# Burden of subclinical coronary atherosclerosis among asymptomatic adults: the REACH–Rural India Study

**Authors:** Avinash Kumar Raghupathy, Mohanraj Sundaresan, Pudhiavan Arun, Dharam J. Kumbhani, Manoj Kumar Baskar, Haritha Thambi, Parthasarathy Ayothi, Karthika Durairaj, Samrat Ashok Vasudevan, Srinidhi Narayani Seenivasan, Buvaneswari Gajendran, Gowdham Manivel, Gowri Subramaniam, Madhavi Sambandam, Velmurugan Ganesan, Balakumaran Jeyakumaran, Jeevithan Shanmugam, Krishnan Swaminathan, Arulraj Ramakrishnan, Mathew Cherian, Thomas Alexander

PMC · DOI: 10.1016/j.lansea.2026.100726 · The Lancet Regional Health - Southeast Asia · 2026-02-11

## TL;DR

This study finds a high prevalence of subclinical coronary atherosclerosis in rural India, highlighting the need for early screening in at-risk populations.

## Contribution

The study provides novel population-based evidence on CAC prevalence and its risk factors in rural India.

## Key findings

- 25.6% of rural Indian adults aged 35–65 had coronary artery calcification (CAC).
- Men had significantly higher CAC prevalence than women, with severe CAC threefold more common in men.
- Diabetes, hypertension, and obesity were independently associated with CAC.

## Abstract

Coronary artery calcification (CAC) serves as a robust marker of subclinical atherosclerosis and an independent predictor of cardiovascular disease (CVD). Despite its clinical significance, population-based evidence on CAC prevalence and its determinants in rural India remains limited. This study aimed to estimate the prevalence of CAC and evaluate its association with cardiometabolic risk factors among adults aged 35–65 years in a rural Indian population.

A total of 3006 individuals aged 35–65 years were selected and invited to participate in the REACH (Risk Evaluation of Subclinical Coronary Health)–Rural India Study. From 2022 to 2024, the study enrolled asymptomatic adults with no history of cardiovascular events from rural communities in the Coimbatore and Tirupur districts of Tamil Nadu, India. Data collection included sociodemographic and clinical profiling, laboratory testing, and carotid intima-media thickness (cIMT). CAC was quantified using the Agatston scoring method from dual-source CT scans.

In total 2961 participants included in the final analysis (mean age 49.8 ± 8.3 years; 52.8% women), the overall prevalence of coronary artery calcification (CAC) was 25.6%. Prevalence was significantly higher in men (33.5%) than in women (18.5%) (p < 0.001). The prevalence of severe CAC (Agatston score >400) was threefold higher in men and most common in those aged 56–65 years. However, no detectable CAC was observed among women aged 35–45 years. The distribution of CAC scores was as follows: 7.0% had minimal CAC (1–10), 11.4% mild (11–100), 5.2% moderate (101–400), and 1.9% severe (>400). Multivariable logistic regression showed that diabetes, hypertension, overweight/obesity, and abnormal CIMT were independently associated with CAC. Among men, current smoking was also significantly associated (OR = 1.51; 95% CI: 1.18–1.93). In total, 83.5% of individuals with CAC had one or more cardiovascular risk factors. No significant associations were observed between CAC and elevated creatinine, reduced eGFR and peripheral artery disease (PAD) after full adjustment.

This study reveals a substantial burden of CAC in a rural Indian population, with prevalence patterns comparable to urban cohorts in Western countries. The findings underscore the need to incorporate CAC screening in individuals with metabolic risk factors, especially in underserved populations, to identify early subclinical atherosclerosis and reduce CVD risk.

10.13039/501100001411Indian Council of Medical Research (ICMR), (REF No. 5/4/1-9/2020-NCD-1).

## Linked entities

- **Diseases:** cardiovascular disease (MONDO:0004995), diabetes (MONDO:0005015)

## Full-text entities

- **Genes:** GPT (glutamic--pyruvic transaminase) [NCBI Gene 2875] {aka AAT1, ALT, ALT1, GPT1, SGPT}, HK1 (hexokinase 1) [NCBI Gene 3098] {aka CNSHA5, HK, HK1-ta, HK1-tb, HK1-tc, HKD}, SLC17A5 (solute carrier family 17 member 5) [NCBI Gene 26503] {aka AST, ISSD, NSD, SD, SIALIN, SIASD}
- **Diseases:** metabolic abnormalities (MESH:D008659), metabolic dysregulation (MESH:D021081), smoking (MESH:D015208), Obesity (MESH:D009765), gestational diabetes (MESH:D016640), NCDs (MESH:D000073296), stroke (MESH:D020521), Overweight (MESH:D050177), chest pain (MESH:D002637), cancer (MESH:D009369), calcification (MESH:D002114), DM (MESH:D003920), CKD (MESH:D051436), angina (MESH:D000787), cardiometabolic disease (MESH:D024821), Disease (MESH:D004194), coronary heart disease (MESH:D003327), Dyslipidemia (MESH:D050171), NCD-1 (MESH:C538557), lipid (MESH:D011017), coronary calcification (MESH:D003323), Abdominal obesity (MESH:D056128), heart failure (MESH:D006333), ischemic attack (MESH:D002546), computed (MESH:C000719218), PAD (MESH:D058729), CAC (MESH:D003324), IHD (MESH:D017202), COVID (MESH:D000086382), atrial fibrillation (MESH:D001281), CVD (MESH:D002318), myocardial infarction (MESH:D009203), carotid and coronary atherosclerosis (MESH:D002340), vascular calcification (MESH:D061205), Atherosclerosis (MESH:D050197), smoker (MESH:C000719328), deaths (MESH:D003643), Hypertension (MESH:D006973)
- **Chemicals:** cholesterol (MESH:D002784), uric acid (MESH:D014527), TG (MESH:D014280), salt (MESH:D012492), pyridoxal phosphate (MESH:D011732), Alcohol (MESH:D000438), calcium (MESH:D002118), Creatinine (MESH:D003404), glucose (MESH:D005947), lipid (MESH:D008055), TC (-)
- **Species:** Nicotiana tabacum (American tobacco, species) [taxon 4097], Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12915248/full.md

## References

30 references — full list in the complete paper: https://tomesphere.com/paper/PMC12915248/full.md

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Source: https://tomesphere.com/paper/PMC12915248