Purpose: Through describing the confusing misdiagnosis process of Liddle syndrome, we try to reveal the importance of accurate aldosterone-renin detection and a genetic test for Liddle syndrome.
Methods: We found a family of hypertension and hypokalaemia with the proband of a 21-year-old female who had been misdiagnosed as primary aldosteronism (PA). She presented with high aldosterone and low renin levels. Aldosterone is not suppressed in the saline infusion test and captopril challenge test. However, treatment with a standard dose of spironolactone has no blood pressure improvement effect. A heterozygous variant of SCNN1G was found with whole exome sequencing and Liddle syndrome is indicated. Treatment with amiloride was effective. We rechecked aldosterone-renin levels with two different aldosterone and renin test kits. Clinical features and the mutant gene SCNN1G of each family member were determined by the Sanger method.
Results: The two kits had nearly opposite results. Among those Liddle syndrome patients confirmed by a genetic test, for Test kit A all ARR were screened positive while for test kit B negative. It seems Test kit B is consistent with the diagnosis while test kit A misleads the diagnosis. A novel SCNN1G mutation, c.1729 C > T, was found in this family, which introduce a premature stop codon in the γ subunit in the epithelial Na+ channel (ENaC) and resulted in a deletion of 72 amino acids at the carboxyl end.
Conclusion: inaccurate ARR detection might misdiagnose Liddle syndrome. A Gene test is an important method for the diagnosis of Liddle syndrome. A novel SCNN1G missense mutation, c.1729 C > T, is found in a Chinese family.
{"title":"Liddle syndrome misdiagnosed as primary aldosteronism is caused by inaccurate aldosterone-rennin detection while a novel <i>SCNN1G</i> mutation is discovered.","authors":"Yaling Yang, Chenwei Wu, Duoduo Qu, Xinyue Xu, Lili Chen, Quanya Sun, Xiaolong Zhao","doi":"10.1080/08037051.2022.2088471","DOIUrl":"https://doi.org/10.1080/08037051.2022.2088471","url":null,"abstract":"<p><strong>Purpose: </strong>Through describing the confusing misdiagnosis process of Liddle syndrome, we try to reveal the importance of accurate aldosterone-renin detection and a genetic test for Liddle syndrome.</p><p><strong>Methods: </strong>We found a family of hypertension and hypokalaemia with the proband of a 21-year-old female who had been misdiagnosed as primary aldosteronism (PA). She presented with high aldosterone and low renin levels. Aldosterone is not suppressed in the saline infusion test and captopril challenge test. However, treatment with a standard dose of spironolactone has no blood pressure improvement effect. A heterozygous variant of <i>SCNN1G</i> was found with whole exome sequencing and Liddle syndrome is indicated. Treatment with amiloride was effective. We rechecked aldosterone-renin levels with two different aldosterone and renin test kits. Clinical features and the mutant gene SCNN1G of each family member were determined by the Sanger method.</p><p><strong>Results: </strong>The two kits had nearly opposite results. Among those Liddle syndrome patients confirmed by a genetic test, for Test kit A all ARR were screened positive while for test kit B negative. It seems Test kit B is consistent with the diagnosis while test kit A misleads the diagnosis. A novel <i>SCNN1G</i> mutation, c.1729 C > T, was found in this family, which introduce a premature stop codon in the γ subunit in the epithelial Na<sup>+</sup> channel (ENaC) and resulted in a deletion of 72 amino acids at the carboxyl end.</p><p><strong>Conclusion: </strong>inaccurate ARR detection might misdiagnose Liddle syndrome. A Gene test is an important method for the diagnosis of Liddle syndrome. A novel <i>SCNN1G</i> missense mutation, c.1729 C > T, is found in a Chinese family.</p>","PeriodicalId":9000,"journal":{"name":"Blood Pressure","volume":" ","pages":"139-145"},"PeriodicalIF":1.8,"publicationDate":"2022-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"40071523","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2021-12-01Epub Date: 2021-10-29DOI: 10.1080/08037051.2021.1995981
Sverre E Kjeldsen, Guido Grassi, Reinhold Kreutz, Giuseppe Mancia
Blood pressure (BP) has been measured as office BP, usually taken after 5 minutes of quiet rest, in all clinical outcome trials in hypertension until recently, when the Systolic Blood Pressure Intervention Trial (SPRINT) was carried out. In the publication of the main SPRINT results it was not evident how BP had been measured (1). Following some literature search (2) it became visible that BP in SPRINT was taken as unattended automated office blood pressure (unattendedAOBP). The more than 100 sites participating in the SPRINT Study in the U.S.A. used the Omron 907 automated device. Personal were additionally trained to use the full capacity of this device by leaving the room prior to the 5 minutes period of rest followed by the preset unattended automated measurements at 5, 6 and 7 minutes. This is properly described in later publications including the article reporting the subgroup data in the elderly participants (3). However, a post hoc investigation in response to the debate suggested that not all investigators had followed the protocol and left the room prior to BP measurement (3). Alternatively, some of the SPRINT investigators years later may in fact not remember how their personal had performed the BP measurement.
