SARC-F with anthropometric add-ons for better sarcopenia detection among elderly outpatients visiting a tertiary care hospital: A cross-sectional study

Authors

  • Dermica EzhilDepartment of Physiotherapy, Sri Ramachandra Institute of Higher Education and Research, Chennai, India
  • Agnes KaaviyaDepartment of Physiotherapy, Sri Ramachandra Institute of Higher Education and Research, Chennai, India
  • Chrysolyte Mohanan Department of Physiotherapy, Sri Ramachandra Institute of Higher Education and Research, Chennai, India
  • Antony Leo Aseer Department of Physiotherapy, Sri Ramachandra Institute of Higher Education and Research, Chennai, India
  • Subbiah Kanthanathan Department of Physiotherapy, Sri Ramachandra Institute of Higher Education and Research, Chennai, India
  • Soundararajan KannanDepartment of Physiotherapy, Sri Ramachandra Institute of Higher Education and Research, Chennai, India

DOI:

Keywords

sarcopenia, SARC- F, calf girth, arm circumference, AWGS

Correspondence

Chrysolyte Mohanan
Email: chrysolyte@sriramachandra.edu.in

Publication history

Received: 2 Feb 2026
Accepted: 16 July 2026
Published online: 25 July 2026

Responsible editor

Reviewers

J: Anonymous

Funding

None

Ethical approval

Approved by the Institutional Review Board of the authors’ affiliated institution (REF: CSP-III/24/JUN/06/196, dated 1 Aug 2024).

Trial registration number

CTRI/2025/04/083920

Copyright

© The Author(s) 2026; all rights reserved. 
Published by Bangladesh Medical University (former Bangabandhu Sheikh Mujib Medical University).
Abstract

Background: Early identification of sarcopenia, a progressive skeletal muscle disorder, remains challenging. Although the Strength, Assistance with walking, Rise from a chair, Climb stairs, and Falls (SARC-F) questionnaire is widely recommended for sarcopenia screening, its limited sensitivity reduces its effectiveness in clinical practice. To improve diagnostic performance, modified versions incorporating anthropometric measurements, calf girth (CalF) and including arm circumference (AC), have been developed and validated in different ethnic populations. This study aimed to evaluate the diagnostic accuracy of the SARC-CalF+AC questionnaire among older adults in Indian population.

Methods: This cross-sectional study included 360 older adults attending the outpatient department of a tertiary care hospital. Participants with preserved cognitive function and independent walking ability were enrolled. The diagnostic performance of the SARC-F and SARC-CalF+AC screening tools was evaluated against the Asian Working Group for Sarcopenia (AWGS) diagnostic criteria.

Results: Approximately one in six were women; Participants mean age was 64 years. Among them 131 were diagnosed with sarcopenia, yielding a prevalence of 36.4% (95% Confidence Interval, 31.6–41.5). The SARC-F questionnaire demonstrated a sensitivity of 22.9% and a specificity of 80.9%. In comparison, the SARC-CalF+AC questionnaire achieved substantially higher sensitivity (75.6%) and specificity (88.2%).

Conclusion: The addition of calf girth and arm circumference measurements significantly improved the diagnostic performance of the SARC-F questionnaire, making SARC-CalF+AC a more effective screening tool for sarcopenia in older adults.

Key messages
The addition of calf girth and arm circumference measurements to the SARC-F questionnaire substantially improves its ability to detect sarcopenia among older adults. SARC-CalF+AC demonstrated markedly higher sensitivity while maintaining good specificity, making it a simple, low-cost, and practical screening tool for early identification of sarcopenia in outpatient settings, particularly in resource-limited healthcare environments.
Introduction

Sarcopenia is a progressive skeletal muscle disorder associated with an increased risk of falls, fractures, physical disability, frailty, and mortality [1]. Muscle weakness is often the earliest manifestation of sarcopenia; however, the condition frequently remains unrecognised in its early stages [2]. International guidelines recommend annual screening for sarcopenia in adults aged 65 years and older or following any major adverse health event.

The Strength, Assistance with walking, Rise from a chair, Climb stairs, and Falls (SARC-F) questionnaire is the most widely recommended screening tool for sarcopenia. Although it demonstrates acceptable specificity, its low-to-moderate sensitivity limits its ability to identify many individuals with the condition [3]. To improve its diagnostic performance, anthropometric measurements have been incorporated into modified screening tools. Calf girth (CalF), recommended by the Asian Working Group for Sarcopenia (AWGS) 2019 and the European Working Group on Sarcopenia in Older People, is considered a simple and reliable surrogate measure of muscle mass and has been endorsed by the World Health Organization as one of the most useful anthropometric indicators. However, calf girth may be influenced by conditions such as lower-limb edema and increased adipose tissue, potentially reducing its diagnostic accuracy [3, 4, 5]. Arm circumference (AC) is another simple anthropometric measure that correlates with muscle mass and has shown potential as a screening marker for sarcopenia. Previous studies have demonstrated that reduced AC is significantly associated with sarcopenia adults [4].

