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Assessment of Dietary Sodium Intake Using the Scored Salt Questionnaire in Autosomal Dominant Polycystic Kidney Disease

The excess intake of dietary sodium is a key modifiable factor for reducing disease progression in autosomal dominant polycystic kidney disease (ADPKD). The aim of this study was to test the hypothesis that the scored salt questionnaire (SSQ; a frequency questionnaire of nine sodium-rich food types)...

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Autores principales: Wong, Annette T. Y., Munt, Alexandra, Allman-Farinelli, Margaret, Badve, Sunil V., Boudville, Neil, Coolican, Helen, Chandra, Ashley N., Coulshed, Susan, Fernando, Mangalee, Grantham, Jared, Haloob, Imad, Harris, David C. H., Hawley, Carmel M., Holt, Jane, Johnson, David W., Kumar, Karthik, Lee, Vincent W., Lonergan, Maureen, Mai, Jun, Rangan, Anna, Roger, Simon D., Saravanabavan, Sayanthooran, Sud, Kamal, Torres, Vicente E., Vilayur, Eswari, Zhang, Jennifer Q. J., Rangan, Gopala K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7692491/
https://www.ncbi.nlm.nih.gov/pubmed/33147804
http://dx.doi.org/10.3390/nu12113376
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author Wong, Annette T. Y.
Munt, Alexandra
Allman-Farinelli, Margaret
Badve, Sunil V.
Boudville, Neil
Coolican, Helen
Chandra, Ashley N.
Coulshed, Susan
Fernando, Mangalee
Grantham, Jared
Haloob, Imad
Harris, David C. H.
Hawley, Carmel M.
Holt, Jane
Johnson, David W.
Kumar, Karthik
Lee, Vincent W.
Lonergan, Maureen
Mai, Jun
Rangan, Anna
Roger, Simon D.
Saravanabavan, Sayanthooran
Sud, Kamal
Torres, Vicente E.
Vilayur, Eswari
Zhang, Jennifer Q. J.
Rangan, Gopala K.
author_facet Wong, Annette T. Y.
Munt, Alexandra
Allman-Farinelli, Margaret
Badve, Sunil V.
Boudville, Neil
Coolican, Helen
Chandra, Ashley N.
Coulshed, Susan
Fernando, Mangalee
Grantham, Jared
Haloob, Imad
Harris, David C. H.
Hawley, Carmel M.
Holt, Jane
Johnson, David W.
Kumar, Karthik
Lee, Vincent W.
Lonergan, Maureen
Mai, Jun
Rangan, Anna
Roger, Simon D.
Saravanabavan, Sayanthooran
Sud, Kamal
Torres, Vicente E.
Vilayur, Eswari
Zhang, Jennifer Q. J.
Rangan, Gopala K.
author_sort Wong, Annette T. Y.
collection PubMed
description The excess intake of dietary sodium is a key modifiable factor for reducing disease progression in autosomal dominant polycystic kidney disease (ADPKD). The aim of this study was to test the hypothesis that the scored salt questionnaire (SSQ; a frequency questionnaire of nine sodium-rich food types) is a valid instrument to identify high dietary salt intake in ADPKD. The performance of the SSQ was evaluated in adults with ADPKD with an estimated glomerular filtration rate (eGFR) ≥ 30 mL/min/1.73 m(2) during the screening visit of the PREVENT-ADPKD trial. High dietary sodium intake (HSI) was defined by a mean 24-h urinary sodium excretion ≥ 100 mmol/day from two collections. The median 24-h urine sodium excretion was 132 mmol/day (IQR: 112–172 mmol/d) (n = 75; mean age: 44.6 ± 11.5 years old; 53% female), and HSI (86.7% of total) was associated with male gender and higher BMI and systolic blood pressure (p < 0.05). The SSQ score (73 ± 23; mean ± SD) was weakly correlated with log(10) 24-h urine sodium excretion (r = 0.29, p = 0.01). Receiving operating characteristic analysis showed that the optimal cut-off point in predicting HSI was an SSQ score of 74 (area under the curve 0.79; sensitivity 61.5%; specificity 90.0%; p < 0.01). The evaluation of the SSQ in participants with a BMI ≥ 25 (n = 46) improved the sensitivity (100%) and the specificity (100%). Consumers with an SSQ score ≥ 74 (n = 41) had higher relative percentage intake of processed meats/seafood and flavourings added to cooking (p < 0.05). In conclusion, the SSQ is a valid tool for identifying high dietary salt intake in ADPKD but its value proposition (over 24-h urinary sodium measurement) is that it may provide consumers and their healthcare providers with insight into the potential origin of sodium-rich food sources.
