With the global increase in life expectancy, the proportion of elderly people in the community is expected to increase gradually. This is referred to as the ‘Coming of the Gray Dawn’ or the ‘Gray Wave’, and highlights the need for current day healthcare professionals to better understand the specific disease processes that occur in the elderly.1,212 One such key change that occurs with increasing age is the alteration in body composition. With each passing year, the body experiences a gradual reduction in muscle mass (sarcopenia) and a relative increase in fat mass (obesity) (Figure 1).3–5345 Though this change occurs in all individuals, it is a modifiable phenotype and depends on the dietary intake and exercise performance of an aging individual.6,767 There is emerging literature on the impact of sarcopenic obesity (SO) on different cardiometabolic risk factors, but a comprehensive review on considering it as a risk factor for cardiovascular disease (CVD) is needed.
Figure 1: Change in body composition with aging
In this manuscript, the authors have attempted to bridge this gap by comprehensively reviewing the available literature regarding the definition, diagnostic criteria, and prevalence of SO, along with the available evidence linking it to CVD, metabolic disease and mortality, and also provide an overview of the current management directives. This will help to better understand the importance of recognising, evaluating and treating SO, to reduce cardiovascular (CV) mortality. Furthermore, the authors have also provided future directions for research on this subject to help identify possible research questions that are currently not addressed in the available literature.
Bidirectional impact
A reduction in muscle mass limits a given individuals’ physical activity and mobility, contributing to obesity.4Expand Reference But an increase in fat mass also compromises muscle mass – adipose tissue can either physically decrease muscle quality by fat infiltration or by its systemic impact of increasing insulin resistance and pro-inflammatory markers (Figure 2).8Expand Reference This leads to a vicious cycle, thus further enhancing progression of declining muscle mass and increasing adiposity at a rapid pace,9Expand Reference especially in the elderly. This bidirectional impact also explains why these two disorders often co-exist rather than occurring in isolation.
Figure 2: The bidirectional impact of sarcopenia and obesity
Definition of sarcopenia and sarcopenic obesity
The term ‘sarcopenic obesity’ was first coined by Baumgartner et al.10Expand Reference SO has been defined by the European Society for Clinical Nutrition and Metabolism (ESPEN) and the European Association for the Study of Obesity (EASO) as a clinical and functional condition characterized by the coexistence of excess fat mass (high body fat percentage) and sarcopenia (low skeletal muscle mass accompanied by low muscle function).11,121112 Sarcopenia is diagnosed based on two or three of the following parameters (varying between different working groups): (a) low muscle mass, (b) low muscle strength, and (c) low physical performance.13–15131415 The perceived prevalence of sarcopenia is lower when all three criteria are utilised, but higher when any two criteria are satisfied.16Expand Reference Sarcopenia may also be defined as the total or appendicular skeletal muscle mass (ASM) in weight/height2 (kg/m2) of an individual being below two standard deviations of a reference population of the same gender.17Expand Reference The prevalence of sarcopenia is higher in women than in men.18Expand Reference Obesity may be defined as a body mass index (BMI) >30 kg/m2,19Expand Reference or a high total or percentage fat mass as assessed by dual-energy X-ray absorptiometry (DXA), bioelectrical impedance analysis or by using other parameters such as visceral fat area or waist circumference (WC). The perceived prevalence of SO in a population aged ≥60 years ranged from 4.4% to 84.0% in men and from 3.6% to 94.0% in women, in a study done between 1999-2004 using the National Health and Nutrition Examination Surveys database in the United States, which may be attributed to the diversity of diagnostic criteria.20Expand Reference
Current gaps in the sarcopenia literature
SO may be associated with significant frailty, disability, and morbidity, as we will see in the latter part of this manuscript. Current diagnostic criteria for SO are heterogenous, ill-defined and do not allow for appropriate patient identification and stratification, in their present form. A 19-26-fold variation in sex-specific rates was noted on reviewing eight definitions for SO.20Expand Reference As can be inferred from the wide variability in the prevalence of SO assessed in various studies, and which highlights the compelling need for further research to ensure uniform diagnostic criteria and management guidelines.
