Skip to main content
Download PDF
Download ePub
  • Original investigation
  • Open access
  • Published:

Diastolic orthostatic hypertension and cardiovascular prognosis in type 2 diabetes: a prospective cohort study

Cardiovascular Diabetology volume 15, Article number: 83 (2016) Cite this article

Abstract

Background

In patients with type 2 diabetes, the prognostic impact of an orthostatic rise in blood pressure is not known. Therefore, the aim of this study was to determine the prognostic implications of the diastolic orthostatic blood pressure response in a cohort of patients with type 2 diabetes. We also evaluated associations between different orthostatic blood pressure responses and markers of subclinical cardiovascular organ damage.

Methods

Office blood pressures were measured in the sitting and in the standing position in 749 patients with type 2 diabetes who participated in the CARDIPP study (Cardiovascular Risk factors in Patients with Diabetes—a Prospective study in Primary care). Diastolic orthostatic hypertension was defined as a rise of diastolic blood pressure ≥10 mmHg and diastolic orthostatic hypotension was defined as a drop of diastolic blood pressure ≥10 mmHg. Recruitment took place between the years 2005–2008, and patients were followed until any of the primary outcome events (cardiovascular death or hospitalization for either myocardial infarction or stroke) occurred or until December 31st, 2014. Measurements of aortic pulse wave velocity and of carotid intima-media thickness were performed at base-line.

Results

Diastolic orthostatic hypertension was found in 140 patients (18.7 %) and was associated with significantly lower risk of cardiovascular events (crude hazard ratio compared with patients with normal systolic and diastolic orthostatic blood pressure response: 0.450, 95 % C.I. 0.206–0.987, P = 0.046). Diastolic orthostatic hypotension was found in 31 patients (4.1 %) and was associated with higher values for aortic pulse wave velocity and carotid intima-media thickness, compared with patients with normal systolic and diastolic orthostatic blood pressure response.

Conclusions

Diastolic orthostatic hypertension is common in patients with type 2 diabetes, and may be a novel marker for decreased cardiovascular risk in these patients.

Background

In patients with type 2 diabetes, orthostatic hypotension is a common clinical finding [1], which is associated with an increased risk for cardiovascular mortality [2]. Orthostatic hypotension is also an established marker for cardiovascular risk in patients with hypertension [3, 4], in the elderly [5–8] and in the general population [9–12]. Considerably less is known, however, about the prevalence and clinical impact of the reverse phenomenon, orthostatic hypertension, which implies an exaggerated rise in blood pressure when assuming an upright position [13, 14]. Orthostatic hypertension has been associated with increased prevalence of silent cerebrovascular lesions in the elderly [15], and with increased risk for incident lacunar strokes in the general population [16]. In patients with type 2 diabetes, an increased prevalence of orthostatic hypertension has been described [17], and orthostatic hypertension has been associated with markers of neuropathy [17] and with altered indices of left atrial volume [18] but prospective studies concerning the predictive value of orthostatic hypertension are lacking. Therefore, we measured the diastolic and systolic blood pressure responses to rising from the sitting to the standing position in a Swedish cohort of middle-aged patients with type 2 diabetes, and analyzed their influence on cardiovascular prognosis. We also explored differences in the extent of subclinical cardiovascular organ damage, measured as aortic pulse wave velocity (PWV) and carotid intima-media thickness (IMT), between patients with differing orthostatic blood pressure responses.

Methods

Population

As described previously [19], CARDIPP (Cardiovascular Risk Factors in Patients with Diabetes—a Prospective Study in Primary Care) is an observational prospective cohort study with the general aim of exploring the impact of cardiovascular risk factors in patients with type 2 diabetes (Clinical Trials.gov number NCT 01049737). Between the years 2005–2008, 761 patients with type 2 diabetes were recruited by nurses specially trained in diabetes care at 22 different primary health care centers in the counties of Östergötland and Jönköping in Sweden. Inclusion criteria were: type 2 diabetes treated in primary care; age 55–65 years; and willingness to participate in the study. The only exclusion criterion was known severe physical or mental disease with short life expectancy. From the total CARDIPP cohort of 761 patients, we excluded for the purpose of this analysis 12 patients for which base-line data were missing for systolic or diastolic blood pressure in either the sitting or the standing position. This yielded a study sample of 749 participants.

Outcomes

The primary endpoint was a composite endpoint of the first non-fatal or fatal event of hospitalization for acute myocardial infarction (ICD-10 code I21), or stroke (ICD-10 codes I60, I61, I63.0–I63.5, I63.8–I63.9, I64) or cardiovascular mortality (ICD-10 codes I00–99). Patients were followed until a primary outcome event occurred, or until December 31st, 2014, by linkage to the Swedish Cause of Death and Inpatient registries (The National Board of Health and Welfare, Stockholm, Sweden) using the national personal identification number of each individual patient, thus ensuring coverage of the entire population.

