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      Association of apolipoproteins A1 and B with type 2 diabetes and fasting blood glucose: a cross-sectional study

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          Abstract

          Background

          Apolipoprotein (Apo) may be associated with type 2 diabetes (T2D), however, little is known whether or not serum apolipoproteins are correlated with fasting blood glucose (FBG) and the prevalence of T2D in Chinese populations. In this study, we examined the association of serum ApoA1, ApoB, and the ratio of ApoB/ApoA1 (ApoB/A1 ratio) with T2D and FBG level, and compared apolipoprotein indicators in predicting T2D in Chinese adults.

          Methods

          A total of 1027 subjects were enrolled in this cross-sectional study. The association of ApoA1, ApoB, and ApoB/A1 ratio with T2D prevalence was determined using logistic regression models. Multivariate-analysis of covariance (ANCOVA) was performed for comparisons of the mean difference in FBG level.

          Results

          We found that ApoB and ApoB/A1 ratio were positively associated with T2D prevalence and FBG, while inverse association was noted between ApoA1 and T2D prevalence as well as FBG. Stratified analyses for sex, age, body mass index (BMI), smoking, and alcohol consumption showed no significant difference for the association of ApoA1, ApoB, and ApoB/A1 ratio with the prevalence of T2D among subgroups (all p-interactions> 0.05). Nonetheless, ApoA1 poorly performed in predicting T2D as it provided an AUC value of 0.310 that was significantly lower than those observed for ApoB (AUC value: 0.631) and ApoB/A1 ratio (AUC value: 0.685). Finally, path analyses indicated that the association between ApoB and T2D was mediated by BMI.

          Conclusions

          This study reveals the association of serum ApoA1, ApoB, and ApoB/A1 ratio with T2D and FBG in Chinese adults, suggesting that ApoB and ApoB/A1 ratio may be early indicators for predicting T2D. Prospective investigation in large cohort is needed.

          Supplementary Information

          The online version contains supplementary material available at 10.1186/s12902-021-00726-5.

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          Most cited references31

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          The moderator-mediator variable distinction in social psychological research: conceptual, strategic, and statistical considerations.

          In this article, we attempt to distinguish between the properties of moderator and mediator variables at a number of levels. First, we seek to make theorists and researchers aware of the importance of not using the terms moderator and mediator interchangeably by carefully elaborating, both conceptually and strategically, the many ways in which moderators and mediators differ. We then go beyond this largely pedagogical function and delineate the conceptual and strategic implications of making use of such distinctions with regard to a wide range of phenomena, including control and stress, attitudes, and personality traits. We also provide a specific compendium of analytic procedures appropriate for making the most effective use of the moderator and mediator distinction, both separately and in terms of a broader causal system that includes both moderators and mediators.
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            Plasma lipoproteins: apolipoprotein structure and function.

            Plasma lipoprotein metabolism is regulated and controlled by the specific apolipoprotein (apo-) constituents of the various lipoprotein classes. The major apolipoproteins include apoE, apoB, apoA-I, apoA-II, apoA-IV, apoC-I, apoC-II, and apoC-III. Specific apolipoproteins function in the regulation of lipoprotein metabolism through their involvement in the transport and redistribution of lipids among various cells and tissues, through their role as cofactors for enzymes of lipid metabolism, or through their maintenance of the structure of the lipoprotein particles. The primary structures of most of the apolipoproteins are now known, and various functional domains of these proteins are being mapped using selective chemical modification, synthetic peptides, and monoclonal antibodies. Furthermore, the establishment of structure-function relationships has been greatly advanced by the identification of genetically determined variants of specific apolipoproteins that are associated with a disorder of lipoprotein metabolism. Future studies will rely heavily on the use of recombinant DNA technology and site-specific mutagenesis to elucidate further the correlations between structure and function and the role of specific apolipoproteins in lipoprotein metabolism.
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              Clinical review 124: Diabetic dyslipidemia: causes and consequences.

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                Author and article information

                Contributors
                xingmin-wang@ntu.edu.cn
                dhljiyi@163.com
                Journal
                BMC Endocr Disord
                BMC Endocr Disord
                BMC Endocrine Disorders
                BioMed Central (London )
                1472-6823
                1 April 2021
                1 April 2021
                2021
                : 21
                : 59
                Affiliations
                [1 ]GRID grid.260483.b, ISNI 0000 0000 9530 8833, Department of Clinical Laboratory, , Affiliated Maternity & Child Health Care Hospital of Nantong University, ; Nantong, 226018 Jiangsu Province China
                [2 ]GRID grid.260483.b, ISNI 0000 0000 9530 8833, Finance Section, , Affiliated Traditional Chinese Medicine Hospital of Nantong University, ; Nantong, 226018 Jiangsu Province China
                [3 ]GRID grid.260483.b, ISNI 0000 0000 9530 8833, Nantong Institute of Genetics and Reproductive Medicine, , Affiliated Maternity & Child Health Care Hospital of Nantong University, ; Nantong, 226018 Jiangsu Province China
                [4 ]GRID grid.260483.b, ISNI 0000 0000 9530 8833, Scientific Education Section, , Affiliated Maternity & Child Health Care Hospital of Nantong University, ; Nantong, 226018 Jiangsu Province China
                Author information
                http://orcid.org/0000-0001-5996-2376
                Article
                726
                10.1186/s12902-021-00726-5
                8017773
                33794863
                fd3314d6-e47b-40fd-b03a-fc80048e344e
                © The Author(s) 2021

                Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

                History
                : 28 September 2020
                : 25 March 2021
                Funding
                Funded by: the 2020 Innovation and Entrepreneurship Program of Jiangsu Province (Doctor Funds of the Innovation and Entrepreneurship Program)
                Categories
                Research Article
                Custom metadata
                © The Author(s) 2021

                Endocrinology & Diabetes
                apolipoprotein a1,apolipoprotein b,apolipoprotein b/a1 ratio,type 2 diabetes,fasting blood glucose

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