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Journal of Human Hypertension
J Hum Hypertens. 2011 Jun; 25(6): 346–353.
Published online 2010 Nov 25. doi:  10.1038/jhh.2010.104
PMCID: PMC3099035

Olmesartan/amlodipine vs olmesartan/hydrochlorothiazide in hypertensive patients with metabolic syndrome: the OLAS study


We studied the effects of treatment with olmesartan/amlodipine and olmesartan/hydrochlorothiazide on inflammatory and metabolic parameters (including new-onset diabetes as a secondary endpoint) in non-diabetic hypertensive patients with metabolic syndrome (MetS). A total of 120 patients with MetS and stage I and II hypertension were randomized to olmesartan 20 mg/amlodipine 5 mg or olmesartan 20 mg/hydrochlorothiazide 12.5 mg. If target systolic blood pressure (<140 mm Hg) was not reached, doses were doubled after 13 weeks; doxazosin 4 mg was added after 26 weeks, and doubled after 39 weeks; follow-up ended at 78 weeks. At each visit, blood pressure (BP), fasting plasma glucose, insulin, adiponectin, tumour necrosis factor-α, C-reactive protein (CRP), intercellular adhesion molecule-1, vascular cell adhesion molecule-1, interleukins-1β, -6 and -8, and albuminuria were measured; BP was similarly reduced in both groups; 80% of patients reached target BP. Reductions in albuminuria were also similar (50%). Only olmesartan/amlodipine reduced the insulin resistance index (24%, P<0.01), increased plasma adiponectin (16%, P<0.05) and significantly reduced all of the inflammation markers studied, except CRP, which showed a similar reduction in each group. The risk of new-onset diabetes was significantly lower with olmesartan/amlodipine (P=0.02). Both olmesartan-based combinations were effective, but the amlodipine combination resulted in metabolic and anti-inflammatory effects that may have advantages over the hydrochlorothiazide combination.

Keywords: metabolic syndrome, olmesartan, amlodipine, hydrochlorothiazide, type 2 diabetes mellitus


The prevalence of metabolic syndrome (MetS) in patients with essential hypertension is very high, and has been estimated as being close to 50%.1 Hypertensive patients with MetS have a much higher cardiovascular (CV) risk than their counterparts without MetS,2 and also have a particularly high risk of developing type 2 diabetes mellitus (T2DM).3 In addition, the choice of antihypertensive therapy can have a large impact on the risk of development of T2DM.4 Renin–angiotensin system blockers, that is, angiotensin-converting enzyme inhibitors and angiotensin receptor blockers (ARBs), improve insulin sensitivity and reduce the risk of developing T2DM compared with placebo, whereas calcium channel blockers (CCBs) have a neutral effect. Thiazide diuretics and β-blockers decrease insulin sensitivity and increase the incidence of T2DM.4 Therefore, the combination of an ARB and a CCB might be particularly beneficial in patients with high metabolic risk.5

The present European Guidelines for the Management of Hypertension acknowledge that most high-risk hypertensive patients require a combination of antihypertensive drugs.6 For patients with MetS, the recommended combinations are renin–angiotensin system blockers combined with low-dose thiazide diuretics or CCBs.6 In spite of the well-known effect of antihypertensive treatment on glucose and lipid metabolism, few studies have been conducted specifically in hypertensive patients with MetS.7, 8 In addition to decreased insulin sensitivity, a low circulating level of adiponectin is a central feature of MetS and is strongly associated with the incidence of T2DM.9 High circulating levels of inflammatory markers such as tumour necrosis factor-α (TNF-α), C-reactive protein (CRP) and interleukins-1β (IL-1β), IL-6 and IL-8 are also a feature of MetS and increase the risk of developing T2DM.10 The adhesion molecules, intercellular adhesion molecule-1 (ICAM-1) and vascular cell adhesion molecule-1 (VCAM-1) are also strongly associated with certain features of MetS,11 particularly postprandial triglyceride and insulin levels, and may therefore be implicated in the development of atherosclerosis and T2DM.11