Despite an increase in the knowledge of the mediators and metabolic pathways involved in the pathogenesis of SO, gross lacunae still persist.21Expand Reference Areas of potential research include investigations into the mediators of the positive effects of exercise, the role of gut hormonal systems and microbiota metabolism in SO, and the interaction of nutritional regulation and skeletal muscle homeostasis.6,22,2362223 These research outcomes would help in the prevention and management of patients with SO.
Areas with scope for further research could also help develop dietary, prevention and treatment protocols for optimising skeletal heath in subjects with obesity. A growing body of evidence lends support for increased protein and amino acid intake, as well as skeletal muscle anabolism with maintenance of lean body mass. A protein intake of 1.0–1.2 g per kg of ideal body weight per day has been suggested as recommended intake in healthy geriatric populations.24–26242526 In addition, exercise training, especially resistance exercise, has been shown to be effective in improving muscle function and mass.27Expand Reference
Unique South Asian phenotype
In India, there is a very high prevalence of individuals who are overweight and obese, and an even higher prevalence of sarcopenia. The overall prevalence of SO in India was noted to be 8.7% in the Longitudinal Aging Study in India.9,28928 The chief predictors of SO were noted to be higher age, urban residence, a geographical location in western or southern India, consumption of tobacco or alcohol, lack of physical activity, ophthalmological comorbidities and the presence of diabetes.9Expand Reference The prevalence of SO in a north Indian cohort of community-dwelling healthy adults as per the Sarcopenic Obesity-Chandigarh Urban Bone Epidemiological Study (SO-CUBES) was determined to be 5.4–6.3% utilizing BMI, WC and DXA-derived fat mass (FM) percentage.29Expand Reference In this study, apparently healthy individuals aged ≥ 20 years with no prior history of any co-morbidities were recruited from the community and underwent body composition analysis, dominant handgrip strength (HGS), and usual gait speed (GS) to assess sarcopenia. However, the younger age is probabaly the reason behind a relatively lower prevalence in this cohort.Asian Indians have been noted to have a small body size with centripetal obesity, as characterised by a high waist-to-hip ratio, WC, visceral fat, and posterior subcutaneous abdominal fat.30,313031 This phenotype has been termed as ‘normal weight obesity’ (normal BMI associated with a high percentage of body fat) and has been noted to have an independent association with increased CV mortality compared to individuals with a normal body fat percentage.32Expand Reference Muscle strength and mass is lower in South Asians than Caucasians. The South Asian community has also been noted to be ethnically and phenotypically different from Eastern and South Eastern Asian nations.9,27927 In view of these differences, international guidelines need to be adapted for the Asian and South Asian community with caution.33Expand Reference
Diagnosis of sarcopenic obesity
SO has various diagnostic criteria, as denoted in Table 1.34–383435363738 Various diagnostic tests are employed in the diagnosis of sarcopenia, including HGS, GS, whole-body DXA, short physical performance battery, squad-jump, countermovement jump, and 10 m and 20 m sprint performance.39,403940 Anthropometric indices such as BMI, WC, waist-to-height ratio (WHtR), weight-adjusted waist index (WWI), along with newer indices as demonstrated in Table 2, may also be employed in screening for SO.41,424142 Higher WWI, WHtR and WC quartiles were associated with higher risk of SO.41Expand Reference A systematic review in 2019 revealed that 19 different measurements of sarcopenia and 10 measurements of adiposity had been applied across various studies; of these, ASM divided by weight (ASM/wt.) or adjusted by height in meters squared (ASM/h2) and BMI were, the most commonly applied measurements of sarcopenia and obesity, respectively. The heterogeneity of the diagnostic assessment was further exacerbated by the application of varying cut-offs for the same measurements.11Expand Reference Hence, a consensus on diagnostic criteria for SO, followed by validation based on homogeneous studies and databases, is the need of the hour as this will ensure an assessment of the correct prevalence, evaluation and treatment of SO across different ethnicities and countries.