Incorporating AC into the SARC-CalF questionnaire (SARC-CalF+AC) has been reported to improve the diagnostic accuracy of sarcopenia screening in several populations [6]. Nevertheless, evidence regarding its performance remains limited, and its applicability across different populations is not well established.

In India, many studies have relied on diagnostic cut-off values derived from Caucasian populations, which may compromise diagnostic accuracy in Indian older adults [7]. The recently published Indian consensus on sarcopenia emphasises the need for region-specific diagnostic criteria, considering ethnic differences in body composition and genetic characteristics, and highlights the importance of validating simple, practical screening tools using population-specific cut-off values [8].

Therefore, this study aimed to examine the diagnostic accuracy of the SARC-F and SARC-CalF+AC questionnaires for screening sarcopenia among elderly outpatients department of a tertiary care hospital, in India.

Methods

Study design

This cross-sectional study recruited older adults attending the outpatient department of a tertiary care hospital. Participants were eligible if they were aged ≥60 years, had intact cognitive function, and were able to stand and walk independently.

Data collection

A total of 391 older adults were screened between May and December 2025, of whom 360 met the eligibility criteria. Thirty-one participants were excluded because of cognitive impairment, walking difficulty, or multiple comorbidities.

Handgrip strength was measured using a Jamar dynamometer, and the highest value from three trials performed with the dominant hand was recorded. Muscle performance was assessed using the five-times chair stand test. Calf girth was measured at its maximum circumference with the participant standing, while arm circumference was measured at the midpoint between the acromion and olecranon processes with the arm relaxed alongside the body.

Procedure

Demographic and clinical information, including age, sex, height, weight, body mass index, comorbidities, and primary diagnosis, was collected using a structured questionnaire. Sarcopenia was diagnosed based on assessments of muscle strength, muscle performance, and muscle mass in accordance with the study's diagnostic criteria. Handgrip strength was used to assess muscle strength, while the five-times chair stand test was used to evaluate muscle performance.

Figure 1 Flowchart of patient enrolment

SARC-F indicate the Strength, Assistance with walking, Rise from a chair, Climb stairs, and Falls; CalF, Calf girth; AC, aim circumference; AWGS, Asian Working Group on Sarcopenia

Measurement of muscle mass

Appendicular skeletal muscle mass (ASM) was estimated using Lee's formula: ASM = (0.244 × weight) + (7.8 × height) + (6.6 × gender) − (0.098 × age) + (race − 3.3), where the race coefficient was −1.28 for Asian individuals [9]. The skeletal muscle index (SMI) was calculated as ASM divided by height squared (ASM/height²). As comprehensive Indian reference values were unavailable, the Asian Working Group for Sarcopenia (AWGS) 2019 cut-off values were used to define low muscle mass: SMI <7.0 kg/m² for men and <5.4 kg/m² for women.

Measurement of muscle strength

Handgrip strength was measured twice for each hand using a Jamar Hydraulic Hand Dynamometer. Participants were seated with the elbow flexed at 90°, and the mean value was recorded in kilograms (kg) [5].

Measurement of muscle performance or function

Lower-limb muscle performance was assessed using the Five-Times Chair Stand Test according to the AWGS 2019 criteria. Participants were instructed to stand up from a chair and sit down five times as quickly as possible with their arms crossed over their chest. The time taken to complete the test was recorded in seconds [3].

Anthropometrics measurements

Anthropometric measurements included body weight, height, mid-upper arm circumference, and calf circumference. Body mass index (BMI) was calculated as weight (kg) divided by height squared (m²). Mid-upper arm circumference was measured at the midpoint between the acromion and olecranon processes of the dominant arm while the participant was standing. Calf circumference was measured at the point of maximum circumference of the relaxed calf with the participant standing and the feet positioned approximately 20 cm apart [10].

Assessment of sarcopenia by using AWGS 2019 criteria

Sarcopenia was diagnosed according to the AWGS 2019 criteria as the presence of low muscle mass (SMI <7.0 kg/m² for men and <5.4 kg/m² for women) together with low muscle strength (handgrip strength <27.5 kg for men and <18 kg for women) and poor physical performance (Five-Times Chair Stand Test ≥12 seconds for both sexes).

