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Research Article | Volume 15 Issue 5 (May, 2025) | Pages 869 - 872
A Cross - Sectional Study on the Prevalence and Risk Factors of Non-alcoholic Fatty Liver Disease Among Patients with Type 2 Diabetes Mellitus
 ,
 ,
1
Associate Professor, Department of General Medicine, Government Medical College, Suryapet, Telangana, India
2
Associate Professor, Department of General Medicine, Government Medical College, Khammam, Telangana, India
Under a Creative Commons license
Open Access
Received
March 28, 2025
Revised
April 23, 2025
Accepted
April 27, 2025
Published
May 13, 2025
Abstract

Background: Non-alcoholic fatty liver disease (NAFLD) is a common comorbidity among patients with Type 2 Diabetes Mellitus (T2DM) and is increasingly recognized as a hepatic manifestation of metabolic syndrome. Identifying its prevalence and associated risk factors in diabetic populations is essential for early intervention and management. Objectives: To determine the prevalence of NAFLD among patients with T2DM and to evaluate the associated clinical and metabolic risk factors. Methods: This cross-sectional study was conducted on 100 adult patients with T2DM attending the outpatient department of a tertiary care hospital. NAFLD was diagnosed using abdominal ultrasonography. Demographic and clinical data, including BMI, duration of diabetes, HbA1c levels, and other metabolic parameters, were recorded. Statistical analysis was performed to identify significant associations, and multivariate logistic regression was used to determine independent predictors. Results: The prevalence of NAFLD was found to be 56%. Higher prevalence was observed in males (62.5%) compared to females (50.0%). Significant associations were noted with BMI ≥25 kg/m² (66.2% vs 26.9%, p<0.001), diabetes duration ≥10 years (68.1% vs 45.3%, p=0.009), and HbA1c ≥7% (61.8% vs 37.5%, p=0.006). On multivariate analysis, BMI ≥25 kg/m² (OR=3.6), HbA1c ≥7% (OR=2.9), and diabetes duration ≥10 years (OR=2.4) were independent predictors of NAFLD. Conclusion: NAFLD is highly prevalent among patients with T2DM. Obesity, poor glycemic control, and longer duration of diabetes are significant risk factors. Routine screening and metabolic optimization are recommended to prevent hepatic complications.

Keywords
INTRODUCTION

Non-alcoholic fatty liver disease (NAFLD) has emerged as the most common chronic liver disorder worldwide, encompassing a spectrum of liver abnormalities ranging from simple hepatic steatosis to non-alcoholic steatohepatitis (NASH), fibrosis, and cirrhosis in individuals with little or no alcohol intake1,2. NAFLD is increasingly recognized as the hepatic manifestation of metabolic syndrome and is closely linked with obesity, insulin resistance, dyslipidemia, and particularly Type 2 Diabetes Mellitus (T2DM)3.

 

The global prevalence of NAFLD is estimated to be around 25%, but this figure rises significantly among patients with T2DM, reaching up to 55–70% in various studies. T2DM accelerates the progression of NAFLD, increasing the risk of advanced fibrosis, cirrhosis, and hepatocellular carcinoma4. The bidirectional relationship between NAFLD and T2DM not only complicates metabolic control but also increases cardiovascular morbidity and all-cause mortality5,6.

 

Despite the growing burden of NAFLD in diabetic populations, it remains underdiagnosed, especially in resource-limited settings, due to the absence of overt symptoms and limited use of imaging in routine diabetic care. Identifying patients at risk using non-invasive methods like abdominal ultrasonography and evaluating associated risk factors are vital steps toward early detection, lifestyle modification, and prevention of long-term hepatic complications.

 

This study was undertaken to determine the prevalence of NAFLD in patients with T2DM attending a tertiary care hospital and to identify clinical and biochemical risk factors associated with its occurrence. The findings aim to contribute to improved screening protocols and patient education in diabetic care.

