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Albuminuria and kidney function as prognostic marker of left ventricular mass among South Asians with hypertension

We aimed to evaluate the association of albuminuria and estimated glomerular filtration rate (eGFR) at baseline and changes in these parameters with left ventricular mass index (LVMI) at 7 years in adults with hypertension from communities in Pakistan. A nested cohort of 539 hypertensives aged 40 ye...

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Autores principales: Feng, Liang, Khan, Aamir Hameed, Jehan, Imtiaz, Allen, John, Jafar, Tazeen H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5736364/
https://www.ncbi.nlm.nih.gov/pubmed/29089200
http://dx.doi.org/10.1016/j.jash.2017.10.003
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author Feng, Liang
Khan, Aamir Hameed
Jehan, Imtiaz
Allen, John
Jafar, Tazeen H.
author_facet Feng, Liang
Khan, Aamir Hameed
Jehan, Imtiaz
Allen, John
Jafar, Tazeen H.
author_sort Feng, Liang
collection PubMed
description We aimed to evaluate the association of albuminuria and estimated glomerular filtration rate (eGFR) at baseline and changes in these parameters with left ventricular mass index (LVMI) at 7 years in adults with hypertension from communities in Pakistan. A nested cohort of 539 hypertensives aged 40 years and older from a community-living population in Karachi, Pakistan, followed up for 7 years in the Control of Blood Pressure and Risk Attenuation trial. Urine spot albumin-to-creatinine ratio (UACR) and serum creatinine-based eGFR were assessed at baseline and 7 years, and echocardiography at 7 years. Mean age of participants was 50.9 ± 9.1 (standard deviation) years; 63% were female. Mean eGFR was 91.0 ± 15.9 (standard deviation) mL/min/1.73 m(2) and median (interquartile range) UACR 6.2 (3.9, 11.3) mg/g. In multivariate analysis, although baseline eGFR was marginally associated with LVMI, a strong association was found between higher LVMI with greater rate of decline in eGFR (β = −1.05; 95% confidence interval [CI]: [−1.94, −0.17]). Higher baseline UACR was significantly associated with higher follow-up LVMI (β = 2.26; 95% CI: [0.87, 3.65]), as was rate of UACR increase of ≥1.07 mg/g/y versus of <0.14 mg/g/y. (β = 4.19; 95% CI: [0.75, 7.63]). Associations with developing left ventricular hypertrophy were found for reduced baseline eGFR, higher baseline UACR, and greater rate of UACR increase, but not for rate of eGFR decline. Comparable results were observed for the outcomes of posterior wall thickness and septal wall thickness. Higher baseline albuminuria, lower baseline eGFR, and their longitudinal worsening were significantly associated with higher LVMI or the development of left ventricular hypertrophy among individuals with hypertension in Pakistan.
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spelling pubmed-57363642017-12-22 Albuminuria and kidney function as prognostic marker of left ventricular mass among South Asians with hypertension Feng, Liang Khan, Aamir Hameed Jehan, Imtiaz Allen, John Jafar, Tazeen H. J Am Soc Hypertens Article We aimed to evaluate the association of albuminuria and estimated glomerular filtration rate (eGFR) at baseline and changes in these parameters with left ventricular mass index (LVMI) at 7 years in adults with hypertension from communities in Pakistan. A nested cohort of 539 hypertensives aged 40 years and older from a community-living population in Karachi, Pakistan, followed up for 7 years in the Control of Blood Pressure and Risk Attenuation trial. Urine spot albumin-to-creatinine ratio (UACR) and serum creatinine-based eGFR were assessed at baseline and 7 years, and echocardiography at 7 years. Mean age of participants was 50.9 ± 9.1 (standard deviation) years; 63% were female. Mean eGFR was 91.0 ± 15.9 (standard deviation) mL/min/1.73 m(2) and median (interquartile range) UACR 6.2 (3.9, 11.3) mg/g. In multivariate analysis, although baseline eGFR was marginally associated with LVMI, a strong association was found between higher LVMI with greater rate of decline in eGFR (β = −1.05; 95% confidence interval [CI]: [−1.94, −0.17]). Higher baseline UACR was significantly associated with higher follow-up LVMI (β = 2.26; 95% CI: [0.87, 3.65]), as was rate of UACR increase of ≥1.07 mg/g/y versus of <0.14 mg/g/y. (β = 4.19; 95% CI: [0.75, 7.63]). Associations with developing left ventricular hypertrophy were found for reduced baseline eGFR, higher baseline UACR, and greater rate of UACR increase, but not for rate of eGFR decline. Comparable results were observed for the outcomes of posterior wall thickness and septal wall thickness. Higher baseline albuminuria, lower baseline eGFR, and their longitudinal worsening were significantly associated with higher LVMI or the development of left ventricular hypertrophy among individuals with hypertension in Pakistan. Elsevier 2017-12 /pmc/articles/PMC5736364/ /pubmed/29089200 http://dx.doi.org/10.1016/j.jash.2017.10.003 Text en © 2017 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Feng, Liang
Khan, Aamir Hameed
Jehan, Imtiaz
Allen, John
Jafar, Tazeen H.
Albuminuria and kidney function as prognostic marker of left ventricular mass among South Asians with hypertension
title Albuminuria and kidney function as prognostic marker of left ventricular mass among South Asians with hypertension
title_full Albuminuria and kidney function as prognostic marker of left ventricular mass among South Asians with hypertension
title_fullStr Albuminuria and kidney function as prognostic marker of left ventricular mass among South Asians with hypertension
title_full_unstemmed Albuminuria and kidney function as prognostic marker of left ventricular mass among South Asians with hypertension
title_short Albuminuria and kidney function as prognostic marker of left ventricular mass among South Asians with hypertension
title_sort albuminuria and kidney function as prognostic marker of left ventricular mass among south asians with hypertension
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5736364/
https://www.ncbi.nlm.nih.gov/pubmed/29089200
http://dx.doi.org/10.1016/j.jash.2017.10.003
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