# Age‐Stratified Associations of Sarcopenic Obesity With Mortality in Type 2 Diabetes

**Authors:** Shinta Yamamoto, Yoshitaka Hashimoto, Fuyuko Takahashi, Moe Murai, Nozomi Yoshioka, Yuto Saijyo, Chihiro Munekawa, Hanako Nakajima, Noriyuki Kitagawa, Takafumi Osaka, Ryosuke Sakai, Hiroshi Okada, Naoko Nakanishi, Saori Majima, Emi Ushigome, Masahide Hamaguchi, Michiaki Fukui

PMC · DOI: 10.1002/jcsm.70211 · Journal of Cachexia, Sarcopenia and Muscle · 2026-01-28

## TL;DR

Sarcopenic obesity increases mortality risk in people with Type 2 diabetes, especially those aged 40–75 years.

## Contribution

This study provides age-stratified evidence on the mortality risk of sarcopenic obesity in Type 2 diabetes patients.

## Key findings

- Sarcopenic obesity significantly increased mortality risk in participants aged 40–75 years.
- In those over 75, sarcopenia alone was linked to higher mortality, but not sarcopenic obesity.
- Compared to non-sarcopenic obesity, sarcopenic obesity had a higher hazard ratio for mortality in younger participants.

## Abstract

Sarcopenic obesity, the coexistence of sarcopenia and obesity, has been linked to adverse health outcomes due to comorbidity. Evidence on the association between sarcopenic obesity and mortality among individuals with Type 2 diabetes remains limited

Sarcopenic obesity was defined using Japan Working Group on Sarcopenic Obesity criteria. Participants were divided into four groups based on the presence of sarcopenia and obesity. Cox proportional hazards models evaluated the mortality risk. Subgroup analyses were performed by age (40–75 vs. >75 years). Sensitivity analysis was performed by dichotomizing participants into sarcopenic obesity and non‐sarcopenic obesity groups.

Of the 799 participants (mean age 68.6 years, 59.3% men), proportions of neither sarcopenia nor obesity, obesity alone, sarcopenia alone and sarcopenic obesity were 56.2%, 34.5%, 6.3% and 3.0%, respectively. During a median follow‐up of 46 months, 41 deaths occurred. Compared with neither of them, the adjusted hazard ratios (aHRs) (95% CI) of mortality in obesity alone, sarcopenia alone and sarcopenic obesity were 0.53 (0.18–1.57) (p = 0.25), 2.36 (0.99–5.6) (p = 0.053) and 2.89 (1.01–8.30) (p = 0.048), respectively. Age‐stratified analyses revealed that sarcopenic obesity markedly increased mortality risk in participants aged 40–75 years (aHR 13.1 [2.93–58.4], p < 0.001), whereas sarcopenia alone (aHR 3.21 [1.07–8.33], p = 0.004), but not sarcopenic obesity (aHR 1.41 [0.34–8.81], p = 0.51), was associated with increased mortality in those aged > 75 years. Compared with non‐sarcopenic obesity, sarcopenic obesity had a significantly higher hazard ratio for mortality (aHR 4.0 [1.44–11.0], p = 0.008). In age‐stratified analysis, this association remained significant in participants aged 40–75 years (aHR 14.1 [3.25–61.5], p < 0.001), but not in those aged > 75 years (aHR 1.55 [0.32–7.46], p = 0.59) (interaction p = 0.03).

In Japanese individuals with Type 2 diabetes, sarcopenic obesity was significantly associated with increased mortality risk. This relationship was particularly pronounced in individuals aged 40–75 years, whereas sarcopenia alone was associated with increased mortality risk rather than sarcopenic obesity in individuals aged > 75.

## Linked entities

- **Diseases:** Type 2 diabetes (MONDO:0005148)

## Full-text entities

- **Genes:** LEP (leptin) [NCBI Gene 3952] {aka LEPD, OB, OBS}, IL15 (interleukin 15) [NCBI Gene 3600] {aka IL-15}, FNDC5 (fibronectin type III domain containing 5) [NCBI Gene 252995] {aka FRCP2, irisin}, ALB (albumin) [NCBI Gene 213] {aka FDAHT, HSA, PRO0883, PRO0903, PRO1341}, CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, IGF1 (insulin like growth factor 1) [NCBI Gene 3479] {aka IGF, IGF-I, IGFI, MGF}, RETN (resistin) [NCBI Gene 56729] {aka ADSF, FIZZ3, RENT, RETN1, RSTN, XCP1}, ADIPOQ (adiponectin, C1Q and collagen domain containing) [NCBI Gene 9370] {aka ACDC, ACRP30, ADIPQTL1, ADPN, APM-1, APM1}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}
- **Diseases:** retinopathy (MESH:D058437), Sarcopenia (MESH:D055948), Hypertension (MESH:D006973), decreased renal function (MESH:D058186), loss of muscle mass (MESH:C536030), Obesity (MESH:D009765), stroke (MESH:D020521), mitochondrial dysfunction (MESH:D028361), visceral adiposity (MESH:D007418), Diabetic nephropathy (MESH:D003928), Diabetic neuropathy (MESH:D003929), Type 2 Diabetes (MESH:D003924), epithelial or non-epithelial malignant neoplasms (MESH:D009375), Malignancy (MESH:D009369), autonomic neuropathy (MESH:D009422), loss of skeletal muscle (MESH:D005207), diabetic complications (MESH:D048909), physical (MESH:D059445), diabetic retinopathy (MESH:D003930), malnutrition (MESH:D044342), Mortality (MESH:D003643), CVD (MESH:D002318), peripheral arterial disease (MESH:D058729), DM (MESH:D009223), insulin resistance (MESH:D007333), gestational diabetes (MESH:D016640), impaired glucose tolerance (MESH:D018149), Type 1 diabetes (MESH:D003922), Diabetes (MESH:D003920), atherosclerosis (MESH:D050197), ischaemic heart disease (MESH:D006331), epithelial or non-epithelial malignancies (MESH:D002277), nephropathy (MESH:D007674), Chronic inflammation (MESH:D007249), impaired (MESH:D060825), polyneuropathy (MESH:D011115), Diabetic Micro (MESH:C536681), adiposity (MESH:D018205), glomerular hypertrophy (MESH:D006984), CKD (MESH:D051436), endothelial dysfunction (MESH:D014652)
- **Chemicals:** glucose (MESH:D005947), lipid (MESH:D008055), creatinine (MESH:D003404), LDL-C (-), TG (MESH:D013866), testosterone (MESH:D013739), triglycerides (MESH:D014280), alcohol (MESH:D000438)
- **Species:** Nicotiana tabacum (American tobacco, species) [taxon 4097], Homo sapiens (human, species) [taxon 9606]

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## References

40 references — full list in the complete paper: https://tomesphere.com/paper/PMC12848597/full.md

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Source: https://tomesphere.com/paper/PMC12848597