Elizabeth Paz-Pacheco, Jose Nevado, Eva Maria Cutiongco-De La Paz, Gabriel Jasul, Aimee Yvonne Criselle Aman, Elizabeth Laurize Alejandro-Ribaya, Mark David Francisco, Ma Luz Vicenta Guanzon, May Uyking-Naranjo, Cecille Añonuevo-Cruz, Maria Patricia Deanna Maningat, Cristina Jaring, Paulette Nacpil-Dominguez, Aniza Pala-Mohamad, Abigail Uy-Canto, John Paul Quisumbing, Annabelle Marie Lat, Diane Carla Bernardo, Noemie Marie Mansibang, Vincent Sean Ribaya, Karell Jo Angelique Calpito, Julius Patrick Ferrer, Jessica Biwang, Jodelyn Melegrito, Christian Deo Deguit, Carlos Emmanuel Panerio
{"title":"菲律宾2型糖尿病患者对磺脲类药物反应性差的遗传变异","authors":"Elizabeth Paz-Pacheco, Jose Nevado, Eva Maria Cutiongco-De La Paz, Gabriel Jasul, Aimee Yvonne Criselle Aman, Elizabeth Laurize Alejandro-Ribaya, Mark David Francisco, Ma Luz Vicenta Guanzon, May Uyking-Naranjo, Cecille Añonuevo-Cruz, Maria Patricia Deanna Maningat, Cristina Jaring, Paulette Nacpil-Dominguez, Aniza Pala-Mohamad, Abigail Uy-Canto, John Paul Quisumbing, Annabelle Marie Lat, Diane Carla Bernardo, Noemie Marie Mansibang, Vincent Sean Ribaya, Karell Jo Angelique Calpito, Julius Patrick Ferrer, Jessica Biwang, Jodelyn Melegrito, Christian Deo Deguit, Carlos Emmanuel Panerio","doi":"10.15605/jafes.037.S8","DOIUrl":null,"url":null,"abstract":"<p><strong>Introduction: </strong>Sulfonylureas (SUs) are commonly used drugs for type 2 diabetes mellitus (T2DM) in the Philippines. This study aimed to associate genetic variants with poor response to gliclazide and glimepiride among Filipinos.</p><p><strong>Methodology: </strong>Two independent, dichotomous longitudinal substudies enrolled 139 and 113 participants in the gliclazide and glimepiride substudies, respectively. DNA from blood samples underwent customized genotyping for candidate genes using microarray. Allelic and genotypic features and clinical associations were determined using exact statistical methods.</p><p><strong>Results: </strong>Three months after sulfonylurea monotherapy, 18 (13%) were found to be poorly responsive to gliclazide, while 7 (6%) had poor response to glimepiride. Seven genetic variants were nominally associated (<i>p</i><0.05) with poor gliclazide response, while three variants were nominally associated with poor glimepiride response. For gliclazide response, 3 carboxypeptidase-associated variants (rs319952 and rs393994 of <i>AGBL4</i> and rs2229437 of <i>PRCP</i>) had the highest genotypic association; other variants include rs9806699, rs7119, rs6465084 and rs1234315. For glimepiride response, 2 variants were nominally associated: <i>CLCN6-NPPA-MTHFR</i> gene cluster - rs5063 and rs17367504 - and rs2299267 from the <i>PON2</i> loci.</p><p><strong>Conclusion: </strong>Genetic variants were found to have a nominal association with sulfonylurea response among Filipinos. These findings can guide for future study directions on pharmacotherapeutic applications for sulfonylurea treatment in this population.</p>","PeriodicalId":41792,"journal":{"name":"Journal of the ASEAN Federation of Endocrine Societies","volume":"38 1","pages":"31-40"},"PeriodicalIF":0.6000,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/ff/70/JAFES-38-S1-31.PMC10207869.pdf","citationCount":"0","resultStr":"{\"title\":\"Genetic Variants Associated with Poor Responsiveness to Sulfonylureas in Filipinos with Type 2 Diabetes Mellitus.\",\"authors\":\"Elizabeth Paz-Pacheco, Jose Nevado, Eva Maria Cutiongco-De La Paz, Gabriel Jasul, Aimee Yvonne Criselle Aman, Elizabeth Laurize Alejandro-Ribaya, Mark David Francisco, Ma Luz Vicenta Guanzon, May Uyking-Naranjo, Cecille Añonuevo-Cruz, Maria Patricia Deanna Maningat, Cristina Jaring, Paulette Nacpil-Dominguez, Aniza Pala-Mohamad, Abigail Uy-Canto, John Paul Quisumbing, Annabelle Marie Lat, Diane Carla Bernardo, Noemie Marie Mansibang, Vincent Sean Ribaya, Karell Jo Angelique Calpito, Julius Patrick Ferrer, Jessica Biwang, Jodelyn Melegrito, Christian Deo Deguit, Carlos Emmanuel Panerio\",\"doi\":\"10.15605/jafes.037.S8\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Introduction: </strong>Sulfonylureas (SUs) are commonly used drugs for type 2 diabetes mellitus (T2DM) in the Philippines. This study aimed to associate genetic variants with poor response to gliclazide and glimepiride among Filipinos.