The role of pulse pressure in navigating the paradigm of chronic kidney disease progression in type 2 diabetes mellitus
Background and aims Arterial stiffness is a risk factor for chronic kidney disease progression (CKD). Pulse pressure is a surrogate marker of arterial stiffness. It is unclear if pulse pressure predicts CKD progression in type 2 diabetes mellitus. Methods This was prospective study involving 1494 pa...
Ausführliche Beschreibung
Autor*in: |
Low, Serena [verfasserIn] Moh, Angela [verfasserIn] Ang, Su Fen [verfasserIn] Lim, Chin Leong [verfasserIn] Liu, Yan Lun [verfasserIn] Wang, Jiexun [verfasserIn] Ang, Keven [verfasserIn] Tang, Wern Ee [verfasserIn] Kwan, Pek Yee [verfasserIn] Lim, Ziliang [verfasserIn] Subramaniam, Tavintharan [verfasserIn] Sum, Chee Fang [verfasserIn] Lim, Su Chi [verfasserIn] |
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E-Artikel |
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Sprache: |
Englisch |
Erschienen: |
2021 |
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Schlagwörter: |
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Anmerkung: |
© Italian Society of Nephrology 2021 |
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Übergeordnetes Werk: |
Enthalten in: Journal of nephrology - Milano : Springer, 1996, 34(2021), 5 vom: 25. Jan., Seite 1429-1444 |
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Übergeordnetes Werk: |
volume:34 ; year:2021 ; number:5 ; day:25 ; month:01 ; pages:1429-1444 |
Links: |
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DOI / URN: |
10.1007/s40620-020-00954-3 |
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Katalog-ID: |
SPR045234817 |
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100 | 1 | |a Low, Serena |e verfasserin |4 aut | |
245 | 1 | 4 | |a The role of pulse pressure in navigating the paradigm of chronic kidney disease progression in type 2 diabetes mellitus |
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520 | |a Background and aims Arterial stiffness is a risk factor for chronic kidney disease progression (CKD). Pulse pressure is a surrogate marker of arterial stiffness. It is unclear if pulse pressure predicts CKD progression in type 2 diabetes mellitus. Methods This was prospective study involving 1494 patients with estimated glomerular filtration rate (eGFR) ≥ 15 ml/min/1.73 $ m^{2} $. Carotid-femoral pulse wave velocity was measured using applanation tonometry. Pulse pressure was calculated as difference between systolic and diastolic blood pressures. CKD progression was defined as worsening of eGFR categories (stage 1, ≥ 90 ml/min/1.73 $ m^{2} $; stage 2, 60–89 ml/min/1.73 $ m^{2} $; stage 3a, 45–59 ml/min/1.73 $ m^{2} $; stage 3b, 30–44 ml/min/1.73 $ m^{2} $; stage 4; 15–29 ml/min/1.73 $ m^{2} $; and stage 5, < 15 ml/min/1.73 $ m^{2} $) with ≥ 25% decrease in eGFR from baseline. Results After follow-up of up to 6 years, CKD progression occurred in 33.5% of subjects. Subjects in 2nd, 3rd and 4th quartiles of peripheral pulse pressure experienced higher risk of CKD progression with unadjusted hazard ratios (HRs) 1.55 [95% confidence interval (CI) 1.13–2.11; p = 0.006], 2.58 (1.93–3.45; p < 0.001) and 3.41 (2.58–4.52; p < 0.001). In the fully adjusted model, the association for 2nd, 3rd and 4th quartiles remained with HRs 1.40 (1.02–1.93; p = 0.038), 1.87 (1.37–2.56; p < 0.001) and 1.75 (1.25–2.44; p = 0.001) respectively. Similarly, 2nd, 3rd and 4th quartiles of aortic pulse pressure were associated with higher hazards of CKD progression with HRs 1.73 (1.25–2.40; p = 0.001), 1.65 (1.18–2.29; p = 0.003) and 1.81 (1.26–2.60; p = 0.001). Increasing urinary albumin-to-creatinine ratio accounted for 44.0% of the association between peripheral pulse pressure and CKD progression. Conclusions Individuals with high pulse pressure were more susceptible to deterioration of renal function. Pulse pressure could potentially be incorporated in clinical practice as an inexpensive and readily available biomarker of renal decline in type 2 diabetes mellitus. Graphic abstract | ||
650 | 4 | |a Pulse pressure |7 (dpeaa)DE-He213 | |
650 | 4 | |a Chronic kidney disease |7 (dpeaa)DE-He213 | |
650 | 4 | |a Type 2 diabetes mellitus |7 (dpeaa)DE-He213 | |
700 | 1 | |a Moh, Angela |e verfasserin |4 aut | |