{"title":"Attended vs. unattended blood pressure - learnings beyond SPRINT.","authors":"Sverre E Kjeldsen, Guido Grassi, Reinhold Kreutz, Giuseppe Mancia","doi":"10.1080/08037051.2021.1995981","DOIUrl":"https://doi.org/10.1080/08037051.2021.1995981","url":null,"abstract":"Blood pressure (BP) has been measured as office BP, usually taken after 5 minutes of quiet rest, in all clinical outcome trials in hypertension until recently, when the Systolic Blood Pressure Intervention Trial (SPRINT) was carried out. In the publication of the main SPRINT results it was not evident how BP had been measured (1). Following some literature search (2) it became visible that BP in SPRINT was taken as unattended automated office blood pressure (unattendedAOBP). The more than 100 sites participating in the SPRINT Study in the U.S.A. used the Omron 907 automated device. Personal were additionally trained to use the full capacity of this device by leaving the room prior to the 5 minutes period of rest followed by the preset unattended automated measurements at 5, 6 and 7 minutes. This is properly described in later publications including the article reporting the subgroup data in the elderly participants (3). However, a post hoc investigation in response to the debate suggested that not all investigators had followed the protocol and left the room prior to BP measurement (3). Alternatively, some of the SPRINT investigators years later may in fact not remember how their personal had performed the BP measurement.","PeriodicalId":9000,"journal":{"name":"Blood Pressure","volume":" ","pages":"439-440"},"PeriodicalIF":1.8,"publicationDate":"2021-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39573998","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2021-12-01Epub Date: 2021-10-26DOI: 10.1080/08037051.2021.1993735
Andreas Skræddergaard, Jakob Nyvad, Kent Lodberg Christensen, Arne Hørlyck, Hossein Mohit Mafi, Mark Reinhard
A 16-year-old patient presented with abdominal pain and sustained hypertension. Thorough evaluation including renography with and without captopril and renal vein renin sampling were normal. Duplex ultrasound, however, raised suspicion of a renal artery stenosis. This was confirmed by computed tomography angiography which showed a severe branch artery stenosis with post-stenotic dilatation consistent with focal fibromuscular dysplasia (FMD). As the hypertension was resistant to 3 classes of antihypertensive treatment, percutaneous transluminal renal angioplasty (PTRA) was offered. The procedure had immediate effect on the blood pressure. Without medication the patient remains normotensive 4 years after and the abdominal pain has only sporadically returned. The presented case illustrates the challenging process of diagnosing FMD-related renal branch artery stenosis as well as the potential benefits of PTRA in this patient group.
{"title":"Difficulty and importance of diagnosing stenosis of renal branch artery in fibromuscular dysplasia: a case report.","authors":"Andreas Skræddergaard, Jakob Nyvad, Kent Lodberg Christensen, Arne Hørlyck, Hossein Mohit Mafi, Mark Reinhard","doi":"10.1080/08037051.2021.1993735","DOIUrl":"https://doi.org/10.1080/08037051.2021.1993735","url":null,"abstract":"<p><p>A 16-year-old patient presented with abdominal pain and sustained hypertension. Thorough evaluation including renography with and without captopril and renal vein renin sampling were normal. Duplex ultrasound, however, raised suspicion of a renal artery stenosis. This was confirmed by computed tomography angiography which showed a severe branch artery stenosis with post-stenotic dilatation consistent with focal fibromuscular dysplasia (FMD). As the hypertension was resistant to 3 classes of antihypertensive treatment, percutaneous transluminal renal angioplasty (PTRA) was offered. The procedure had immediate effect on the blood pressure. Without medication the patient remains normotensive 4 years after and the abdominal pain has only sporadically returned. The presented case illustrates the challenging process of diagnosing FMD-related renal branch artery stenosis as well as the potential benefits of PTRA in this patient group.</p>","PeriodicalId":9000,"journal":{"name":"Blood Pressure","volume":" ","pages":"416-420"},"PeriodicalIF":1.8,"publicationDate":"2021-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39557815","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2021-12-01DOI: 10.1080/08037051.2021.1963666
Tomáš Seeman, Kryštof Staněk, Jakub Slížek, Jan Filipovský, Janusz Feber
Purpose: We studied the performance of unattended automated office blood pressure (uAOBP) measurement in children, in relation to oscillometric office BP (OBP) and ambulatory blood pressure monitoring (ABPM).
Materials and methods: One hundred and eleven stable treated and untreated outpatients investigated for hypertension underwent uAOBP measurements (seated unattended in a quiet room separate from the renal clinic room, six times after a 5 min rest with the BpTRU device), and immediately before using the oscillometric device. Ambulatory 24 h blood pressure monitoring (ABPM) was performed on the same day in a subgroup of 42 children.
Results: UAOBP measurements were successful in 106 children (95%), 5 pre-school children did not tolerate to be alone in the room. The mean ± SD systolic/diastolic uAOBP, OBP and daytime ABP were 109.1 ± 14.0/70.8 ± 10.7 mmHg, 121.6 ± 16.5/77.6 ± 10.5 mmHg and 123.5 ± 11.3/73.7 ± 6.8 mmHg, respectively. Systolic/diastolic uAOBP was significantly lower than OBP by 13.6/7.6 mmHg (p < 0.0001) and lower than daytime ABP by 14.4 ± 0.5/2.9 ± 0.3 mmHg (p < 0.0001). The heart rate was not significantly different during uAOBP than during OBP measurements. On Bland Altman analysis the uAOBP underestimated OBP by a mean of 15.6 mmHg for systolic BP and by 8.6 mmHg for diastolic BP. In all 9 children with white-coat systolic hypertension uAOBP was within the normal range (<95th pc for OBP), in six of nine children with white-coat diastolic hypertension uAOBP was within the normal range however, in three of them it was elevated despite normal ABP.