Olmesartan is the latest ARB to become available in clinical practice. A systematic review of the efficacy of ARBs in studies that used 24-h ambulatory blood pressure (BP) monitoring revealed that olmesartan may achieve greater ambulatory BP reductions than other ARBs, even though reductions in office BP were similar.12 Fixed-dose combinations of olmesartan with amlodipine and with hydrochlorothiazide have recently become available. In addition to other ancillary actions, amlodipine has been shown to have a modest insulin-sensitising effect that is additive to the effect of an ARB.13, 14

The primary objective of this stand-alone study, OLAS (OLmesartan/Amlodipine vs olmesartan/hydrochlorothiazide in metabolic Syndrome), was to investigate the effects of olmesartan/amlodipine and olmesartan/hydrochlorothiazide combination therapy on inflammatory (including TNF-α, CRP, IL-1β, -6 and -8, ICAM-1 and VCAM-1) and metabolic parameters (including insulin sensitivity and adiponectin), with new-onset T2DM as a secondary outcome measure, in non-diabetic hypertensive patients with MetS.


The patients recruited for this study were all Europid, aged 25–75 years and had stage I and II hypertension (systolic BP (SBP) 140–179 mm Hg) and MetS, as defined by the International Diabetes Federation for Europid populations15 (waist circumference >94 cm in men and >80 cm in women, and at least two of the following criteria: triglycerides >1.7 mmol l−1; high-density lipoprotein-cholesterol <1.03 mmol l−1 in men and <1.29 mmol l−1 in women; fasting blood glucose >5.6 mmol l−1; BP >135/80 mm Hg). Previous antihypertensive therapy, if any, was withdrawn during a washout period of 3–5 weeks before inclusion.

Patients with diabetes mellitus were excluded from the study and, in order to unmask hidden diabetes, a standard oral glucose tolerance test was performed in patients with fasting blood glucose >5.6 mmol l−1. Patients were also excluded if they showed evidence of unstable angina, acute coronary syndrome, myocardial infarction, decompensated congestive heart failure, stroke or transient ischemic attack within the previous 6 months, left ventricular outflow obstruction, liver dysfunction (serum bilirubin >1.5 × or plasma aminotransferases 2 × the upper normal limit), renal insufficiency (plasma creatinine >133 mmol l−1 in men and >124 mmol l−1 in women) or overt proteinuria (>300 mg per day). Patients with known hypersensitivity or a history of severe adverse effects with any ARB, CCB, thiazide diuretic or α-adrenergic blocker were excluded, as well as those with any contraindication for olmesartan, amlodipine, hydrochlorothiazide or doxazosin (based on the prescribing information for each drug). Pregnant women, nursing mothers, women of childbearing potential not using adequate contraceptive methods and patients with a history of mental illness or psychiatric disorders were also excluded.

The study was conducted according to standard good clinical practice guidelines and approved by the local ethics committee of participating centres. All participants provided written informed consent before inclusion.

A parallel-group, prospective, randomized, open-label, blinded end point design (PROBE) was used, and all measurements and procedures were performed by personnel blinded to the treatment allocation.16 The study design is shown in Figure 1. After baseline measurements were taken, patients were randomized to receive olmesartan (20 mg)+ amlodipine (5 mg) daily (OA group), or olmesartan (20 mg) + hydrochlorothiazide (12.5 mg) daily (OH group). After 13±2, 26±2, 39±2 and 78±2 weeks (approximately 3, 6, 9 and 18 months) all measurements were repeated. Those patients not reaching the SBP target (<140 mm Hg) were successively uptitrated to a double dose of the initial treatment after 13 weeks, an additional 4 mg of doxazosin (long-acting formulation) after 26 weeks, and 8 mg of doxazosin after week 39. Additional visits were performed after 52±2 and 65±2 weeks (12 and 15 months) but only BP, fasting blood glucose, compliance and tolerance data were obtained. Patients who had already been uptitrated to the maximum treatment doses but still had SBP >160 mm Hg were removed from the study. In all patients with fasting glycaemia >5.6 mmol l−1 but <7 mmol l−1 at any visit after the first, a standard oral glucose tolerance test was performed within the following 10 days. New-onset T2DM was diagnosed in patients with fasting glycaemia ⩾7 mmol l−1 or 120 min post-load glycaemia >11.1 mmol l−1, in the absence of clinical signs of type 1 or secondary diabetes mellitus, according to the current World Health Organization guidelines.17

Figure 1
Design of the OLAS study showing the antihypertensive treatment schedule. The treatment was uptitrated if the target systolic blood pressure (<140 mm Hg) had not been reached. A, amlodipine; D, doxazosin; H: hydrochlorothiazide; ...

