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Editorial
Sarcopenia and Frailty in Type 2 Diabetes Mellitus: An Overlooked Challenge
Chul-Hee Kimorcid
Diabetes & Metabolism Journal 2026;50(4):666-668.
DOI: https://doi.org/10.4093/dmj.2026.0339
Published online: July 1, 2026
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Division of Endocrinology and Metabolism, Department of Internal Medicine, Soonchunhyang University Bucheon Hospital, Bucheon, Korea

corresp_icon Corresponding author: Chul-Hee Kim orcid Division of Endocrinology and Metabolism, Department of Internal Medicine, Soonchunhyang University Bucheon Hospital, 170 Jomaru-ro, Wonmi-gu, Bucheon 14584, Korea, E-mail: chkimem@schmc.ac.kr

Copyright © 2026 Korean Diabetes Association

This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (https://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

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Sarcopenia and frailty are both age-related conditions that share significant common features and are associated with higher comorbidities and mortality in the general population. With the global increase in the aging population, these conditions have become major health concerns in patients with type 2 diabetes mellitus (T2DM). The relationship between sarcopenia, frailty, and diabetes is complicated as they often coexist and are related to other factors, especially aging.
Sarcopenia—low muscle strength and/or low muscle quantity/quality—is a comorbidity of diabetes with rising prevalence in recent decades [1]. Moreover, it is an independent predictor of incident all-cause mortality in older adults with T2DM [25].
Frailty, a state of increased vulnerability to stressors resulting from reduced physiologic reserve and impaired homeostatic capacity across multiple organ systems, is associated with decreased quality of life and increased risk of falls, disability, hospitalization, and mortality [6]. T2DM and frailty also frequently co-occur and are increasingly prevalent in older patients. Frailty not only affects the management of diabetes in older adults with T2DM, but is also associated with increased mortality in multiple settings [7,8].
Mortality is expected to be even higher when both conditions are present. Both sarcopenia and frailty are consistently associated with higher all-cause mortality, and their co-occurrence generally confers the highest risk [9]. Because definitions vary for sarcopenia and frailty, absolute hazard ratios differ by study, but the risk gradient (neither < one condition < both) is fairly consistent across various settings (community aging cohorts [9], oncology [10], and diabetes-related foot disease [11], among others). However, few studies have investigated the joint association of sarcopenia and frailty with mortality in older people with T2DM.
In this issue, Cengiz et al. [12] reported 5-year mortality in a cohort study of 447 T2DM patients aged 60 years or over after assessing muscle mass, strength, and frailty. The results showed that 11% had isolated sarcopenia, 22.4% isolated frailty, and 9.8% both. Co-existing sarcopenia and frailty significantly increased 5-year mortality risk; frailty alone had a hazard ratio of 2.59, while combined sarcopenia and frailty had a hazard ratio of 3.29 compared to those without these conditions.
This study reveals the current real-world situation of sarcopenia and frailty and their impact on mortality in patients with T2DM. However, it also has several limitations in research design and areas for improvement. First of all, the study population was not large, and was recruited from a single center, and thus is not representative of the general population. Second, the 5-year follow-up period may not be long enough for evaluation of median survival in chronic diseases. Third, further consideration of the diagnostic criteria for sarcopenia and frailty is crucial. The main limitations of studies up to now were non-uniform definitions, measurement heterogeneity, and imperfect construct validity across diabetes phenotypes. Different definitions of sarcopenia by different working groups (different entry points, cutoffs, and adjustment indices) yielded marked inconsistencies in prevalence and prognostic performance [13,14]. The frailty instrument chosen can also affect outcome associations in diabetes cohorts. The fatigue, resistance, ambulation, illnesses, and loss of weight (FRAIL) scale, which was used in this study, showed good diagnostic accuracy against the Fried phenotype in community-dwelling older adults with diabetes, but classified more people as frail than the Fried [15]. Studies comparing FRAIL-derived categories to a frailty index showed only moderate correlation, and outcome associations can differ by instrument [16].
In older diabetes patients, coexistence of diabetes and sarcopenia was associated with substantially higher frailty prevalence, and low muscle mass mediated part of the diabetes-frailty relationship, with synergistic interactions between diabetes and low strength/poor performance further increasing frailty odds [17]. This supports treating ‘sarcopenia+frailty’ as a higher-risk state than either alone, but it also underscores the construct overlap: low strength/poor performance influences both sarcopenia staging (European Working Group on Sarcopenia in Older People 2 [EWGSOP2]) and FRAIL scoring (via resistance/ambulation). Sarcopenia and frailty share core domains (weakness/slowness), so ‘double-positive’ groups can in part reflect definitional overlap rather than two independent pathologies; this is important when interpreting ‘combined phenotype’ mortality signals. Frailty captures multisystem vulnerability (energy dysregulation, neuroendocrine/inflammatory burden, comorbidity load, and reduced stress response), while sarcopenia captures a more specific end-organ manifestation closely tied to mobility limitation, falls, disability, and reduced cardiopulmonary reserve. Co-occurrence therefore often identifies patients with both systemic vulnerability and critical functional limitations, which plausibly increases death risk. It still remains unclear whether there is a specific diabetes-related pathway linking sarcopenia/frailty to mortality or if they are merely overlapping comorbid conditions. This needs to be elucidated more clearly in future studies.
In patients with T2DM, especially older adults and those with complications, screening for sarcopenia and frailty can identify patients at substantially higher mortality risk, including those with obesity, wherein sarcopenia may be under-recognized. The strongest phenotype signal in available data appears when sarcopenia/frailty co-occur and in sarcopenic obesity groups. Recently, a multicomponent intervention (16-week resistance exercise program, nutritional-educational sessions, optimization of diabetes care) showed improvement of frailty status and physical function in older people with T2DM [18]. We need more large-scale, long-term intervention studies to provide a strong supportive evidence base for functional outcomes and mortality impact.
In summary, although this study sounds the alarm about the current challenges of sarcopenia and frailty in T2DM patients, many unanswered questions remain. First of all, we urgently need a globally unified definition of sarcopenia and frailty. More large-scale, long-term follow-up studies in various populations are also needed. Furthermore, research on the mechanisms or pathways linking T2DM with sarcopenia/frailty could provide insight into future interventions.

CONFLICTS OF INTEREST

Chul-Hee Kim has served as an international editorial board member of Diabetes & Metabolism Journal since 2023 but was not involved in the review process for this manuscript. The author declares no competing interests related to this work.

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        Sarcopenia and Frailty in Type 2 Diabetes Mellitus: An Overlooked Challenge
        Diabetes Metab J. 2026;50(4):666-668.   Published online July 1, 2026
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      Sarcopenia and Frailty in Type 2 Diabetes Mellitus: An Overlooked Challenge
      Kim CH. Sarcopenia and Frailty in Type 2 Diabetes Mellitus: An Overlooked Challenge. Diabetes Metab J. 2026;50(4):666-668.
      DOI: https://doi.org/10.4093/dmj.2026.0339.

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