Conclusion: uAOBP measurement is feasible in school-aged children, its values are considerably lower than OBP as well as daytime ABP and it could help with detection of white-coat systolic hypertension. The clinical applicability of uAOBP in children should be confirmed in further studies.
{"title":"Unattended automated office blood pressure measurement in children.","authors":"Tomáš Seeman, Kryštof Staněk, Jakub Slížek, Jan Filipovský, Janusz Feber","doi":"10.1080/08037051.2021.1963666","DOIUrl":"https://doi.org/10.1080/08037051.2021.1963666","url":null,"abstract":"<p><strong>Purpose: </strong>We studied the performance of unattended automated office blood pressure (uAOBP) measurement in children, in relation to oscillometric office BP (OBP) and ambulatory blood pressure monitoring (ABPM).</p><p><strong>Materials and methods: </strong>One hundred and eleven stable treated and untreated outpatients investigated for hypertension underwent uAOBP measurements (seated unattended in a quiet room separate from the renal clinic room, six times after a 5 min rest with the BpTRU device), and immediately before using the oscillometric device. Ambulatory 24 h blood pressure monitoring (ABPM) was performed on the same day in a subgroup of 42 children.</p><p><strong>Results: </strong>UAOBP measurements were successful in 106 children (95%), 5 pre-school children did not tolerate to be alone in the room. The mean ± SD systolic/diastolic uAOBP, OBP and daytime ABP were 109.1 ± 14.0/70.8 ± 10.7 mmHg, 121.6 ± 16.5/77.6 ± 10.5 mmHg and 123.5 ± 11.3/73.7 ± 6.8 mmHg, respectively. Systolic/diastolic uAOBP was significantly lower than OBP by 13.6/7.6 mmHg (<i>p</i> < 0.0001) and lower than daytime ABP by 14.4 ± 0.5/2.9 ± 0.3 mmHg (<i>p</i> < 0.0001). The heart rate was not significantly different during uAOBP than during OBP measurements. On Bland Altman analysis the uAOBP underestimated OBP by a mean of 15.6 mmHg for systolic BP and by 8.6 mmHg for diastolic BP. In all 9 children with white-coat systolic hypertension uAOBP was within the normal range (<95th pc for OBP), in six of nine children with white-coat diastolic hypertension uAOBP was within the normal range however, in three of them it was elevated despite normal ABP.</p><p><strong>Conclusion: </strong>uAOBP measurement is feasible in school-aged children, its values are considerably lower than OBP as well as daytime ABP and it could help with detection of white-coat systolic hypertension. The clinical applicability of uAOBP in children should be confirmed in further studies.</p>","PeriodicalId":9000,"journal":{"name":"Blood Pressure","volume":"30 6","pages":"359-366"},"PeriodicalIF":1.8,"publicationDate":"2021-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10664529","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2021-12-01Epub Date: 2021-10-19DOI: 10.1080/08037051.2021.1991778
Minh Ngoc Nguyen, Karin Skov, Birgitte Bang Pedersen, Niels Henrik Buus
Purpose: Hypertension is common in kidney transplant recipients (KTRs). For the evaluation of blood pressure (BP), 24-h ambulatory BP measurements (ABPM) are considered superior to usual office measurements but are also resource demanding and troublesome to many patients. We therefore evaluated the use of unattended automated office BP (AOBP) during the first year following living donor kidney transplantation and compared AOBP with ABPM as obtained 12 months after transplantation.
Materials and methods: Data were retrieved from a cohort of 57 KTRs (mean age 45 ± 14 years, 75% males) who all received kidneys from living donors and had a good graft function (estimated glomerular filtration rate (eGFR) 52 ± 16 ml/min/1.73 m2 at 12 months). Unattended AOBP was measured at each visit to the outpatient clinic using the BpTru® device, while ABPM was obtained by Spacelabs® equipment before and 12 months after transplantation.
Results: AOBP remained stable from month 2 (130.2 ± 10.8/82.2 ± 7.8 mmHg) to month 12 (129.0 ± 12.8/83.1 ± 9.6 mmHg) post-transplantation. At 12 months follow-up, ambulatory daytime systolic BP was slightly higher than AOBP (132.7 ± 10.7 vs. 129.4 ± 12.2 mmHg, p = 0.04), while diastolic BP was similar (82.7 ± 7.7 vs. 82.0 ± 10.2 mmHg). Using Bland-Altman plots, 95% limits of agreements were -17.9 to 24.5 mmHg for systolic and -16.5 to 15.1 mmHg for diastolic BP. When considering a target BP of ≤130/<80 mmHg, 62% had sustained hypertension, 9% white coat hypertension and 11% masked hypertension. Using multiple linear regression analysis, only urine albumin-creatinine ratio tended to predict a higher systolic AOBP (p = 0.07).