Weight, height, waist circumference, fasting plasma glucose and insulin, lipid profile (that is, total cholesterol, high-density lipoprotein-cholesterol and triglycerides), creatinine, sodium, potassium, bilirubin, aminotransferases, high-sensitivity-CRP, and urinary albumin and creatinine (in early morning samples) were measured by standard clinical procedures. Heart rate and BP were measured according to current guidelines,6 using a validated semi-automatic device (OMRON 705P), in the morning (between 08:30 and 11:30) after 5 min of rest in a sitting position with the back supported; patients were advised to avoid smoking and caffeinated drinks 30 min before the measurement. The values for BP and heart rate obtained at each visit were the average of two measurements separated by at least 2 min; a third reading was obtained if there was a difference of 5 mm Hg or 5 beats per minute between the two readings.

Plasma TNF-α was measured using a commercial enzyme-linked immunosorbent assay (ARCUS Biologicals, Modena, Italy); plasma adiponectin, ICAM-1, VCAM-1 and interleukins-1β, -6 and -8 were also measured with a commercial enzyme-linked immunosorbent assay (LINCO Research Inc., MO, USA). The insulin resistance index (IRI) was estimated by the homeostasis model assessment formula:18 IRI=fasting plasma insulin × fasting plasma glucose/135, with insulin in pmol l−1 (1 mU per l=6.00 pmol l−1) and glucose in mmol l−1. Compliance was assessed by returned pill counts and tolerance by questionnaire.

An intention-to-treat analysis was performed in all patients who received at least one dose of study medication and had a subsequent efficacy observation. All analyses were specified a priori, except where otherwise indicated. All calculations were performed using the statistical software SPSS 15.0 (SPSS Inc., Chicago, IL, USA) for Microsoft Windows, including logistic regression modelling. The sample size was calculated with the assumption (based on a pilot trial) of a 25% difference in the means between the groups for most of the main variables (namely IRI, adiponectin, TNF-α, IL-1β, IL-6, ICAM-1, and VCAM-1), and a 40% variation coefficient within the groups, yielding 54 patients per group for a 90% statistical power with α=0.05. Assuming a 10% patient loss, a sample size of 60 per group was required. However, the study could be underpowered for the secondary objective (new-onset T2DM), as we did not have enough information to calculate an adequate sample size.

The data are presented as mean±s.d., with 95% confidence intervals for differences as appropriate. Changes from baseline and between groups in BP, heart rate and laboratory parameters were evaluated using a Student's t-test for paired or unpaired data, or analysis of variance, as appropriate. Categorical variables were compared using the χ2 or the Fisher's exact tests, as appropriate. The survival analysis for new-onset T2DM was performed using the Kaplan–Meier model followed by the log-rank test. The standard Pearson model was used for correlation analysis. All statistical tests were two-tailed and a P-value of <0.05 was considered statistically significant.


Enrolment for this trial began in May 2005, including a 6-month, 8-patient pilot trial to check for feasibility and to confirm the sample size calculation. A total of 256 patients were screened, of whom 120 were randomized. At baseline, the mean age was 59.3±8.1 years, 55% of patients were female, and the mean body mass index was 31.2±3.7 kg m−2. There were 60 patients in each group. The flowchart of the study is shown in Figure 2.

Figure 2
Flowchart of the OLAS study. Doses are mg per day. A, amlodipine; D, doxazosin; H, hydrochlorothiazide; O, olmesartan; OGTT, oral glucose tolerance test; SBP, systolic blood pressure; T2DM, type 2 diabetes mellitus.

Of the 120 patients randomized, 31 (25.8%) had received previous antihypertensive treatment; 17 in the OA group and 14 in the OH group. None had received combination treatment and all had a SBP >140 mm Hg; three had received a thiazide diuretic, two a β-blocker, nine a CCB (seven dihydropyridinic, two non-dihydropyridinic), nine an angiotensin-converting enzyme inhibitor, seven an ARB and one a direct renin inhibitor. A post hoc χ2-test showed that these drugs were evenly distributed between the groups.

