Sarah L. White
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Previous Organizations / Institutes
The organizations / institutes from the scholar's other articles in the past ten years
Research Subjects
Sarah L. White has a total of 32 co-authors. Here are the top co-authors by number of shared publications:
- Kevan R. Polkinghorne
Department of Medicine, Monash University, Clayton, Victoria, Australia
5 shared publications Steven J. Chadban
Sydney Medical School, University of Sydney, Sydney, Australia
4 shared publicationsAlan Cass
The George Institute, Faculty of Medicine, University of Sydney, Sydney, Australia
3 shared publications- Jonathan C. Craig
College of Medicine and Public Health, Flinders University, Adelaide, South Australia, Australia
2 shared publications Robert C. Atkins
Baker IDI Heart and Diabetes Institute, Melbourne, Australia
2 shared publications- Vlado Perkovic
The George Institute for Global Health, University of New South Wales, Sydney, New South Wales, Australia
2 shared publications
Latest Publications
- Open Access
- 11 December 2013
- Published by Springer Nature in BMC Cardiovascular Disorders
- Vol. 13 (1) , 115
Uric acid is a risk factor for ischemic stroke and all-cause mortality in the general population: a gender specific analysis from The Tromsø Study
Background: The role of serum uric acid as an independent predictor of cardiovascular disease and death is uncertain in the general population. Adjustments for additional cardiovascular risk factors have not been consistent. We examined the association of serum uric acid with all-cause mortality, ischemic stroke and myocardial infarction in a prospective population based study, with several traditional and non-traditional risk factors for cardiovascular disease included in the model. Methods: A population-based prospective cohort study was performed among 2696 men and 3004 women. Endpoints were all-cause mortality after 15 years, and fatal or non-fatal myocardial infarction (MI) and ischemic stroke after 12 years. Results: 1433 deaths, 659 MIs and 430 ischemic strokes occurred during follow-up. Fully adjusted Cox regression analyses showed that per 1 SD (87 μmol/L) increase in serum uric acid level, the risk of all-cause mortality increased in both genders (hazard ratios, HR men; 1.11, 95% CI 1.02-1.20, women; 1.16, 1.05-1.29). HRs and 95% CI for stroke were 1.31, 1.14-1.50 in men, 1.13, 0.94-1.36 in women, and 1.22 (1.09, 1.35) in the overall population. No independent associations were observed with MI. Conclusion: Serum uric acid was associated with all-cause mortality in men and women, even after adjustment for blood pressure, estimated GFR, urinary albumin/creatinine ratio, drug intake and traditional cardiovascular risk factors. After the same adjustments, serum uric acid was associated with 31% increased risk of stroke in men.
- 11 December 2013
- Published by Springer Nature in BMC Cardiovascular Disorders
- Vol. 13 (1) , 115
Open AccessUric acid is a risk factor for ischemic stroke and all-cause mortality in the general population: a gender specific analysis from The Tromsø Study
Background: The role of serum uric acid as an independent predictor of cardiovascular disease and death is uncertain in the general population. Adjustments for additional cardiovascular risk factors have not been consistent. We examined the association of serum uric acid with all-cause mortality, ischemic stroke and myocardial infarction in a prospective population based study, with several traditional and non-traditional risk factors for cardiovascular disease included in the model. Methods: A population-based prospective cohort study was performed among 2696 men and 3004 women. Endpoints were all-cause mortality after 15 years, and fatal or non-fatal myocardial infarction (MI) and ischemic stroke after 12 years. Results: 1433 deaths, 659 MIs and 430 ischemic strokes occurred during follow-up. Fully adjusted Cox regression analyses showed that per 1 SD (87 μmol/L) increase in serum uric acid level, the risk of all-cause mortality increased in both genders (hazard ratios, HR men; 1.11, 95% CI 1.02-1.20, women; 1.16, 1.05-1.29). HRs and 95% CI for stroke were 1.31, 1.14-1.50 in men, 1.13, 0.94-1.36 in women, and 1.22 (1.09, 1.35) in the overall population. No independent associations were observed with MI. Conclusion: Serum uric acid was associated with all-cause mortality in men and women, even after adjustment for blood pressure, estimated GFR, urinary albumin/creatinine ratio, drug intake and traditional cardiovascular risk factors. After the same adjustments, serum uric acid was associated with 31% increased risk of stroke in men.