700 | 1 | |a Ang, Su Fen |e verfasserin |4 aut | |
700 | 1 | |a Lim, Chin Leong |e verfasserin |4 aut | |
700 | 1 | |a Liu, Yan Lun |e verfasserin |4 aut | |
700 | 1 | |a Wang, Jiexun |e verfasserin |4 aut | |
700 | 1 | |a Ang, Keven |e verfasserin |4 aut | |
700 | 1 | |a Tang, Wern Ee |e verfasserin |4 aut | |
700 | 1 | |a Kwan, Pek Yee |e verfasserin |4 aut | |
700 | 1 | |a Lim, Ziliang |e verfasserin |4 aut | |
700 | 1 | |a Subramaniam, Tavintharan |e verfasserin |4 aut | |
700 | 1 | |a Sum, Chee Fang |e verfasserin |4 aut | |
700 | 1 | |a Lim, Su Chi |e verfasserin |4 aut | |
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10.1007/s40620-020-00954-3 doi (DE-627)SPR045234817 (SPR)s40620-020-00954-3-e DE-627 ger DE-627 rakwb eng 610 ASE Low, Serena verfasserin aut The role of pulse pressure in navigating the paradigm of chronic kidney disease progression in type 2 diabetes mellitus 2021 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Italian Society of Nephrology 2021 Background and aims Arterial stiffness is a risk factor for chronic kidney disease progression (CKD). Pulse pressure is a surrogate marker of arterial stiffness. It is unclear if pulse pressure predicts CKD progression in type 2 diabetes mellitus. Methods This was prospective study involving 1494 patients with estimated glomerular filtration rate (eGFR) ≥ 15 ml/min/1.73 $ m^{2} $. Carotid-femoral pulse wave velocity was measured using applanation tonometry. Pulse pressure was calculated as difference between systolic and diastolic blood pressures. CKD progression was defined as worsening of eGFR categories (stage 1, ≥ 90 ml/min/1.73 $ m^{2} $; stage 2, 60–89 ml/min/1.73 $ m^{2} $; stage 3a, 45–59 ml/min/1.73 $ m^{2} $; stage 3b, 30–44 ml/min/1.73 $ m^{2} $; stage 4; 15–29 ml/min/1.73 $ m^{2} $; and stage 5, < 15 ml/min/1.73 $ m^{2} $) with ≥ 25% decrease in eGFR from baseline. Results After follow-up of up to 6 years, CKD progression occurred in 33.5% of subjects. Subjects in 2nd, 3rd and 4th quartiles of peripheral pulse pressure experienced higher risk of CKD progression with unadjusted hazard ratios (HRs) 1.55 [95% confidence interval (CI) 1.13–2.11; p = 0.006], 2.58 (1.93–3.45; p < 0.001) and 3.41 (2.58–4.52; p < 0.001). In the fully adjusted model, the association for 2nd, 3rd and 4th quartiles remained with HRs 1.40 (1.02–1.93; p = 0.038), 1.87 (1.37–2.56; p < 0.001) and 1.75 (1.25–2.44; p = 0.001) respectively. Similarly, 2nd, 3rd and 4th quartiles of aortic pulse pressure were associated with higher hazards of CKD progression with HRs 1.73 (1.25–2.40; p = 0.001), 1.65 (1.18–2.29; p = 0.003) and 1.81 (1.26–2.60; p = 0.001). Increasing urinary albumin-to-creatinine ratio accounted for 44.0% of the association between peripheral pulse pressure and CKD progression. Conclusions Individuals with high pulse pressure were more susceptible to deterioration of renal function. Pulse pressure could potentially be incorporated in clinical practice as an inexpensive and readily available biomarker of renal decline in type 2 diabetes mellitus. Graphic abstract Pulse pressure (dpeaa)DE-He213 Chronic kidney disease (dpeaa)DE-He213 Type 2 diabetes mellitus (dpeaa)DE-He213 Moh, Angela verfasserin aut Ang, Su Fen verfasserin aut Lim, Chin Leong verfasserin aut Liu, Yan Lun verfasserin aut Wang, Jiexun verfasserin aut Ang, Keven verfasserin aut Tang, Wern Ee verfasserin aut Kwan, Pek Yee verfasserin aut Lim, Ziliang verfasserin aut Subramaniam, Tavintharan verfasserin aut Sum, Chee Fang verfasserin aut Lim, Su Chi verfasserin aut Enthalten in Journal of nephrology Milano : Springer, 1996 34(2021), 5 vom: 25. Jan., Seite 1429-1444 (DE-627)269534512 (DE-600)1475007-7 1724-6059 nnns volume:34 year:2021 number:5 day:25 month:01 pages:1429-1444 https://dx.doi.org/10.1007/s40620-020-00954-3 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 AR 34 2021 5 25 01 1429-1444 |