METHODOLOGY

Study Design and Setting:
This was a hospital-based, cross-sectional observational study conducted in the Department of General Medicine at Government Medical College (GMC), Suryapet. The study was carried out over a period of nine months, from May 2024 to January 2025.

 

Study Population:
The study included adult patients (aged ≥18 years) with a confirmed diagnosis of Type 2 Diabetes Mellitus (T2DM) attending the outpatient and inpatient services of GMC Suryapet during the study period.

 

Inclusion Criteria:

Patients diagnosed with T2DM for at least one year.

Age ≥18 years.

 

Patients who gave written informed consent.

 

Exclusion Criteria:

History of significant alcohol consumption (>20 g/day for men, >10 g/day for women).

 

Known chronic liver diseases (viral hepatitis, autoimmune hepatitis, Wilson’s disease, etc.).

 

Use of hepatotoxic drugs (e.g., methotrexate, tamoxifen, amiodarone).

Pregnancy.

 

Patients with Type 1 Diabetes Mellitus.

 

Sample Size:
A total of 100 eligible patients with T2DM were included in the study by convenient sampling.

 

Data Collection:
Demographic and clinical data including age, gender, BMI, duration of diabetes, and presence of comorbidities (hypertension, dyslipidemia) were recorded. Laboratory parameters such as fasting blood glucose, postprandial glucose, HbA1c, lipid profile, and liver function tests were documented.

 

Diagnosis of NAFLD:
NAFLD was diagnosed using abdominal ultrasonography, performed by an experienced radiologist. The diagnosis was based on characteristic features of hepatic steatosis, including increased echogenicity of the liver parenchyma with posterior beam attenuation and loss of visualization of intrahepatic vessels.

 

Statistical Analysis:
Data were entered in Microsoft Excel and analyzed using SPSS version 25. Descriptive statistics were used for demographic variables. Associations between NAFLD and risk factors were assessed using Chi-square test for categorical variables and independent t-test for continuous variables. Multivariate logistic regression was performed to identify independent predictors of NAFLD. A p-value <0.05 was considered statistically significant.

 

Ethical Considerations:
The study was approved by the Institutional Ethics Committee of Government Medical College, Suryapet. Written informed consent was obtained from all participants prior to inclusion.

RESULTS

Out of the 100 patients with Type 2 Diabetes Mellitus (T2DM) enrolled in the study, 56% were diagnosed with Non-Alcoholic Fatty Liver Disease (NAFLD) based on ultrasonographic findings. The prevalence was higher among males (62.5%) compared to females (50.0%) (Table 1).

 

Table 1: Prevalence of NAFLD by Gender

Gender

NAFLD Present (n)

NAFLD Absent (n)

Total (n)

Prevalence (%)

Male

30

18

48

62.5

Female

26

26

52

50.0

Total

56

44

100

56.0

 

Body Mass Index (BMI) showed a strong association with NAFLD. Among patients with BMI ≥25 kg/m², the prevalence of NAFLD was significantly higher (66.2%) compared to those with BMI <25 kg/m² (26.9%) (Table 2). This difference was statistically significant and suggests that overweight and obesity are major contributing factors to hepatic fat accumulation.

 

Table 2: Association of NAFLD with Body Mass Index (BMI)

BMI Category

NAFLD Present (n)

NAFLD Absent (n)

Total (n)

Prevalence (%)

< 25 kg/m²

7

19

26

26.9

≥ 25 kg/m²

49

25

74

66.2

Total

56

44

100

56.0

 

Duration of diabetes also demonstrated a notable relationship with NAFLD. Patients with a diabetes duration of ≥10 years exhibited a higher prevalence of NAFLD (68.1%) compared to those with <10 years of disease (45.3%) (Table 3).

 

Table 3: NAFLD Prevalence by Duration of Diabetes

Duration of Diabetes

NAFLD Present (n)

NAFLD Absent (n)

Total (n)

Prevalence (%)

< 10 years

24

29

53

45.3

≥ 10 years

32

15

47

68.1

Total

56

44

100

56.0

This indicates that chronicity of hyperglycemia may exacerbate hepatic steatosis over time.

