# Changes in leisure time physical activity, obesity-related morbidities, fatal and non-fatal CVD events and total mortality: Over 20-year follow-up in the opera study

**Authors:** Asla Suutari-Jääskö, Karri Parkkila, Hannu Vähänikkilä, Mikko Tulppo, Juha Perkiömäki, Heikki Huikuri, Olavi Ukkola

PMC · DOI: 10.1371/journal.pone.0342429 · PLOS One · 2026-02-23

## TL;DR

This study shows that maintaining regular leisure-time physical activity reduces the risk of obesity-related diseases and cardiovascular events, while quitting activity increases these risks, especially in office workers.

## Contribution

The study provides long-term evidence on how changes in leisure-time physical activity affect cardiovascular and mortality outcomes, considering occupational activity levels.

## Key findings

- Maintaining regular leisure-time physical activity is linked to lower rates of hypertension, diabetes, and metabolic syndrome.
- Quitting physical activity increases non-fatal CVD events in occupationally active individuals and raises fatal CVD and mortality risks in sedentary groups.
- Office workers who are sedentary or quit physical activity face significantly higher risks of fatal CVD and all-cause mortality.

## Abstract

The impact of changes in leisure time physical activity (LTPA) is not well-documented, especially when considering occupational physical activity (OPA). This study examines the effects of LTPA changes in workers with varying physical activity demands.

Part of the OPERA study, we tracked morbidities for over 20 years (P1, from 1993 to 2014) and mortality for over 8 years (P2, from 2014 to 2021–2022) with 599 participants. They were categorized into four LTPA groups (“sedentary,” “started,” “quit,” “active”) and two OPA groups (“office workers” and “occupationally physically active”).

Maintaining regular LTPA was associated with lower incidence of hypertension, diabetes and metabolic syndrome (p-values 0.007, < 0.001 and <0.001 respectively). Non-fatal cardiovascular disease (CVD) events were more common (p = 0.006, HR 1.99, CI95% 1.22–3.26) in the “quit” group during P1, especially among “occupationally physically active” (p < 0.001, HR 2.29, CI95% 1.23–4.29). During P2, fatal CVD events were associated with being in the “sedentary” group (p = 0.042, HR 2.67, CI95% 1.04–7.03). This association was particularly evident among “office workers,” where belonging to the “sedentary” and “quit” groups was associated with a higher risk of fatal CVD events (p = 0.017, HR 5.45, CI95%1.36–21.91, and p = 0.025, HR 4.55, CI95% 1.21–17.19, respectively). Furthermore, total mortality was associated with being in the “sedentary” or “quit” groups (p = 0.029, HR 3.69, CI95% 1.14–11.93, and p = 0.009, HR 4.61, CI95%1.47–14.49, respectively).

Stopping LTPA in middle age was associated to higher risk for non-fatal CVD events in “occupationally physically active” individuals. Fatal CVD events were associated with a sedentary lifestyle in whole study population. Among “office workers,” both a sedentary lifestyle and stopping regular LTPA were associated with higher risks of fatal CVD events and all-cause mortality.

## Linked entities

- **Diseases:** diabetes (MONDO:0005015), metabolic syndrome (MONDO:0000816), cardiovascular disease (MONDO:0004995)

## Full-text entities

- **Genes:** H6PD (hexose-6-phosphate dehydrogenase/glucose 1-dehydrogenase) [NCBI Gene 9563] {aka CORTRD1, G6PDH, GDH, H6PDH}, INS (insulin) [NCBI Gene 3630] {aka IDDM, IDDM1, IDDM2, ILPR, IRDN, MODY10}
- **Diseases:** Stroke (MESH:D020521), overweight (MESH:D050177), obese (MESH:D009765), weight gain (MESH:D015430), LTPA (MESH:C000719197), DM (MESH:D009223), Diabetes (MESH:D003920), CHD (MESH:D003327), MetS (MESH:D024821), artery disease (MESH:D002539), unstable angina (MESH:D000789), OPA (MESH:D009784), CAD (MESH:D003324), HC (MESH:D006937), heart failure (MESH:D006333), TIA (MESH:D002546), Type 2 diabetes (MESH:D003924), ischemic stroke (MESH:D002544), CVD (MESH:D002318), AMI (MESH:D009203), Atherosclerosis (MESH:D050197), SAH (MESH:D013345), Death (MESH:D003643), Hypertension (MESH:D006973)
- **Chemicals:** cholesterol (MESH:D002784), triglycerides (MESH:D014280), manganese (MESH:D008345), glucose (MESH:D005947), heparin (MESH:D006493), Alcohol (MESH:D000438), HC drug (-)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

37 references — full list in the complete paper: https://tomesphere.com/paper/PMC12928424/full.md

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Source: https://tomesphere.com/paper/PMC12928424