<?xml version="1.0" encoding="utf-8"?>
<journal>
<title>Caspian Journal of Internal Medicine</title>
<title_fa></title_fa>
<short_title>Caspian J Intern Med</short_title>
<subject>Medical Sciences</subject>
<web_url>http://caspjim.com</web_url>
<journal_hbi_system_id>1</journal_hbi_system_id>
<journal_hbi_system_user>admin</journal_hbi_system_user>
<journal_id_issn>2008-6164</journal_id_issn>
<journal_id_issn_online>2008-6172</journal_id_issn_online>
<journal_id_pii>8</journal_id_pii>
<journal_id_doi>10.22088/cjim</journal_id_doi>
<journal_id_iranmedex></journal_id_iranmedex>
<journal_id_magiran></journal_id_magiran>
<journal_id_sid>14</journal_id_sid>
<journal_id_nlai>8888</journal_id_nlai>
<journal_id_science>13</journal_id_science>
<language>en</language>
<pubdate>
	<type>jalali</type>
	<year>1405</year>
	<month>3</month>
	<day>1</day>
</pubdate>
<pubdate>
	<type>gregorian</type>
	<year>2026</year>
	<month>6</month>
	<day>1</day>
</pubdate>
<volume>17</volume>
<number>3</number>
<publish_type>online</publish_type>
<publish_edition>1</publish_edition>
<article_type>fulltext</article_type>
<articleset>
	<article>


	<language>en</language>
	<article_id_doi></article_id_doi>
	<title_fa></title_fa>
	<title>Serum β2-microglobulin as a marker of renal tubular damage in transfusion-dependent β-thalassemia</title>
	<subject_fa>Nephrology</subject_fa>
	<subject>Nephrology</subject>
	<content_type_fa>Original Article</content_type_fa>
	<content_type>Original Article</content_type>
	<abstract_fa></abstract_fa>
	<abstract>&lt;span style=&quot;font-size:14px;&quot;&gt;&lt;span style=&quot;font-family:Times New Roman;&quot;&gt;&lt;span style=&quot;line-height:14pt&quot;&gt;&lt;b&gt;&lt;i&gt;&lt;span style=&quot;color:blue&quot;&gt;Background: &lt;/span&gt;&lt;/i&gt;&lt;/b&gt;&amp;beta;-thalassemia major is a hereditary disorder characterized by transfusion-dependent anemia and associated complications. In patients with &amp;beta;-thalassemia major, one of the long-term complications of regular blood transfusion is renal dysfunction. This study aimed to evaluate serum &amp;beta;2-microglobulin as a marker of the severity of renal tubular dysfunction and to examine the clinical factors associated with the severity of renal tubular dysfunction in children with &amp;beta;-thalassemia major.&lt;/span&gt;&lt;br&gt;
&lt;span style=&quot;line-height:14pt&quot;&gt;&lt;b&gt;&lt;i&gt;&lt;span style=&quot;color:blue&quot;&gt;Methods: &lt;/span&gt;&lt;/i&gt;&lt;/b&gt;This cross-sectional analytical study was conducted on 134 non-diabetic children with &amp;beta;-thalassemia major who attended thalassemia centers in Mazandaran Province, Iran. Data were collected using a structured checklist that included demographic information, laboratory findings, and clinical parameters. The severity of renal tubular dysfunction was assessed using serum &amp;beta;2-microglobulin levels. Glomerular filtration rate was estimated using the revised Schwartz formula. Pearson correlation analysis was used for statistical analysis.&lt;/span&gt;&lt;br&gt;
&lt;span style=&quot;line-height:14pt&quot;&gt;&lt;b&gt;&lt;i&gt;&lt;span style=&quot;color:blue&quot;&gt;Results: &lt;/span&gt;&lt;/i&gt;&lt;/b&gt;A significant positive correlation was observed between &amp;beta;2-microglobulin levels and age (r = 0.311, p &lt; 0.001), number of blood transfusions per year (r = 0.390, p &lt; 0.001), serum creatinine (r = 0.732, p &lt; 0.001), blood urea nitrogen (r = 0.715, p &lt; 0.001), and serum ferritin (r = 0.505, p &lt; 0.001). In contrast, significant negative correlations were found with serum hemoglobin (r = &amp;minus;0.433, p &lt; 0.001) and creatinine clearance (r = &amp;minus;0.383, p &lt; 0.001).&lt;/span&gt;&lt;br&gt;
&lt;span style=&quot;line-height:14pt&quot;&gt;&lt;b&gt;&lt;i&gt;&lt;span style=&quot;color:blue&quot;&gt;Conclusion: &lt;/span&gt;&lt;/i&gt;&lt;/b&gt;Renal tubular dysfunction in children with &amp;beta;-thalassemia major showed significant correlations with age, iron overload, anemia severity, and transfusion frequency. Serum &amp;beta;2-microglobulin may serve as a useful marker for the early detection of tubular damage and may help guide preventive strategies in clinical practice.&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&lt;br&gt;
&amp;nbsp;</abstract>
	<keyword_fa></keyword_fa>
	<keyword>Beta-thalassemia major, Pediatrics, Renal tubular dysfunction, β2-microglobulin, Iron overload, Biomarker</keyword>
	<start_page>549</start_page>
	<end_page>554</end_page>
	<web_url>http://caspjim.com/browse.php?a_code=A-10-2467-2&amp;slc_lang=en&amp;sid=1</web_url>