Table 1: Measurement cut-offs for sarcopenia and obesity from various studies34–383435363738
Author (year) |
Sarcopenia measure |
Sarcopenia measurement (cut-off value) |
Obesity indicator |
Study population |
Baumgartner (2004)34Expand Reference |
ASM/height2 |
DXA (male <7.26 kg/m2, female <5.45 kg/m2) |
Body fat ( male ≥28%, female ≥40%) |
New Mexico Elder Health Survey |
Villareal (2005)35Expand Reference |
ASM/height2 |
ASM (<5.45 kg/m2, sex not specified) |
BMI (≥30 kg/m2) |
Young healthy population |
Bouchard (2009)36Expand Reference |
ASM/height2 |
DXA (male <8.51 kg/m2, female <6.29 kg/m2) |
Body fat ( male ≥28%, female ≥35%) |
Nutrition as a Determinant of Successful Aging Study |
Kim (2009)37Expand Reference |
ASM/height2 |
DXA (male <7.40 kg/m2, female <5.14 kg/m2) |
Body fat ( male ≥20.2%, female ≥31.7%) |
Korean Sarcopenic Obesity Study |
Levine (2012)38Expand Reference |
(ASM x 100)/ (body mass) |
DXA (male <25.7%, female <19.4%) |
WC (male <102 cm, female <88 cm) |
National Health and Nutrition Examination Survey |
ASM = appendicular skeletal muscle; BMI = body mass index; DXA = dual-energy X-ray absorptiometry; WC = waist circumference.
Table 2: Various anthropometric indices for sarcopenic obesity
|
|
Waist–calf circumference ratio Waist circumference/calf circumference |
Normal <2.5 Suspected SO 2.5–3.5 Confirmed SO >3.5 |
Calf central index Calf circumference/waist–hip ratio |
Normal >30 Suspected SO 30–40 Confirmed SO <40 |
Body–calf index BMI/calf circumference |
Normal <0.6 Suspected SO 0.6–1.0 Confirmed SO >1.0 |
BMI = body mass index; SO = sarcopenic obesity.
Impact of sarcopenic obesity on cardiovascular risk factors
Sarcopenic obesity and diabetes
SO has been demonstrated to have an association with hyperglycaemia and insulin resistance in numerous studies. In a cross-sectional study conducted in 2020, in Singapore with 1,235 patients with type 2 diabetes, SO was detected in >20% of patients with type 2 diabetes mellitus aged more than 45 years of age.43Expand Reference Similarly, subjects with SO were observed to have the highest risk of insulin resistance and dysglycaemia in a cross-sectional analysis of 14,528 adults from the NHANES III cohort.44Expand Reference In the Korean Sarcopenic Obesity Study (KSOS), which included 810 subjects (414 patients with diabetes and 396 control subjects) who were examined using DXA, SO was noted to be associated with insulin resistance, inflammation, and vitamin D deficiency.45Expand Reference Furthermore, SO was associated with insulin resistance, metabolic syndrome, dyslipidemia, and vitamin D deficiency in a cross-sectional analysis of 2,943 participants aged 60 years or above from the Korea National Health and Nutrition Examination Survey (KNHANES).46Expand Reference Another Korean study reported a higher risk of diabetes in patients with SO (odds ratio [OR]: 2.16, 95% confidence interval [CI]: 1.08–3.27) than in the sarcopenia group (OR: 1.24, 95% CI: 0.86–2.15).47Expand Reference
Sarcopenic obesity and hypertension
A cross-sectional study of older adults from the KNHANES database noted that SO had a greater association with increased risk of hypertension.48Expand Reference The risk of hypertension was higher in the sarcopenia (OR: 2.48, 95% CI: 1.89–6.16), obesity (OR: 3.15, 95% CI: 2.76–3.59), and SO (OR: 6.42, 95% CI: 4.85–8.48) groups than in the non-sarcopenia, non-obesity group.48,494849 The 10-year risk of hypertension was found to be higher in patients with SO than in those with sarcopenia alone or those who did not have sarcopenia or obesity, but similar to those with obesity alone.50 Expand ReferenceStudies have also demonstrated that the prevalence of SO is much higher in patients with chronic diseases such as hypertension, diabetes, and dyslipidaemia.51Expand Reference