Sitting and standing blood pressure measurements

Office blood pressure was measured by specially trained nurses [20]. Measurements were made manually with the auscultatory method, with appropriately sized cuffs, following a 5 minute wait, with the patient sitting comfortably in a relaxed position with the arm supported at heart level. Three sitting measurements were made, with 1 minute between each measurement. Thereafter, the patient was asked to rise, and one additional measurement was made when the patient had been standing for 2 minutes. Blood pressures were determined to the nearest 2 mmHg. The blood pressure value obtained at the third sitting measurement is referred to as the sitting blood pressure in this report. The orthostatic blood pressure response was calculated as the difference between the third sitting measurement and the standing measurement. The cut-off for abnormal systolic orthostatic blood pressure responses was ≥20 mmHg, as has been proposed for both hypotensive [21] and hypertensive [13] orthostatic blood pressure reactions. Thus, systolic orthostatic hypertension was defined as a rise of systolic blood pressure ≥20 mmHg, with or without an accompanying diastolic blood pressure rise, and systolic orthostatic hypotension was defined as a drop of systolic blood pressure ≥20 mmHg, with or without an accompanying diastolic blood pressure drop. For diastolic orthostatic hypotensive reactions the cut-off was ≥10 mmHg [21] and we applied the same numerical threshold for diastolic orthostatic hypertension, since no consensus criteria exist for this entity [13]. Accordingly, diastolic orthostatic hypertension was defined as a rise of diastolic blood pressure ≥10 mmHg, with or without an accompanying systolic blood pressure rise, and diastolic orthostatic hypotension was defined as a drop of diastolic blood pressure ≥10 mmHg, with or without an accompanying drop of systolic blood pressure. Thus, a normal systolic orthostatic blood pressure response was defined as a change of systolic blood pressure within the range of −19 to +19 mmHg, and a normal diastolic orthostatic blood pressure response was defined as a change of diastolic blood pressure within the range of −9 to +9 mmHg.

Aortic pulse wave velocity measurements

To measure aortic PWV, electrocardiogram-gated pulse wave analyses of the carotid and femoral arteries were performed with a Millar pressure tonometer and the SphygmoCor system (Model MM3, AtCor Medical, Sydney, Australia). The pulse wave transit time was calculated by subtracting the time between the ECG R-wave and the arrival of the pulse wave to the carotid measurement site from the time between the ECG R-wave and the arrival of the pulse wave to the femoral measurement site. The surface distance was defined as the distance between the suprasternal notch and the femoral measurement site, subtracted by the distance between the suprasternal notch and the carotid measurement site. The PWV was calculated by dividing the surface distance with the pulse wave transit time. Applanation tonometry measurements were performed in duplicate, and reported as means of the two measurements. Measures of PWV were successfully obtained in 692 patients at base-line.

Carotid ultrasonography

Carotid IMT was measured in B-mode, using Philips ATL HDI 5000 (Philips Ultrasound, Seattle, USA) with a 4–7 MHz linear transducer [22]. Three consecutive longitudinal images, frozen in diastole, were analyzed with software for off-line measurement of intima-media thickness (Artery Measurement System II; Image and Data Analysis, Gothenburg, Sweden). A section of 10 mm 1–2 cm proximal to the carotid bulb was measured manually by tracing a cursor along the echo wedges. A mean value from the right and left carotid arteries was calculated. Measures of carotid IMT were successfully obtained in 729 patients at base-line.

Laboratory analyses

Blood samples were drawn in the morning following a 10 h over-night fast. The Swedish Mono-S HPLC standard was used for HbA1c analyses [23], but the values were subsequently converted to the International Federation of Clinical Chemistry and Laboratory Medicine (IFCC) units (mmol/mol). Creatinine-based values of estimated glomerular filtration rate (eGFR) were calculated according to the Modification of Diet in Renal Disease (MDRD) study equation [24].

Statistics

For the statistical analyses, SPSS software (IBM SPSS Statistics 23, Chicago, IL, USA) was used. In the main comparisons, the reference group was defined as patients who had a normal systolic and diastolic orthostatic blood pressure response. Differences of base-line characteristics were tested for statistical significance with two-sided independent t test, Chi square test or, where appropriate, Fisher's exact test. With the use of Cox regression models, the associations between the time to a first endpoint event and the presence of diastolic or systolic orthostatic hypertension or hypotension, were calculated as the hazard ratio (HR) for each group with a corresponding 95 % confidence interval (C.I.). Crude HRs were first calculated, and if they were significant, adjusted HRs were then calculated by using multivariate Cox regression models which adjusted for traditional cardiovascular risk factors. The first multivariate model adjusted for age, sex and sitting systolic blood pressure, and the second multivariate model adjusted additionally for smoking status, low density lipoprotein (LDL) cholesterol, body mass index and use of any antihypertensive medication. If the crude hazard ratios were not statistically significant, no further adjustments were made. Statistical significance was defined as P < 0.05. Since the purpose of the study was to present adjusted HRs, and not to screen for independent predictors, no adjustments for multiple testing were performed.

Ethics

All participants gave written informed consent. The merging of study data with other registries was approved by the National Board of Health and Welfare and by the Swedish Data Inspection Board. The study was approved by the Regional Ethical Review Board in Linköping, Sweden. The study protocol followed the principles expressed in the Declaration of Helsinki.