- Top Cited PapersOpen Access
- 1 July 2011
- Published by Elsevier in American Journal of Kidney Diseases
- Vol. 58 (1) , 19-28
Diagnostic Accuracy of Urine Dipsticks for Detection of Albuminuria in the General Community
- 1 July 2011
- Published by Elsevier in American Journal of Kidney Diseases
- Vol. 58 (1) , 19-28
Top Cited PapersOpen AccessDiagnostic Accuracy of Urine Dipsticks for Detection of Albuminuria in the General Community
- 1 April 2010
- Published by Elsevier in American Journal of Kidney Diseases
- Vol. 55 (4) , 660-670
Comparison of the Prevalence and Mortality Risk of CKD in Australia Using the CKD Epidemiology Collaboration (CKD-EPI) and Modification of Diet in Renal Disease (MDRD) Study GFR Estimating Equations: The AusDiab (Australian Diabetes, Obesity and Lifestyle) Study
- 1 April 2010
- Published by Elsevier in American Journal of Kidney Diseases
- Vol. 55 (4) , 660-670
Comparison of the Prevalence and Mortality Risk of CKD in Australia Using the CKD Epidemiology Collaboration (CKD-EPI) and Modification of Diet in Renal Disease (MDRD) Study GFR Estimating Equations: The AusDiab (Australian Diabetes, Obesity and Lifestyle) Study
- Top Cited Papers
- 1 August 2009
- Published by Elsevier in American Journal of Kidney Diseases
- Vol. 54 (2) , 248-261
Is Low Birth Weight an Antecedent of CKD in Later Life? A Systematic Review of Observational Studies
- 1 August 2009
- Published by Elsevier in American Journal of Kidney Diseases
- Vol. 54 (2) , 248-261
Top Cited PapersIs Low Birth Weight an Antecedent of CKD in Later Life? A Systematic Review of Observational Studies
- 22 March 2009
- Published by Oxford University Press (OUP) in Nephrology Dialysis Transplantation
- Vol. 24 (8) , 2464-2472
Alcohol consumption and 5-year onset of chronic kidney disease: the AusDiab study
Excessive alcohol consumption is a risk factor for hypertension and stroke; however, evidence for an association with chronic kidney disease is conflicting. A total of 6259 adults >or=25 years of age, without a history of alcohol dependence, participating in baseline (1999-2000) and follow-up (2004-2005) phases of an Australian population-representative study (AusDiab) were the subject of this analysis. Alcohol consumption status and volume/frequency were collected by standardized interviewer administered questionnaires and self-administered food frequency questionnaires. The outcomes were as follows: (i) 5-year decline in estimated glomerular filtration rate (eGFR) >or=10%, with baseline eGFR >or= 60 and final eGFR or= 2.5 (males)/>or= 3.5 (females) mg/mmol, in the absence of albuminuria at baseline. Self-identification as a moderate or heavy, versus light, drinker was associated with elevated risk of albuminuria in males and females or=30 g/day was associated with an increased risk of albuminuria after adjustment for age, sex and baseline kidney function (OR = 1.59, 95% CI 1.07-2.36), but a reduced risk of eGFR <60 mL/min/1.73 m(2) (OR = 0.59, 95% CI 0.37-0.95), compared with consumption of <10 g/day. Moderate-heavy alcohol consumption may be an important modifiable risk factor for albuminuria in the general population. The natural history of alcohol-induced kidney damage and how this relates to markers of kidney function in the general population warrant further research.
