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Semmelweis University | Molecular Medicine Research Group - Academia.edu
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var $lessLink = $(".js-mobile-nav-collapse-trigger"); var $section = $('.js-mobile-nav-expand-section'); $moreLink.click(function(ev){ ev.preventDefault(); $moreLink.hide(); $lessLink.show(); $section.collapse('show'); }); $lessLink.click(function(ev){ ev.preventDefault(); $moreLink.show(); $lessLink.hide(); $section.collapse('hide'); }); })() if ($a.is_logged_in() || false) { new Aedu.NavigationController({ el: '.js-main-nav', showHighlightedNotification: false }); } else { $(".js-header-login-url").attr("href", $a.loginUrlWithRedirect()); } Aedu.autocompleteSearch = new AutocompleteSearch({el: '.js-SiteSearch-form'});</script></div></div> <div id='site' class='fixed'> <div id="content" class="clearfix"> <script>document.addEventListener('DOMContentLoaded', function(){ var $dismissible = $(".dismissible_banner"); $dismissible.click(function(ev) { $dismissible.hide(); }); });</script> <div class="DesignSystem" style="margin-top:-40px"><div class="PageHeader"><div class="container"><div class="row"><div class="col-xs-12 clearfix"><div class="u-floatLeft u-fs24 u-tcGrayDarkest"><span class="PageHeader-title u-m0x u-fw700 u-mr5x u-pr5x u-borderColorGrayLight u-borderRight1"><a href="https://sote.academia.edu/"><span class="u-linkUnstyled u-tcGrayDarkest">Semmelweis University</span></a></span><h1 class="u-m0x u-fw300 u-fs24 u-displayInline">Molecular Medicine Research Group</h1></div><div class="u-floatRight u-mt1x"></div></div></div></div></div><div class="TabbedNavigation"><div class="container"><div class="row"><div class="col-xs-12 clearfix"><ul class="nav u-m0x u-p0x list-inline"><li class="u-floatLeft u-pr5x u-mr5x u-borderColorGrayLight u-borderRight1"><a href="https://sote.academia.edu/"><span><i class="fa fa-arrow-left"></i> All Departments</span></a></li><li class="u-floatLeft active"><a href="https://sote.academia.edu/Departments/Molecular_Medicine_Research_Group/Documents">11 Papers</a></li><li class="u-floatLeft"><a href="https://sote.academia.edu/Departments/Molecular_Medicine_Research_Group">1 Researchers</a></li></ul></div></div></div></div><div class="container"><div class="row"><div class="col-xs-12"><div class="u-displayFlex"><div class="u-flexGrow1"><div class="u-ph0x"><div class="works"><div class="u-borderBottom1 u-borderColorGrayLighter"><div class="clearfix u-pv7x u-mb0x js-work-card work_24511069 coauthored" data-work_id="24511069" itemscope="itemscope" itemtype="https://schema.org/ScholarlyArticle"><div class="header"><div class="title u-fontSerif u-fs22 u-lineHeight1_3"><a class="u-tcGrayDarkest js-work-link" href="https://www.academia.edu/24511069/Common_Genetic_Variants_of_the_Human_Steroid_21_Hydroxylase_Gene_CYP21A2_Are_Related_to_Differences_in_Circulating_Hormone_Levels">Common Genetic Variants of the Human Steroid 21- Hydroxylase Gene (CYP21A2) Are Related to Differences in Circulating Hormone Levels</a></div></div><div class="u-pb4x u-mt3x"><div class="summary u-fs14 u-fw300 u-lineHeight1_5 u-tcGrayDarkest"><div class="summarized">Purpose: Systematic evaluation of the potential relationship between the common genetic variants of CYP21A2 and hormone levels. Methods: The relationships of CYP21A2 intron 2 polymorphisms and haplotypes with diverse baseline and... <a class="more_link u-tcGrayDark u-linkUnstyled" data-container=".work_24511069" data-show=".complete" data-hide=".summarized" data-more-link-behavior="true" href="#">more</a></div><div class="complete hidden">Purpose: Systematic evaluation of the potential