Results

Population characteristics

The study population consisted of 257 women (34.3 %) and 492 men. The majority (88.5 %) were born in Sweden. The most common anti-diabetic treatment strategy was oral anti-diabetics (OAD) and/or non-insulin injectables (NNI) which were used by 40.9 percent of the participants, followed by life-style advice only (28.2 %), combined use of insulin with OAD/NNI (18.0 %) and insulin only (13.0 %). There were 462 participants (61.7 %) who reported a previous diagnosis of hypertension, 67 participants (8.9 %) who reported having had a myocardial infarction and 18 participants (2.4 %) who reported having had a stroke. Background characteristics are presented according to the orthostatic blood pressure reaction (Table 1). During a median follow-up time of 7.8 years (range: 38–3537 days), there were 75 end-point events (42 events related to ischemic heart disease including 37 myocardial infarctions, 27 events related to ischemic stroke, four events related to intracerebral hemorrhage, one event related to subdural bleeding and one event related to congestive heart failure). Fifty-eight events occurred among the 534 patients with normal systolic and diastolic orthostatic blood pressure responses (10.9 %), five events occurred among the 45 patients with systolic orthostatic hypertension (11.1 %), two events occurred among the 24 patients with systolic orthostatic hypotension (8.3 %), seven events occurred among the 140 patients with diastolic orthostatic hypertension (5.0 %) and six events occurred among the 31 patients with diastolic orthostatic hypotension (19.4 %).

Table 1 Clinical characteristics and medications at base-line in 749 patients with type 2 diabetes, stratified according to their orthostatic blood pressure reactions
Full size table

Orthostatic blood pressure response

The difference between the sitting blood pressure and the standing blood pressure followed normal distribution curves (Fig. 1) for both systolic and diastolic measurements. For the systolic blood pressure change, mean (SD) was 1.1 (10.9) mmHg, median was 0 mmHg and the range was −40 to +50 mmHg (inter-quartile range −6 to +8 mmHg). For the diastolic blood pressure change, mean (SD) was 2.6 (6.8) mmHg, median was 2.0 mmHg and the range was −24 to +25 mmHg (inter-quartile range −2 to +8 mmHg). The most common orthostatic abnormality was diastolic hypertension which was found in 140 patients (18.7 %) followed by systolic hypertension which was found in 45 patients (6.0 %), diastolic hypotension which was found in 31 patients (4.1 %) and systolic hypotension which was found in 24 patients (3.2 %). There were 25 patients (3.4 %) with more than one orthostatic blood pressure abnormality: Thirteen of the patients with systolic orthostatic hypertension also had diastolic orthostatic hypertension, six of the patients with systolic orthostatic hypotension also had diastolic orthostatic hypotension, four of the patients with diastolic orthostatic hypertension also had systolic orthostatic hypotension, and two of the patients with diastolic orthostatic hypotension also had systolic orthostatic hypertension. Overall, there were 534 patients (71.3 %) who had a normal orthostatic blood pressure response, defined as a change of systolic blood pressure within the range of −19 to +19 mmHg and a change of diastolic blood pressure within the range of −9 to +9 mmHg. This group was used as the reference group in all main comparisons. Sitting and standing blood pressures are presented according to the systolic and diastolic orthostatic blood pressure reactions in Table 2.

Fig. 1
figure 1

Distribution of systolic (left panel) and diastolic (right panel) orthostatic blood pressure changes, in 749 patients with type 2 diabetes

Full size image
Table 2 Blood pressure variables and markers of target organ damage in 749 patients with type 2 diabetes, stratified according to their orthostatic blood pressure reactions
Full size table

Systolic orthostatic hypertension

In a Cox regression analysis that compared patients with systolic orthostatic hypertension (n = 45) with the 534 patients who had a normal systolic and diastolic orthostatic blood pressure response, systolic orthostatic hypertension was not significantly associated with the risk of the combined end-point (HR 1.095, 95 % C.I. 0.439–2.731, P = 0.486). Similar results were obtained when the 45 patients with systolic orthostatic hypertension were compared with the 704 patients without systolic orthostatic hypertension (HR 1.201, 95 % C.I. 0.485–2.976, P = 0.693) or with the 680 patients who had a normal systolic blood pressure response (HR 1.191, 95 % C.I. 0.480–2.954, P = 0.706). Patients with systolic blood pressure rise ≥20 mmHg had significantly (P = 0.001) higher PWV than patients with a normal orthostatic blood pressure response, but similar IMT (Table 2).

Systolic orthostatic hypotension

In a Cox regression analysis that compared patients with systolic orthostatic hypotension (n = 24) with the 534 patients who had a normal systolic and diastolic orthostatic blood pressure response, systolic orthostatic hypotension was not significantly associated with the risk of the combined end-point (HR 0.750, 95 % C.I. 0.183–3.073, P = 0.690). Similar results were obtained when the 24 patients with systolic orthostatic hypotension were compared with the 725 patients without systolic orthostatic hypotension (HR 0.810, 95 % C.I. 0.199–3.301, P = 0.769) or with the 680 patients who had a normal systolic blood pressure response (HR 0.819, 95 % C.I. 0.201–3.340, P = 0.780). Patients with systolic blood pressure fall ≥ 20 mmHg had non-significantly higher PWV and IMT compared with patients with a normal orthostatic blood pressure response (Table 2).