BP decreased significantly in each group vs baseline (P<0.001), but there were no significant differences in BP control between the groups (analysis of variance, P=0.39). Figure 3 shows the BP values obtained during the study. The final SBP values were 126.5±9.0 and 129.9±10.9 mm Hg for the OA and OH groups, respectively, and the final diastolic BP values were 84.9±7.3 and 86.3±8.6 mm Hg. The mean differences between groups throughout the study were 1.5 mm Hg for SBP (−1.4 to 4.4) and 0.8 mm Hg for diastolic BP (−1.8 to 3.6). In the OA group, 53.3% of patients required doubling of the initial drug doses, and 30.0% required the addition of doxazosin. The respective figures for the OH group were 53.3 and 31.7%. By week 26, before the addition of doxazosin, 68.3% of patients in the OA group and 66.7% in the OH group had reached the target BP; at the end of the study, the respective figures were 81.7 and 78.3%.

Figure 3
Systolic and diastolic blood pressures during the OLAS study. Those patients who did not achieve systolic blood pressure target (<140 mm Hg) received 4 mg of doxazosin at week 26, which was doubled to 8 mg of doxazosin ...

The baseline values for all of the quantitative variables in both groups are presented in Table 1. There were no significant differences between groups at baseline. For body mass index, waist circumference, fasting plasma glucose, sodium, potassium, creatinine, lipid profile, bilirubin and aminotransferases, no differences between the treatment groups were found throughout the study; the final values are presented in Table 2.

Table 1
Baseline values for all of the quantitative variables in both groups
Table 2
Final values (week 78) for the quantitative variables that did not change significantly in both groups

The albumin excretion rate decreased significantly in both groups (P<0.01), with no between-group differences. In the OA group, the percentage reductions were 34.1% at week 26 and 50.0% at week 78; in the OH group, the reductions were 36.2 and 53.7%, respectively. The 95% confidence intervals for the differences were, respectively, −7.5 to 11.8% and −5.9 to 13.4%. The IRI and plasma fasting insulin were significantly reduced in the OA group (by 24.1 and 25.0%, respectively, both P<0.01), whereas adiponectin was increased by 16.3% (P<0.01). In the OH group, changes in IRI, plasma fasting insulin and adiponectin were not significant. These differences between the two groups were significant. Figure 4a shows the percentage changes in albuminuria, fasting insulin, IRI and adiponectin; the percentage changes in adiponectin showed an inverse correlation with the percentage changes in the IRI (Pearson's R test=−0.54, P<0.001).

Figure 4
(a) Percentage change from baseline in urinary albumin/creatinine quotient, fasting plasma insulin, homeostasis model assessment index of insulin resistance and plasma adiponectin. (b) Percentage changes from baseline in inflammatory markers: tumour necrosis ...

Of the inflammation markers studied, only CRP was significantly reduced in both groups (by 16.7 and 14.1% in the OA and OH groups, respectively, both P<0.05; 95% confidence intervals for the difference was −2.1 to 7.2%), with no significant difference between the two groups. The other inflammation markers were significantly reduced in the OA group only (by 16.1% for TNF-α, 18.5% for IL-1β, 18.1% for IL-6, 12.8% for IL-8, 20.8% for ICAM-1 and 30.8% for VCAM-1); the between-group differences were significant for all of these inflammation markers. Figure 4b shows the percentage changes in all of the inflammation markers studied.

A post hoc analysis was performed within each group in order to assess the effect of the addition of doxazosin (after week 26) on the studied variables. With the exception of a significant reduction in SBP and diastolic BP (similar for both groups), no differences could be found between the patients taking doxazosin and those not receiving doxazosin. After week 26, the only variables that underwent significant changes were SBP and diastolic BP (Figure 3), and new-onset T2DM (Figure 5).

Figure 5
Kaplan–Meier survival analysis for the incidence of type 2 diabetes mellitus. A, amlodipine; ARR, absolute risk reduction; H, hydrochlorothiazide; O, olmesartan; OR, odds ratio.