Sarcopenia screening tools

The risk of sarcopenia was assessed using the SARC-F, SARC-CalF, and SARC-CalF+AC questionnaires. The SARC-F questionnaire assesses five domains: strength, assistance with walking, rising from a chair, climbing stairs, and falls. Scores range from 0 to 10, with a score of ≥4 indicating a risk of sarcopenia [3].

The SARC-CalF questionnaire incorporates calf circumference (CC) into the SARC-F by assigning 10 points if CC is ≤33 cm in women or ≤34 cm in men, and 0 points otherwise. Total scores range from 0 to 20, with a score of ≥11 indicating a risk of sarcopenia [3].

The SARC-CalF+AC questionnaire further incorporates arm circumference (AC) using cut-off values of ≤27.5 cm for women and ≤28.6 cm for men [7, 11 ]. The screening cut-offs for SARC-F and SARC-CalF+AC were ≥4 and ≥11, respectively [3]. Both CC and AC contribute 10 points each if their respective values are at or below the cut-off, resulting in a maximum possible score of 30. The optimal cut-off value for the SARC-CalF+AC questionnaire was determined according to the method described by Zhou et al [12].

Data analysis

Statistical analyses were performed using IBM SPSS Statistics version 20. Continuous and categorical variables were compared using the Student's t test and the chi-square (χ²) test, respectively. Using the AWGS 2019 criteria as the reference standard, the diagnostic performance of the SARC-F and SARC-CalF+AC questionnaires was evaluated by calculating sensitivity, specificity, positive and negative predictive values, overall diagnostic accuracy, and their corresponding 95% confidence intervals (CIs). The accuracy was defined as the proportion of combined true positives and true negatives.

Results

A total of 360 participants meeting the inclusion criteria were enrolled. Females comprised 57.8% and males 42.2%, with a mean age of 68.6 (6.1) years. Participants with sarcopenia were significantly older and had lower BMI, arm circumference, calf circumference, chair stand performance, handgrip strength and skeletal muscle mass index than non-sarcopenic participants (all P<0.001). Most participants were aged 60-69 years (64%) followed by 70–79 years (29%) and 80-89 years (7%) (Table 1). Among the 360 participants, 131 were diagnosed with sarcopenia, yielding a prevalence of 36.4% (95% CI, 31.6–41.5).

Table 1 Participants' characteristics categorised using the AWGS criteria

Characteristics

Total

(n=360)

With  sarcopenia

(n=141)

Without  sarcopenia

(n=219)

P

Age

Men

69.2 (6.5)

72.3 (5.5)

67.5 (6.2)

 

Women

68.1 (5.8)

71.2 (5.0)

66.2 (5.5)

 

Total

68.6 (6.1)

71.7 (5.3)

66.8 (5.9)

0.47

Gender, n (%) 

Men

152 (42.2)

64 (48.1)

88 (40.5)

0.2

Women

208 (57.7)

77 (51.8)

131 (59.4)

0.17

Body mass index (kg/m2)

Men

25.2 (4.8)

23.1 (4.0)

27.1 (4.5)

 

Women

24.4 (4.2)

22.0 (3.5)

25.9 (3.9)

 

Total

24.8 (4.5)

22.6 (3.8)

26.5 (4.2)

<0.001

Arm circumference (cm)

Men

28.2 (4.3)

27.2 (6.0)

31.0 (4.4)

 

Women

27.1 (3.8)

25.7 (5.2)

29.4 (3.8)

 

Total

27.7 (4.1)

26.5 (5.7)

30.2 (4.1)

<0.001

Chair stand test(s)

16.8 (6.0)

19.0 (5.5)

9.4 (2.4)

<0.001

Hand grip strength (kg)

Men

30.5 (7.8)

20.0 (5.0)

26.5 (7.0)

 

Women

27.5 (6.9)

18.3 (4.2)

24.0 (6.1)

 

Total

29.1 (7.4)

19.2 (4.6)

25.3 (6.6)

<0.001

Results are mean (standard deviation) unless otherwise indicated

Comparison of SARC-F and SARC-CalF+AC for sarcopenia screening

The SARC-F questionnaire demonstrated a sensitivity of 22.9% and a specificity of 80.9%. In comparison, the SARC-CalF+AC questionnaire showed substantially higher sensitivity (75.6%) and specificity (88.2%), indicating superior diagnostic performance (Table 2). The overall diagnostic accuracy was 59.4% (95% CI: 54.2–64.6) for the SARC-F questionnaire and 83.6% (95% CI: 79.4–87.3) for the SARC-CalF+AC questionnaire.