- 22 March 2009
- Published by Oxford University Press (OUP) in Nephrology Dialysis Transplantation
- Vol. 24 (8) , 2464-2472
Alcohol consumption and 5-year onset of chronic kidney disease: the AusDiab study
Excessive alcohol consumption is a risk factor for hypertension and stroke; however, evidence for an association with chronic kidney disease is conflicting. A total of 6259 adults >or=25 years of age, without a history of alcohol dependence, participating in baseline (1999-2000) and follow-up (2004-2005) phases of an Australian population-representative study (AusDiab) were the subject of this analysis. Alcohol consumption status and volume/frequency were collected by standardized interviewer administered questionnaires and self-administered food frequency questionnaires. The outcomes were as follows: (i) 5-year decline in estimated glomerular filtration rate (eGFR) >or=10%, with baseline eGFR >or= 60 and final eGFR or= 2.5 (males)/>or= 3.5 (females) mg/mmol, in the absence of albuminuria at baseline. Self-identification as a moderate or heavy, versus light, drinker was associated with elevated risk of albuminuria in males and females or=30 g/day was associated with an increased risk of albuminuria after adjustment for age, sex and baseline kidney function (OR = 1.59, 95% CI 1.07-2.36), but a reduced risk of eGFR <60 mL/min/1.73 m(2) (OR = 0.59, 95% CI 0.37-0.95), compared with consumption of <10 g/day. Moderate-heavy alcohol consumption may be an important modifiable risk factor for albuminuria in the general population. The natural history of alcohol-induced kidney damage and how this relates to markers of kidney function in the general population warrant further research.
- 1 July 2008
- Published by American Public Health Association in American Journal of Public Health
- Vol. 98 (7) , 1306-1313
Socioeconomic Disadvantage and Kidney Disease in the United States, Australia, and Thailand
Objectives. We sought to determine whether an elevated burden of chronic kidney disease is found among disadvantaged groups living in the United States, Australia, and Thailand. Methods. We used data on participants 35 years or older for whom a valid serum creatinine measurement was available from studies in the United States, Thailand, and Australia. We used logistic regression to analyze the association of income, education, and employment with the prevalence of chronic kidney disease (estimated glomerular filtration rate2). Results. Age- and gender-adjusted odds of having chronic kidney disease were increased 86% for US Whites in the lowest income quartile versus the highest quartile (odds ratio [OR] = 1.86; 95% confidence interval [CI] = 1.27, 2.72). Odds were increased 2 times and 6 times, respectively, among unemployed (not retired) versus employed non-Hispanic Black and Mexican American participants (OR=2.89; 95% CI=1.53, 5.46; OR=6.62; 95% CI=1.94, 22.64. respectively). Similar associations were not evident for the Australian or Thai populations. Conclusions. Higher kidney disease prevalence among financially disadvantaged groups in the United States should be considered when chronic kidney disease prevention and management strategies are created. This approach is less likely to be of benefit to the Australian and Thai populations.
- 1 July 2008
- Published by American Public Health Association in American Journal of Public Health
- Vol. 98 (7) , 1306-1313
Socioeconomic Disadvantage and Kidney Disease in the United States, Australia, and Thailand
Objectives. We sought to determine whether an elevated burden of chronic kidney disease is found among disadvantaged groups living in the United States, Australia, and Thailand. Methods. We used data on participants 35 years or older for whom a valid serum creatinine measurement was available from studies in the United States, Thailand, and Australia. We used logistic regression to analyze the association of income, education, and employment with the prevalence of chronic kidney disease (estimated glomerular filtration rate2). Results. Age- and gender-adjusted odds of having chronic kidney disease were increased 86% for US Whites in the lowest income quartile versus the highest quartile (odds ratio [OR] = 1.86; 95% confidence interval [CI] = 1.27, 2.72). Odds were increased 2 times and 6 times, respectively, among unemployed (not retired) versus employed non-Hispanic Black and Mexican American participants (OR=2.89; 95% CI=1.53, 5.46; OR=6.62; 95% CI=1.94, 22.64. respectively). Similar associations were not evident for the Australian or Thai populations. Conclusions. Higher kidney disease prevalence among financially disadvantaged groups in the United States should be considered when chronic kidney disease prevention and management strategies are created. This approach is less likely to be of benefit to the Australian and Thai populations.
- 18 February 2008
- Published by AMPCo in Medical Journal of Australia
- Vol. 188 (4) , 204-208
Limited knowledge of kidney disease in a survey of AusDiab study participants
Objectives: To explore awareness of the causes of kidney disease and recollection of kidney function testing in a cohort of Australian adults. Design, setting and participants: An interviewer‐adminis...
- 18 February 2008
- Published by AMPCo in Medical Journal of Australia
- Vol. 188 (4) , 204-208
Limited knowledge of kidney disease in a survey of AusDiab study participants
Objectives: To explore awareness of the causes of kidney disease and recollection of kidney function testing in a cohort of Australian adults. Design, setting and participants: An interviewer‐adminis...