Diastolic orthostatic hypertension

Patients with diastolic orthostatic hypertension (n = 140) had a significantly lower risk of experiencing the combined end-point compared with the 534 patients who had a normal systolic and diastolic orthostatic blood pressure reaction (HR 0.450, 95 % C.I. 0.206–0.987, P = 0.046). Diastolic orthostatic hypertension remained significantly associated with a decreased risk for cardiovascular events following adjustment for age, sex and sitting systolic blood pressure (HR 0.452, 95 % C.I. 0.206–0.990, P = 0.047, cumulative event rate 65/674) as well as following additional adjustment for smoking status, LDL cholesterol, body mass index and use of any antihypertensive medication (HR 0.335, 95 % C.I. 0.133–0.839, P = 0.020, cumulative event rate 59/616). The results of the fully adjusted model are presented in Table 3. Patients with diastolic orthostatic hypertension did not differ significantly from patients with a normal orthostatic blood pressure response in terms of PWV and IMT (Table 2). Among the patients with diastolic orthostatic hypertension, 88 (62.9 %) had a standing diastolic blood pressure ≤90 mmHg and 72 (51.4 %) had a standing systolic blood pressure ≤140 mmHg.

Table 3 Adjusted hazard ratios for a composite end-point consisting of cardiovascular death or hospitalization for either myocardial infarction or stroke, based on a multivariate Cox regression model in 616 patients with type 2 diabetes
Full size table

Diastolic orthostatic hypotension

There was a non-significant trend towards increased risk for the combined end-point when patients with diastolic orthostatic hypotension (n = 31) were compared with the 534 patients who had a normal systolic and diastolic blood pressure response (HR 1.804, 95 % C.I. 0.778–4.183, P = 0.169). The same non-significant trend was observed when patients with diastolic orthostatic hypotension were compared with the 718 patients without diastolic orthostatic hypotension (HR 2.039, 95 % C.I. 0.885–4.696, P = 0.094) or with the 578 patients who had a normal diastolic blood pressure response (HR 1.818, 95 % C.I. 0.786–4.204, P = 0.162). Patients with diastolic orthostatic hypotension had significantly (P = 0.013) higher PWV and significantly (P = 0.010) higher IMT than patients with a normal orthostatic blood pressure response (Table 2).

Combined groups

When patients who had either systolic or diastolic orthostatic hypertension or both (n = 172) were grouped together and compared with the 534 patients with a normal orthostatic blood pressure response, the presence of any hypertensive orthostatic blood pressure response was associated with a decreased risk for the composite end-point of borderline statistical significance (HR 0.530, 95 % C.I. 0.271–1.036, P = 0.064) and with significantly higher PWV (10.8 ± 2.2 m/s vs. 10.2 ± 2.1 m/s, P = 0.006) but similar IMT (0.75 ± 0.19 mm vs. 0.73 ± 0.17 mm, P = 0.156). When patients who had either systolic or diastolic orthostatic hypotension or both (n = 49) were compared with the 534 patients with a normal orthostatic blood pressure response, there was no significant association with the presence of any hypotensive orthostatic blood pressure response and the composite end-point (HR 1.308, 95 % C.I. 0.597–2.866, P = 0.502) but significantly higher values were found for both PWV (11.0 ± 2.4 m/s vs. 10.2 ± 2.1 m/s, P = 0.022) and IMT (0.82 ± 0.25 mm vs. 0.73 ± 0.17 mm, P = 0.014).

Sensitivity analysis

Since previous cardiovascular disease is a risk factor for recurrent events, we performed a sensitivity analysis, in which 86 patients were excluded due to reporting either previous myocardial infarction or previous stroke, or due to missing baseline data concerning these variables. When compared with patients with a normal orthostatic blood pressure response, the hazard ratio for the combined end-point was 1.010 (95 % C.I. 0.312–3.272, P = 0.986, n = 510) for systolic orthostatic hypertension, 1.119 (95 % C.I. 0.270–4.637, P = 0.877, n = 493) for systolic orthostatic hypotension, 0.285 (95 % C.I. 0.088–0.923, P = 0.036, n = 595) for diastolic orthostatic hypertension, and 1.728 (95 % C.I. 0.617–4.837, P = 0.298, n = 499) for diastolic orthostatic hypotension. For patients with either systolic or diastolic orthostatic hypertension or both, the hazard ratio was 0.394 (95 % C.I. 0.155–0.999, P = 0.050, n = 624) and for patients with either systolic or diastolic orthostatic hypotension or both, the hazard ratio was 1.342 (95 % C.I. 0.529–3.404, P = 0.536, n = 516).

Discussion

The principal finding of this prospective observational cohort study was that diastolic orthostatic hypertension was found in nearly one in five patients with type 2 diabetes, and that this condition was associated with a decreased risk for incident cardiovascular events, independently of classical cardiovascular risk factors.

The prevalence of orthostatic hypertension in our cohort was similar to previously reported data from patients with long term type 1 diabetes [25] and middle- aged [17] or elderly [18] patients with type 2 diabetes. It is difficult, however, to make comparisons between studies, since several different definitions of orthostatic hypertension have been used. In some studies [17, 25], a change from sitting systolic blood pressure < 140 mmHg to standing blood pressure ≥140 mmHg and/or a change from sitting diastolic blood pressure <90 mmHg to standing blood pressure ≥90 mmHg have been used, whereas other authors applied systolic cut-offs of 10 mmHg [18] or 20 mmHg [15, 26]. Diastolic cut-off values of 10 mmHg have been applied in two previous studies only [16, 27], none of which were confined to patients with type 2 diabetes. In the Atherosclerosis Risk in Communities Study [16], a diastolic blood pressure rise >10 mmHg was found in 9.2 % of participants. No association between diastolic orthostatic hypertension and stroke risk was found, but a linear relationship between diastolic orthostatic blood pressure change and incident non-lacunar thrombotic strokes was noted. In the Normative Aging Study [27], which included only presumably healthy men, diastolic blood pressure rise ≥10 mmHg was found in a similar proportion of participants (20.8 %) as in our cohort. The prognostic impact of diastolic orthostatic hypertension was not evaluated, but sitting diastolic blood pressure was a significant risk factor for myocardial infarctions only in patients with an exaggerated diastolic blood pressure rising reaction.