Conclusion: In a cohort of stable living donor KTRs, mean values of unattended AOBP using BpTru® are comparable to daytime ABPM with a misclassification rate of approximately 20%.
目的:高血压在肾移植受者(KTRs)中很常见。对于血压(BP)的评估,24小时动态血压测量(ABPM)被认为优于通常的办公室测量,但对许多患者来说也需要资源和麻烦。因此,我们评估了活体肾移植后第一年无人值机自动办公血压(AOBP)的使用情况,并将AOBP与移植后12个月获得的ABPM进行了比较。材料和方法:数据来自一组57名ktr患者(平均年龄45±14岁,75%为男性),他们都接受了活体供体肾脏,移植物功能良好(12个月时估计肾小球滤过率(eGFR) 52±16 ml/min/1.73 m2)。在每次门诊就诊时,使用BpTru®设备测量无人值机的AOBP,而在移植前和移植后12个月,使用Spacelabs®设备测量ABPM。结果:AOBP在移植后第2个月(130.2±10.8/82.2±7.8 mmHg)至第12个月(129.0±12.8/83.1±9.6 mmHg)保持稳定。在12个月的随访中,日间动态收缩压略高于AOBP(132.7±10.7 vs 129.4±12.2 mmHg, p = 0.04),而舒张压相似(82.7±7.7 vs 82.0±10.2 mmHg)。使用Bland-Altman图,95%的一致性限制为收缩压-17.9 ~ 24.5 mmHg,舒张压-16.5 ~ 15.1 mmHg。当考虑目标血压≤130/p = 0.07时)。结论:在稳定的活体供体ktr队列中,使用BpTru®的无人值守AOBP的平均值与日间ABPM相当,误分类率约为20%。
{"title":"Unattended automated office blood pressure in living donor kidney transplant recipients.","authors":"Minh Ngoc Nguyen, Karin Skov, Birgitte Bang Pedersen, Niels Henrik Buus","doi":"10.1080/08037051.2021.1991778","DOIUrl":"https://doi.org/10.1080/08037051.2021.1991778","url":null,"abstract":"<p><strong>Purpose: </strong>Hypertension is common in kidney transplant recipients (KTRs). For the evaluation of blood pressure (BP), 24-h ambulatory BP measurements (ABPM) are considered superior to usual office measurements but are also resource demanding and troublesome to many patients. We therefore evaluated the use of unattended automated office BP (AOBP) during the first year following living donor kidney transplantation and compared AOBP with ABPM as obtained 12 months after transplantation.</p><p><strong>Materials and methods: </strong>Data were retrieved from a cohort of 57 KTRs (mean age 45 ± 14 years, 75% males) who all received kidneys from living donors and had a good graft function (estimated glomerular filtration rate (eGFR) 52 ± 16 ml/min/1.73 m<sup>2</sup> at 12 months). Unattended AOBP was measured at each visit to the outpatient clinic using the BpTru® device, while ABPM was obtained by Spacelabs® equipment before and 12 months after transplantation.</p><p><strong>Results: </strong>AOBP remained stable from month 2 (130.2 ± 10.8/82.2 ± 7.8 mmHg) to month 12 (129.0 ± 12.8/83.1 ± 9.6 mmHg) post-transplantation. At 12 months follow-up, ambulatory daytime systolic BP was slightly higher than AOBP (132.7 ± 10.7 <i>vs.</i> 129.4 ± 12.2 mmHg, <i>p</i> = 0.04), while diastolic BP was similar (82.7 ± 7.7 <i>vs.</i> 82.0 ± 10.2 mmHg). Using Bland-Altman plots, 95% limits of agreements were -17.9 to 24.5 mmHg for systolic and -16.5 to 15.1 mmHg for diastolic BP. When considering a target BP of ≤130/<80 mmHg, 62% had sustained hypertension, 9% white coat hypertension and 11% masked hypertension. Using multiple linear regression analysis, only urine albumin-creatinine ratio tended to predict a higher systolic AOBP (<i>p</i> = 0.07).</p><p><strong>Conclusion: </strong>In a cohort of stable living donor KTRs, mean values of unattended AOBP using BpTru® are comparable to daytime ABPM with a misclassification rate of approximately 20%.</p>","PeriodicalId":9000,"journal":{"name":"Blood Pressure","volume":" ","pages":"386-394"},"PeriodicalIF":1.8,"publicationDate":"2021-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39531272","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2021-12-01Epub Date: 2021-07-06DOI: 10.1080/08037051.2021.1907174
Erietta Polychronopoulou, Michel Burnier, Georg Ehret, Renate Schoenenberger-Berzins, Maxime Berney, Belen Ponte, Paul Erne, Murielle Bochud, Antoinette Pechère-Bertschi, Gregoire Wuerzner
Purpose: Poor adherence to drug therapy and inadequate drug regimens are two frequent factors responsible for the poor blood pressure (BP) control observed in patients with apparent resistant hypertension. We evaluated the efficacy of an antihypertensive management strategy combining a standardised therapy with three long acting drugs and electronic monitoring of drug adherence in patients with apparent resistant hypertension.