relationship between the common genetic variants of CYP21A2 and hormone levels. Methods: The relationships of CYP21A2 intron 2 polymorphisms and haplotypes with diverse baseline and stimulated blood hormone levels were studied in 106 subjects with non-functioning adrenal incidentaloma (NFAI). The rationale for using NFAI subjects is dual: i) their baseline hormone profiles do not differ from those of healthy subjects and ii) hormone levels after stimulation tests are available. Results: The carriers (N = 27) of a well-defined CYP21A2 haplotype cluster (c5) had significantly elevated levels of cortisol (p = 0.0110), and 17-hydroxyprogesterone (p = 0.0001) after ACTH stimulation, and 11-deoxycortisol after metyrapone administration (p = 0.0017), but the hormone values were in normal ranges. In addition, the carriers (N = 33) of the C allele of the rs6462 polymorphism had a higher baseline aldosterone level (p = 0.0006). The prevalence of these genetic variants of CYP21A2 did not differ between NFAI and healthy subjects. Conclusions: The common CYP21A2 variants presumably exert the same effect on hormone levels in the healthy and disease-affected populations. Therefore, they may contribute to complex diseases such as some cardiovascular diseases, and may influence the genotype-phenotype correlation in patients with congenital adrenal hyperplasia (CAH) including the individual need for hormone substitution.</div></div></div><ul class="InlineList u-ph0x u-fs13"><li class="InlineList-item logged_in_only"><div class="share_on_academia_work_button"><a class="academia_share Button Button--inverseBlue Button--sm js-bookmark-button" data-academia-share="Work/24511069" data-share-source="work_strip" data-spinner="small_white_hide_contents"><i class="fa fa-plus"></i><span class="work-strip-link-text u-ml1x" data-content="button_text">Bookmark</span></a></div></li><li class="InlineList-item"><div class="download"><a id="51370109d3b4fbb421d40274591bca5f" rel="nofollow" data-download="{"attachment_id":44843265,"asset_id":24511069,"asset_type":"Work","always_allow_download":false,"track":null,"button_location":"work_strip","source":null,"hide_modal":null}" class="Button Button--sm Button--inverseGreen js-download-button prompt_button doc_download" href="https://www.academia.edu/attachments/44843265/download_file?st=MTczMjc2NTc5OCw4LjIyMi4yMDguMTQ2&s=work_strip"><i class="fa fa-arrow-circle-o-down fa-lg"></i><span class="u-textUppercase u-ml1x" data-content="button_text">Download</span></a></div></li><li class="InlineList-item"><ul class="InlineList InlineList--bordered u-ph0x"><li class="InlineList-item InlineList-item--bordered"><span class="InlineList-item-text">by <span itemscope="itemscope" itemprop="author" itemtype="https://schema.org/Person"><a class="u-tcGrayDark u-fw700" data-has-card-for-user="46696509" href="https://sote.academia.edu/MartonDoleschall">Marton Doleschall</a><script data-card-contents-for-user="46696509" type="text/json">{"id":46696509,"first_name":"Marton","last_name":"Doleschall","domain_name":"sote","page_name":"MartonDoleschall","display_name":"Marton Doleschall","profile_url":"https://sote.academia.edu/MartonDoleschall","photo":"/images/s65_no_pic.png"}</script></span></span><span class="u-displayInlineBlock InlineList-item-text"> and <span class="u-textDecorationUnderline u-clickable InlineList-item-text js-work-more-authors-24511069">+1</span><div class="hidden js-additional-users-24511069"><div><span itemscope="itemscope" itemprop="author" itemtype="https://schema.org/Person"><a href="https://sote.academia.edu/KlaraKoncz">Klara Koncz</a></span></div></div></span><script>(function(){ var popoverSettings = { el: $('.js-work-more-authors-24511069'), placement: 'bottom', hide_delay: 200, html: true, content: function(){ return $('.js-additional-users-24511069').html(); 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Methods: The relationships of CYP21A2 intron 2 polymorphisms and haplotypes with diverse baseline and stimulated blood hormone levels were studied in 106 subjects with non-functioning adrenal incidentaloma (NFAI). The rationale for using NFAI subjects is dual: i) their baseline hormone profiles do not differ from those of healthy subjects and ii) hormone levels after stimulation tests are available. Results: The carriers (N = 27) of a well-defined CYP21A2 haplotype cluster (c5) had significantly elevated levels of cortisol (p = 0.0110), and 17-hydroxyprogesterone (p = 0.0001) after ACTH stimulation, and 11-deoxycortisol after metyrapone administration (p = 0.0017), but the hormone values were in normal ranges. In addition, the carriers (N = 33) of the C allele of the rs6462 polymorphism had a higher baseline aldosterone level (p = 0.0006). The prevalence of these genetic variants of CYP21A2 did not differ between NFAI and healthy subjects. Conclusions: The common CYP21A2 variants presumably exert the same effect on hormone levels in the healthy and disease-affected populations. Therefore, they may contribute to complex diseases such as some cardiovascular diseases, and may influence the genotype-phenotype correlation in patients with congenital adrenal hyperplasia (CAH) including the individual need for hormone substitution.","publication":null,"publication_with_fallback":"PLOS ONE","downloadable_attachments":[{"id":44843265,"asset_id":24511069,"asset_type":"Work","always_allow_download":false,"scribd_thumbnail_url":"https://attachments.academia-assets.com/44843265/thumbnails/1.jpg","download_url":"https://d1wqtxts1xzle7.cloudfront.net/44843265/CYP21A2_incidentaloma_Doleschall__2014-libre.pdf?1460963345=\u0026response-content-disposition=attachment%3B+filename%3DCommon_Genetic_Variants_of_the_Human_Ste.pdf\u0026Expires=1732766622\u0026Signature=YUgwaaqRdItm7neOZh4JOcU~0-5TW7a2wiDDG8dCw9an5Ak~DjTJKthwlk~DLLYEeRStxsbu~lT8WpX5hzC-9ThIeP2xYOVhIf~X3KY1n1GsvBnx~nVCadZ5ti1HtB~wz4nYQYpGe3qVNn4PzYg0TLIDIE~wBXK7l0foULsCb7~NnXhCvJhLr-q1c-cGQqdg-P3kolM4R7crVR-GlK3vl7hf32spWwAos9Xpdcd6v5IFkZqeeaYCikPe6xgfXJ4uXU8Dv8J2ie7baP~4~bunWYDQNSH6kIWYmOEGOT1V0sTgbvrKDiPD9iVjSQ7FQpJH1X4wbUDrmQOZhbHyIuez2g__\u0026Key-Pair-Id=APKAJLOHF5GGSLRBV4ZA","download_file_url":"https://www.academia.edu/attachments/44843265/download_file?st=MTczMjc2NTc5OCw4LjIyMi4yMDguMTQ2&","full_thumbnail_url":"https://0.academia-photos.com/attachment_thumbnails/44843265/mini_magick20220704-26657-lttrdb.png?1656938725"}],"downloadable_attachments_with_full_thumbnails":[{"id":44843265,"asset_id":24511069,"asset_type":"Work","always_allow_download":false,"scribd_thumbnail_url":"https://attachments.academia-assets.com/44843265/thumbnails/1.jpg","download_url":"https://d1wqtxts1xzle7.cloudfront.net/44843265/CYP21A2_incidentaloma_Doleschall__2014-libre.pdf?1460963345=\u0026response-content-disposition=attachment%3B+filename%3DCommon_Genetic_Variants_of_the_Human_Ste.pdf\u0026Expires=1732766622\u0026Signature=YUgwaaqRdItm7neOZh4JOcU~0-5TW7a2wiDDG8dCw9an5Ak~DjTJKthwlk~DLLYEeRStxsbu~lT8WpX5hzC-9ThIeP2xYOVhIf~X3KY1n1GsvBnx~nVCadZ5ti1HtB~wz4nYQYpGe3qVNn4PzYg0TLIDIE~wBXK7l0foULsCb7~NnXhCvJhLr-q1c-cGQqdg-P3kolM4R7crVR-GlK3vl7hf32spWwAos9Xpdcd6v5IFkZqeeaYCikPe6xgfXJ4uXU8Dv8J2ie7baP~4~bunWYDQNSH6kIWYmOEGOT1V0sTgbvrKDiPD9iVjSQ7FQpJH1X4wbUDrmQOZhbHyIuez2g__\u0026Key-Pair-Id=APKAJLOHF5GGSLRBV4ZA","download_file_url":"https://www.academia.edu/attachments/44843265/download_file?st=MTczMjc2NTc5OCw4LjIyMi4yMDguMTQ2&","full_thumbnail_url":"https://0.academia-photos.com/attachment_thumbnails/44843265/mini_magick20220704-26657-lttrdb.png?1656938725"}],"has_pdf":true,"has_fulltext":true,"page_count":10,"ordered_authors":[{"id":46696509,"first_name":"Marton","last_name":"Doleschall","domain_name":"sote","page_name":"MartonDoleschall","display_name":"Marton