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<records>

  <record>
    <language>eng</language>
          <publisher>Oriental Scientific Publishing Company</publisher>
        <journalTitle>Biomedical and Pharmacology Journal</journalTitle>
          <issn>0974-6242</issn>
            <publicationDate>2025-06-30</publicationDate>
    
        <volume>18</volume>
        <issue>2</issue>

 
    <startPage>1545</startPage>
    <endPage>1558</endPage>

	 
      <doi>10.13005/bpj/3192</doi>
        <publisherRecordId>65889</publisherRecordId>
    <documentType>article</documentType>
    <title language="eng">Effect of Semaglutide Add-on to Metformin on Visceral Adiposity Index and Markers of Visceral Adipose Tissue Activity in Type 2 Diabetic Patients</title>

    <authors>
	 


      <author>
       <name>Abid Shaheer</name>

 
		
	<affiliationId>1</affiliationId>
      </author>
    

	 


      <author>
       <name>Mahir Jallo</name>


		
	<affiliationId>2</affiliationId>

      </author>
    

	 


      <author>
       <name>Shahid Akhtar</name>

		
	<affiliationId>3</affiliationId>
      </author>
    

	


	


	
    </authors>
    
	    <affiliationsList>
	    
		
		<affiliationName affiliationId="1">Department of Biomedical Sciences, College of Medicine, Gulf Medical University, United Arab Emirates.</affiliationName>
    

		
		<affiliationName affiliationId="2">Department of Internal Medicine, Thumbay University Hospital, United Arab Emirates. </affiliationName>
    
		
		<affiliationName affiliationId="3">Department of Clinical Biochemistry, Thumbay Labs, United Arab Emirates</affiliationName>
    
		
		
		
	  </affiliationsList>






    <abstract language="eng">The objective of the study was to find out the effect of semaglutide add-on to metformin on the visceral adiposity index and markers of visceral adipose tissue activity in type 2 diabetic patients based on body mass. A total of 90 patients with type 2 diabetes (both genders aged 30-60 years) were included in the study. The participants were divided into three groups based on their Body Mass Index (BMI), which includes the subjects with normal body weight (BMI between 18.5 - 24.9 kg/m<sup>2</sup>), overweight (BMI between 25 - 29.9 kg/m<sup>2</sup>) and obesity (BMI ≥30 kg/m<sup>2</sup>). Enzyme-linked immunosorbent assay was used to analyze serum leptin and adiponectin. Visceral Adiposity Index (VAI) was determined by the formula: Waist Circumference/(39.68 + [1.88 × BMI]) × Triglycerides/1.03 × 1.31/High-Density Lipoproteins. VAI showed minimal changes with metformin alone but decreased significantly with semaglutide add-on (p &lt; 0.05), with the greatest reduction in the obesity group (-0.70). Leptin levels remained unchanged after metformin but significantly declined following semaglutide treatment (p &lt; 0.05). The reduction was most pronounced in the obesity group (-5.10 ng/mL), followed by overweight (-3.40 ng/mL) and normal-weight individuals (-2.60 ng/mL). Adiponectin levels increased significantly post-semaglutide add-on therapy (p &lt; 0.05). The greatest increase was observed in the obesity group (+3.70 μg/mL), followed by overweight (+3.30 μg/mL) and normal-weight participants (+3.30 μg/mL). Semaglutide presents a promising long-term solution for reducing the visceral adiposity index and enhancing metabolic health by modulating markers of visceral fat activity in patients with poorly controlled type 2 diabetes. This study highlights the importance of personalized treatment approaches, suggesting that semaglutide can be strategically utilized to prevent excess fat accumulation in the abdominal cavity.</abstract>

    <fullTextUrl format="html">https://biomedpharmajournal.org/vol18no2/effect-of-semaglutide-add-on-to-metformin-on-visceral-adiposity-index-and-markers-of-visceral-adipose-tissue-activity-in-type-2-diabetic-patients/</fullTextUrl>

<keywords language="eng">

      
        <keyword>Adipokine</keyword>
      

      
        <keyword> Adiponectin</keyword>
      

      
        <keyword> Diabetes</keyword>
      

      
        <keyword> Leptin</keyword>
      

      
        <keyword> Obesity</keyword>
      
</keywords>
  </record>
</records>