Longitudinal trajectories of albuminuria and risk of subclinical and clinical heart failure, atrial fibrillation, and coronary heart disease: the MESA study - Scorecard - MDSpire

Longitudinal trajectories of albuminuria and risk of subclinical and clinical heart failure, atrial fibrillation, and coronary heart disease: the MESA study

  • By

  • Soroush Masrouri

  • Parag A Chevli

  • Michael P Bancks

  • Saeid Mirzai

  • João A C Lima

  • David A Bluemke

  • Neha J Pagidipati

  • Michael D Shapiro

  • November 3, 2025

  • 0 min

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Clinical Scorecard: Analysis of Albuminuria Patterns and Their Association with Subclinical and Clinical Heart Failure, Atrial Fibrillation, and Coronary Heart Disease: Insights from the MESA Study

At a Glance

CategoryDetail
ConditionAlbuminuria and its association with heart failure (HF), atrial fibrillation (AF), and coronary heart disease (CHD)
Key MechanismsProgressive increases in urine albumin-creatinine ratio (UACR) reflect glomerular injury and are linked to elevated cardiac biomarkers and interstitial myocardial fibrosis, contributing to HF and cardiovascular risk
Target PopulationAdults aged approximately 62 years from a multi-ethnic cohort, including those with normoalbuminuria at baseline
Care SettingCardiovascular risk assessment and monitoring in outpatient and research settings

Key Highlights

  • Distinct UACR trajectory groups over 5 and 10 years identify subgroups at elevated risk for HF, AF, and CHD, independent of baseline UACR levels.
  • Sustained medium to high or rapid rise in UACR is associated with 1.5- to 3.7-fold increased risk of HF, HF subtypes, AF, and CHD.
  • Elevated UACR trajectories correlate with increased NT-proBNP, hs-TnT, and myocardial fibrosis measured by cardiac MRI T1 mapping, linking albuminuria to subclinical cardiac injury.

Guideline-Based Recommendations

Diagnosis

  • Use longitudinal monitoring of urine albumin-creatinine ratio (UACR) to identify progressive albuminuria trajectories.
  • Consider UACR trajectories even in individuals with normoalbuminuria at baseline for cardiovascular risk stratification.

Management

  • Target individuals with sustained or rapidly rising UACR for intensified cardiovascular risk management to prevent HF and related conditions.
  • Incorporate cardiac biomarker assessment (NT-proBNP, hs-TnT) and imaging (cardiac MRI T1 mapping) for evaluation of subclinical myocardial injury in high-risk patients.

Monitoring & Follow-up

  • Regularly monitor UACR over time rather than relying on single measurements to detect progressive albuminuria.
  • Follow cardiac biomarkers and imaging findings to assess progression of myocardial fibrosis and risk of HF.

Risks

  • Progressive albuminuria increases risk for heart failure, particularly HF with preserved ejection fraction (HFpEF), atrial fibrillation, and coronary heart disease.
  • Risk associations persist independent of baseline UACR and are not fully explained by interim AF or CHD events.

Patient & Prescribing Data

Middle-aged to older adults from a multi-ethnic cohort, including those initially normoalbuminuric

Identification of high-risk UACR trajectories may guide early intervention to prevent progression to clinical HF and cardiovascular events; monitoring cardiac biomarkers and myocardial fibrosis can inform treatment response.

Clinical Best Practices

  • Incorporate serial UACR measurements into routine cardiovascular risk assessments to detect progressive albuminuria.
  • Recognize that even low-level increases in UACR below clinical thresholds carry significant cardiovascular risk.
  • Use combined biomarker and imaging approaches to detect subclinical myocardial injury in patients with rising albuminuria.
  • Focus preventive strategies on patients with sustained medium to high or rapidly rising UACR trajectories to reduce HF and cardiovascular event incidence.

References

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