Doleschall","profile_url":"https://sote.academia.edu/MartonDoleschall","photo":"/images/s65_no_pic.png"},{"id":47491285,"first_name":"Klara","last_name":"Koncz","domain_name":"sote","page_name":"KlaraKoncz","display_name":"Klara Koncz","profile_url":"https://sote.academia.edu/KlaraKoncz","photo":"/images/s65_no_pic.png"}],"research_interests":[{"id":1135,"name":"Human Genetics","url":"https://www.academia.edu/Documents/in/Human_Genetics","nofollow":false},{"id":24856,"name":"STEROIDS","url":"https://www.academia.edu/Documents/in/STEROIDS","nofollow":false},{"id":74235,"name":"Copy Number Variation of DNA","url":"https://www.academia.edu/Documents/in/Copy_Number_Variation_of_DNA","nofollow":false},{"id":589853,"name":"Adrenal Gland","url":"https://www.academia.edu/Documents/in/Adrenal_Gland","nofollow":false},{"id":1399723,"name":"Steroid","url":"https://www.academia.edu/Documents/in/Steroid"}],"publication_year":null,"publication_year_with_fallback":2014,"paper_rank":null,"all_time_views":22,"active_discussion":{}}, }) } })();</script></ul></li></ul></div></div><div class="u-borderBottom1 u-borderColorGrayLighter"><div class="clearfix u-pv7x u-mb0x js-work-card work_24554752" data-work_id="24554752" itemscope="itemscope" itemtype="https://schema.org/ScholarlyArticle"><div class="header"><div class="title u-fontSerif u-fs22 u-lineHeight1_3"><a class="u-tcGrayDarkest js-work-link" href="https://www.academia.edu/24554752/Intraspecific_Evolution_of_Human_RCCX_Copy_Number_Variation_Traced_by_Haplotypes_of_the_CYP21A2_Gene">Intraspecific Evolution of Human RCCX Copy Number Variation Traced by Haplotypes of the CYP21A2 Gene</a></div></div><div class="u-pb4x u-mt3x"><div class="summary u-fs14 u-fw300 u-lineHeight1_5 u-tcGrayDarkest"><div class="summarized">The RCCX region is a complex, multiallelic, tandem copy number variation (CNV). Two complete genes, complement component 4 (C4) and steroid 21-hydroxylase (CYP21A2, formerly CYP21B), reside in its variable region. RCCX is prone to... <a class="more_link u-tcGrayDark u-linkUnstyled" data-container=".work_24554752" data-show=".complete" data-hide=".summarized" data-more-link-behavior="true" href="#">more</a></div><div class="complete hidden">The RCCX region is a complex, multiallelic, tandem copy number variation (CNV). Two complete genes, complement component 4 (C4) and steroid 21-hydroxylase (CYP21A2, formerly CYP21B), reside in its variable region. RCCX is prone to nonallelic homologous recombination (NAHR) such as unequal crossover, generating duplications and deletions of RCCX modules, and gene conversion. A series of allele-specific long-range polymerase chain reaction coupled to the whole-gene sequencing of CYP21A2 was developed for molecular haplotyping. By means of the developed techniques, 35 different kinds of CYP21A2 haplotype variant were experimentally determined from 112 unrelated European subjects. The number of the resolved CYP21A2 haplotype variants was increased to 61 by bioinformatic haplotype reconstruction. The CYP21A2 haplotype variants could be assigned to the haplotypic RCCX CNV structures (the copy number of RCCX modules) in most cases. The genealogy network constructed from the CYP21A2 haplotype variants delineated the origin of RCCX structures. The different RCCX structures were located