Key result
Systolic-diastolic hypertension is linked to ~2.5-fold higher odds of concurrent diabetic kidney disease.
Why the study?
Although hypertension is a key modifiable risk factor for diabetic kidney disease (DKD), the associations between specific blood pressure phenotypes and concurrent DKD risk in adults with diabetes remain poorly understood.
Are specific blood pressure phenotypes (ISH, IDH, SDH) associated with concurrent diabetic kidney disease in adults with diabetes, and can machine learning models using routine clinical variables discriminate this concurrent risk pattern?
Cross-Sectional (n=1,240)
No
Are specific blood pressure phenotypes (ISH, IDH, SDH) associated with concurrent diabetic kidney disease in adults with diabetes, and can machine learning models using routine clinical variables discriminate this concurrent risk pattern?
Isolated systolic hypertension and systolic-diastolic hypertension are strongly associated with concurrent diabetic kidney disease in community-dwelling adults with diabetes, and integrating these phenotypes with routine clinical variables offers moderate discrimination for opportunistic risk pattern recognition.
Answers are grounded in this paper and cite their sources.
May support opportunistic DKD recognition via BP phenotypes in diabetes; extends cross-sectional associations but leaves causal inference open.
Background Diabetic kidney disease (DKD) is a leading cause of end-stage renal disease, with hypertension being a key modifiable risk factor. However, associations between specific blood pressure (BP) phenotypes and concurrent DKD risk remain poorly understood. Methods This cross-sectional study analyzed 1,240 adults with diabetes from community health records in Shanghai. Concurrent DKD was defined by UACR ≥30 mg/g or eGFR <60 mL/min/1.73 m 2 . BP phenotypes (140/90 mmHg threshold) were classified as normal (NBP), isolated systolic (ISH), isolated diastolic (IDH), and systolic-diastolic hypertension (SDH). Multivariable logistic regression (LR) estimated adjusted odds ratios (aORs). The cohort was split 80:20 into training (n = 992) and test (n = 248) sets. Five machine learning algorithms were evaluated using strict within-training-fold preprocessing. Results Concurrent DKD was present in 331/1,240 participants (26.69%). After adjustment, ISH and SDH were significantly associated with higher DKD odds versus NBP. On the independent test set, ROC-AUCs were 0.776 for XGBoost and 0.771 for LR, with no statistically significant discrimination difference. XGBoost showed a slightly lower Brier score, while LR offered superior calibration stability and nomogram interpretability. Conclusion ISH and SDH are associated with a higher prevalence of concurrent DKD in adults with diabetes. Routine clinical features and BP phenotypes provide moderate discrimination. These models function for opportunistic concurrent risk pattern recognition rather than predictive screening, supporting further external validation prior to clinical implementation.
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Song et al. (2026) conducted a cross-sectional in Diabetes mellitus and concurrent diabetic kidney disease (DKD) (n=1,240). Systolic-diastolic hypertension (SDH, SBP ≥140 and DBP ≥90 mmHg) and isolated systolic hypertension (ISH, SBP ≥140 and DBP <90 mmHg) vs. Normal blood pressure (NBP, SBP <140 and DBP <90 mmHg) was evaluated on Concurrent diabetic kidney disease (DKD) phenotype (UACR ≥30 mg/g or eGFR <60 mL/min/1.73 m2) (OR 2.465, 95% CI 1.634-3.717, p=<0.001).
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