% of participants.
Results
Anaemia and metabolic acidosis showed clear gradients of increasing prevalence with lower estimated glomerular filtration rate and higher albuminuria.
Both complications increased with lower eGFR and higher albuminuria across KDIGO G-A strata.
The associations between complications and G-A strata remained significant after multivariable adjustment.
These patterns were observed across primary aetiologies and geographic regions.
Results
Secondary hyperparathyroidism occurred across all CKD stages but was most frequent in G5, while hyperphosphatemia was mainly observed in G5.
Secondary hyperparathyroidism was present across all stages (G3a through G5).
Hyperphosphatemia was mainly observed in G5.
Hyperkalaemia remained rare across all G-A categories.
Complication prevalence varied by primary aetiology and geographic region.
Results
The prevalence of CKD complications varied significantly by both primary aetiology and geographic region after multivariable adjustment.
Associations between complications and geographic region remained significant after multivariable adjustment.
Associations between complications and primary aetiology also remained significant after multivariable adjustment.
The study drew from 41 hospitals across multiple Thai geographic regions.
Demographic, clinical, and laboratory data were collected at baseline from the multicentre THAI-CKD cohort.
Conclusions
KDIGO G-A staging and regional profiles are recommended to prioritise etiologic evaluation and tailor laboratory monitoring in low- and middle-income settings.
The study aimed to optimise screening and monitoring in resource-constrained settings.
Stage- and albuminuria-dependent patterns of metabolic complications were identified.
Pronounced regional and etiologic heterogeneity in CKD was demonstrated at the national level.
The findings support differentiated approaches to laboratory monitoring based on KDIGO G-A category.
What This Means
This research examined why people develop chronic kidney disease (CKD) and what complications they experience across different regions of Thailand. The study analyzed data from over 3,300 adults with moderate-to-severe CKD (stages 3-5) recruited from 41 hospitals nationwide. The most common causes of CKD were diabetes-related kidney damage (41%) and high blood pressure-related kidney damage (34%). Notably, about 22% of cases had no identifiable cause — a condition called CKDu (CKD of unknown aetiology) — which was particularly concentrated in the Central and Western regions of Thailand and tended to occur at earlier, less severe disease stages.
The study found that certain complications followed predictable patterns based on how advanced the CKD was. For example, anemia and metabolic acidosis became more common as kidney function worsened and as more protein appeared in the urine. A condition called secondary hyperparathyroidism (abnormal parathyroid hormone levels) appeared at all stages of CKD, while abnormally high phosphate levels were mainly seen in the most severe stage (G5). High potassium levels were surprisingly rare across all disease stages. Importantly, the frequency of these complications also differed depending on what caused someone's kidney disease and which part of Thailand they lived in, even after accounting for other factors.
This research suggests that a 'one-size-fits-all' approach to monitoring CKD patients may not be the most efficient use of limited medical resources in lower-income countries. Instead, tailoring laboratory testing schedules and screening priorities based on a patient's disease stage, the amount of protein in their urine, the underlying cause of their kidney disease, and their geographic region could help healthcare systems better target resources. The findings are particularly relevant for other low- and middle-income countries facing similar challenges in managing CKD at a population level.