Variables  

Frequency (%)

Indication of colposcopy

 

Visual inspection of the cervix with acetic acid positive

200 (66.7)

Abnormal pap test

13 (4.3)

Human papilloma virus DNA positive

4 (1.3)

Suspicious looking cervix

14 (4.7)

Others (per vaginal discharge, post-coital bleeding)

69 (23.0)

Histopathological diagnosis

Cervical Intraepithelial Neoplasia 1

193 (64.3)

Cervical Intraepithelial Neoplasia 2

26 (8.7)

Cervical Intraepithelial Neoplasia 3

32 (10.7)

Invasive cervical cancer

27 (9.0)

Chronic cervicitis

17 (5.6)

Squamous metaplasia

5 (1.7)

Groups based on pre-test marks

Pretest
marks (%)

Posttest

Marks (%)

Difference in pre and post-test marks (mean improvement)

P

Didactic lecture classes

<50%

36.6 (4.8)

63.2 (9.4)

26.6

<0.001

≥50%

52.8 (4.5)

72.4 (14.9)

19.6

<0.001

Flipped classes

<50%

36.9 (4.7)

82.2 (10.8)

45.4

<0.001

≥50%

52.8 (4.6)

84.2 (10.3)

31.4

<0.001

Data presented as mean (standard deviation)

Background characteristics

Number (%)

Age at presentation (weeks)a

14.3 (9.2)

Gestational age at birth (weeks)a

37.5 (2.8)

Birth weight (grams)a

2,975.0 (825.0)

Sex

 

Male

82 (41)

Female

118 (59)

Affected side

 

Right

140 (70)

Left

54 (27)

Bilateral

6 (3)

Delivery type

 

Normal vaginal delivery

152 (76)

Instrumental delivery

40 (20)

Cesarean section

8 (4)

Place of delivery

 

Home delivery by traditional birth attendant

30 (15)

Hospital delivery by midwife

120 (60)

Hospital delivery by doctor

50 (25)

Prolonged labor

136 (68)

Presentation

 

Cephalic

144 (72)

Breech

40 (20)

Transverse

16 (8)

Shoulder dystocia

136 (68)

Maternal diabetes

40 (20)

Maternal age (years)a

27.5 (6.8)

Parity of mother

 

Primipara

156 (78)

Multipara

156 (78)

aMean (standard deviation), all others are n (%)

Background characteristics

Number (%)

Age at presentation (weeks)a

14.3 (9.2)

Gestational age at birth (weeks)a

37.5 (2.8)

Birth weight (grams)a

2,975.0 (825.0)

Sex

 

Male

82 (41)

Female

118 (59)

Affected side

 

Right

140 (70)

Left

54 (27)

Bilateral

6 (3)

Delivery type

 

Normal vaginal delivery

152 (76)

Instrumental delivery

40 (20)

Cesarean section

8 (4)

Place of delivery

 

Home delivery by traditional birth attendant

30 (15)

Hospital delivery by midwife

120 (60)

Hospital delivery by doctor

50 (25)

Prolonged labor

136 (68)

Presentation

 

Cephalic

144 (72)

Breech

40 (20)

Transverse

16 (8)

Shoulder dystocia

136 (68)

Maternal diabetes

40 (20)

Maternal age (years)a

27.5 (6.8)

Parity of mother

 

Primipara

156 (78)

Multipara

156 (78)

aMean (standard deviation), all others are n (%)

Mean escape latency of acquisition day

Groups                 

NC

SC

ColC

Pre-SwE Exp

Post-SwE Exp

Days

 

 

 

 

 

1st

26.2 (2.3)

30.6 (2.4) 

60.0 (0.0)b

43.2 (1.8)b

43.8 (1.6)b

2nd

22.6 (1.0) 

25.4 (0.6)

58.9 (0.5)b

38.6 (2.0)b

40.5 (1.2)b

3rd

14.5 (1.8) 

18.9 (0.4) 

56.5 (1.2)b

34.2 (1.9)b 

33.8 (1.0)b

4th

13.1 (1.7) 

17.5 (0.8) 

53.9 (0.7)b

35.0 (1.6)b

34.9 (1.6)b

5th

13.0 (1.2) 

15.9 (0.7) 

51.7 (2.0)b

25.9 (0.7)b 

27.7 (0.9)b

6th

12.2 (1.0) 

13.3 (0.4) 

49.5 (2.0)b

16.8 (1.1)b

16.8 (0.8)b

Average of acquisition days

5th and 6th 

12.6 (0.2)

14.6 (0.8)

50.6 (0.7)b

20.4 (2.1)a

22.4 (3.2)a

NC indicates normal control; SC, Sham control; ColC, colchicine control; SwE, swimming exercise exposure.

aP <0.05; bP <0.01.