</p><p><strong>Methodology: </strong>Two independent, dichotomous longitudinal substudies enrolled 139 and 113 participants in the gliclazide and glimepiride substudies, respectively. DNA from blood samples underwent customized genotyping for candidate genes using microarray. Allelic and genotypic features and clinical associations were determined using exact statistical methods.</p><p><strong>Results: </strong>Three months after sulfonylurea monotherapy, 18 (13%) were found to be poorly responsive to gliclazide, while 7 (6%) had poor response to glimepiride. Seven genetic variants were nominally associated (<i>p</i><0.05) with poor gliclazide response, while three variants were nominally associated with poor glimepiride response. For gliclazide response, 3 carboxypeptidase-associated variants (rs319952 and rs393994 of <i>AGBL4</i> and rs2229437 of <i>PRCP</i>) had the highest genotypic association; other variants include rs9806699, rs7119, rs6465084 and rs1234315. For glimepiride response, 2 variants were nominally associated: <i>CLCN6-NPPA-MTHFR</i> gene cluster - rs5063 and rs17367504 - and rs2299267 from the <i>PON2</i> loci.</p><p><strong>Conclusion: </strong>Genetic variants were found to have a nominal association with sulfonylurea response among Filipinos. 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Genetic Variants Associated with Poor Responsiveness to Sulfonylureas in Filipinos with Type 2 Diabetes Mellitus.
Introduction: Sulfonylureas (SUs) are commonly used drugs for type 2 diabetes mellitus (T2DM) in the Philippines. This study aimed to associate genetic variants with poor response to gliclazide and glimepiride among Filipinos.
Methodology: Two independent, dichotomous longitudinal substudies enrolled 139 and 113 participants in the gliclazide and glimepiride substudies, respectively. DNA from blood samples underwent customized genotyping for candidate genes using microarray. Allelic and genotypic features and clinical associations were determined using exact statistical methods.
Results: Three months after sulfonylurea monotherapy, 18 (13%) were found to be poorly responsive to gliclazide, while 7 (6%) had poor response to glimepiride. Seven genetic variants were nominally associated (p<0.05) with poor gliclazide response, while three variants were nominally associated with poor glimepiride response. For gliclazide response, 3 carboxypeptidase-associated variants (rs319952 and rs393994 of AGBL4 and rs2229437 of PRCP) had the highest genotypic association; other variants include rs9806699, rs7119, rs6465084 and rs1234315. For glimepiride response, 2 variants were nominally associated: CLCN6-NPPA-MTHFR gene cluster - rs5063 and rs17367504 - and rs2299267 from the PON2 loci.
Conclusion: Genetic variants were found to have a nominal association with sulfonylurea response among Filipinos. These findings can guide for future study directions on pharmacotherapeutic applications for sulfonylurea treatment in this population.
期刊介绍:
The Journal of the ASEAN Federation of Endocrine Societies (JAFES) is an OPEN ACCESS, internationally peer-reviewed, English language, medical and health science journal that is published in print two times a year by the ASEAN Federation of Endocrine Societies. It shall serve as the endocrine window between the ASEAN region and the world, featuring original papers and publishing key findings from specialists and experts of endocrinology.