Elsevier

Journal of Diabetes and its Complications

Volume 30, Issue 7, September–October 2016, Pages 1326-1332
Journal of Diabetes and its Complications

Nocturnal blood pressure is associated with the progression of microvascular complications and hypertension in patients with type 1 diabetes mellitus

https://doi.org/10.1016/j.jdiacomp.2016.05.021Get rights and content

Abstract

Aims

To evaluate relationships between early alterations in blood pressure and the progression of microvascular complications of diabetes in clinically-normotensive patients with type 1 diabetes (T1DM).

Methods

In a prospective observational study of 85 normotensive T1DM patients without microalbuminuria, blood pressure (BP) was monitored over 24 h using the ambulatory blood pressure monitoring (ABPM) system at baseline and 7 years later. Development or progression of microalbuminuria, retinopathy and hypertension was evaluated.

Results

Initially, 20 patients (24%) were diagnosed with masked hypertension and 31 (37%) with non-dipper pattern as the only pathological findings. At 7 years: 1) twenty-seven patients (32%) had progression of retinopathy related to the nocturnal diastolic blood pressure (BPD) (OR:1.122; p = 0.034) and final non-dipper pattern (OR:5.857; p = 0.005); 2) seven patients (10%) developed microalbuminuria for which nocturnal systolic blood pressure (BPS) was a risk factor (OR:1.129; p = 0.007); 3) five of the normotensive patients (9%) progressed to hypertension; historic HbA1c (OR:2.767; p = 0.046) and nocturnal BPD (OR:1.243; p = 0.046) being the related risk factors. BPD level ≥ 65 mmHg was associated with an increase in progression of retinopathy and hypertension.

Conclusions

In T1DM patients there is an elevated prevalence of BP alterations, detected using ABPM. Alterations in nocturnal BP predispose to development/progression of microvascular complications and overt hypertension.

Introduction

In patients with type 1 diabetes (T1DM), the presence of hypertension (HT) is considered one of the principal factors for the development and progression of microvascular complications (Rodrigues, Canani, Schvartzman, & Gross, 2011) such as nephropathy (Chillarón et al., 2013) and retinopathy (Hammes et al., 2011), as well as cardiovascular disease (Bild and Teutsch, 1987, Miller et al., 2013). Several intervention studies have demonstrated the benefit of BP control not only in patients with diabetes but also in the general population (Heart Outcomes Prevention Evaluation Study Investigators, 2000, Patel and ADVANCE Collaborative Group, 2007).

It is becoming progressively more usual to employ ambulatory blood pressure monitoring (ABPM). The technique has better reproducibility, reduces the patient's alarm or “white coat hypertension” and whose results correlate better with target organ involvement and cardiovascular morbid-mortality (Bliziotis et al., 2012, Gaborieau et al., 2008). Further, it enables the detection of subclinical alterations of blood pressure (BP), such as the circadian rhythm alteration and/or the presence of masked hypertension (Pickering, Shimbo, & Haas, 2006). These alterations can be missed when isolated BP measurements are made, and are more prevalent in patients with diabetes than in the general population (Chatterjee et al., 2009, Darcan et al., 2006, Flores et al., 2000, Lurbe et al., 2001). Our group observed (Vílchez-López et al., 2011) an elevated prevalence of masked hypertension [up to 32% presented with pathological average systolic (BPS) or diastolic (BPD) values during activity period] and the non-dipper pattern in 42% of patients with T1DM who were normotensive based on single measurement of BP. These findings were related to the deterioration of metabolic control and an atherogenic lipid profile.

Despite there being considerable evidence that the coexistence of hypertension and diabetes increases the risk of development and progression of chronic complications (Bild and Teutsch, 1987, De Boer et al., 2008), there is insufficient information on the role of subclinical blood pressure alterations in relation to the progression of microangiopathy complications in diabetes, and on the development of overt HT.

The objective of the present study was to evaluate the relationships between the presence of early subclinical BP alterations (detected using ABPM) and the progression of retinopathy, the development of microalbuminuria and the appearance of overt HT in clinically-normotensive T1DM patients.

Section snippets

Subjects and study design

The study design was observational, of a cohort of 85 T1DM clinically normotensive patients who, on screening, had consistently negative microalbuminuria. The patients were prospectively monitored for 7 years. They were selected consecutively from the diabetes clinic of our Endocrinology and Nutrition Unit at the University Hospital Puerta del Mar (Cádiz, Spain). The period of evaluation was from Oct. 2005 to Sept. 2006, with a re-evaluation between Oct. 2012 and Sept. 2013. The inclusion

Baseline examination

Of the 89 patients who initially fulfilled the inclusion criteria, 4 were excluded for having < 75% of valid BP readings in the initial ABPM. The principal clinical characteristics, demographics and the BP values measured with the ABPM system are summarized in Table 1. Of the 85 patients included in the study, 55% (n = 47) were females. In the ABPM measurements, despite all the patients presenting with normal office BP values (i.e. an inclusion criterion), 20 (24%) were diagnosed as masked HT and

Discussion

Our results highlight the relevance of early alterations in BP, such as the elevation of nocturnal BP, as a risk marker of the development and progression of chronic complications in patients with T1DM but who are clinically normotensive. Nocturnal BPD was related to the progression of retinopathy and the development of overt HT, while nocturnal BPS was related to the development of microalbuminuria. These BP alterations would not have been noted in the standard single-measurement BP.

Further,

Acknowledgments

This study was financed by grants from the Spanish Diabetes Society and National Plan of I+D+I 2008–2011 of ISCIII (PI11/02924) Junta de Andalucia (PI-0322-2011) and FEDER. Editorial assistance was by Dr. Peter R Turner.

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    Disclosure: The authors declare that there are no conflicts of interest in the conduct of this study.

    This work was presented as an abstract at the 17th European Congress of Endocrinology (Dublin, Ireland); May 16–20, 2015 (published in Endocrine Abstracts 2015; vol. 37).

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