Categories

Number (%)

Sex

 

   Male

36 (60.0)

   Female

24 (40.0)

Age in yearsa

8.8 (4.2)

Education

 

   Pre-school

20 (33.3)

   Elementary school

24 (40.0)

   Junior high school

16 (26.7)

Cancer diagnoses

 

Acute lymphoblastic leukemia

33 (55)

Retinoblastoma

5 (8.3)

Acute myeloid leukemia

4 (6.7)

Non-Hodgkins lymphoma

4 (6.7)

Osteosarcoma

3 (5)

Hepatoblastoma

2 (3.3)

Lymphoma

2 (3.3)

Neuroblastoma

2 (3.3)

Medulloblastoma

1 (1.7)

Neurofibroma

1 (1.7)

Ovarian tumour

1 (1.7)

Pancreatic cancer

1 (1.7)

Rhabdomyosarcoma

1 (1.7)

aMean (standard deviation)

Test results

Disease

Sensitivity (%)

Specificity (%)

PPV (%)

NPV (%)

Yes

No

Reid’s score ≥ 5

Positive

10

15

37.0

94.5

40.1

93.8

Negative

17

258

 

 

 

 

Swede score ≥ 5

Positive

20

150

74.1

45.0

11.8

94.6

Negative

7

123

 

 

 

 

Swede score ≥ 8

Positive

3

21

11.1

92.3

12.5

91.3

Negative

24

252

 

 

 

 

High-grade indicates a score of ≥5 in both tests; PPV indicates positive predictive value; NPV, negative predictive value

Test

Sensitivity (%)

Specificity (%)

Positive predictive value (%)

Negative predictive value (%)

Reid’s score ≥ 5

37.0

94.5

40.0

93.8

Swede score ≥ 5

74.1

45

11.8

94.6

Swede score ≥ 8

11.1

92.3

12.5

91.3

Test

Sensitivity (%)

Specificity (%)

Positive predictive value (%)

Negative predictive value (%)

Reid’s score ≥ 5

37.0

94.5

40.0

93.8

Swede score ≥ 5

74.1

45

11.8

94.6

Swede score ≥ 8

11.1

92.3

12.5

91.3

Narakas classification

Total

200 (100%)

Grade 1

72 (36%)

Grade 2

64 (32%)

Grade 3

50 (25%)

Grade 4

14 (7%)

Complete recoverya

107 (54)

60 (83)

40 (63)

7 (14)

-

Near complete functional recovery but partial deformitya

22 (11)

5 (7)

10 (16)

6 (12)

1 (7)

Partial recovery with gross functional defect    and deformity

31 (16)

7 (10)

13 (20)

10 (20)

1 (7)

No significant improvement 

40 (20)

-

1 (1.5)

27 (54)

12 (86)

aSatisfactory recovery

bGrade 1, C5, 6, 7 improvement; Grade 2, C5, 6, 7 improvement; Grade 3, panpalsy C5, 6, 7, 8, 9, Grade 4, panpalsy with Hornon’s syndrome.

Narakas classification

Total

200 (100%)

Grade-1

72 (36%)

Grade-2

64 (32%)

Grade-3

50 (25%)

Grade-4

14 (7%)

Complete recoverya

107 (54)

60 (83)

40 (63)

7 (14)

-

Near complete functional recovery but partial deformitya

22 (11)

5 (7)

10 (16)

6 (12)

1 (7)

Partial recovery with gross functional defect    and deformity

31 (16)

7 (10)

13 (20)

10 (20)

1 (7)

No significant improvement 

40 (20)

-

1 (1.5)

27 (54)

12 (86)

aSatisfactory recovery

bGrade 1, C5, 6, 7 improvement; Grade 2, C5, 6, 7 improvement; Grade 3, panpalsy C5, 6, 7,8,9, Grade 4, panpalsy with Hornon’s syndrome.

Variables in probe trial day

Groups

NC

SC

ColC

Pre-SwE Exp

Post-SwE Exp

Target crossings

8.0 (0.3)

7.3 (0.3) 

1.7 (0.2)a

6.0 (0.3)a

5.8 (0.4)a

Time spent in target

18.0 (0.4) 

16.2 (0.7) 

5.8 (0.8)a

15.3 (0.7)a

15.2 (0.9)a

NC indicates normal control; SC, Sham control; ColC, colchicine control; SwE, swimming exercise exposure.

aP <0.01.