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10.1007/s40620-020-00954-3 doi (DE-627)SPR045234817 (SPR)s40620-020-00954-3-e DE-627 ger DE-627 rakwb eng 610 ASE Low, Serena verfasserin aut The role of pulse pressure in navigating the paradigm of chronic kidney disease progression in type 2 diabetes mellitus 2021 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Italian Society of Nephrology 2021 Background and aims Arterial stiffness is a risk factor for chronic kidney disease progression (CKD). Pulse pressure is a surrogate marker of arterial stiffness. It is unclear if pulse pressure predicts CKD progression in type 2 diabetes mellitus. Methods This was prospective study involving 1494 patients with estimated glomerular filtration rate (eGFR) ≥ 15 ml/min/1.73 $ m^{2} $. Carotid-femoral pulse wave velocity was measured using applanation tonometry. Pulse pressure was calculated as difference between systolic and diastolic blood pressures. CKD progression was defined as worsening of eGFR categories (stage 1, ≥ 90 ml/min/1.73 $ m^{2} $; stage 2, 60–89 ml/min/1.73 $ m^{2} $; stage 3a, 45–59 ml/min/1.73 $ m^{2} $; stage 3b, 30–44 ml/min/1.73 $ m^{2} $; stage 4; 15–29 ml/min/1.73 $ m^{2} $; and stage 5, < 15 ml/min/1.73 $ m^{2} $) with ≥ 25% decrease in eGFR from baseline. Results After follow-up of up to 6 years, CKD progression occurred in 33.5% of subjects. Subjects in 2nd, 3rd and 4th quartiles of peripheral pulse pressure experienced higher risk of CKD progression with unadjusted hazard ratios (HRs) 1.55 [95% confidence interval (CI) 1.13–2.11; p = 0.006], 2.58 (1.93–3.45; p < 0.001) and 3.41 (2.58–4.52; p < 0.001). In the fully adjusted model, the association for 2nd, 3rd and 4th quartiles remained with HRs 1.40 (1.02–1.93; p = 0.038), 1.87 (1.37–2.56; p < 0.001) and 1.75 (1.25–2.44; p = 0.001) respectively. Similarly, 2nd, 3rd and 4th quartiles of aortic pulse pressure were associated with higher hazards of CKD progression with HRs 1.73 (1.25–2.40; p = 0.001), 1.65 (1.18–2.29; p = 0.003) and 1.81 (1.26–2.60; p = 0.001). Increasing urinary albumin-to-creatinine ratio accounted for 44.0% of the association between peripheral pulse pressure and CKD progression. Conclusions Individuals with high pulse pressure were more susceptible to deterioration of renal function. Pulse pressure could potentially be incorporated in clinical practice as an inexpensive and readily available biomarker of renal decline in type 2 diabetes mellitus. Graphic abstract Pulse pressure (dpeaa)DE-He213 Chronic kidney disease (dpeaa)DE-He213 Type 2 diabetes mellitus (dpeaa)DE-He213 Moh, Angela verfasserin aut Ang, Su Fen verfasserin aut Lim, Chin Leong verfasserin aut Liu, Yan Lun verfasserin aut Wang, Jiexun verfasserin aut Ang, Keven verfasserin aut Tang, Wern Ee verfasserin aut Kwan, Pek Yee verfasserin aut Lim, Ziliang verfasserin aut Subramaniam, Tavintharan verfasserin aut Sum, Chee Fang verfasserin aut Lim, Su Chi verfasserin aut Enthalten in Journal of nephrology Milano : Springer, 1996 34(2021), 5 vom: 25. Jan., Seite 1429-1444 (DE-627)269534512 (DE-600)1475007-7 1724-6059 nnns volume:34 year:2021 number:5 day:25 month:01 pages:1429-1444 https://dx.doi.org/10.1007/s40620-020-00954-3 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 AR 34 2021 5 25 01 1429-1444 |
allfields_unstemmed |
10.1007/s40620-020-00954-3 doi (DE-627)SPR045234817 (SPR)s40620-020-00954-3-e DE-627 ger DE-627 rakwb eng 610 ASE Low, Serena verfasserin aut The role of pulse pressure in navigating the paradigm of chronic kidney disease progression in type 2 diabetes mellitus 2021 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Italian Society of Nephrology 2021 Background and aims Arterial stiffness is a risk factor for chronic kidney disease progression (CKD). Pulse pressure is a surrogate marker of arterial stiffness. It is unclear if pulse pressure predicts CKD progression in type 2 diabetes mellitus. Methods This was prospective study involving 1494 patients with estimated glomerular filtration rate (eGFR) ≥ 15 ml/min/1.73 $ m^{2} $. Carotid-femoral pulse wave velocity was measured using applanation tonometry. Pulse pressure was calculated as difference between systolic and diastolic blood pressures. CKD progression was defined as worsening of eGFR categories (stage 1, ≥ 90 ml/min/1.73 $ m^{2} $; stage 2, 60–89 ml/min/1.73 $ m^{2} $; stage 3a, 45–59 ml/min/1.73 $ m^{2} $; stage 3b, 30–44 ml/min/1.73 $ m^{2} $; stage 4; 15–29 ml/min/1.73 $ m^{2} $; and stage 5, < 15 ml/min/1.73 $ m^{2} $) with ≥ 25% decrease in eGFR from baseline. Results After follow-up of up to 6 years, CKD progression occurred in 33.5% of subjects. Subjects in 2nd, 