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spelling pubmed-76924912020-11-28 Assessment of Dietary Sodium Intake Using the Scored Salt Questionnaire in Autosomal Dominant Polycystic Kidney Disease Wong, Annette T. Y. Munt, Alexandra Allman-Farinelli, Margaret Badve, Sunil V. Boudville, Neil Coolican, Helen Chandra, Ashley N. Coulshed, Susan Fernando, Mangalee Grantham, Jared Haloob, Imad Harris, David C. H. Hawley, Carmel M. Holt, Jane Johnson, David W. Kumar, Karthik Lee, Vincent W. Lonergan, Maureen Mai, Jun Rangan, Anna Roger, Simon D. Saravanabavan, Sayanthooran Sud, Kamal Torres, Vicente E. Vilayur, Eswari Zhang, Jennifer Q. J. Rangan, Gopala K. Nutrients Article The excess intake of dietary sodium is a key modifiable factor for reducing disease progression in autosomal dominant polycystic kidney disease (ADPKD). The aim of this study was to test the hypothesis that the scored salt questionnaire (SSQ; a frequency questionnaire of nine sodium-rich food types) is a valid instrument to identify high dietary salt intake in ADPKD. The performance of the SSQ was evaluated in adults with ADPKD with an estimated glomerular filtration rate (eGFR) ≥ 30 mL/min/1.73 m(2) during the screening visit of the PREVENT-ADPKD trial. High dietary sodium intake (HSI) was defined by a mean 24-h urinary sodium excretion ≥ 100 mmol/day from two collections. The median 24-h urine sodium excretion was 132 mmol/day (IQR: 112–172 mmol/d) (n = 75; mean age: 44.6 ± 11.5 years old; 53% female), and HSI (86.7% of total) was associated with male gender and higher BMI and systolic blood pressure (p < 0.05). The SSQ score (73 ± 23; mean ± SD) was weakly correlated with log(10) 24-h urine sodium excretion (r = 0.29, p = 0.01). Receiving operating characteristic analysis showed that the optimal cut-off point in predicting HSI was an SSQ score of 74 (area under the curve 0.79; sensitivity 61.5%; specificity 90.0%; p < 0.01). The evaluation of the SSQ in participants with a BMI ≥ 25 (n = 46) improved the sensitivity (100%) and the specificity (100%). Consumers with an SSQ score ≥ 74 (n = 41) had higher relative percentage intake of processed meats/seafood and flavourings added to cooking (p < 0.05). In conclusion, the SSQ is a valid tool for identifying high dietary salt intake in ADPKD but its value proposition (over 24-h urinary sodium measurement) is that it may provide consumers and their healthcare providers with insight into the potential origin of sodium-rich food sources. MDPI 2020-11-02 /pmc/articles/PMC7692491/ /pubmed/33147804 http://dx.doi.org/10.3390/nu12113376 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Wong, Annette T. Y.
Munt, Alexandra
Allman-Farinelli, Margaret
Badve, Sunil V.
Boudville, Neil
Coolican, Helen
Chandra, Ashley N.
Coulshed, Susan
Fernando, Mangalee
Grantham, Jared
Haloob, Imad
Harris, David C. H.
Hawley, Carmel M.
Holt, Jane
Johnson, David W.
Kumar, Karthik
Lee, Vincent W.
Lonergan, Maureen
Mai, Jun
Rangan, Anna
Roger, Simon D.
Saravanabavan, Sayanthooran
Sud, Kamal
Torres, Vicente E.
Vilayur, Eswari
Zhang, Jennifer Q. J.
Rangan, Gopala K.
Assessment of Dietary Sodium Intake Using the Scored Salt Questionnaire in Autosomal Dominant Polycystic Kidney Disease
title Assessment of Dietary Sodium Intake Using the Scored Salt Questionnaire in Autosomal Dominant Polycystic Kidney Disease
title_full Assessment of Dietary Sodium Intake Using the Scored Salt Questionnaire in Autosomal Dominant Polycystic Kidney Disease
title_fullStr Assessment of Dietary Sodium Intake Using the Scored Salt Questionnaire in Autosomal Dominant Polycystic Kidney Disease
title_full_unstemmed Assessment of Dietary Sodium Intake Using the Scored Salt Questionnaire in Autosomal Dominant Polycystic Kidney Disease
title_short Assessment of Dietary Sodium Intake Using the Scored Salt Questionnaire in Autosomal Dominant Polycystic Kidney Disease
title_sort assessment of dietary sodium intake using the scored salt questionnaire in autosomal dominant polycystic kidney disease
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7692491/
https://www.ncbi.nlm.nih.gov/pubmed/33147804
http://dx.doi.org/10.3390/nu12113376
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