Sarcopenic obesity and dyslipidaemia
SO has been noted to have a significant association with dyslipidaemia.52Expand Reference Studies from the KHNANES cohort have demonstrated that male patients with SO had a higher risk of dyslipidaemia (OR: 2.82, 95% CI: 1.76–4.51) compared with those with obesity alone (OR: 2.12, 95% CI: 1.11–4.07) or sarcopenia alone (OR: 1.46, 95% CI: 1.01–2.11).52Expand Reference
Sarcopenic obesity and metabolic syndrome
SO has been found to be significantly associated with metabolic syndrome. A greater risk of metabolic syndrome was noted by Lim et al. among adults with SO (OR: 8.28, 95% CI: 4.45–15.40) than among those with obesity (OR: 5.51, 95% CI: 2.81–10.80) or sarcopenia (OR: 2.64, 95% CI: 1.08– 6.44) in a cross-sectional study of 565 patients aged ≥65 years from the Korean Longitudinal Study on Health and Aging (KLoSA).47Expand Reference Another study conducted among 600 older adults from Taiwan showed that the group with SO had a higher risk of metabolic syndrome (OR: 11.59, 95% CI: 6.72–19.98) than the group with obesity alone (OR: 7.53, 95% CI: 4.01–14.14) or sarcopenia alone (OR: 1.98, 95% CI: 1.25–3.16).53Expand Reference
Sarcopenic obesity and osteoporosis
A study conducted across 3,385 males and 4,064 females from the KHNANES cohort demonstrated that the risk of osteoporosis was higher in the SO group (OR: 8.67, 95% CI: 4.19–17.94 in men; OR: 2.93, 95% CI: 1.99–4.32 in women).54Expand Reference Another cross-sectional study using data from 2,893 subjects from the KNHANES database showed a greater risk of knee osteoarthritis in the SO (OR: 3.51, 95% CI: 2.15–5.75) and non-SO (OR: 2.38, 95% CI: 1.80–3.15) groups, but not in the sarcopenic, non-obesity group.55Expand Reference Yet another study reported lower bone mineral density and a higher risk of non-vertebral fracture in older adults with SO than in those without sarcopenia, without obesity, and with only obesity.56Expand Reference
Sarcopenic obesity and coronary artery disease
A cross-sectional analysis of Korean adults from the KNHANES database assessing the association between the 10-year CVD risk (estimated using the Framingham risk score) and SO revealed a higher 10-year CVD risk in the SO group compared with the non-sarcopenia non-obesity group (OR: 2.49, 95% CI: 1.53–4.06 in men; OR: 1.87; 95% CI: 1.02–3.41 in women), even though the risk of CVD was not high in the groups with sarcopenia or obesity alone.57Expand Reference However, contrasting reports were seen in a prospective cohort study of older men from the British Regional Heart Study.57Expand Reference In this study, no significant increase in the risk of coronary heart disease (fatal or non-fatal myocardial infarction) or CVD events (non-fatal myocardial infarction, non-fatal stroke, or fatal CVD) were noted in men with SO.57Expand Reference Numerous cross-sectional studies have also reported that older adults with SO did not have a significantly higher prevalence of CVD than those without sarcopenia or obesity.58,595859
Sarcopenic obesity and mortality
Various studies have shown an association between SO and increased mortality risk. In the British Regional Heart Study, an analysis of 4,107 men aged 60–79 years revealed that the risk of all-cause mortality was increased in men with SO.53Expand Reference Subjects with a high WC (>102 cm) and in the lowest quartile of midarm muscle circumference had a 55% increase in mortality risk compared with non-sarcopenic, non-obese men over 6 years of follow up.60Expand Reference On further follow up of the cohort after 11 years, there was a 72% increased risk of mortality in men with SO compared with the non-sarcopenic, non-obese group after adjustment for lifestyle and CV risk factors.61Expand Reference A prospective analysis of 4,652 participants aged ≥60 years from the NHANES III cohort showed higher risk of all-cause mortality in women with SO (HR: 1.29, 95% CI: 1.03–1.60) than in women without sarcopenia or obesity over a 14-year follow-up period.62Expand Reference A meta-analysis of 12 prospective cohort studies found that the risk of mortality was highest in patients with SO (HR 1.24, 95% CI 1.12–1.37) compared with healthy individuals.63Expand Reference