3rd and 4th quartiles of peripheral pulse pressure experienced higher risk of CKD progression with unadjusted hazard ratios (HRs) 1.55 [95% confidence interval (CI) 1.13–2.11; p = 0.006], 2.58 (1.93–3.45; p < 0.001) and 3.41 (2.58–4.52; p < 0.001). In the fully adjusted model, the association for 2nd, 3rd and 4th quartiles remained with HRs 1.40 (1.02–1.93; p = 0.038), 1.87 (1.37–2.56; p < 0.001) and 1.75 (1.25–2.44; p = 0.001) respectively. Similarly, 2nd, 3rd and 4th quartiles of aortic pulse pressure were associated with higher hazards of CKD progression with HRs 1.73 (1.25–2.40; p = 0.001), 1.65 (1.18–2.29; p = 0.003) and 1.81 (1.26–2.60; p = 0.001). Increasing urinary albumin-to-creatinine ratio accounted for 44.0% of the association between peripheral pulse pressure and CKD progression. Conclusions Individuals with high pulse pressure were more susceptible to deterioration of renal function. Pulse pressure could potentially be incorporated in clinical practice as an inexpensive and readily available biomarker of renal decline in type 2 diabetes mellitus. Graphic abstract Pulse pressure (dpeaa)DE-He213 Chronic kidney disease (dpeaa)DE-He213 Type 2 diabetes mellitus (dpeaa)DE-He213 Moh, Angela verfasserin aut Ang, Su Fen verfasserin aut Lim, Chin Leong verfasserin aut Liu, Yan Lun verfasserin aut Wang, Jiexun verfasserin aut Ang, Keven verfasserin aut Tang, Wern Ee verfasserin aut Kwan, Pek Yee verfasserin aut Lim, Ziliang verfasserin aut Subramaniam, Tavintharan verfasserin aut Sum, Chee Fang verfasserin aut Lim, Su Chi verfasserin aut Enthalten in Journal of nephrology Milano : Springer, 1996 34(2021), 5 vom: 25. Jan., Seite 1429-1444 (DE-627)269534512 (DE-600)1475007-7 1724-6059 nnns volume:34 year:2021 number:5 day:25 month:01 pages:1429-1444 https://dx.doi.org/10.1007/s40620-020-00954-3 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 AR 34 2021 5 25 01 1429-1444 |
allfieldsGer |
10.1007/s40620-020-00954-3 doi (DE-627)SPR045234817 (SPR)s40620-020-00954-3-e DE-627 ger DE-627 rakwb eng 610 ASE Low, Serena verfasserin aut The role of pulse pressure in navigating the paradigm of chronic kidney disease progression in type 2 diabetes mellitus 2021 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Italian Society of Nephrology 2021 Background and aims Arterial stiffness is a risk factor for chronic kidney disease progression (CKD). Pulse pressure is a surrogate marker of arterial stiffness. It is unclear if pulse pressure predicts CKD progression in type 2 diabetes mellitus. Methods This was prospective study involving 1494 patients with estimated glomerular filtration rate (eGFR) ≥ 15 ml/min/1.73 $ m^{2} $. Carotid-femoral pulse wave velocity was measured using applanation tonometry. Pulse pressure was calculated as difference between systolic and diastolic blood pressures. CKD progression was defined as worsening of eGFR categories (stage 1, ≥ 90 ml/min/1.73 $ m^{2} $; stage 2, 60–89 ml/min/1.73 $ m^{2} $; stage 3a, 45–59 ml/min/1.73 $ m^{2} $; stage 3b, 30–44 ml/min/1.73 $ m^{2} $; stage 4; 15–29 ml/min/1.73 $ m^{2} $; and stage 5, < 15 ml/min/1.73 $ m^{2} $) with ≥ 25% decrease in eGFR from baseline. Results After follow-up of up to 6 years, CKD progression occurred in 33.5% of subjects. Subjects in 2nd, 3rd and 4th quartiles of peripheral pulse pressure experienced higher risk of CKD progression with unadjusted hazard ratios (HRs) 1.55 [95% confidence interval (CI) 1.13–2.11; p = 0.006], 2.58 (1.93–3.45; p < 0.001) and 3.41 (2.58–4.52; p < 0.001). In the fully adjusted model, the association for 2nd, 3rd and 4th quartiles remained with HRs 1.40 (1.02–1.93; p = 0.038), 1.87 (1.37–2.56; p < 0.001) and 1.75 (1.25–2.44; p = 0.001) respectively. Similarly, 2nd, 3rd and 4th quartiles of aortic pulse pressure were associated with higher hazards of CKD progression with HRs 1.73 (1.25–2.40; p = 0.001), 1.65 (1.18–2.29; p = 0.003) and 1.81 (1.26–2.60; p = 0.001). Increasing urinary albumin-to-creatinine ratio accounted for 44.0% of the association between peripheral pulse pressure and CKD progression. Conclusions Individuals with high pulse pressure were more susceptible to deterioration of renal function. Pulse pressure could potentially be incorporated in clinical practice as an inexpensive and readily available