{"title":"一项横断面研究表明,在严重肥胖患者的CIDE家族亚型中,cdec与人体脂肪组织中的脂肪储存关系最为密切。","authors":"Yasuyuki Iwahashi, Seiji Nishikage, Yusei Hosokawa, Tomoko Yamada, Yasushi Nakagawa, Yushi Hirota, Kazuhiko Sakaguchi, Yuki Nishimoto, Shinsuke Nakajima, Seiichi Kitahama, Yasuyoshi Yamamoto, Tomoichiro Mukai, Wataru Ogawa, Yoshikazu Tamori","doi":"10.1007/s13340-025-00806-0","DOIUrl":null,"url":null,"abstract":"<p><p>The cell death-inducing DFF45-like effector (CIDE) family comprises CIDEA, CIDEB, and CIDEC (fat-specific protein of 27 kDa), all of which are lipid droplet-associated proteins and contribute to fat storage and energy homeostasis. However, the relative impacts of these isoforms on fat storage in adipose tissue and obesity in humans have been unclear. We here examined the expression of CIDE family genes in visceral adipose tissue (VAT) of obese individuals who underwent laparoscopic sleeve gastrectomy and explored its relation to adiposity-related parameters. RNA-sequencing analysis revealed that <i>CIDEA</i> and <i>CIDEC</i> were highly expressed in VAT, whereas <i>CIDEB</i> was expressed at a substantially lower level. <i>CIDEA</i> and <i>CIDEC</i> expression levels were positively correlated with body fat mass and subcutaneous adipose tissue (SAT) area, whereas <i>CIDEB</i> expression was negatively correlated with these markers. In addition, <i>CIDEC</i> and <i>CIDEB</i> expression levels showed positive and negative correlations, respectively, with BMI. Multivariable regression analysis showed that only <i>CIDEC</i> expression was significantly associated with body fat mass. Stratification of the subjects according to tertiles of <i>CIDEC</i> expression revealed that BMI, body fat mass, and SAT area were significantly greater in the highest <i>CIDEC</i> expression group than in the other two groups. Our findings thus suggest that, among CIDE isoforms, CIDEC is the most closely associated with fat storage in human adipose tissue.</p><p><strong>Supplementary information: </strong>The online version contains supplementary material available at 10.1007/s13340-025-00806-0.</p>","PeriodicalId":11340,"journal":{"name":"Diabetology International","volume":"16 3","pages":"538-545"},"PeriodicalIF":1.2000,"publicationDate":"2025-04-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12209148/pdf/","citationCount":"0","resultStr":"{\"title\":\"CIDEC is most closely associated with fat storage in human adipose tissue among CIDE family isoforms in severely obese subjects: a cross-sectional study.\",\"authors\":\"Yasuyuki Iwahashi, Seiji Nishikage, Yusei Hosokawa, Tomoko Yamada, Yasushi Nakagawa, Yushi Hirota, Kazuhiko Sakaguchi, Yuki Nishimoto, Shinsuke Nakajima, Seiichi Kitahama, Yasuyoshi Yamamoto, Tomoichiro Mukai, Wataru Ogawa, Yoshikazu Tamori\",\"doi\":\"10.1007/s13340-025-00806-0\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>The cell death-inducing DFF45-like effector (CIDE) family comprises CIDEA, CIDEB, and CIDEC (fat-specific protein of 27 kDa), all of which are lipid droplet-associated proteins and contribute to fat storage and energy homeostasis. However, the relative impacts of these isoforms on fat storage in adipose tissue and obesity in humans have been unclear. We here examined the expression of CIDE family genes in visceral adipose tissue (VAT) of obese individuals who underwent laparoscopic sleeve gastrectomy and explored its relation to adiposity-related parameters. RNA-sequencing analysis revealed that <i>CIDEA</i> and <i>CIDEC</i> were highly expressed in VAT, whereas <i>CIDEB</i> was expressed at a substantially lower level. <i>CIDEA</i> and <i>CIDEC</i> expression levels were positively correlated with body fat mass and subcutaneous adipose tissue (SAT) area, whereas <i>CIDEB</i> expression was negatively correlated with these markers. In addition, <i>CIDEC</i> and <i>CIDEB</i> expression levels showed positive and negative correlations, respectively, with BMI. Multivariable regression analysis showed that only <i>CIDEC</i> expression was significantly associated with body fat mass. Stratification of the subjects according to tertiles of <i>CIDEC</i> expression revealed that BMI, body fat mass, and SAT area were significantly greater in the highest <i>CIDEC</i> expression group than in the other two groups. Our findings thus suggest that, among CIDE isoforms, CIDEC is the most closely associated with fat storage in human adipose tissue.