# Asia at the Epicenter of the Global Cardiometabolic Shift

**Authors:** Shaun Khanna, Gary C.H. Gan, Andrew P. Sindone, Jasper Tromp, Javed Butler, Roger Foo, Nitesh Nerlekar, Aditya Bhat

PMC · DOI: 10.1016/j.jacasi.2026.01.001 · JACC Asia · 2026-03-03

## TL;DR

Cardiometabolic diseases are rising rapidly in Asia due to biological factors and weak health systems, requiring tailored prevention and treatment strategies.

## Contribution

Highlights how biological susceptibility and health-system limitations uniquely drive cardiometabolic disease in Asia.

## Key findings

- Metabolic risk in Asians emerges at lower BMI than in Western populations.
- Life-course prevention and improved primary care are critical for managing cardiometabolic conditions.
- Access to therapies and risk tools tailored for Asian populations is essential for progress.

## Abstract

Cardiometabolic disease has become the dominant noncommunicable health challenge of the 21st century, with its burden increasingly centered in Asia. Rising obesity, type 2 diabetes mellitus, hypertension, and dyslipidemia now account for more than one-third of cardiovascular mortality. This escalation reflects the interaction of biological susceptibility with rapid urbanization, digitalized food environments, physical inactivity, and persistent tobacco exposure. Health-system limitations, including low diagnosis rates, poor risk-factor control, and uneven access to essential therapies, further amplify vulnerability across South, East, and Southeast Asia. Environmental pressures such as air pollution and extreme heat compound these risks, while migrant data illustrate how biological predisposition is magnified in obesogenic settings. This review synthesizes evolving epidemiology, biological diversity, behavioral and environmental drivers, and health-system gaps shaping cardiometabolic risk across Asia. It also outlines policy and therapeutic strategies, including strengthened primary care, prevention-focused interventions, and emerging therapeutics needed to reduce cardiometabolic disease in the region.

•Cardiometabolic disease is increasing fastest in Asia due to biological vulnerability and health-system constraints.•Metabolic risk develops at lower BMI in Asian populations, limiting the use of Western risk thresholds.•Life-course prevention and stronger primary care are central to managing cardiometabolic multimorbidity.•Progress will depend on fair access to effective therapies and risk tools tailored to Asian populations.

Cardiometabolic disease is increasing fastest in Asia due to biological vulnerability and health-system constraints.

Metabolic risk develops at lower BMI in Asian populations, limiting the use of Western risk thresholds.

Life-course prevention and stronger primary care are central to managing cardiometabolic multimorbidity.

Progress will depend on fair access to effective therapies and risk tools tailored to Asian populations.

## Linked entities

- **Diseases:** type 2 diabetes mellitus (MONDO:0005148), dyslipidemia (MONDO:0002525)

## Full-text entities

- **Genes:** MC4R (melanocortin 4 receptor) [NCBI Gene 4160] {aka BMIQ20}, SLC5A2 (solute carrier family 5 member 2) [NCBI Gene 6524] {aka SGLT2}, REN (renin) [NCBI Gene 5972] {aka ADTKD4, HNFJ2, RTD}, HECTD4 (HECT domain E3 ubiquitin protein ligase 4) [NCBI Gene 283450] {aka C12ord51, C12orf51, HEEL, NEDSSCC, POTAGE}, NID2 (nidogen 2) [NCBI Gene 22795] {aka NID-2}, GCG (glucagon) [NCBI Gene 2641] {aka GLP-1, GLP1, GLP2, GRPP}, GLP1R (glucagon like peptide 1 receptor) [NCBI Gene 2740] {aka GLP-1, GLP-1-R, GLP-1R}, INS (insulin) [NCBI Gene 3630] {aka IDDM, IDDM1, IDDM2, ILPR, IRDN, MODY10}
- **Diseases:** glucose dysregulation (MESH:D018149), abdominal obesity (MESH:D056128), coronary artery disease (MESH:D003324), T2D (MESH:D003924), adiposity (MESH:D018205), renal disease (MESH:D007674), heart failure (MESH:D006333), familial hypercholesterolemia (MESH:D006938), weight loss (MESH:D015431), health (OMIM:603663), insulin resistance (MESH:D007333), cardiovascular deaths (MESH:D002318), myocardial infarction (MESH:D009203), end-organ injury (MESH:C564816), COVID-19 (MESH:D000086382), ischemic heart disease (MESH:D017202), deaths (MESH:D003643), undernutrition (MESH:D044342), Hypertension (MESH:D006973), atherosclerosis (MESH:D050197), cardio-renal-metabolic disease (MESH:D059347), visceral adiposity (MESH:D007418), metabolic disease (MESH:D008659), metabolic dysregulation (MESH:D021081), cardiomyopathy (MESH:D009202), non-communicable disease (MESH:D000073296), overweight (MESH:D050177), stroke (MESH:D020521), weight gain (MESH:D015430), Obesity (MESH:D009765), chronic kidney disease (MESH:D051436), Diabetes mellitus (MESH:D003920), endothelial dysfunction (MESH:D014652), atherogenic dyslipidemia (MESH:D050171), hyperkalemia (MESH:D006947), Physical (MESH:D059445), inflammation (MESH:D007249), disease (MESH:D004194), Cardiometabolic Disease (MESH:D024821), hyperglycemia (MESH:D006943)
- **Chemicals:** glucose (MESH:D005947), alcohol (MESH:D000438), lipid (MESH:D008055), carbohydrates (MESH:D002241), catecholamine (MESH:D002395), potassium (MESH:D011188), Sodium (MESH:D012964), amino (-), glycemia (MESH:D001786), aspirin (MESH:D001241), metformin (MESH:D008687), aldosterone (MESH:D000450), triglycerides (MESH:D014280), nitrogen dioxide (MESH:D009585), cortisol (MESH:D006854), Salt (MESH:D012492)
- **Species:** Homo sapiens (human, species) [taxon 9606], Nicotiana tabacum (American tobacco, species) [taxon 4097]

## Full text

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## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12959306/full.md

## References

137 references — full list in the complete paper: https://tomesphere.com/paper/PMC12959306/full.md

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Source: https://tomesphere.com/paper/PMC12959306