biomarker of renal decline in type 2 diabetes mellitus. Graphic abstract Pulse pressure (dpeaa)DE-He213 Chronic kidney disease (dpeaa)DE-He213 Type 2 diabetes mellitus (dpeaa)DE-He213 Moh, Angela verfasserin aut Ang, Su Fen verfasserin aut Lim, Chin Leong verfasserin aut Liu, Yan Lun verfasserin aut Wang, Jiexun verfasserin aut Ang, Keven verfasserin aut Tang, Wern Ee verfasserin aut Kwan, Pek Yee verfasserin aut Lim, Ziliang verfasserin aut Subramaniam, Tavintharan verfasserin aut Sum, Chee Fang verfasserin aut Lim, Su Chi verfasserin aut Enthalten in Journal of nephrology Milano : Springer, 1996 34(2021), 5 vom: 25. Jan., Seite 1429-1444 (DE-627)269534512 (DE-600)1475007-7 1724-6059 nnns volume:34 year:2021 number:5 day:25 month:01 pages:1429-1444 https://dx.doi.org/10.1007/s40620-020-00954-3 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 AR 34 2021 5 25 01 1429-1444 |
allfieldsSound |
10.1007/s40620-020-00954-3 doi (DE-627)SPR045234817 (SPR)s40620-020-00954-3-e DE-627 ger DE-627 rakwb eng 610 ASE Low, Serena verfasserin aut The role of pulse pressure in navigating the paradigm of chronic kidney disease progression in type 2 diabetes mellitus 2021 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Italian Society of Nephrology 2021 Background and aims Arterial stiffness is a risk factor for chronic kidney disease progression (CKD). Pulse pressure is a surrogate marker of arterial stiffness. It is unclear if pulse pressure predicts CKD progression in type 2 diabetes mellitus. Methods This was prospective study involving 1494 patients with estimated glomerular filtration rate (eGFR) ≥ 15 ml/min/1.73 $ m^{2} $. Carotid-femoral pulse wave velocity was measured using applanation tonometry. Pulse pressure was calculated as difference between systolic and diastolic blood pressures. CKD progression was defined as worsening of eGFR categories (stage 1, ≥ 90 ml/min/1.73 $ m^{2} $; stage 2, 60–89 ml/min/1.73 $ m^{2} $; stage 3a, 45–59 ml/min/1.73 $ m^{2} $; stage 3b, 30–44 ml/min/1.73 $ m^{2} $; stage 4; 15–29 ml/min/1.73 $ m^{2} $; and stage 5, < 15 ml/min/1.73 $ m^{2} $) with ≥ 25% decrease in eGFR from baseline. Results After follow-up of up to 6 years, CKD progression occurred in 33.5% of subjects. Subjects in 2nd, 3rd and 4th quartiles of peripheral pulse pressure experienced higher risk of CKD progression with unadjusted hazard ratios (HRs) 1.55 [95% confidence interval (CI) 1.13–2.11; p = 0.006], 2.58 (1.93–3.45; p < 0.001) and 3.41 (2.58–4.52; p < 0.001). In the fully adjusted model, the association for 2nd, 3rd and 4th quartiles remained with HRs 1.40 (1.02–1.93; p = 0.038), 1.87 (1.37–2.56; p < 0.001) and 1.75 (1.25–2.44; p = 0.001) respectively. Similarly, 2nd, 3rd and 4th quartiles of aortic pulse pressure were associated with higher hazards of CKD progression with HRs 1.73 (1.25–2.40; p = 0.001), 1.65 (1.18–2.29; p = 0.003) and 1.81 (1.26–2.60; p = 0.001). Increasing urinary albumin-to-creatinine ratio accounted for 44.0% of the association between peripheral pulse pressure and CKD progression. Conclusions Individuals with high pulse pressure were more susceptible to deterioration of renal function. Pulse pressure could potentially be incorporated in clinical practice as an inexpensive and readily available biomarker of renal decline in type 2 diabetes mellitus. Graphic abstract Pulse pressure (dpeaa)DE-He213 Chronic kidney disease (dpeaa)DE-He213 Type 2 diabetes mellitus (dpeaa)DE-He213 Moh, Angela verfasserin aut Ang, Su Fen verfasserin aut Lim, Chin Leong verfasserin aut Liu, Yan Lun verfasserin aut Wang, Jiexun verfasserin aut Ang, Keven verfasserin aut Tang, Wern Ee verfasserin aut Kwan, Pek Yee verfasserin aut Lim, Ziliang verfasserin aut Subramaniam, Tavintharan verfasserin aut Sum, Chee Fang verfasserin aut Lim, Su Chi verfasserin aut Enthalten in Journal of nephrology Milano : Springer, 1996 34(2021), 5 vom: 25. Jan., Seite 1429-1444 (DE-627)269534512 (DE-600)1475007-7 1724-6059 nnns volume:34 year:2021 number:5 day:25 month:01 pages:1429-1444 https://dx.doi.org/10.1007/s40620-020-00954-3 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 AR 34 2021 5 25 01 1429-1444 |
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Pulse pressure Chronic kidney disease Type 2 diabetes mellitus |