</p><p><strong>Supplementary information: </strong>The online version contains supplementary material available at 10.1007/s13340-025-00806-0.</p>\",\"PeriodicalId\":11340,\"journal\":{\"name\":\"Diabetology International\",\"volume\":\"16 3\",\"pages\":\"538-545\"},\"PeriodicalIF\":1.2000,\"publicationDate\":\"2025-04-08\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12209148/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Diabetology International\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1007/s13340-025-00806-0\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2025/7/1 0:00:00\",\"PubModel\":\"eCollection\",\"JCR\":\"Q4\",\"JCRName\":\"ENDOCRINOLOGY & METABOLISM\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Diabetology International","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1007/s13340-025-00806-0","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/7/1 0:00:00","PubModel":"eCollection","JCR":"Q4","JCRName":"ENDOCRINOLOGY & METABOLISM","Score":null,"Total":0}
CIDEC is most closely associated with fat storage in human adipose tissue among CIDE family isoforms in severely obese subjects: a cross-sectional study.
The cell death-inducing DFF45-like effector (CIDE) family comprises CIDEA, CIDEB, and CIDEC (fat-specific protein of 27 kDa), all of which are lipid droplet-associated proteins and contribute to fat storage and energy homeostasis. However, the relative impacts of these isoforms on fat storage in adipose tissue and obesity in humans have been unclear. We here examined the expression of CIDE family genes in visceral adipose tissue (VAT) of obese individuals who underwent laparoscopic sleeve gastrectomy and explored its relation to adiposity-related parameters. RNA-sequencing analysis revealed that CIDEA and CIDEC were highly expressed in VAT, whereas CIDEB was expressed at a substantially lower level. CIDEA and CIDEC expression levels were positively correlated with body fat mass and subcutaneous adipose tissue (SAT) area, whereas CIDEB expression was negatively correlated with these markers. In addition, CIDEC and CIDEB expression levels showed positive and negative correlations, respectively, with BMI. Multivariable regression analysis showed that only CIDEC expression was significantly associated with body fat mass. Stratification of the subjects according to tertiles of CIDEC expression revealed that BMI, body fat mass, and SAT area were significantly greater in the highest CIDEC expression group than in the other two groups. Our findings thus suggest that, among CIDE isoforms, CIDEC is the most closely associated with fat storage in human adipose tissue.
Supplementary information: The online version contains supplementary material available at 10.1007/s13340-025-00806-0.
期刊介绍:
Diabetology International, the official journal of the Japan Diabetes Society, publishes original research articles about experimental research and clinical studies in diabetes and related areas. The journal also presents editorials, reviews, commentaries, reports of expert committees, and case reports on any aspect of diabetes. Diabetology International welcomes submissions from researchers, clinicians, and health professionals throughout the world who are interested in research, treatment, and care of patients with diabetes. All manuscripts are peer-reviewed to assure that high-quality information in the field of diabetes is made available to readers. Manuscripts are reviewed with due respect for the author''s confidentiality. At the same time, reviewers also have rights to confidentiality, which are respected by the editors. The journal follows a single-blind review procedure, where the reviewers are aware of the names and affiliations of the authors, but the reviewer reports provided to authors are anonymous. Single-blind peer review is the traditional model of peer review that many reviewers are comfortable with, and it facilitates a dispassionate critique of a manuscript.