Materials and methods: In this multicentric observational study, adult patients with residual hypertension on 24 h ambulatory BP monitoring (ABMP) despite the use of three or more antihypertensive drugs could be included. Olmesartan/amlodipine (40/10 mg, single pill fixed-dose combination) and chlorthalidone (25 mg) were prescribed for 3 months in two separated electronic pills boxes (EPB). The primary outcome was 24 h ambulatory systolic BP (SBP) control at 3 months, defined as mean SBP <130 mmHg.
Results: We enrolled 48 patients (36.0% women) of whom 35 had complete EPB data. After 3 months, 52.1% of patients had 24 h SBP <130 mmHg. 24 h SBP decreased by respectively -9.1 ± 15.5 mmHg, -22.8 ± 30.6 mmHg and -27.7 ± 16.6 mmHg from the tertile with the lowest adherence to the tertile with the highest adherence to the single pill combination (p = 0.024). A similar trend was observed with tertiles of adherence to chlorthalidone. Adherence superior to 90% was associated with 24 h systolic and diastolic blood pressure control in multiple logistic regression analysis (odds ratio = 14.1 (95% confidence interval 1.1-173.3, p = 0.039).
Conclusions: A simplified standardised antihypertensive therapy combined with electronic monitoring of adherence normalises SBP in about half of patients with apparent resistant hypertension. Such combined management strategy enables identifying patients who need complementary investigations and those who rather need a long-term support of their adherence.
{"title":"Assessment of a strategy combining ambulatory blood pressure, adherence monitoring and a standardised triple therapy in resistant hypertension.","authors":"Erietta Polychronopoulou, Michel Burnier, Georg Ehret, Renate Schoenenberger-Berzins, Maxime Berney, Belen Ponte, Paul Erne, Murielle Bochud, Antoinette Pechère-Bertschi, Gregoire Wuerzner","doi":"10.1080/08037051.2021.1907174","DOIUrl":"https://doi.org/10.1080/08037051.2021.1907174","url":null,"abstract":"<p><strong>Purpose: </strong>Poor adherence to drug therapy and inadequate drug regimens are two frequent factors responsible for the poor blood pressure (BP) control observed in patients with apparent resistant hypertension. We evaluated the efficacy of an antihypertensive management strategy combining a standardised therapy with three long acting drugs and electronic monitoring of drug adherence in patients with apparent resistant hypertension.</p><p><strong>Materials and methods: </strong>In this multicentric observational study, adult patients with residual hypertension on 24 h ambulatory BP monitoring (ABMP) despite the use of three or more antihypertensive drugs could be included. Olmesartan/amlodipine (40/10 mg, single pill fixed-dose combination) and chlorthalidone (25 mg) were prescribed for 3 months in two separated electronic pills boxes (EPB). The primary outcome was 24 h ambulatory systolic BP (SBP) control at 3 months, defined as mean SBP <130 mmHg.</p><p><strong>Results: </strong>We enrolled 48 patients (36.0% women) of whom 35 had complete EPB data. After 3 months, 52.1% of patients had 24 h SBP <130 mmHg. 24 h SBP decreased by respectively -9.1 ± 15.5 mmHg, -22.8 ± 30.6 mmHg and -27.7 ± 16.6 mmHg from the tertile with the lowest adherence to the tertile with the highest adherence to the single pill combination (<i>p</i> = 0.024). A similar trend was observed with tertiles of adherence to chlorthalidone. Adherence superior to 90% was associated with 24 h systolic and diastolic blood pressure control in multiple logistic regression analysis (odds ratio = 14.1 (95% confidence interval 1.1-173.3, <i>p</i> = 0.039).</p><p><strong>Conclusions: </strong>A simplified standardised antihypertensive therapy combined with electronic monitoring of adherence normalises SBP in about half of patients with apparent resistant hypertension. Such combined management strategy enables identifying patients who need complementary investigations and those who rather need a long-term support of their adherence.</p>","PeriodicalId":9000,"journal":{"name":"Blood Pressure","volume":" ","pages":"332-340"},"PeriodicalIF":1.8,"publicationDate":"2021-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1080/08037051.2021.1907174","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39154566","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2021-12-01Epub Date: 2021-10-29DOI: 10.1080/08037051.2021.1995975
Sverre E Kjeldsen, Krzysztof Narkiewicz, Michel Burnier, Suzanne Oparil
Renal denervation (RDN) may be a new treatment modality for patients with hypertension. Initially, efforts to test the efficacy of RDN in lowering blood pressure (BP) have focussed on patients with apparent treatment resistant hypertension (aTRH). The SYMPLICITY HTN2 trial [1] reported a major reduction in systolic BP with RDN in patients with aTRH using office-based BP measurement. However, using ambulatory BP, the state-ofthe art technique for measuring BP in patients with aTRH [2], BP reductions were less evident [1]. Further, since poor drug adherence, which is common in aTRH [3], was not monitored in SYMPLICITY HTN-2, interpretation of the study results could be confounded by the Hawthorne effect i.e. patients started taking their drugs as prescribed in response to the attention devoted to them [4]. SYMPLICITY HTN-3 [5] included a sham control group and ambulatory BP measurements that balanced the Hawthorne and white-coat, placebo, and regressionto-the–mean effects, resulting in a BP reduction of 2mmHg in the RDN treatment group compared to the sham control. Further, meta-analyses