Pain level

Number (%)

P

Pre

Post 1

Post 2

Mean (SD)a pain score

4.7 (1.9)

2.7 (1.6)

0.8 (1.1)

<0.001

Pain categories

    

   No pain (0)

-

(1.7)

31 (51.7)

<0.001

   Mild pain (1-3)

15 (25.0)

43 (70.0)

27 (45.0)

 

   Moderete pain (4-6)

37 (61.7)

15 (25.0)

2 (3.3)

 

   Severe pain (7-10)

8 (13.3)

2 (3.3)

-

 

aPain scores according to the visual analogue scale ranging from 0 to 10; SD indicates standard deviation

Surgeries

Number  

(%)

Satisfactory outcomes n (%)

Primary surgery (n=24)

 

 

Upper plexus

6 (25)

5 (83)

Pan-palsy

18 (75)

6 (33)

All

24 (100)

11 (46)

Secondary Surgery (n=26)

 

 

Shoulder deformity

15 (58)

13 (87)

Wrist and forearm deformity

11 (42)

6 (54)

All

26 (100)

19 (73)

Primary and secondary surgery

50 (100)

30 (60)

Mallet score 14 to 25 or Raimondi score 2-3 or Medical Research grading >3 to 5.

Narakas classification

Total

200 (100%)

Grade-1

72 (36%)

Grade-2

64 (32%)

Grade-3

50 (25%)

Grade-4

14 (7%)

Complete recoverya

107 (54)

60 (83)

40 (63)

7 (14)

-

Near complete functional recovery but partial deformitya

22 (11)

5 (7)

10 (16)

6 (12)

1 (7)

Partial recovery with gross functional defect    and deformity

31 (16)

7 (10)

13 (20)

10 (20)

1 (7)

No significant improvement 

40 (20)

-

1 (1.5)

27 (54)

12 (86)

aSatisfactory recovery

bGrade 1, C5, 6, 7 improvement; Grade 2, C5, 6, 7 improvement; Grade 3, panpalsy C5, 6, 7,8,9, Grade 4, panpalsy with Hornon’s syndrome.

Trials

Groups

NC

SC

ColC

Pre-SwE Exp

Post-SwE Exp

1

20.8 (0.6)

22.1 (1.8)

41.1 (1.3)b

31.9 (1.9)b

32.9 (1.8)a, b

2

10.9 (0.6)

14.9 (1.7)

37.4 (1.1)b

24.9 (2.0)b

26.8 (2.5)b

3

8.4 (0.5)

9.9 (2.0)

32.8 (1.2)b

22.0 (1.4)b

21.0 (1.4)b

4

7.8 (0.5)

10.4 (1.3)

27.6(1.1)b

12.8 (1.2)b

13.0 (1.4)b

Savings (%)c

47.7 (3.0)

33.0 (3.0)

10.0 (0.9)b

23.6 (2.7)b

18.9 (5.3)b

NC indicates normal control; SC, Sham control; ColC, colchicine control; SwE, swimming exercise exposure.

aP <0.05; bP <0.01.

cThe difference in latency scores between trials 1 and 2, expressed as the percentage of savings increased from trial 1 to trial 2

 Lesion-size

Histopathology report

Total

CIN1

CIN2

CIN3

ICC

CC

SM

0–5 mm

73

0

0

0

5

5

83

6–15 mm

119

18

1

4

0

0

142

>15 mm

1

8

31

23

12

0

75

Total

193

26

32

27

17

5

300

CIN indicates cervical intraepithelial neoplasia; ICC, invasive cervical cancer; CC, chronic cervicitis; SM, squamous metaplasia

 

Histopathology report

Total

CIN1

CIN2

CIN3

ICC

CC

SM

Lesion -Size

0-5  mm

73

0

0

0

5

5

83

6-15  mm

119

18

1

4

0

0

142

>15  mm

1

8

31

23

12

0

75

Total

193

26

32

27

17

5

300

CIN indicates Cervical intraepithelial neoplasia; ICC, Invasive cervical cancer; CC, Chronic cervicitis; SM, Squamous metaplasia

Group

Didactic posttest marks (%)

Flipped posttest marks (%)

Difference in marks (mean improvement)

P

<50%

63.2 (9.4)

82.2 (10.8)

19.0

<0.001

≥50%

72.4 (14.9)

84.2 ( 10.3)

11.8

<0.001

Data presented as mean (standard deviation)

Table 2 Sensitivity, specificity, likelihood ratios, disease prevalence, predictive values, and accuracy for SARC-F and SARC-CalF+AC questionnaires in sarcopenia screening (n=360)

Statistic

SARC-F

SARC-CalF+AC

Sensitivity

22.9 (16.0–1.1)

75.6 (67.3–82.7)

Specificity

80.9 (74.6–85.9)

88.2 (83.3–92.1)

Positive predictive value

44.0 (30.7–50.1)

78.6 (71.8–84.1)

Negative predictive value

64.6 (61.9–67.1)

86.3 (82.3–89.5)

Accuracya

59.4 (54.2–64.6)

83.6 (79.4–87.3)

SARC-F indicate the Strength, Assistance with walking, Rise from a chair, Climb stairs, and Falls; CalF, Calf girth; AC, aim circumference; AWGS, Asian Working Group on Sarcopenia.
Results are percents (95% confidence intervals) using the Asian Working Group for Sarcopenia 2019 criteria as the gold standard.
aAccuracy was defined as the true positives plus true negatives divided by all subjects.