 

In terms of glycemic control, NAFLD was more prevalent in patients with poor glycemic status (HbA1c ≥7%), with a prevalence of 61.8%, compared to 37.5% in those with HbA1c <7% (Table 4). This supports the hypothesis that persistent hyperglycemia is a significant contributor to the development of hepatic fat accumulation.

 

Table 4: Association of HbA1c with NAFLD

HbA1c Level

NAFLD Present (n)

NAFLD Absent (n)

Total (n)

Prevalence (%)

< 7%

9

15

24

37.5

≥ 7%

47

29

76

61.8

Total

56

44

100

56.0

 

On multivariate logistic regression analysis, three variables emerged as statistically significant independent predictors of NAFLD: BMI ≥25 kg/m² (OR: 3.6; 95% CI: 1.5–8.6; p=0.004), HbA1c ≥7% (OR: 2.9; 95% CI: 1.2–6.9; p=0.014), and duration of diabetes ≥10 years (OR: 2.4; 95% CI: 1.0–5.8; p=0.041) (Table 5).

 

Table 5: Multivariate Logistic Regression Analysis of Risk Factors for NAFLD

Variable

Odds Ratio (OR)

95% Confidence Interval

P-value

BMI ≥ 25 kg/m²

3.6

1.5 – 8.6

0.004

HbA1c ≥ 7%

2.9

1.2 – 6.9

0.014

Duration ≥ 10 years

2.4

1.0 – 5.8

0.041

 

These findings highlight the multifactorial nature of NAFLD in patients with T2DM, with obesity, poor glycemic control, and longer disease duration being the primary determinants in this cohort.

CONCLUSION

In this cross-sectional study conducted at Government Medical College, Suryapet, we found that 56% of patients with Type 2 Diabetes Mellitus (T2DM) had sonographic evidence of Non-Alcoholic Fatty Liver Disease (NAFLD). This prevalence aligns with findings from earlier studies which report NAFLD prevalence rates of 50–70% among diabetic populations. The high burden observed in our study reinforces the strong interrelationship between hepatic steatosis and T2DM.

 

Male predominance in NAFLD prevalence (62.5%) is consistent with prior literature, possibly due to gender-related differences in visceral adiposity and hormonal profiles. Obesity emerged as a major risk factor, with 66.2% of overweight/obese patients (BMI ≥25 kg/m²) showing evidence of NAFLD. This corroborates existing evidence that insulin resistance associated with obesity plays a central role in hepatic fat accumulation7,8.

 

We also observed a significantly higher prevalence of NAFLD in patients with longer duration of diabetes (≥10 years) and those with poor glycemic control (HbA1c ≥7%), findings echoed by studies such as those by Leite et al. and Targher et al., where prolonged hyperglycemia and insulin resistance have been implicated in the pathogenesis and progression of NAFLD9.

 

Our multivariate logistic regression analysis confirmed BMI ≥25 kg/m², HbA1c ≥7%, and diabetes duration ≥10 years as independent predictors of NAFLD. These factors should prompt clinicians to actively screen for hepatic involvement in T2DM patients even in the absence of clinical symptoms10.

 

The non-invasive and cost-effective utility of ultrasonography makes it a practical tool in routine diabetic care, particularly in low-resource settings like ours. Early identification can allow for lifestyle interventions and pharmacologic strategies to reverse or arrest disease progression11.

 

Limitations of this study include its single-center design and relatively small sample size, which may affect generalizability. Additionally, ultrasonography, though practical, is operator-dependent and less sensitive for early or mild steatosis compared to MRI or liver biopsy.