of the first generation of randomised controlled studies of RDN did not show BP lowering effects of RDN (Figures 1 and 2), whether or not SYMPLICITY HTN-3 was included [6], and whether or not a sham control (Figures 3 and 4) was a part of the design [7]. However, these disappointments [5–7] did not end the interest in RDN for many reasons. First, total abdominal sympathectomy resulting from surgical splanchnicectomy was highly effective in the treatment of severe hypertension in cohorts of patients reported in the 1930s [8] and 1950s [9,10]. Second, the meta-analyses showed that RDN did not lead to severe adverse events and could be considered safe [6,7]. Third, the role of the sympathetic nervous system in the pathophysiology of hypertension is strong [11,12]. Further, the procedural problems that contributed to the failure of early RDN trials to lower BP could be overcome [13,14]. Therefore, new protocols were designed to assess the antihypertensive efficacy of RDN. One new approach was to perform clinical studies in untreated hypertensive
{"title":"The five RADIANCE-HTN and SPYRAL-HTN randomised studies suggest that the BP lowering effect of RDN corresponds to the effect of one antihypertensive drug.","authors":"Sverre E Kjeldsen, Krzysztof Narkiewicz, Michel Burnier, Suzanne Oparil","doi":"10.1080/08037051.2021.1995975","DOIUrl":"https://doi.org/10.1080/08037051.2021.1995975","url":null,"abstract":"Renal denervation (RDN) may be a new treatment modality for patients with hypertension. Initially, efforts to test the efficacy of RDN in lowering blood pressure (BP) have focussed on patients with apparent treatment resistant hypertension (aTRH). The SYMPLICITY HTN2 trial [1] reported a major reduction in systolic BP with RDN in patients with aTRH using office-based BP measurement. However, using ambulatory BP, the state-ofthe art technique for measuring BP in patients with aTRH [2], BP reductions were less evident [1]. Further, since poor drug adherence, which is common in aTRH [3], was not monitored in SYMPLICITY HTN-2, interpretation of the study results could be confounded by the Hawthorne effect i.e. patients started taking their drugs as prescribed in response to the attention devoted to them [4]. SYMPLICITY HTN-3 [5] included a sham control group and ambulatory BP measurements that balanced the Hawthorne and white-coat, placebo, and regressionto-the–mean effects, resulting in a BP reduction of 2mmHg in the RDN treatment group compared to the sham control. Further, meta-analyses of the first generation of randomised controlled studies of RDN did not show BP lowering effects of RDN (Figures 1 and 2), whether or not SYMPLICITY HTN-3 was included [6], and whether or not a sham control (Figures 3 and 4) was a part of the design [7]. However, these disappointments [5–7] did not end the interest in RDN for many reasons. First, total abdominal sympathectomy resulting from surgical splanchnicectomy was highly effective in the treatment of severe hypertension in cohorts of patients reported in the 1930s [8] and 1950s [9,10]. Second, the meta-analyses showed that RDN did not lead to severe adverse events and could be considered safe [6,7]. Third, the role of the sympathetic nervous system in the pathophysiology of hypertension is strong [11,12]. Further, the procedural problems that contributed to the failure of early RDN trials to lower BP could be overcome [13,14]. Therefore, new protocols were designed to assess the antihypertensive efficacy of RDN. One new approach was to perform clinical studies in untreated hypertensive","PeriodicalId":9000,"journal":{"name":"Blood Pressure","volume":" ","pages":"327-331"},"PeriodicalIF":1.8,"publicationDate":"2021-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39573756","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2021-12-01Epub Date: 2021-10-29DOI: 10.1080/08037051.2021.1996220
Di Zhang, Qi-Fang Huang, Chang-Sheng Sheng, Yan Li, Ji-Guang Wang
Purpose: We investigated serum uric acid changes in relation to the achieved clinic and ambulatory blood pressure after 8 weeks of antihypertensive therapy with two dihydropyridine calcium channel blockers.
Materials and methods: The study participants were patients with clinic and ambulatory hypertension, enrolled in a randomised controlled trial that compared amlodipine (5-10 mg, n = 215) and nifedipine gastrointestinal therapeutic system (GITS, 30-60 mg, n = 203). Hyperuricaemia was defined as a serum uric acid concentration of ≥420 µmol/L in men and ≥360 µmol/L in women. Analysis of covariance and multiple regression analyses were performed to study the associations between serum uric acid changes and the achieved clinic and ambulatory blood pressure during follow-up.
Results: At baseline, 67 (16.0%) of the 418 patients had hyperuricaemia. Antihypertensive treatment reduced clinic and 24-h daytime and night-time systolic/diastolic blood pressure by a mean (±standard error [SE]) change of -17.4 ± 0.6/-8.6 ± 0.4 mm Hg and -13.7 ± 0.5/-8.3 ± 0.3 mm Hg, -13.8 ± 0.6/-8.4 ± 0.4 mm Hg, and -12.7 ± 0.7/-8.0 ± 0.4 mm Hg, respectively. Antihypertensive treatment reduced serum uric acid by a mean (±SE) change of -9.3 ± 2.8 μmol/L. The serum uric acid changes differed according to the achieved clinic and ambulatory blood pressure, and were statistically significant (mean ± SE -20.6 ± 6.6 to -10.7 ± 2.9 μmol/L, p ≤ 0.04) at the systolic/diastolic ranges of 130-139/≥90 mm Hg in clinic pressure, and <130/75-84 mm Hg, <145/80-84 mm Hg and <120/65-69 mm Hg in 24-h, daytime and night-time ambulatory pressure.