Considering previously reported data from patients with diabetes mellitus [1, 2], we found a lower than expected prevalence of orthostatic hypotensive blood pressure reactions in our cohort. A possible explanation may be that we measured blood pressure in the sitting rather than in the supine position. Although this is in accordance with recent guidelines for resting blood pressure measurements [28], it may have contributed to an underestimation of the prevalence of orthostatic hypotensive reactions. Furthermore, delayed orthostatic hypotension has been found to be quite common in patients undergoing head-up tilt tests [29] and since we measured the standing blood pressure 2 minutes after the patients had risen, patients with later orthostatic hypotension may not have been identified. Indeed, previous studies in which orthostatic hypotension occurred more frequently [1, 2] included systolic measurements obtained after 3 minutes of standing. This discrepancy in methodology may have contributed to the relatively low prevalence of orthostatic hypotension in our cohort. We also did not find any statistically significant associations between orthostatic hypotension and any particular antihypertensive drug class, which is in contrast to other reports, where beta blockers [30] and calcium antagonists and alpha blockers [31] have been associated with this condition.

Since diastolic blood pressure control is particularly important in patients with diabetes mellitus [32], our finding that diastolic orthostatic hypertension was associated with a lower risk for cardiovascular events may at first seem counter-intuitive. However, it is important to bear in mind that the definition of diastolic orthostatic hypertension in our study was based on the change of the diastolic blood pressure, not on absolute diastolic blood pressure levels. In fact, sitting diastolic blood pressure was significantly lower in patients with diastolic orthostatic hypertension, and only a minority of patients with diastolic orthostatic hypertension had standing blood pressure >90 mmHg. The majority of the endpoint events in our trial were related to ischemic heart disease. Since myocardial perfusion occurs mainly during diastole, it could be speculated that an inability to raise the diastolic blood pressure during orthostasis puts the myocardium at increased risk for episodes of hypoperfusion, particularly in the presence of coronary artery disease. Supporting this theory is the finding that in the Captoril Prevention Project, diastolic orthostatic hypotension was a predictor of myocardial infarctions but not of strokes, whereas systolic orthostatic hypotension predicted strokes but not myocardial infarctions [3]. Possibly, this could be a consequence of the cerebral perfusion being more dependent than the myocardial perfusion on systolic blood pressure. The low number of patients with systolic orthostatic hypotension, as well as the relatively low number of strokes that occurred in our cohort, may have precluded us from elucidating any associations between systolic orthostatic hypotension and cerebrovascular disease. It should also be noted that previous investigations have shown an association between a marked blood pressure elevation during exercise stress testing and a good prognosis [33, 34], although the impact of the diastolic blood pressure response has not been studied in detail in these circumstances.

Early pathogenetic studies [35] on orthostatic hypertension showed that in patients with this condition, excessive gravitational pooling of blood in the lower extremities causes a reduction of cardiac output, which leads to a compensatory sympathetic hyperactivity followed by an abnormally intense arterial vasoconstriction which raises the diastolic blood pressure. Increased peripheral vascular resistance has been demonstrated in patients with orthostatic hypertension who underwent a head-up tilt test [36]. Further support of a role for peripheral resistance in the pathogenesis of this condition comes from a case report in which a patient with severe symptomatic orthostatic hypertension was successfully treated with an alpha blocker [37]. We did not perform measurements of endothelial function in our study, but it could be speculated that diastolic orthostatic hypertension is associated with preserved endothelial function, which would help explain the decreased risk associated with this condition in our cohort. In patients with type 2 diabetes, baroreflex hypersensitivity has been suggested as a factor contributing to orthostatic hypertension [17]. Increased arterial stiffness may also be a relevant contributing condition, and we found an association between the presence of systolic orthostatic hypertension and high aortic PWV in our cohort, which is in contrast to what has previously been reported in a smaller pioneering study [38].

In the present study, we did not find a statistically significant increased risk in patients with orthostatic hypotension, regardless of whether diastolic or systolic diagnostic criteria were applied. This is in contrast to several previously published reports [2–12]. This discrepancy may be due simply to a lack of power, since relatively few patients exhibited these blood pressure reactions in our cohort. Therefore, these results should be cautiously interpreted. Furthermore, since we did find an association between diastolic orthostatic hypotension and markers of increased arterial stiffness (PWV) and atherosclerosis (carotid IMT), this condition may not be entirely harmless. Since the value of diastolic rather than systolic orthostatic hypotension as a marker of risk for myocardial infarction has been described previously in three studies [3, 5, 10], our results may suggest that the diastolic orthostatic hypotensive reaction is of particular importance in terms of risk stratification, at least in patients at high risk for coronary artery disease.

