Abstract
Background
Moderately increased albuminuria (MIA) is strongly associated with hypertension (HTN) in patients with type 2 diabetic mellitus (T2DM). However, the association between risk factors and coexisting HTN and MIA remains unassessed.
Objectives
This study aimed to determine both cross-sectional and longitudinal associations of risk factors with HTN and MIA comorbidity in patients with T2DM.
Methods
A total of 1,600 patients with T2DM were examined at baseline and longitudinal data were obtained from 1,337 T2DM patients with at least 2 follow-up visits to assess the presence of HTN alone (yes/no), MIA alone (yes/no) and the coexistence of both (yes/no) in a 9-year open cohort study between 2004 and 2013. Bivariate mixed-effects logistic regression with a Bayesian approach was employed to evaluate associations of risk factors with HTN and MIA comorbidity in the longitudinal assessment.
Results
After adjustment for age and BMI, patients with uncontrolled plasma glucose, as a combined index of the glucose profile, were more likely to have HTN [odds ratio (OR): 1.73 with 95% Bayesian credible intervals (BCI) 1.29–2.20] and MIA [OR: 1.34 (95% BCI 1.13–1.62)]. The risks of having HTN and MIA were increased by a one-year raise in diabetes duration [with 0.89 (95% BCI 0.84–0.96) and 0.81 (95% BCI 0.73–0.92) ORs, respectively] and a one-unit increase in non-high-density lipoprotein-cholesterol (Non-HDL-C) [with 1.30 (95% BCI 1.23–1.34) and 1.24 (95% BCI 1.14–1.33) ORs, respectively].
Conclusions
T2DM patients with HTN, MIA, and the coexistence of both had uncontrolled plasma glucose, significantly higher Non-HDL-C, and shorter diabetes duration than the other T2DM patients. Duration of diabetes and uncontrolled plasma glucose index showed the stronger effects on HTN and MIA comorbidity than on each condition separately.
Acknowledgments
The authors would like to thank all participants. We are thankful to Mrs Maryam Zare and Mr Majid Abyar who assisted authors in using the recorded data of Isfahan Endocrine and Metabolism Research Center. We would also like to thank the Student Research Center, School of Health, Endocrine and Metabolism Research Centre, Isfahan University of Medical Sciences, Isfahan, Iran. This research was funded by the Student Research Center, School of Health, Endocrine and Metabolism Research Centre, Isfahan University of Medical Sciences, Isfahan, Iran (No. 394909).
Ethics approval and informed consent
The present study conforms to the principles outlined in the Declaration of Helsinki. The protocol of the IDOPS was also approved by the Ethics Committee of the Isfahan University of Medical Sciences (IUMS) and Research Ethics Committee of Isfahan Endocrine and Metabolism Research Center (IEMRC) (No. 394909). Informed consent was obtained from all individual participants included in the study.
Data availability
The data used to support the findings of the present study are available from the corresponding authors upon request.
Supplementary materials
Abbreviations: MIA, moderately increased albuminuria; HTN, hypertension; FPG, fasting plasma glucose; PPG, postprandial plasma glucose; HbA1C, glycosylated hemoglobin; Total-Chol, total cholesterol; Non-HDL-Chol, non-high-density lipoprotein cholesterol; LDL-Chol, low density lipoprotein cholesterol.
Author contributions
All authors contributed toward data analysis, drafting and critically revising the paper, gave final approval of the version to be published, and agree to be accountable for all aspects of the work.
Disclosure
The authors report no conflicts of interest in regard to this work.