During the study, three patients (5.0%) developed T2DM in the OA group, compared with 11 (18.3%) in the OH group (odds ratio 4.24 for OA vs OH; absolute risk reduction 13.3%). The Kaplan–Meier survival analysis is plotted in Figure 5. The log-rank test showed a significant difference between the groups (P=0.02). A logistic regression modelling analysis determined that the predictors of T2DM development (after adjustement for gender and baseline values of age, body mass index, waist circumference and fasting plasma glucose) were: the IRI (OR 1.27 per 0.5 AU increment, P=0.013), OH treatment (OR 3.98, P=0.023) and low adiponectin (OR 2.26 per 1 μg ml−1 decrement, P=0.043). The addition of doxazosin showed no correlation with new-onset T2DM.

The compliance rate was high: 96.1% for the OA group up to week 26 and 92.7% at the end of the study; the respective figures were 94.1 and 91.8% for the OH group. Only one patient withdrew from the study because of side effects (malleolar oedema, in the OA group) but minor side effects were reported by low proportions of patients in the OA group (oedema (8.3%), headache (6.7%) and flushing or dizziness (1.7%)) and in the OH group (oedema (3.3%), headache (5.0%) and flushing or dizziness (5.0%)). Three patients (5.0%) in each group were withdrawn from the study because of poor BP control, with SBP >160 mm Hg despite full treatment. There were no differences in the incidence of side effects between the groups (Fisher's exact test). None of the patients had hypokalaemia during the study, and the correlation studies between potassium and insulin, glucose or IRI were negative (data not shown).


The findings of this study demonstrate that both antihypertensive combinations—olmesartan plus amlodipine and olmesartan plus hydrochlorothiazide—are well tolerated and effective in non-diabetic hypertensive subjects with MetS, and allow achievement of adequate BP control in the majority of patients using a simple treatment strategy. Combination treatment has been shown to increase the efficacy of treatment and reduce adverse effects.19 A recent large meta-analysis has shown that the extra BP reduction that can be obtained with a combination of drugs from different classes is approximately five times greater than the BP reduction produced by doubling the dose of one drug.20 The olmesartan/amlodipine combination was factorially evaluated in the COACH trial, a large, multicentre, randomized, double-blind, placebo-controlled study.21 The olmesartan/hydrochlorothiazide combination has also been extensively studied.22 Each of these olmesartan-based combinations has been found to be well tolerated and effective. However, to the best of our knowledge, neither of the combinations has been studied specifically in patients with MetS, and data on their effects in obese hypertensive patients are very scarce. Most of our patients were obese, as expected in a group with MetS; moreover, the prevalence of obesity in our community is among the highest in Europe.23 The validity of the MetS concept has been recently challenged for CV risk prediction,24 but it remains a useful predictor of T2DM development.

In the present study, significant reductions in urinary albumin/creatinine quotient were also observed in both treatment arms. Microalbuminuria is highly prevalent in non-diabetic hypertensive subjects with MetS,25 and is a well-known marker of both renal and CV risk.26 The LIFE trial, in hypertensive patients with left ventricular hypertrophy, showed that reductions in albumin excretion during treatment translate into a reduction in the risk of CV events.27

The OLAS study also shows that there are clear differences between the two olmesartan-based combinations with regard to metabolic and inflammatory markers. It has long been established that thiazide diuretics impair insulin sensitivity and increase the incidence of T2DM.4 This adverse effect can only partially be explained by hypokalaemia; a systematic review of the available evidence found that thiazides are diabetogenic even in the absence of changes in the plasma potassium level.28

Thiazide diuretics have been shown to reduce hard CV endpoints in many large controlled trials, and are recommended as first-line treatment for hypertension in the current guidelines.6, 29 However, most of these trials have been based on chlorthalidone or indapamide, whereas the currently recommended low doses (up to 25 mg per day) of hydrochlorothiazide have never been shown to reduce CV morbidity and mortality.30 Nevertheless, hydrochlorothiazide is, by far, the most prescribed thiazide diuretic worldwide, and the one used in almost all of the available single-pill combinations containing a diuretic.