Strengths of our study include the community-based approach, in which patients were recruited from primary care with few exclusion criteria and with no patients lost to follow-up. In our opinion, the most important study limitation was that few patients fulfilled the criteria for diastolic or systolic orthostatic hypotension. Thus, the lack of statistically significant associations between orthostatic hypotension and the combined end-point may be attributable to a lack of statistical power. Furthermore, there were relatively few events, which precludes us from exploring possible gender differences, and from separately studying patients with or without antihypertensive medications. Larger studies that directly compare the predictive value of different orthostatic blood pressure reactions, as well as the impact of different antihypertensive drugs on orthostatic blood pressure reactions, should be encouraged in patients with type 2 diabetes. Finally, it should be noted that the orthostatic blood pressure response was diagnosed at one single occasion. Since the reproducibility of orthostatic blood pressure reactions has been shown to be poor [39], it is possible that some patients would have changed orthostatic status if the measurement had been repeated at several occasions. Thus, although diastolic orthostatic hypertension diagnosed at one single occasion was a significant and independent predictor of decreased cardiovascular risk in our cohort, it would seem justified in clinical practice to repeat the measurement on several occasions in order to enhance the prognostic performance.

Conclusions

Diastolic orthostatic hypertension was common in patients with type 2 diabetes, and was associated with a decreased cardiovascular risk, whereas diastolic orthostatic hypotension was associated with significantly increased degree of sub-clinical target organ damage. Evaluation of the orthostatic blood pressure reaction is easy to perform in everyday clinical praxis, and should be encouraged in patients with type 2 diabetes. We suggest that health care providers pay attention to the diastolic orthostatic blood pressure response, which was frequently abnormal in our cohort, and which may add independent prognostic information beyond traditional risk factors. Larger studies aiming at determining the optimal definitions of orthostatic blood pressure reactions, as well as the number of measurements required to confirm the diagnosis, seem warranted in patients with type 2 diabetes.

Abbreviations

CARDIPP:

cardiovascular risk factors in patients with diabetes—a prospective study in primary care

CI:

confidence interval

ECG:

electrocardiogram

eGFR:

estimated glomerular filtration rate

HbA1c:

glycosylated hemoglobinA1

HDL:

high-density lipoprotein

HR:

hazard ratio

IMT:

intima-media thickness

LDL:

low-density lipoprotein

PWV:

pulse wave velocity

References

  1. Wu JS, Yang YC, Lu FH, Wu CH, Wang RH, Chang CJ. Population-based study on the prevalence and risk factors of orthostatic hypotension in subjects with pre-diabetes and diabetes. Diabetes Care. 2009;32:69–74.

    Article  PubMed  PubMed Central  Google Scholar 

  2. Luukinen H, Airaksinen KE. Orthostatic hypotension predicts vascular death in older diabetic patients. Diabetes Res Clin Pract. 2005;67:163–6.

    Article  PubMed  Google Scholar 

  3. Fedorowski A, Wahlstrand B, Hedner T, Melander O. Systolic and diastolic component of orthostatic hypotension and cardiovascular events in hypertensive patients: the captopril prevention project. J Hypertens. 2014;32:75–81.

    Article  CAS  PubMed  Google Scholar 

  4. Davis BR, Langford HG, Blaufox MD, Curb JD, Polk BF, Shulman NB. The association of postural changes in systolic blood pressure and mortality in persons with hypertension: the hypertension detection and follow-up program experience. Circulation. 1987;75:340–6.

    Article  CAS  PubMed  Google Scholar 

  5. Luukinen H, Koski K, Laippala P, Airaksinen KE. Orthostatic hypotension and the risk of myocardial infarction in the home-dwelling elderly. J Intern Med. 2004;255:486–93.

    Article  CAS  PubMed  Google Scholar 

  6. Luukinen H, Koski K, Laippala P, Kivela SL. Prognosis of diastolic and systolic orthostatic hypotension in older persons. Arch Intern Med. 1999;159:273–80.

    Article  CAS  PubMed  Google Scholar 

  7. Masaki KH, Schatz IJ, Burchfiel CM, Sharp DS, Chiu D, Foley D, et al. Orthostatic hypotension predicts mortality in elderly men: the honolulu heart program. Circulation. 1998;98:2290–5.

    Article  CAS  PubMed  Google Scholar 

  8. Fagard RH, De Cort P. Orthostatic hypotension is a more robust predictor of cardiovascular events than nighttime reverse dipping in elderly. Hypertension. 2010;56:56–61.

    Article  CAS  PubMed  Google Scholar 

  9. Rose KM, Tyroler HA, Nardo CJ, Arnett DK, Light KC, Rosamond W, et al. Orthostatic hypotension and the incidence of coronary heart disease: the atherosclerosis risk in communities study. Am J Hypertens. 2000;13:571–8.

    Article  CAS  PubMed  Google Scholar 

  10. Fedorowski A, Stavenow L, Hedblad B, Berglund G, Nilsson PM, Melander O. Orthostatic hypotension predicts all-cause mortality and coronary events in middle-aged individuals (the malmo preventive project). Eur Heart J. 2010;31:85–91.