Conclusion: Our study showed that antihypertensive therapy with a dihydropyridine calcium channel blocker was associated with reduced serum uric acid, especially when 24-h ambulatory systolic blood pressure was controlled.
目的:研究两种二氢吡啶钙通道阻滞剂抗高血压治疗8周后血清尿酸变化与临床和动态血压的关系。材料和方法:研究对象为临床和动态高血压患者,纳入随机对照试验,比较氨氯地平(5-10 mg, n = 215)和硝苯地平胃肠道治疗系统(GITS, 30-60 mg, n = 203)。高尿酸血症定义为男性血清尿酸浓度≥420µmol/L,女性血清尿酸浓度≥360µmol/L。采用协方差分析和多元回归分析研究随访期间血清尿酸变化与临床及动态血压的相关性。结果:在基线时,418例患者中有67例(16.0%)患有高尿酸血症。降压治疗使临床和24小时白天和夜间收缩压/舒张压的平均(±标准误差[SE])变化分别为-17.4±0.6/-8.6±0.4 mm Hg、-13.7±0.5/-8.3±0.3 mm Hg、-13.8±0.6/-8.4±0.4 mm Hg和-12.7±0.7/-8.0±0.4 mm Hg。降压治疗降低血清尿酸的平均(±SE)变化为-9.3±2.8 μmol/L。在130 ~ 139/≥90 mm Hg收缩压/舒张压范围内,血清尿酸的变化随临床和动态血压的不同而不同,且具有统计学意义(平均值±SE -20.6±6.6 ~ -10.7±2.9 μmol/L, p≤0.04)。结论:本研究表明,应用二氢吡啶钙通道阻滞剂降压可降低血清尿酸,特别是在控制24 h动态收缩压的情况下。
{"title":"Serum uric acid change in relation to antihypertensive therapy with the dihydropyridine calcium channel blockers.","authors":"Di Zhang, Qi-Fang Huang, Chang-Sheng Sheng, Yan Li, Ji-Guang Wang","doi":"10.1080/08037051.2021.1996220","DOIUrl":"https://doi.org/10.1080/08037051.2021.1996220","url":null,"abstract":"<p><strong>Purpose: </strong>We investigated serum uric acid changes in relation to the achieved clinic and ambulatory blood pressure after 8 weeks of antihypertensive therapy with two dihydropyridine calcium channel blockers.</p><p><strong>Materials and methods: </strong>The study participants were patients with clinic and ambulatory hypertension, enrolled in a randomised controlled trial that compared amlodipine (5-10 mg, <i>n</i> = 215) and nifedipine gastrointestinal therapeutic system (GITS, 30-60 mg, <i>n</i> = 203). Hyperuricaemia was defined as a serum uric acid concentration of ≥420 µmol/L in men and ≥360 µmol/L in women. Analysis of covariance and multiple regression analyses were performed to study the associations between serum uric acid changes and the achieved clinic and ambulatory blood pressure during follow-up.</p><p><strong>Results: </strong>At baseline, 67 (16.0%) of the 418 patients had hyperuricaemia. Antihypertensive treatment reduced clinic and 24-h daytime and night-time systolic/diastolic blood pressure by a mean (±standard error [SE]) change of -17.4 ± 0.6/-8.6 ± 0.4 mm Hg and -13.7 ± 0.5/-8.3 ± 0.3 mm Hg, -13.8 ± 0.6/-8.4 ± 0.4 mm Hg, and -12.7 ± 0.7/-8.0 ± 0.4 mm Hg, respectively. Antihypertensive treatment reduced serum uric acid by a mean (±SE) change of -9.3 ± 2.8 μmol/L. The serum uric acid changes differed according to the achieved clinic and ambulatory blood pressure, and were statistically significant (mean ± SE -20.6 ± 6.6 to -10.7 ± 2.9 μmol/L, <i>p</i> ≤ 0.04) at the systolic/diastolic ranges of 130-139/≥90 mm Hg in clinic pressure, and <130/75-84 mm Hg, <145/80-84 mm Hg and <120/65-69 mm Hg in 24-h, daytime and night-time ambulatory pressure.</p><p><strong>Conclusion: </strong>Our study showed that antihypertensive therapy with a dihydropyridine calcium channel blocker was associated with reduced serum uric acid, especially when 24-h ambulatory systolic blood pressure was controlled.</p>","PeriodicalId":9000,"journal":{"name":"Blood Pressure","volume":" ","pages":"395-402"},"PeriodicalIF":1.8,"publicationDate":"2021-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39573762","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2021-12-01Epub Date: 2021-10-29DOI: 10.1080/08037051.2021.1996221
Olívia Moraes Ruberti, Juan Carlos Yugar-Toledo, Heitor Moreno, Bruno Rodrigues
Purpose: Hypertensive patients with access to telemedicine can receive telemonitoring of blood pressure and cardiovascular risk factors such as sedentary lifestyle, diet, and remote supervision of treatment compliance. Faced with this challenge, electronic devices for telemonitoring of BP have gained space. They have shown to be effective in the follow-up of hypertensive patients and assist in the adherence and control of associated risk factors such as physical inactivity and obesity.
