Darryl P. Leong

Dr. Darryl P. Leong


Research Focus & Metrics

Academic Career Length

17Years (2010-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 July 2015 in The Lancet
Verified
Journal Article
Closed access
DLDarryl P. Leong
Darryl P. Leong
KTKoon K Teo
Koon K Teo
SRSumathy Rangarajan
Sumathy Rangarajan
PLPatricio López-Jaramillo
Patricio López-Jaramillo
AAAlvaro Avezum
Alvaro Avezum
SYSalim Yusuf
Salim Yusuf

1 September 2017 in Circulation Research
Verified
Journal Article
Closed access
DLDarryl P. Leong
Darryl P. Leong
PJPhilip G. Joseph
Philip G. Joseph
MMMartin McKee
Martin McKee
SASonia S. Anand
Sonia S. Anand
KTKoon K. Teo
Koon K. Teo
SYSalim Yusuf
Salim Yusuf
In this second part of a 2-part series on the global burden of cardiovascular disease, we review the proven, effective approaches to the prevention and treatment of cardiovascular disease. We specifically review the management of acute cardiovascular diseases, including acute coronary syndromes and stroke; the care of cardiovascular disease in the ambulatory setting, including medical strategies for vascular disease, atrial fibrillation, and heart failure; surgical strategies for arterial revascularization, rheumatic and other valvular heart disease, and symptomatic bradyarrhythmia; and approaches to the prevention of cardiovascular disease, including lifestyle factors, blood pressure control, cholesterol-lowering, antithrombotic therapy, and fixed-dose combination therapy. We also discuss cardiovascular disease prevention in diabetes mellitus; digital health interventions; the importance of socioeconomic status and universal health coverage. We review building capacity for conduction cardiovascular intervention through strengthening healthcare systems, priority setting, and the role of cost effectiveness.

12 April 2016 in Journal of Cachexia, Sarcopenia and Muscle
Verified
Journal Article
Open access
PDF file
DLDarryl P. Leong
Darryl P. Leong
KTKoon K. Teo
Koon K. Teo
SRSumathy Rangarajan
Sumathy Rangarajan
VKV. Raman Kutty
V. Raman Kutty
FLFernando Lanas
Fernando Lanas
SYSalim Yusuf
Salim Yusuf
Background: The measurement of handgrip strength (HGS) has prognostic value with respect to all‐cause mortality, cardiovascular mortality and cardiovascular disease, and is an important part of the evaluation of frailty. Published reference ranges for HGS are mostly derived from Caucasian populations in high‐income countries. There is a paucity of information on normative HGS values in non‐Caucasian populations from low‐ or middle‐income countries. The objective of this study was to develop reference HGS ranges for healthy adults from a broad range of ethnicities and socioeconomically diverse geographic regions.Methods: HGS was measured using a Jamar dynamometer in 125,462 healthy adults aged 35‐70 years from 21 countries in the Prospective Urban Rural Epidemiology (PURE) study.Results: HGS values differed among individuals from different geographic regions. HGS values were highest among those from Europe/North America, lowest among those from South Asia, South East Asia and Africa, and intermediate among those from China, South America, and the Middle East. Reference ranges stratified by geographic region, age, and sex are presented. These ranges varied from a median (25th–75th percentile) 50 kg (43–56 kg) in men 60 years from South East Asia. Reference ranges by ethnicity and body‐mass index are also reported.Conclusions: Individual HGS measurements should be interpreted using region/ethnic‐specific reference ranges.

29 July 2014 in Circulation
Verified
Journal Article
Closed access
PDF file
DLDarryl P. Leong
Darryl P. Leong
ASAndrew Smyth
Andrew Smyth
KTKoon K. Teo
Koon K. Teo
MMMartin McKee
Martin McKee
SRSumathy Rangarajan
Sumathy Rangarajan
SYSalim Yusuf
Salim Yusuf
Background—: Although moderate alcohol use is associated with protection against myocardial infarction (MI), it is not known whether this effect is generalizable to populations worldwide. It is also uncertain whether differences in the pattern of alcohol use (and in particular heavy episodic consumption) between different regions negate any beneficial effect. Methods and Results—: We included 12 195 cases of first MI and 15 583 age- and sex-matched controls from 52 countries. Current alcohol use was associated with a reduced risk of MI (compared with nonusers: adjusted odds ratio, 0.87; 95% confidence interval, 0.80–0.94; P =0.001); however, the strength of this association was not uniform across different regions (region-alcohol interaction P 65 years: odds ratio, 5.3; 95% confidence interval, 1.6–18; P =0.008). Conclusions—: In most participants, low levels of alcohol use are associated with a moderate reduction in the risk of MI; however, the strength of this association may not be uniform across different countries. An episode of heavy drinking is associated with an increased risk of acute MI in the subsequent 24 hours, particularly in older individuals.

1 August 2018 in Canadian Journal of Cardiology
Verified
Journal Article
Closed access
HMHassan Mir
Hassan Mir
MAMuhammad Alhussein
Muhammad Alhussein
SASulaiman Alrashidi
Sulaiman Alrashidi
HAHussain Alzayer
Hussain Alzayer
AAAhmad Alshatti
Ahmad Alshatti
DLDarryl P. Leong
Darryl P. Leong

4 February 2020 in Journal of the American Heart Association
Verified
Journal Article
Open access
PDF file
MFMohammed A. M. Farooqi
Mohammed A. M. Farooqi
HGHertzel Gerstein
Hertzel Gerstein
SYSalim Yusuf
Salim Yusuf
DLDarryl P. Leong
Darryl P. Leong
Background: Frailty is associated with higher mortality in individuals at high cardiovascular disease ( CVD ) risk. We hypothesize that frailty is a more important prognostic factor than CVD risk factors and aim to determine the prognostic value of a cumulative deficit frailty index in patients with or at high risk for CVD . Methods and Results: We conducted an individual‐level pooled analysis of participants with or at risk for CVD , recruited in 14 multicenter clinical trials. The cumulative deficit index was calculated as the proportion of 26 deficits exhibited. Individuals were categorized as nonfrail, prefrail, or frail if they had indexes of ≤0.1, >0.1 to 0.21, or >0.21, respectively. CVD risk was assessed using the Framingham score. Outcomes included CVD event (new or recurrent myocardial infarction, stroke, or heart failure) and mortality. We studied 154 696 patients (mean age, 70.8 years; 63% men) with median follow‐up of 3.2 years. There were 17 535 CVD events and 15 067 deaths. The frail group (n=13 872) had higher risk of a CVD event (incidence rate ratio, 1.97; 95% CI , 1.85–2.08), all‐cause mortality (hazard ratio, 1.91; 95% CI , 1.79–2.03), and CVD mortality (hazard ratio, 1.91; 95% CI , 1.77–2.05) than the nonfrail group (n=101 343). Associations remained unchanged after adjusting for CVD risk factors. The index statistically outperformed the Framingham score in its ability to discriminate CVD events (C‐statistic, 0.60 [95% CI , 0.60–0.61] versus 0.58 [95% CI , 0.57–0.58], respectively; P <0.001). Conclusions: In individuals with or at high risk of developing CVD , the cumulative deficit index is associated with increased CVD events and mortality, independent of CVD risk factors, and adds incremental prognostic value.