The MEchanisms for the DIabetes preventing effect of CAndesartan (MEDICA) study found that, compared with candesartan, hydrochlorothiazide increased insulin resistance in a manner that was not related to hypokalaemia, but was associated with fat redistribution, an increase in visceral adiposity, steatohepatitis and low-grade inflammation.31 The Pharmacogenomic Evaluation of Antihypertensive Responses study found that the adverse metabolic effects (including new-onset T2DM) of hydrochlorothiazide, alone or associated with atenolol, were more frequent and severe in patients with abdominal obesity.32 The Study of Trandolapril/Verapamil SR And Insulin Resistance (STAR), showed that in non-diabetic hypertensive patients with MetS, an angiotensin-converting enzyme inhibitor/CCB combination was associated with a much lower risk of developing diabetes than an ARB/hydrochlorothiazide combination, despite similar reduction in BP;7 a correlation with potassium levels was also excluded. Our results regarding the development of T2DM are comparable, and also ruled out thiazide-induced hypokalaemia as the cause. Moreover, we were able to establish the predictive role of low adiponectin levels in this model, even independently of the changes in the insulin sensitivity index. In fact, low adiponectin is a powerful independent predictor of T2DM.9

The clinical relevance of the changes in these metabolic parameters is unknown, although a higher incidence of T2DM may not be trivial. The importance of new-onset T2DM in hypertension trials has been challenged, as it does not seem to be associated with a higher risk of mortality or clinical events in the short term,33 and for some authors its possible occurrence should not influence the selection of antihypertensive drug.34 Moreover, the STAR Long-Term Extension Trial showed that it is partially reversible.35 The risk associated with new-onset T2DM may become apparent only in very long-term studies, except in very high-risk situations. In the VALIANT trial, after an acute myocardial infarction, patients with previously known or newly diagnosed diabetes mellitus had similarly increased risks of mortality and CV events, much higher than non-diabetic patients.36

Recently, the Avoiding Cardiovascular events through COMbination therapy in Patients LIving with Systolic Hypertension (ACCOMPLISH) trial showed a 20% reduction in the risk of CV events and mortality with the use of a fixed-dose combination of benazepril/amlodipine, compared with a fixed-dose combination of benazepril/hydrochlorothiazide, despite similar reduction in BP.37 These results point to an, as yet, unknown BP-independent mechanism, although a reduction in central BP may also be implied.38 Although an ARB was prescribed instead of an angiotensin-converting enzyme inhibitor in the OLAS study, these treatment strategies are generally similar, and our results suggest that the different effects on inflammatory mediators could contribute to the results shown in ACCOMPLISH. Blockade of the renin–angiotensin system has anti-inflammatory actions and, in particular, olmesartan has been shown to reduce CRP, TNF-α, IL-6 and monocyte chemotactic protein-1 in the EUropean Trial on Olmesartan and Pravastatin in Inflammation and Atherosclerosis (EUTOPIA).39 Amlodipine also has anti-inflammatory properties,13 whereas hydrochlorothiazide elicits microinflammation and increases the circulating levels of CRP.31 The clinical relevance of these findings is, however, not yet established.

The PROBE design may introduce investigator bias but has been validated in many hypertension trials to date, and reflects usual clinical practice more closely than a randomized controlled design.40 Another limitation of the present study is a small, not significant but consistent difference in blood pressure (1.5/0.8 mm Hg lower in the OA group). However, a post hoc analysis did not find a significant correlation between this difference and the observed changes in metabolic and inflammation parameters.

In conclusion, both the olmesartan/amlodipine and olmesartan/hydrochlorothiazide combinations were effective and well tolerated in this study, but the effects on metabolic and inflammatory markers and on new-onset T2DM were possibly more favourable for the combination containing the CCB. The impressive results of the ACCOMPLISH trial on hard CV endpoints have not been explained, but our study may be hypothesis-generating and stimulate further research that may eventually elucidate the BP-independent protection afforded by the renin–angiotensin system blocker/CCB combination.

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The authors gratefully acknowledge the altruistic collaboration of the nurses and auxiliary personnel in our Hypertension Clinic, and also of the laboratory personnel. The authors would also like to thank Jo Bentley (inScience Communications, a Wolters Kluwer business), whose services were funded by Daiichi-Sankyo, for editing this manuscript for English language. This study was supported by a grant from the Fundación Canaria COMLP #01501008.


Francisco Javier Martinez-Martin has received lecture fees from Daiichi-Sankyo, Pfizer, Menarini, Chiesi, Takeda and others and also grant funding from Pfizer and Chiesi, but none directly related to this study. The authors have no other relevant affiliations or financial involvement with any entity with a financial interest or conflict related with the subject of this article.


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