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Change in ankle-brachial index over time and mortality in diabetics with proteinuria
Sirin Jiwakanon1, Sharon Adler, Rajnish Mehrotra
1Hatyai Hospital, Hatyai, Songkhla, Thailand.
Insights
In diabetic chronic kidney disease (CKD) patients, a low or decreasing ankle-brachial index (ABI) significantly predicts a higher risk of all-cause mortality. Routine ABI measurement aids in risk stratification for these individuals.
Area of Science:
- Nephrology
- Cardiology
- Vascular Medicine
Background:
- Peripheral arterial disease (PAD) is prevalent in diabetic chronic kidney disease (CKD).
- Ankle-brachial index (ABI) abnormalities (low or high) are common in this population.
- The prognostic significance of different ABI levels and changes is not well understood.
Purpose of the Study:
- To investigate the association between baseline ABI and all-cause mortality in proteinuric diabetic CKD patients.
- To determine if changes in ABI over time predict mortality in this cohort.
- To evaluate the utility of ABI measurement for risk stratification in diabetic CKD.
Main Methods:
- Prospective study of 167 proteinuric diabetic CKD patients.
- Baseline ABI measurement and assessment of all-cause mortality over a mean follow-up of 40 months.
- ABI change analysis in 75 subjects with normal baseline ABI over 23 months.
Main Results:
- 41% of participants had abnormal baseline ABI (<0.9 or >1.3).
- Low baseline ABI (<0.9) was associated with significantly higher all-cause mortality (HR: 2.23).
- A decrease in ABI over time in initially normal ABI subjects strongly predicted mortality (adjusted HR: 7.41).
Conclusions:
- Peripheral arterial disease is common and progresses rapidly in diabetic CKD.
- Both low baseline ABI and a declining ABI are potent predictors of all-cause mortality.
- Routine ABI measurement offers a simple method for risk stratification in diabetic CKD patients.
Abstract:
Peripheral arterial disease is common in diabetic chronic kidney disease (CKD) and is characterized either by abnormally low or high ankle-brachial index (ABI). Whether low or high ABI carries similar prognostic value is unknown. The association of baseline ABI with all-cause mortality over 40 ± 21 months (mean ± SD) was ascertained in 167 proteinuric diabetics (age 57 ± 7 years; median urine protein-creatinine, 2.5 mg/mg). Association of change in ABI with all-cause mortality was determined in 75 subjects with normal ABI (0.9 - 1.3) at baseline. Among 167 participants, 41% had an abnormal ABI: < 0.9, 18%; and > 1.3 or non-compressible arteries, 23%. Only individuals with low ABI had a significantly higher risk for all-cause mortality (hazards ratio (95% confidence interval), HR: 2.23 (1.07, 4.65)). In subjects with normal ABI at baseline with follow-up measurement (n = 75), vascular disease worsened in 39% over 23 ± 6 months: 17% had either a decrease in ABI by ≥ 0.1 or a final ABI < 0.9, and 21% had a final ABI > 1.3 or noncompressible arteries. Only individuals who had a decrease in ABI over time had a significantly higher risk for death (adjusted HR, 7.41 (1.63, 33.65)). Peripheral arterial disease is not uncommon and progresses rapidly in individuals with diabetes and proteinuria. Low or declining ABI is a strong predictor of all-cause mortality. Routine measurement of ABI is a simple bed-side procedure that may permit easy risk-stratification in diabetic CKD patients.
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