    Article  PubMed  PubMed Central  Google Scholar 

  11. Eigenbrodt ML, Rose KM, Couper DJ, Arnett DK, Smith R, Jones D. Orthostatic hypotension as a risk factor for stroke: the atherosclerosis risk in communities (ARIC) study, 1987–1996. Stroke. 2000;31:2307–13.

    Article  CAS  PubMed  Google Scholar 

  12. Rose KM, Eigenbrodt ML, Biga RL, Couper DJ, Light KC, Sharrett AR, et al. Orthostatic hypotension predicts mortality in middle-aged adults: the atherosclerosis risk in communities (aric) study. Circulation. 2006;114:630–6.

    Article  PubMed  Google Scholar 

  13. Fessel J, Robertson D. Orthostatic hypertension: when pressor reflexes overcompensate. Nat Clin Pract Nephrol. 2006;2:424–31.

    Article  PubMed  Google Scholar 

  14. Buddineni JP, Chauhan L, Ahsan ST, Whaley-Connell A. An emerging role for understanding orthostatic hyp’er’tension in the cardiorenal syndrome. Cardiorenal Med. 2011;1:113–22.

    Article  PubMed  PubMed Central  Google Scholar 

  15. Kario K, Eguchi K, Hoshide S, Hoshide Y, Umeda Y, Mitsuhashi T, et al. U-curve relationship between orthostatic blood pressure change and silent cerebrovascular disease in elderly hypertensives: orthostatic hypertension as a new cardiovascular risk factor. J Am Coll Cardiol. 2002;40:133–41.

    Article  PubMed  Google Scholar 

  16. Yatsuya H, Folsom AR, Alonso A, Gottesman RF, Rose KM. Postural changes in blood pressure and incidence of ischemic stroke subtypes: the ARIC study. Hypertension. 2011;57:167–73.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  17. Yoshinari M, Wakisaka M, Nakamura U, Yoshioka M, Uchizono Y, Iwase M. Orthostatic hypertension in patients with type 2 diabetes. Diabetes Care. 2001;24:1783–6.

    Article  CAS  PubMed  Google Scholar 

  18. Mesquita P, Queiroz D, de Lima Lamartine, Silva V, Texeira Vde C, Vilaca de Lima YR, Junior ER, et al. Prevalence of orthostatic hypertension in elderly patients with type 2 diabetes. Int J Endocrinol. 2015;2015:463487.

    Article  PubMed  PubMed Central  Google Scholar 

  19. Wijkman M, Lanne T, Engvall J, Lindstrom T, Ostgren CJ, Nystrom FH. Masked nocturnal hypertension–a novel marker of risk in type 2 diabetes. Diabetologia. 2009;52:1258–64.

    Article  CAS  PubMed  Google Scholar 

  20. Wijkman M, Lanne T, Grodzinsky E, Ostgren CJ, Engvall J, Nystrom FH. Ambulatory systolic blood pressure predicts left ventricular mass in type 2 diabetes, independent of central systolic blood pressure. Blood Press Monit. 2012;17:139–44.

    Article  PubMed  Google Scholar 

  21. Freeman R, Wieling W, Axelrod F, Benditt D, Benarroch E, Biaggioni I, et al. Consensus statement on the definition of orthostatic hypotension, neurally mediated syncope and the postural tachycardia syndrome. Clin Auton Res. 2011;21:69–72.

    Article  PubMed  Google Scholar 

  22. Dahlen EM, Lanne T, Engvall J, Lindstrom T, Grodzinsky E, Nystrom FH, et al. Carotid intima-media thickness and apolipoprotein B/apolipoprotein A-I ratio in middle-aged patients with Type 2 diabetes. Diabet Med. 2009;26:384–90.

    Article  CAS  PubMed  Google Scholar 

  23. Hoelzel W, Weykamp C, Jeppsson JO, Miedema K, Barr JR, Goodall I, et al. IFCC reference system for measurement of hemoglobin A1c in human blood and the national standardization schemes in the United States, Japan, and Sweden: a method-comparison study. Clin Chem. 2004;50:166–74.

    Article  CAS  PubMed  Google Scholar 

  24. Levey AS, Bosch JP, Lewis JB, Greene T, Rogers N, Roth D. A more accurate method to estimate glomerular filtration rate from serum creatinine: a new prediction equation. Modification of diet in renal disease study group. Ann Intern Med. 1999;130:461–70.

    Article  CAS  PubMed  Google Scholar 

  25. Hirai FE, Moss SE, Klein BE, Klein R. Postural blood pressure changes and associated factors in long-term type 1 diabetes: wisconsin epidemiologic study of diabetic retinopathy. J Diabetes Complications. 2009;23:83–8.

    Article  PubMed  PubMed Central  Google Scholar 

  26. Nardo CJ, Chambless LE, Light KC, Rosamond WD, Sharrett AR, Tell GS, et al. Descriptive epidemiology of blood pressure response to change in body position. The ARIC study. Hypertension. 1999;33:1123–9.

    Article  CAS  PubMed  Google Scholar 

  27. Sparrow D, Tifft CP, Rosner B, Weiss ST. Postural changes in diastolic blood pressure and the risk of myocardial infarction: the normative aging study. Circulation. 1984;70:533–7.