in tight groups. The minority of groups with identical RCCX structure occurred once in the network, implying monophyletic origin, but the majority of groups occurred several times and in different locations, indicating polyphyletic origin. The monophyletic groups were often created by single unequal crossover, whereas recurrent unequal crossover events generated some of the polyphyletic groups. As a result of recurrent NAHR events, more CYP21A2 haplotype variants with different allele patterns belonged to the same RCCX structure. The intraspecific evolution of RCCX CNV described here has provided a reasonable expectation for that of complex, multiallelic, tandem CNVs in humans.</div></div></div><ul class="InlineList u-ph0x u-fs13"><li class="InlineList-item logged_in_only"><div class="share_on_academia_work_button"><a class="academia_share Button Button--inverseBlue Button--sm js-bookmark-button" data-academia-share="Work/24554752" data-share-source="work_strip" data-spinner="small_white_hide_contents"><i class="fa fa-plus"></i><span class="work-strip-link-text u-ml1x" data-content="button_text">Bookmark</span></a></div></li><li class="InlineList-item"><div class="download"><a id="fd83579278e54b73b7979089a964dda6" rel="nofollow" data-download="{"attachment_id":44884827,"asset_id":24554752,"asset_type":"Work","always_allow_download":false,"track":null,"button_location":"work_strip","source":null,"hide_modal":null}" class="Button Button--sm Button--inverseGreen js-download-button prompt_button doc_download" href="https://www.academia.edu/attachments/44884827/download_file?st=MTczMjc2NTc5OCw4LjIyMi4yMDguMTQ2&s=work_strip"><i class="fa fa-arrow-circle-o-down fa-lg"></i><span class="u-textUppercase u-ml1x" data-content="button_text">Download</span></a></div></li><li class="InlineList-item"><ul class="InlineList InlineList--bordered u-ph0x"><li class="InlineList-item InlineList-item--bordered"><span class="InlineList-item-text">by <span itemscope="itemscope" itemprop="author" itemtype="https://schema.org/Person"><a class="u-tcGrayDark u-fw700" data-has-card-for-user="46696509" href="https://sote.academia.edu/MartonDoleschall">Marton Doleschall</a><script data-card-contents-for-user="46696509" type="text/json">{"id":46696509,"first_name":"Marton","last_name":"Doleschall","domain_name":"sote","page_name":"MartonDoleschall","display_name":"Marton Doleschall","profile_url":"https://sote.academia.edu/MartonDoleschall","photo":"/images/s65_no_pic.png"}</script></span></span></li><li class="js-paper-rank-work_24554752 InlineList-item InlineList-item--bordered hidden"><span class="js-paper-rank-view hidden u-tcGrayDark" data-paper-rank-work-id="24554752"><i class="u-m1x fa fa-bar-chart"></i><strong class="js-paper-rank"></strong></span><script>$(function() { new Works.PaperRankView({ workId: 24554752, container: ".js-paper-rank-work_24554752", }); 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Two complete genes, complement component 4 (C4) and steroid 21-hydroxylase (CYP21A2, formerly CYP21B), reside in its variable region. RCCX is prone to nonallelic homologous recombination (NAHR) such as unequal crossover, generating duplications and deletions of RCCX modules, and gene conversion. A series of allele-specific long-range polymerase chain reaction coupled to the whole-gene sequencing of CYP21A2 was developed for molecular haplotyping. By means of the developed techniques, 35 different kinds of CYP21A2 haplotype variant were experimentally determined from 112 unrelated European subjects. The number of the resolved CYP21A2 haplotype variants was increased to 61 by bioinformatic haplotype reconstruction. The CYP21A2 haplotype