CONCLUSION

This cross-sectional study highlights a high prevalence of Non-Alcoholic Fatty Liver Disease (NAFLD) among patients with Type 2 Diabetes Mellitus (T2DM), with more than half of the studied population affected. Obesity, poor glycemic control (HbA1c ≥7%), and longer duration of diabetes (≥10 years) were identified as significant and independent risk factors. These findings underscore the need for routine screening of NAFLD in diabetic patients, especially those with additional metabolic risk factors. Early detection through ultrasonography can facilitate timely lifestyle modifications and appropriate interventions, potentially reducing the burden of hepatic and cardiovascular complications. Integration of NAFLD assessment into diabetic care protocols is strongly recommended.

REFERENCES
  1. Yi M, Chen RP, Yang R, et al. Increased prevalence and risk of non-alcoholic fatty liver disease in overweight and obese patients with type 2 diabetes in South China. Diabet Med. 2017;34(4):505–13.
  2. Targher G, Byrne CD. Metabolically healthy obesity and NAFLD. Nat Rev Gastroenterol Hepatol. 2016;13(8):442–4.
  3. Mantovani A, Grani G. Thyroid dysfunction and nonalcoholic fatty liver disease: we need new larger and well-designed longitudinal studies. Dig Dis Sci. 2018;63(8):1970–6.
  4. Bohte AE, van Werven JR, Bipat S, et al. The diagnostic accuracy of US, CT, MRI and 1H-MRS for the evaluation of hepatic steatosis compared with liver biopsy: a meta-analysis. Eur Radiol. 2011;21(1):87–97.
  5. Alizadeh A, Mansour-Ghanaei F, Roozdar A, et al. Laboratory tests, liver vessels color doppler sonography, and fibroscan findings in patients with nonalcoholic fatty liver disease: an observation study. J Clin Imaging Sci. 2018;8:13.
  6. Doycheva I, Cui J, Nguyen P, et al. Non-invasive screening of diabetics in primary care for NAFLD and advanced fibrosis by MRI and MRE. Aliment Pharmacol Ther. 2016;43(1):83–95.
  7. Pais R, Charlotte F, Fedchuk L, et al. A systematic review of follow-up biopsies reveals disease progression in patients with non-alcoholic fatty liver. J Hepatol. 2013;59(3):550–6.
  8. Takeuchi Y, Ito H, Komatsu Y, et al. Non-alcoholic fatty liver disease is an independent predictor for macroangiopathy in Japanese type 2 diabetic patients: a cross-sectional study. Intern Med. 2012;51(13):1667–75.
  9. Motamed N, Rabiee B, Hemasi GR, et al. Body roundness index and waist-to-height ratio are strongly associated with non-alcoholic fatty liver disease: a population-based study. Hepat Mon. 2016;16(10):e39575.
  10. Zhou Q, Wang Y, Wang J, Liu Y, Qi D, Yao W, Jiang H, Li T, Huang K, Zhang W, Huo X. Prevalence and risk factor analysis for the nonalcoholic fatty liver disease in patients with type 2 diabetes mellitus. Medicine (Baltimore). 2021 Mar 12;100(10):e24940. doi: 10.1097/MD.0000000000024940. PMID: 33725855; PMCID: PMC7969325.
  11. Alsabaani AA, Mahfouz AA, Awadalla NJ, Musa MJ, Al Humayed SM. Non-Alcoholic Fatty Liver Disease among Type-2 Diabetes Mellitus Patients in Abha City, South Western Saudi Arabia. Int J Environ Res Public Health. 2018 Nov 11;15(11):2521. doi: 10.3390/ijerph15112521. PMID: 30423871; PMCID: PMC6266142.
  12. Zhou Q, Wang Y, Wang J, Liu Y, Qi D, Yao W, Jiang H, Li T, Huang K, Zhang W, Huo X. Prevalence and risk factor analysis for the nonalcoholic fatty liver disease in patients with type 2 diabetes mellitus. Medicine (Baltimore). 2021 Mar 12;100(10):e24940. doi: 10.1097/MD.0000000000024940. PMID: 33725855; PMCID: PMC7969325.
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