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Low, Serena @@aut@@ Moh, Angela @@aut@@ Ang, Su Fen @@aut@@ Lim, Chin Leong @@aut@@ Liu, Yan Lun @@aut@@ Wang, Jiexun @@aut@@ Ang, Keven @@aut@@ Tang, Wern Ee @@aut@@ Kwan, Pek Yee @@aut@@ Lim, Ziliang @@aut@@ Subramaniam, Tavintharan @@aut@@ Sum, Chee Fang @@aut@@ Lim, Su Chi @@aut@@ |
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Pulse pressure is a surrogate marker of arterial stiffness. It is unclear if pulse pressure predicts CKD progression in type 2 diabetes mellitus. Methods This was prospective study involving 1494 patients with estimated glomerular filtration rate (eGFR) ≥ 15 ml/min/1.73 $ m^{2} $. Carotid-femoral pulse wave velocity was measured using applanation tonometry. Pulse pressure was calculated as difference between systolic and diastolic blood pressures. CKD progression was defined as worsening of eGFR categories (stage 1, ≥ 90 ml/min/1.73 $ m^{2} $; stage 2, 60–89 ml/min/1.73 $ m^{2} $; stage 3a, 45–59 ml/min/1.73 $ m^{2} $; stage 3b, 30–44 ml/min/1.73 $ m^{2} $; stage 4; 15–29 ml/min/1.73 $ m^{2} $; and stage 5, < 15 ml/min/1.73 $ m^{2} $) with ≥ 25% decrease in eGFR from baseline. Results After follow-up of up to 6 years, CKD progression occurred in 33.5% of subjects. Subjects in 2nd, 3rd and 4th quartiles of peripheral pulse pressure experienced higher risk of CKD progression with unadjusted hazard ratios (HRs) 1.55 [95% confidence interval (CI) 1.13–2.11; p = 0.006], 2.58 (1.93–3.45; p < 0.001) and 3.41 (2.58–4.52; p < 0.001). In the fully adjusted model, the association for 2nd, 3rd and 4th quartiles remained with HRs 1.40 (1.02–1.93; p = 0.038), 1.87 (1.37–2.56; p < 0.001) and 1.75 (1.25–2.44; p = 0.001) respectively. Similarly, 2nd, 3rd and 4th quartiles of aortic pulse pressure were associated with higher hazards of CKD progression with HRs 1.73 (1.25–2.40; p = 0.001), 1.65 (1.18–2.29; p = 0.003) and 1.81 (1.26–2.60; p = 0.001). Increasing urinary albumin-to-creatinine ratio accounted for 44.0% of the association between peripheral pulse pressure and CKD progression. Conclusions Individuals with high pulse pressure were more susceptible to deterioration of renal function. Pulse pressure could potentially be incorporated in clinical practice as an inexpensive and readily available biomarker of renal decline in type 2 diabetes mellitus. 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Low, Serena |
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Low, Serena ddc 610 misc Pulse pressure misc Chronic kidney disease misc Type 2 diabetes mellitus The role of pulse pressure in navigating the paradigm of chronic kidney disease progression in type 2 diabetes mellitus |
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610 ASE The role of pulse pressure in navigating the paradigm of chronic kidney disease progression in type 2 diabetes mellitus Pulse pressure (dpeaa)DE-He213 Chronic kidney disease (dpeaa)DE-He213 Type 2 diabetes mellitus (dpeaa)DE-He213 |
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Low, Serena Moh, Angela Ang, Su Fen Lim, Chin Leong Liu, Yan Lun Wang, Jiexun Ang, Keven Tang, Wern Ee Kwan, Pek Yee Lim, Ziliang Subramaniam, Tavintharan Sum, Chee Fang Lim, Su Chi |
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role of pulse pressure in navigating the paradigm of chronic kidney disease progression in type 2 diabetes mellitus |
title_auth |
The role of pulse pressure in navigating the paradigm of chronic kidney disease progression in type 2 diabetes mellitus |
abstract |
Background and aims Arterial stiffness is a risk factor for chronic kidney disease progression (CKD). Pulse pressure is a surrogate marker of arterial stiffness. It is unclear if pulse pressure predicts CKD progression in type 2 diabetes mellitus. Methods This was prospective study involving 1494 patients with estimated glomerular filtration rate (eGFR) ≥ 15 ml/min/1.73 $ m^{2} $. Carotid-femoral pulse wave velocity was measured using applanation tonometry. Pulse pressure was calculated as difference between systolic and diastolic blood pressures. CKD progression was defined as worsening of eGFR categories (stage 1, ≥ 90 ml/min/1.73 $ m^{2} $; stage 2, 60–89 ml/min/1.73 $ m^{2} $; stage 3a, 45–59 ml/min/1.73 $ m^{2} $; stage 3b, 30–44 ml/min/1.73 $ m^{2} $; stage 4; 15–29 ml/min/1.73 $ m^{2} $; and stage 5, < 15 ml/min/1.73 $ m^{2} $) with ≥ 25% decrease in eGFR from baseline. Results After follow-up of up to 6 years, CKD progression occurred in 33.5% of subjects. Subjects in 2nd, 3rd and 4th quartiles of peripheral pulse pressure experienced higher risk of CKD progression with unadjusted hazard ratios (HRs) 1.55 [95% confidence interval (CI) 1.13–2.11; p = 0.006], 2.58 (1.93–3.45; p < 0.001) and 3.41 (2.58–4.52; p < 0.001). In the fully adjusted model, the association for 2nd, 3rd and 4th quartiles remained with HRs 1.40 (1.02–1.93; p = 0.038), 1.87 (1.37–2.56; p < 0.001) and 1.75 (1.25–2.44; p = 0.001) respectively. Similarly, 2nd, 3rd and 4th quartiles of aortic pulse pressure were associated with higher hazards of CKD progression with HRs 1.73 (1.25–2.40; p = 0.001), 1.65 (1.18–2.29; p = 0.003) and 1.81 (1.26–2.60; p = 0.001). Increasing urinary albumin-to-creatinine ratio accounted for 44.0% of the association between peripheral pulse pressure and CKD progression. Conclusions Individuals with high pulse pressure were more susceptible to deterioration of renal function. Pulse pressure could potentially be incorporated in clinical practice as an inexpensive and readily available biomarker of renal decline in type 2 diabetes mellitus. Graphic abstract © Italian Society of Nephrology 2021 |
abstractGer |
Background and aims Arterial stiffness is a risk factor for chronic kidney disease progression (CKD). Pulse pressure is a surrogate marker of arterial stiffness. It is unclear if pulse pressure predicts CKD progression in type 2 diabetes mellitus. Methods This was prospective study involving 1494 patients with estimated glomerular filtration rate (eGFR) ≥ 15 ml/min/1.73 $ m^{2} $. Carotid-femoral pulse wave velocity was measured using applanation tonometry. Pulse pressure was calculated as difference between systolic and diastolic blood pressures. CKD progression was defined as worsening of eGFR categories (stage 1, ≥ 90 ml/min/1.73 $ m^{2} $; stage 2, 60–89 ml/min/1.73 $ m^{2} $; stage 3a, 45–59 ml/min/1.73 $ m^{2} $; stage 3b, 30–44 ml/min/1.73 $ m^{2} $; stage 4; 15–29 ml/min/1.73 $ m^{2} $; and stage 5, < 15 ml/min/1.73 $ m^{2} $) with ≥ 25% decrease in eGFR from baseline. Results After follow-up of up to 6 years, CKD progression occurred in 33.5% of subjects. Subjects in 2nd, 3rd and 4th quartiles of peripheral pulse pressure experienced higher risk of CKD progression with unadjusted hazard ratios (HRs) 1.55 [95% confidence interval (CI) 1.13–2.11; p = 0.006], 2.58 (1.93–3.45; p < 0.001) and 3.41 (2.58–4.52; p < 0.001). In the fully adjusted model, the association for 2nd, 3rd and 4th quartiles remained with HRs 1.40 (1.02–1.93; p = 0.038), 1.87 (1.37–2.56; p < 0.001) and 1.75 (1.25–2.44; p = 0.001) respectively. Similarly, 2nd, 3rd and 4th quartiles of aortic pulse pressure were associated with higher hazards of CKD progression with HRs 1.73 (1.25–2.40; p = 0.001), 1.65 (1.18–2.29; p = 0.003) and 1.81 (1.26–2.60; p = 0.001). Increasing urinary albumin-to-creatinine ratio accounted for 44.0% of the association between peripheral pulse pressure and CKD progression. Conclusions Individuals with high pulse pressure were more susceptible to deterioration of renal function. Pulse pressure could potentially be incorporated in clinical practice as an inexpensive and readily available biomarker of renal decline in type 2 diabetes mellitus. Graphic abstract © Italian Society of Nephrology 2021 |
abstract_unstemmed |
Background and aims Arterial stiffness is a risk factor for chronic kidney disease progression (CKD). Pulse pressure is a surrogate marker of arterial stiffness. It is unclear if pulse pressure predicts CKD progression in type 2 diabetes mellitus. Methods This was prospective study involving 1494 patients with estimated glomerular filtration rate (eGFR) ≥ 15 ml/min/1.73 $ m^{2} $. Carotid-femoral pulse wave velocity was measured using applanation tonometry. Pulse pressure was calculated as difference between systolic and diastolic blood pressures. CKD progression was defined as worsening of eGFR categories (stage 1, ≥ 90 ml/min/1.73 $ m^{2} $; stage 2, 60–89 ml/min/1.73 $ m^{2} $; stage 3a, 45–59 ml/min/1.73 $ m^{2} $; stage 3b, 30–44 ml/min/1.73 $ m^{2} $; stage 4; 15–29 ml/min/1.73 $ m^{2} $; and stage 5, < 15 ml/min/1.73 $ m^{2} $) with ≥ 25% decrease in eGFR from baseline. Results After follow-up of up to 6 years, CKD progression occurred in 33.5% of subjects. Subjects in 2nd, 3rd and 4th quartiles of peripheral pulse pressure experienced higher risk of CKD progression with unadjusted hazard ratios (HRs) 1.55 [95% confidence interval (CI) 1.13–2.11; p = 0.006], 2.58 (1.93–3.45; p < 0.001) and 3.41 (2.58–4.52; p < 0.001). In the fully adjusted model, the association for 2nd, 3rd and 4th quartiles remained with HRs 1.40 (1.02–1.93; p = 0.038), 1.87 (1.37–2.56; p < 0.001) and 1.75 (1.25–2.44; p = 0.001) respectively. Similarly, 2nd, 3rd and 4th quartiles of aortic pulse pressure were associated with higher hazards of CKD progression with HRs 1.73 (1.25–2.40; p = 0.001), 1.65 (1.18–2.29; p = 0.003) and 1.81 (1.26–2.60; p = 0.001). Increasing urinary albumin-to-creatinine ratio accounted for 44.0% of the association between peripheral pulse pressure and CKD progression. Conclusions Individuals with high pulse pressure were more susceptible to deterioration of renal function. Pulse pressure could potentially be incorporated in clinical practice as an inexpensive and readily available biomarker of renal decline in type 2 diabetes mellitus. Graphic abstract © Italian Society of Nephrology 2021 |
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title_short |
The role of pulse pressure in navigating the paradigm of chronic kidney disease progression in type 2 diabetes mellitus |
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https://dx.doi.org/10.1007/s40620-020-00954-3 |
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author2 |
Moh, Angela Ang, Su Fen Lim, Chin Leong Liu, Yan Lun Wang, Jiexun Ang, Keven Tang, Wern Ee Kwan, Pek Yee Lim, Ziliang Subramaniam, Tavintharan Sum, Chee Fang Lim, Su Chi |
author2Str |
Moh, Angela Ang, Su Fen Lim, Chin Leong Liu, Yan Lun Wang, Jiexun Ang, Keven Tang, Wern Ee Kwan, Pek Yee Lim, Ziliang Subramaniam, Tavintharan Sum, Chee Fang Lim, Su Chi |
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doi_str |
10.1007/s40620-020-00954-3 |
up_date |
2024-07-03T14:40:09.492Z |
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Pulse pressure is a surrogate marker of arterial stiffness. It is unclear if pulse pressure predicts CKD progression in type 2 diabetes mellitus. Methods This was prospective study involving 1494 patients with estimated glomerular filtration rate (eGFR) ≥ 15 ml/min/1.73 $ m^{2} $. Carotid-femoral pulse wave velocity was measured using applanation tonometry. Pulse pressure was calculated as difference between systolic and diastolic blood pressures. CKD progression was defined as worsening of eGFR categories (stage 1, ≥ 90 ml/min/1.73 $ m^{2} $; stage 2, 60–89 ml/min/1.73 $ m^{2} $; stage 3a, 45–59 ml/min/1.73 $ m^{2} $; stage 3b, 30–44 ml/min/1.73 $ m^{2} $; stage 4; 15–29 ml/min/1.73 $ m^{2} $; and stage 5, < 15 ml/min/1.73 $ m^{2} $) with ≥ 25% decrease in eGFR from baseline. Results After follow-up of up to 6 years, CKD progression occurred in 33.5% of subjects. Subjects in 2nd, 3rd and 4th quartiles of peripheral pulse pressure experienced higher risk of CKD progression with unadjusted hazard ratios (HRs) 1.55 [95% confidence interval (CI) 1.13–2.11; p = 0.006], 2.58 (1.93–3.45; p < 0.001) and 3.41 (2.58–4.52; p < 0.001). In the fully adjusted model, the association for 2nd, 3rd and 4th quartiles remained with HRs 1.40 (1.02–1.93; p = 0.038), 1.87 (1.37–2.56; p < 0.001) and 1.75 (1.25–2.44; p = 0.001) respectively. Similarly, 2nd, 3rd and 4th quartiles of aortic pulse pressure were associated with higher hazards of CKD progression with HRs 1.73 (1.25–2.40; p = 0.001), 1.65 (1.18–2.29; p = 0.003) and 1.81 (1.26–2.60; p = 0.001). Increasing urinary albumin-to-creatinine ratio accounted for 44.0% of the association between peripheral pulse pressure and CKD progression. Conclusions Individuals with high pulse pressure were more susceptible to deterioration of renal function. Pulse pressure could potentially be incorporated in clinical practice as an inexpensive and readily available biomarker of renal decline in type 2 diabetes mellitus. 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score |
7.3972797 |