variants could be assigned to the haplotypic RCCX CNV structures (the copy number of RCCX modules) in most cases. The genealogy network constructed from the CYP21A2 haplotype variants delineated the origin of RCCX structures. The different RCCX structures were located in tight groups. The minority of groups with identical RCCX structure occurred once in the network, implying monophyletic origin, but the majority of groups occurred several times and in different locations, indicating polyphyletic origin. The monophyletic groups were often created by single unequal crossover, whereas recurrent unequal crossover events generated some of the polyphyletic groups. As a result of recurrent NAHR events, more CYP21A2 haplotype variants with different allele patterns belonged to the same RCCX structure. 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href="https://www.academia.edu/53252353/Serum_chromogranin_A_level_continuously_rises_with_the_progression_of_type_1_diabetes_and_indicates_the_presence_of_both_enterochromaffin_like_cell_hyperplasia_and_autoimmune_gastritis">Serum chromogranin A level continuously rises with the progression of type 1 diabetes, and indicates the presence of both enterochromaffin‐like cell hyperplasia and autoimmune gastritis</a></div></div><div class="u-pb4x u-mt3x"></div><ul class="InlineList u-ph0x u-fs13"><li class="InlineList-item logged_in_only"><div class="share_on_academia_work_button"><a class="academia_share Button Button--inverseBlue Button--sm js-bookmark-button" data-academia-share="Work/53252353" data-share-source="work_strip" data-spinner="small_white_hide_contents"><i class="fa fa-plus"></i><span class="work-strip-link-text u-ml1x" data-content="button_text">Bookmark</span></a></div></li><li class="InlineList-item"><div class="download"><a id="3d5115d0650d241aaece00b655b26bdc" 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$(".js-view-count-work_53252353").removeClass('hidden') })</script></div></li></ul></li></ul></div></div><div class="u-borderBottom1 u-borderColorGrayLighter"><div class="clearfix u-pv7x u-mb0x js-work-card work_53252354" data-work_id="53252354" itemscope="itemscope" itemtype="https://schema.org/ScholarlyArticle"><div class="header"><div class="title u-fontSerif u-fs22 u-lineHeight1_3"><a class="u-tcGrayDarkest js-work-link" href="https://www.academia.edu/53252354/Lower_serum_chromogranin_B_level_is_associated_with_type_1_diabetes_and_with_type_2_diabetes_patients_with_intensive_conservative_insulin_treatment">Lower serum chromogranin B level is associated with type 1 diabetes and with type 2 diabetes patients with intensive conservative insulin treatment</a></div></div><div class="u-pb4x u-mt3x"><div class="summary u-fs14 u-fw300 u-lineHeight1_5 u-tcGrayDarkest"><div class="summarized">Background Chromogranin B (CgB) plays an important role in the physiological insulin secretion of pancreatic beta cells. Serum CgB levels were investigated in type 1 and type 2 diabetes patients in a cross-sectional study. Methods An... <a class="more_link u-tcGrayDark u-linkUnstyled" data-container=".work_53252354" data-show=".complete" data-hide=".summarized" data-more-link-behavior="true" href="#">more</a></div><div class="complete hidden">Background Chromogranin B (CgB) plays an important role in the physiological insulin secretion of pancreatic beta cells. Serum CgB levels were investigated in type 1 and type 2 diabetes patients in a cross-sectional study. Methods An observational cross-sectional study was performed with the inclusion of 94 control subjects, 100 type 1 and 100 type 2 diabetes patients, at the Metabolic Outpatient Clinic of the Department of Internal Medicine