Discussion

Sarcopenia is a common age-related skeletal muscle disorder associated with reduced physical function, falls, fractures, frailty, and increased mortality. Early identification is essential for timely intervention and prevention of adverse health outcomes in the growing older population. Although the SARC-F questionnaire is the most widely recommended screening tool, its diagnostic performance varies across populations and is influenced by factors such as age, comorbidities, ethnicity, and body composition.

Previous studies have reported considerable variation in the sensitivity and specificity of the SARC-F questionnaire. For example, a study conducted in Vietnam reported a sensitivity of 65.8% and a specificity of 71.4% based on the AWGS 2019 criteria, whereas a study from Hong Kong reported high specificity (98.8% in men and 94.2% in women) but comparatively lower sensitivity [13]. These findings highlight the limited sensitivity of the SARC-F questionnaire and the need to improve its ability to identify individuals with sarcopenia.

The incorporation of anthropometric measurements into the SARC-F questionnaire has been proposed as a practical approach to improving its diagnostic performance. Previous studies from Brazil and China demonstrated that adding calf circumference to the SARC-F increased the sensitivity of sarcopenia screening [14]. Consistent with these findings, our study showed that incorporating both calf circumference and arm circumference (SARC-CalF+AC) substantially improved the sensitivity of the screening tool (75.6%) compared with the original SARC-F questionnaire (22.9%), while maintaining good specificity. These findings support the value of anthropometric measurements as simple and effective additions to conventional sarcopenia screening. The optimal arm circumference cut-off values identified in our study were lower than those reported in a Chinese population [14], emphasising the importance of population-specific cut-off values.

Appropriate diagnostic cut-off values are essential for maximizing screening accuracy. Differences in ethnicity, body composition, nutritional status, and genetic background may influence anthropometric measurements and the prevalence of sarcopenia. The recently published Indian Consensus on Sarcopenia also emphasizes the need for region-specific diagnostic criteria to improve the identification and management of sarcopenia in Indian older adults.

The SARC-CalF+AC questionnaire is a simple, inexpensive, non-invasive, and practical screening tool that can be easily implemented in routine clinical practice, particularly in primary healthcare and resource-limited settings. Its improved diagnostic performance may facilitate earlier identification of individuals at risk of sarcopenia and support timely intervention. Given the influence of socioeconomic, ethnic, and lifestyle factors on sarcopenia, further validation of this screening tool in diverse populations is warranted [2].

This study has several limitations. First, the sample size was relatively small and participants were recruited from a single tertiary care hospital, which may limit the generalisability of the findings. Second, skeletal muscle mass was estimated using Lee's predictive equation rather than direct measurement techniques such as bioelectrical impedance analysis or dual-energy X-ray absorptiometry. Third, we did not evaluate the severity of sarcopenia among affected participants. Future multicentre studies involving larger and more diverse populations and using gold-standard methods for muscle mass assessment are needed to further validate the diagnostic performance of the SARC-CalF+AC questionnaire.

Conclusion

SARC-CalF+AC showed substantially higher sensitivity than SARC-F alone for detecting sarcopenia in this Indian population, supporting its use as a practical screening tool in primary care and outpatient settings. Incorporating ethnicity-specific and socioeconomic factors into future cut-off values will further improve screening accuracy.