<author_list>
	<author>
	<first_name>Roghayeh</first_name>
	<middle_name></middle_name>
	<last_name>Akbari</last_name>
	<suffix></suffix>
	<first_name_fa></first_name_fa>
	<middle_name_fa></middle_name_fa>
	<last_name_fa></last_name_fa>
	<suffix_fa></suffix_fa>
	<email>Roghayeh.akbari@yahoo.com</email>
	<code>100319475328460057784</code>
	<orcid>100319475328460057784</orcid>
	<coreauthor>No</coreauthor>
	<affiliation>Infectious Diseases and Tropical Medicine Research Center, Health Research Institute, Babol University of Medical Sciences, Babol, Iran</affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


	<author>
	<first_name>Hassan</first_name>
	<middle_name></middle_name>
	<last_name>Mahmoodi Nesheli</last_name>
	<suffix></suffix>
	<first_name_fa></first_name_fa>
	<middle_name_fa></middle_name_fa>
	<last_name_fa></last_name_fa>
	<suffix_fa></suffix_fa>
	<email>mahmoodi86@yahoo.com</email>
	<code>100319475328460057785</code>
	<orcid>100319475328460057785</orcid>
	<coreauthor>No</coreauthor>
	<affiliation>Non-Communicable Pediatric Diseases Research Center, Health Research Institute, Babol University of Medical Sciences, Babol, IR Iran</affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


	<author>
	<first_name>Soha</first_name>
	<middle_name></middle_name>
	<last_name>Salehi</last_name>
	<suffix></suffix>
	<first_name_fa></first_name_fa>
	<middle_name_fa></middle_name_fa>
	<last_name_fa></last_name_fa>
	<suffix_fa></suffix_fa>
	<email>smmalekshah@gmail.com</email>
	<code>100319475328460057786</code>
	<orcid>100319475328460057786</orcid>
	<coreauthor>No</coreauthor>
	<affiliation>Student Research Committee, Babol University of Medical Sciences, Babol, Iran</affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


	<author>
	<first_name>Mahmoud</first_name>
	<middle_name></middle_name>
	<last_name>Hajiahmadi</last_name>
	<suffix></suffix>
	<first_name_fa></first_name_fa>
	<middle_name_fa></middle_name_fa>
	<last_name_fa></last_name_fa>
	<suffix_fa></suffix_fa>
	<email>hajiahmadi@yahoo.com</email>
	<code>100319475328460057787</code>
	<orcid>100319475328460057787</orcid>
	<coreauthor>No</coreauthor>
	<affiliation>Clinical Research Development Unit of Amirkola Children&#039;s Hospital, Babol University of Medical Sciences, Babol, Iran</affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


	<author>
	<first_name>Sahar</first_name>
	<middle_name></middle_name>
	<last_name>Sadr Moharerpour</last_name>
	<suffix></suffix>
	<first_name_fa></first_name_fa>
	<middle_name_fa></middle_name_fa>
	<last_name_fa></last_name_fa>
	<suffix_fa></suffix_fa>
	<email>drsaharsadr@gmail.com</email>
	<code>100319475328460057788</code>
	<orcid>100319475328460057788</orcid>
	<coreauthor>Yes
</coreauthor>
	<affiliation>Non-Communicable Pediatric Diseases Research Center, Health Research Institute, Babol University of Medical Sciences, Babol, IR Iran</affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


</author_list>


	</article>
</articleset>
</journal>