Materials and methods: Narrative Review.
Results: The use of advanced smartwatches, smartphone apps, and online software for monitoring physical activity is increasingly common. Electronic equipment is briefly presented here as a support for better addressing some cardiovascular variables. Using various automated feedback services with a follow-up multidisciplinary clinical team is the ideal strategy.
Conclusion: Mobile health can improve risk factors and health status, particularly for hypertensive patients, improving access to cardiac rehabilitation and reducing the cost.
{"title":"Hypertension telemonitoring and home-based physical training programs.","authors":"Olívia Moraes Ruberti, Juan Carlos Yugar-Toledo, Heitor Moreno, Bruno Rodrigues","doi":"10.1080/08037051.2021.1996221","DOIUrl":"https://doi.org/10.1080/08037051.2021.1996221","url":null,"abstract":"<p><strong>Purpose: </strong>Hypertensive patients with access to telemedicine can receive telemonitoring of blood pressure and cardiovascular risk factors such as sedentary lifestyle, diet, and remote supervision of treatment compliance. Faced with this challenge, electronic devices for telemonitoring of BP have gained space. They have shown to be effective in the follow-up of hypertensive patients and assist in the adherence and control of associated risk factors such as physical inactivity and obesity.</p><p><strong>Materials and methods: </strong>Narrative Review.</p><p><strong>Results: </strong>The use of advanced smartwatches, smartphone apps, and online software for monitoring physical activity is increasingly common. Electronic equipment is briefly presented here as a support for better addressing some cardiovascular variables. Using various automated feedback services with a follow-up multidisciplinary clinical team is the ideal strategy.</p><p><strong>Conclusion: </strong>Mobile health can improve risk factors and health status, particularly for hypertensive patients, improving access to cardiac rehabilitation and reducing the cost.</p>","PeriodicalId":9000,"journal":{"name":"Blood Pressure","volume":" ","pages":"428-438"},"PeriodicalIF":1.8,"publicationDate":"2021-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39826339","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2021-12-01Epub Date: 2021-11-18DOI: 10.1080/08037051.2021.2003180
Nikolina Bukal, Dražen Pekov, Luka Penezić, Bojan Jelaković, Živka Dika
We report the case of 39-year-old Caucasian man presenting in emergency department with new onset of severe hypertension with hypokalaemia eight weeks after renal colic. Patient was referred to a hypertension unit for further investigation. Hormonal analysis confirmed secondary aldosteronism and slightly impaired kidney function. Imaging revealed smaller right kidney, 'string of beads appearance' of distal part of right renal artery, a short zone of dissection and renal infarction. Renal scintigraphy showed significant blood flow reduction and severe functional damage of the right kidney. Despite multidrug antihypertensive treatment patient's hypertension was resistant and target organ damage evolved. After initial patient's refusal, he was later successfully treated with laparoscopic simple nephrectomy. Histopathological analysis confirmed renal artery dissection and medial fibroplasia. Thereafter, hypertension was controlled with trandalopril monotherapy. This is a first case report of the patient with renovascular multifocal fibromuscular dysplasia, dissection and renal infarction whose diagnosis of the disease was confirmed by angiography and histopathologic analysis. Resistant hypertension was successfully treated with nephrectomy.
{"title":"Resistant hypertension after renal infarction in a man with fibromuscular dysplasia.","authors":"Nikolina Bukal, Dražen Pekov, Luka Penezić, Bojan Jelaković, Živka Dika","doi":"10.1080/08037051.2021.2003180","DOIUrl":"https://doi.org/10.1080/08037051.2021.2003180","url":null,"abstract":"<p><p>We report the case of 39-year-old Caucasian man presenting in emergency department with new onset of severe hypertension with hypokalaemia eight weeks after renal colic. Patient was referred to a hypertension unit for further investigation. Hormonal analysis confirmed secondary aldosteronism and slightly impaired kidney function. Imaging revealed smaller right kidney, 'string of beads appearance' of distal part of right renal artery, a short zone of dissection and renal infarction. Renal scintigraphy showed significant blood flow reduction and severe functional damage of the right kidney. Despite multidrug antihypertensive treatment patient's hypertension was resistant and target organ damage evolved. After initial patient's refusal, he was later successfully treated with laparoscopic simple nephrectomy. Histopathological analysis confirmed renal artery dissection and medial fibroplasia. Thereafter, hypertension was controlled with trandalopril monotherapy. This is a first case report of the patient with renovascular multifocal fibromuscular dysplasia, dissection and renal infarction whose diagnosis of the disease was confirmed by angiography and histopathologic analysis. Resistant hypertension was successfully treated with nephrectomy.</p>","PeriodicalId":9000,"journal":{"name":"Blood Pressure","volume":" ","pages":"421-427"},"PeriodicalIF":1.8,"publicationDate":"2021-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39634971","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}