Acknowledgements
We would like to thank all the patients who participated in the study.
Author contributions
Concept or design of the work; or the acquisition, analysis, or interpretation of data for the work: DE, AK, CM. Drafting the work or reviewing it critically for important intellectual content: DE, AK, CM, AL. Final approval of the version to be published: DE, AK, CM, ALA, SK, SK. Accountable for all aspects of the work in ensuring that questions related to the accuracy or integrity of any part of the work are appropriately investigated and resolved: DE, AK, CM, AL.
Conflict of interest
We do not have any conflict of interest.
Data availability statement
We confirm that the data supporting the findings of the study will be shared upon reasonable request.
AI disclosure
None
Supplementary file
None
    References
    1. Tagliafico AS, Bignotti B, Torri L, Rossi F. Sarcopenia: how to measure, when and why. Radiol Med. 2022;127(3):228-237. doi: https://doi.org/10.1007/s11547-022-01450-3
    2. Endo K, Sato T, Kakisaka K, Takikawa Y. Calf and arm circumference as simple markers for screening sarcopenia in patients with chronic liver disease. Hepatol Res. 2021;51(2):176-189. doi: https://doi.org/10.1111/hepr.13589
    3. Krzymińska-Siemaszko R, Deskur-Śmielecka E, Kaluźniak-Szymanowska A, Murawiak M, Wieczorowska-Tobis K. Comparison of diagnostic value of the SARC-F and its four modified versions in Polish community-dwelling older adults. Clin Interv Aging. 2023;18:783-797. doi: https://doi.org/10.2147/CIA.S408616
    4. Hu FJ, Liu H, Liu XL, Jia SL, Hou LS, Xia X, Dong BR. Mid-Upper Arm Circumference as an Alternative Screening Instrument to Appendicular Skeletal Muscle Mass Index for Diagnosing Sarcopenia. Clin Interv Aging. 2021 Jun 15;16:1095-1104. doi: https://doi.org/10.2147/CIA.S311081
    5. Chen LK, Woo J, Assantachai P, Auyeung TW, Chou MY, Iijima K, et al. Asian Working Group for Sarcopenia: 2019 consensus update on sarcopenia diagnosis and treatment. J Am Med Dir Assoc. 2020;21(3):300-307.e2. doi: https://doi.org/10.1016/j.jamda.2019.12.012
    6. Zhou J, Li T, Chen X, Wang M, Jiang W, Jia H. Comparison of the diagnostic value of SARC-F and its three modified versions for screening sarcopenia in Chinese community-dwelling older adults. J Nutr Health Aging. 2022;26(1):77-83. doi: https://doi.org/10.1007/s12603-021-1718-z
    7. Kalra S, Shaikh IA, Shende S, Kapoor N, Unnikrishnan AG, Sharma OP, et al. An Indian consensus on sarcopenia: epidemiology, etiology, clinical impact, screening, and therapeutic approaches. Int J Gen Med. 2025;18:1731-1745. doi: https://doi.org/10.2147/IJGM.S510412
    8. Pal R, Aggarwal A, Singh T, Sharma S, Khandelwal N, Garg A, Bhansali A, Kumar A, Yadav U, Singh P, Dhiman V, Dutta P, Bhadada SK. Diagnostic cut-offs, prevalence, and biochemical predictors of sarcopenia in healthy Indian adults: The Sarcopenia-Chandigarh Urban Bone Epidemiological Study (Sarco-CUBES). Eur Geriatr Med. 2020 Oct;11(5):725-736. doi: https://doi.org/10.1007/s41999-020-00332-z
    9. Lee RC, Wang Z, Heo M, Ross R, Janssen I, Heymsfield SB. Total-body skeletal muscle mass: development and cross-validation of anthropometric prediction models. Am J Clin Nutr. 2000;72(3):796-803. doi: https://doi.org/10.1093/ajcn/72.3.796
    10. Barbosa-Silva TG, Menezes AM, Bielemann RM, Malmstrom TK, Gonzalez MC, Grupo de Estudos em Composição Corporal e Nutrição (COCONUT). Enhancing SARC-F: improving sarcopenia screening in the clinical practice. J Am Med Dir Assoc. 2016;17(12):1136-1141. doi: https://doi.org/10.1016/j.jamda.2016.08.004
    11. Nguyen TN, Nguyen AT, Khuong LQ, Nguyen TX, Nguyen HTT, Nguyen TTH, Hoang MV, Pham T, Nguyen TN, Vu HTT. Reliability and Validity of SARC-F Questionnaire to Assess Sarcopenia Among Vietnamese Geriatric Patients. Clin Interv Aging. 2020 Jun 9;15:879-886. doi: https://doi.org/10.2147/CIA.S254397
    12. Woo J, Leung J, Morley JE. Validating the SARC-F: a suitable community screening tool for sarcopenia? J Am Med Dir Assoc. 2014;15(9):630-634. doi: https://doi.org/10.1016/j.jamda.2014.04.021
    13. Krzymińska-Siemaszko R, Deskur-Śmielecka E, Kaluźniak-Szymanowska A, Lewandowicz M, Wieczorowska-Tobis K. Comparison of diagnostic performance of SARC-F and its two modified versions (SARC-CalF and SARC-F+EBM) in community-dwelling older adults from Poland. Clin Interv Aging. 2020;15:583-594. doi: https://doi.org/10.2147/CIA.S250508
    14. Jeng C, Zhao LJ, Wu K, Zhou Y, Chen T, Deng HW. Race and socioeconomic effect on sarcopenia and sarcopenic obesity in the Louisiana Osteoporosis Study (LOS). JCSM Clin Rep. 2018 Jul-Dec;3(2):e00027. PMID: 31463425