    Article  CAS  PubMed  Google Scholar 

  28. Mancia G, Fagard R, Narkiewicz K, Redón J, Zanchetti A, Böhm M, et al. 2013 ESH/ESC guidelines for the management of arterial hypertension. J Hypertens. 2013;31:1281–357.

    Article  CAS  PubMed  Google Scholar 

  29. Gibbons CH, Freeman R. Delayed orthostatic hypotension. Neurology. 2006;67:28–32.

    Article  PubMed  Google Scholar 

  30. Canney M, O`Connell MDL, Murphy CM, O`Leary N, Little MA, O`Seaghdha CM, et al. Single agent antihypertensive therapy and orthostatic blood pressure behaviour in older adults using beat-to-beat measurements: the irish longitudinal study on ageing. PLoS One. 2016;11(1):e0146156.

    Article  PubMed  PubMed Central  Google Scholar 

  31. Wecht JM, Weir JP, Martinez S, Eraifej M, Bauman WA. Orthostatic hypotension and orthostatic hypertension in American veterans. Clin Auton Res. 2016;26:49–58.

    Article  PubMed  Google Scholar 

  32. Hansson L, Zanchetti A, Carruthers SG, Dahlof B, Elmfeldt D, Julius S, et al. Effects of intensive blood-pressure lowering and low-dose aspirin in patients with hypertension: principal results of the Hypertension Optimal Treatment (HOT) randomised trialHOT Study Group. Lancet. 1998;351:1755–62.

    Article  CAS  PubMed  Google Scholar 

  33. Habibzadeh MR, Farzaneh-Far R, Sarna P, Na B, Schiller NB, Whooley MA. Association of blood pressure and heart rate response during exercise with cardiovascular events in the heart and soul study. J Hypertens. 2010;28:2236–42.

    Article  CAS  PubMed  Google Scholar 

  34. Hedberg P, Ohrvik J, Lonnberg I, Nilsson G. Augmented blood pressure response to exercise is associated with improved long-term survival in older people. Heart. 2009;95:1072–8.

    Article  CAS  PubMed  Google Scholar 

  35. Streeten DH, Auchincloss JH Jr, Anderson GH Jr, Richardson RL, Thomas FD, Miller JW. Orthostatic hypertension. Pathogenetic studies. Hypertension. 1985;7:196–203.

    Article  CAS  PubMed  Google Scholar 

  36. Lee H, Kim H-A. Orthostatic hypertension: an underestimated cause of orthostatic intolerance. Clin Neurophysiol. 2016;127:2102–7.

    Article  PubMed  Google Scholar 

  37. Chhabra L, Spodick D. Orthostatic Hypertension: recognizing an underappreciated clinical condition. Indian Heart J. 2013;65:454–6.

    Article  PubMed  PubMed Central  Google Scholar 

  38. Hoshide S, Kario K, Eguchi K, Ishikawa J, Morinari M, Shimada K. Altered aortic properties in elderly orthostatic hypertension. Hypertens Res. 2005;28:15–9.

    Article  Google Scholar 

  39. Vara-Gonzalez L, Arauzo Alonso S, Gonzalez Fernandez RM, Marin-Gil Vecilla M, Virseda Marin N, Munoz Cacho P. Reproducibility of postural changes of blood pressure in hypertensive elderly patients in primary care. Blood Press Monit. 2006;11:17–20.

    Article  PubMed  Google Scholar 

Download references

Authors’ contributions

MW researched data and wrote the manuscript. TL collected and researched data, contributed to the discussion and reviewed the manuscript. CJÖ collected and researched data, contributed to the discussion and reviewed the manuscript. FHN collected and researched data, contributed to the discussion and reviewed the manuscript. All authors read and approved the final manuscript.

Acknowledgements

This work was supported by Grant support from FORSS, the Research Council of Southeastern Sweden, and the by grants from the King Gustaf V and Queen Victoria Freemason Foundation, Sweden.

Competing interests

The authors declare that they have no competing interests.

Author information

Authors and Affiliations

  1. Department of Internal Medicine and Department of Medical and Health Sciences, Linköping University, Norrköping, Sweden

    Magnus Wijkman

  2. Department of Medical and Health Sciences, Linköping University, Linköping, Sweden

    Toste Länne, Carl Johan Östgren & Fredrik H. Nystrom

  3. Department of Internal Medicine, Vrinnevi Hospital, Gamla Övägen 25, 603 79, Norrköping, Sweden

    Magnus Wijkman

Authors
  1. Magnus Wijkman
    View author publications

    You can also search for this author in PubMed Google Scholar

  2. Toste Länne
    View author publications

    You can also search for this author in PubMed Google Scholar

  3. Carl Johan Östgren
    View author publications

    You can also search for this author in PubMed Google Scholar

  4. Fredrik H. Nystrom
    View author publications

    You can also search for this author in PubMed Google Scholar

Corresponding author

Correspondence to Magnus Wijkman.

Rights and permissions

Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 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.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Wijkman, M., Länne, T., Östgren, C.J. et al. Diastolic orthostatic hypertension and cardiovascular prognosis in type 2 diabetes: a prospective cohort study. Cardiovasc Diabetol 15, 83 (2016). https://doi.org/10.1186/s12933-016-0399-0

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: https://doi.org/10.1186/s12933-016-0399-0

Keywords

Cardiovascular Diabetology

ISSN: 1475-2840