Clinical implications
With a steady increase in the global geriatric population and the concurrent obesity epidemic, SO is a rapidly burgeoning health phenomenon. As sarcopenia and obesity share pathological factors including aging, hormones, and immunological factors, SO has a greater cumulative risk of negative health outcomes when compared to sarcopenia or obesity alone. In the absence of a global consensus definition and diagnostic criteria, SO is probably underdiagnosed as a clinical entity. As we may note from the aforementioned evidence, SO is associated with an increased risk of disability, mortality, metabolic diseases, CVD, and other comorbidities, compared with sarcopenia or obesity alone. In terms of assessing the overall health burden of SO, we are probably witnessing only the tip of the iceberg. The various clinical implications have been summarized in Table 3 and are now discussed in more detail.
Table 3: Clinical implications of sarcopenic obesity on cardiometabolic health*
1 |
SO is grossly underdiagnosed due to lack of awareness and criteria |
2 |
SO is associated with increased risks of disability, mortality, metabolic diseases and cardiovascular diseases compared with individuals with obesity or sarcopenia alone |
3 |
A combination of aerobic and resistance exercises is helpful to address both obesity and sarcopenia, respectively |
4 |
A daily protein intake of 1.2–1.6 g/kg/day has been proposed in patients with SO; caution is to be exercised in patients with renal impairment |
5 |
The utility of anti-obesity medications in the management of SO is not well studied |
6 |
Many novel drug targets (such as tesamorelin [a growth-hormone-releasing hormone analog], myostatin antibodies [LY2495655, bimagrumab, REGN1033, PF-06252616, BMS-986089, PINTA-745] and recombinant irisin) are currently in different stages of drug development |
*Clinical implications are based on the authors experience in this area
SO = sarcopenic obesity.
Sarcopenic obesity and exercise
There is a relative scarcity of data with regard to the management of SO. A regimen of weight loss without exercise leads to a simultaneous reduction of both fat mass and lean mass, which further aggravates sarcopenia. In a systematic review conducted by Weinheimer EM et al., it was reported that the addition of exercise to energy restriction can attenuate the loss of lean mass, despite not appearing to have any significant additive effect on weight reduction.22Expand Reference A fat-free mass (FFM)>15% was observed in approximately 81% of overweight/obese individuals following energy restriction alone compared with 39% using energy restriction and exercise, respectively.22Expand Reference This suggests that exercise is an effective tool to help preserve FFM after moderate energy restriction induced weight loss, which is important for combating SO.
In view of the possible benefits of exercise in countering SO, prescribing a good exercise regimen is essential.64Expand Reference Evidence indicates that a combination of aerobic and resistance exercise is the best possible regimen.65Expand Reference Resistance training has been shown to be more useful against sarcopenia, while aerobic exercise has a better efficacy against obesity. Hence, it could be concluded that their combination could provides the best results in SO, although evidence is currently lacking.