and Hematology, Semmelweis University. Serum CgB levels were measured with enzyme-linked immunosorbent assay. Results Serum CgB level was lower in type 1 diabetes patients than in matched control subjects (p = 0.0241), while they were equal in type 2 diabetes patients and controls (p = 0.1698). The subgroup of type 2 diabetes patients who received intensive conservative insulin treatment had significantly lower CgB levels compared to those with other regimens of antidiabetic therapies (p = 0.0283). Conclusion The lower serum CgB levels in the pa...</div></div></div><ul class="InlineList u-ph0x u-fs13"><li class="InlineList-item logged_in_only"><div class="share_on_academia_work_button"><a class="academia_share Button Button--inverseBlue Button--sm js-bookmark-button" data-academia-share="Work/53252354" data-share-source="work_strip" data-spinner="small_white_hide_contents"><i class="fa fa-plus"></i><span class="work-strip-link-text u-ml1x" data-content="button_text">Bookmark</span></a></div></li><li class="InlineList-item"><div class="download"><a id="21ed925752e18178a79c1635852fe49b" rel="nofollow" data-download="{"attachment_id":70133639,"asset_id":53252354,"asset_type":"Work","always_allow_download":false,"track":null,"button_location":"work_strip","source":null,"hide_modal":null}" class="Button Button--sm Button--inverseGreen js-download-button prompt_button doc_download" href="https://www.academia.edu/attachments/70133639/download_file?st=MTczMjc2NTc5OSw4LjIyMi4yMDguMTQ2&s=work_strip"><i class="fa fa-arrow-circle-o-down fa-lg"></i><span class="u-textUppercase u-ml1x" data-content="button_text">Download</span></a></div></li><li class="InlineList-item"><ul class="InlineList InlineList--bordered u-ph0x"><li class="InlineList-item InlineList-item--bordered"><span class="InlineList-item-text">by <span itemscope="itemscope" itemprop="author" itemtype="https://schema.org/Person"><a class="u-tcGrayDark u-fw700" data-has-card-for-user="46696509" href="https://sote.academia.edu/MartonDoleschall">Marton Doleschall</a><script data-card-contents-for-user="46696509" type="text/json">{"id":46696509,"first_name":"Marton","last_name":"Doleschall","domain_name":"sote","page_name":"MartonDoleschall","display_name":"Marton Doleschall","profile_url":"https://sote.academia.edu/MartonDoleschall","photo":"/images/s65_no_pic.png"}</script></span></span></li><li class="js-paper-rank-work_53252354 InlineList-item InlineList-item--bordered hidden"><span class="js-paper-rank-view hidden u-tcGrayDark" data-paper-rank-work-id="53252354"><i class="u-m1x fa fa-bar-chart"></i><strong class="js-paper-rank"></strong></span><script>$(function() { new Works.PaperRankView({ workId: 53252354, container: ".js-paper-rank-work_53252354", }); 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Serum CgB levels were investigated in type 1 and type 2 diabetes patients in a cross-sectional study. Methods An observational cross-sectional study was performed with the inclusion of 94 control subjects, 100 type 1 and 100 type 2 diabetes patients, at the Metabolic Outpatient Clinic of the Department of Internal Medicine and Hematology, Semmelweis University. Serum CgB levels were measured with enzyme-linked immunosorbent assay. Results Serum CgB level was lower in type 1 diabetes patients than in matched control subjects (p = 0.0241), while they were equal in type 2 diabetes patients and controls (p = 0.1698). The subgroup of type 2 diabetes patients who received intensive conservative insulin treatment had significantly lower CgB levels compared to those with other regimens of antidiabetic therapies (p = 0.0283). 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