A randomized controlled trial conducted in older adults with obesity demonstrated an improvement in the physical performance test which was greater in the combination exercise group than in the resistance-only or aerobic-only groups (29%, 14%, and 14%, respectively) over 6 months of follow up. The decrease in lean mass was smaller in the combination and resistance groups than in the aerobic group (3%, 2%, and 5%, respectively).66Expand Reference
A few trials have compared resistance exercise with no exercise.67,686768 Resistance exercise has been shown to increase lean mass and physical capacity in older female subjects with SO.67,686768
Periodization, a systematic variation in the specificity of physical training, intensity and volume, has also emerged as a potential strategy to improve muscle performance.69Expand Reference
Sarcopenic obesity and diet
With regard to dietary regimens in patients with SO, there is evidence to suggest that adequate protein intake is essential in SO.70Expand Reference Protein supplementation in addition to resistance exercise was shown to reduce fat mass and increase lean mass, upper body strength, and leg strength compared with resistance exercise alone.70Expand Reference A daily protein intake of 1.2–1.6 g/kg/day has been proposed in patients with SO; caution is to be exercised in patients with renal impairment.71Expand Reference Limited evidence exists to suggest that a dietary supplementation with vitamin D, amino-acid supplementation, tea catechins, and combination exercise (aerobic plus resistance) for 3 months can improve body fat mass and physical function, but not muscle mass, in elderly women with SO.72Expand Reference
Sarcopenic obesity and anti-obesity medications
There is a relative paucity of trials on the utility of conventional anti-obesity medications (orlistat, phentermine, lorcaserin, liraglutide etc.) on SO.73Expand Reference The rapidity of weight reduction following the use of anti-obesity medications may cause rapid simultaneous loss of muscle mass, though this is has not yet been confirmed in SO by any published studies. Drugs such as tesamorelin (a growth hormone-releasing hormone analog), myostatin antibodies (LY2495655, bimagrumab, REGN1033, PF-06252616, BMS-986089, PINTA-745) and recombinant irisin have been shown to have beneficial effects in patients with SO.74–7774757677
Sarcopenic obesity and bariatric surgery
There is limited evidence on the effects of bariatric surgery in patients with SO.78Expand Reference A risk of excessive loss of muscle mass is present in the event of weight loss, and if surgery is not followed by regular exercise.78Expand Reference A prospective cohort trial comparing the effect of gastric bypass and sleeve gastrectomy in patients with SO and non-SO showed that despite baseline differences in muscle mass between both groups, there was no difference between the groups 12 months after bariatric surgery.79Expand Reference This indicates that patients with sarcopenia do not lose more muscle mass despite similar weight loss. However, more randomized trials are required before recommending bariatric surgery in patients with SO.
Summary
SO is a chronic condition and an emerging health challenge, connected to the confluence of the rise in the elderly population and the obesity epidemic. The disparity in diagnostic criteria was a disadvantage faced by previous trials on SO, when defining inclusion criteria for subjects in a clinical trial; this has been resolved to an extent by the ESPEN/EASO consensus on definition and diagnostic criteria, published in 2022.11Expand Reference Screening for SO in the elderly population should be prioritized to permit early diagnosis of SO and early initiation of treatment in order to minimize unfavourable outcomes and improve quality of life. As this review has highlighted, SO is associated with a vast burden of metabolic disorders, morbidity, risk of CVD and mortality. Therapeutic regimens are in the nascent stages of development and need a multi-specialty and multi-modality approach to tackle this challenge with changes in diet, exercise regimens, pharmacological management and rarely, surgical intervention. This review also stresses the need for an increased awareness of SO, including amongst medical specialties beyond geriatrics. A broader recognition is crucial for a comprehensive understanding of the true health burden of SO, as it will enable us to discern, for example, the incidence of SO under different conditions, such as malignancies and other medical conditions.