Evidence map›Paper›PMID 28180242›Full record

ArticleAmerican journal of hypertension2017

11-Beta Dehydrogenase Type 2 Activity Is Not Reduced in Treatment Resistant Hypertension.

Lama Ghazi, Tanja Dudenbostel, Maria El Hachem, Mohammed Siddiqui, Chee Paul Lin, Suzanne Oparil, David A Calhoun

Open access · bronzeAbstract read
In one paragraph

Article in American journal of hypertension, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.9field-weighted citation impact, top 25% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed, 10 citations in OpenAlex.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 1 institution in 1 country.

Lama GhaziVascular Biology and Hypertension Program, Cardiovascular Disease, Department of Medicine, University of Birmingham at Alabama, Birmingham, Alabama, USA.
Tanja DudenbostelVascular Biology and Hypertension Program, Cardiovascular Disease, Department of Medicine, University of Birmingham at Alabama, Birmingham, Alabama, USA.
Maria El HachemVascular Biology and Hypertension Program, Cardiovascular Disease, Department of Medicine, University of Birmingham at Alabama, Birmingham, Alabama, USA.
Mohammed SiddiquiVascular Biology and Hypertension Program, Cardiovascular Disease, Department of Medicine, University of Birmingham at Alabama, Birmingham, Alabama, USA.
Chee Paul LinCenter for Clinical and Translational Science, University of Birmingham at Alabama, Birmingham, Alabama, USA.
Suzanne OparilVascular Biology and Hypertension Program, Cardiovascular Disease, Department of Medicine, University of Birmingham at Alabama, Birmingham, Alabama, USA.
David A CalhounVascular Biology and Hypertension Program, Cardiovascular Disease, Department of Medicine, University of Birmingham at Alabama, Birmingham, Alabama, USA.
University of Alabama at Birmingham · US

Funding

UAB Center for Clinical and Translational Science (CCTS)UL1TR001417 · NCATS · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI KIMBERLY, ROBERT P. · 2015 to 2018
$31.4M
University of Alabama at Birmingham's Diabetes Research CenterP30DK079626 · NIDDK · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI Kirk Michael Habegger · 2013 to 2026
$19.5M
MECHANISMS OF HYPERTENSION AND CARDIOVASCULAR DISEASEST32HL007457 · NHLBI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI Martin E Young · 1985 to 2026
$8.6M
Mechanisms of Refractory HypertensionR01HL113004 · NHLBI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI OPARIL, SUZANNE · 2014 to 2018
$2.5M
NCATS NIH HHS UL1 TR001417NHLBI NIH HHS R01 HL113004NHLBI NIH HHS T32 HL007457NIDDK NIH HHS P30 DK079626
6 · The paper itself

Abstract

BACKGROUND AND

objectiveDecreased renal 11-beta dehydrogenase type 2 (11β-HSD2) activity, as reflected by an increased urinary free cortisol to cortisone ratio (UFF/UFE), is associated with having hypertension (HTN). The current study was conducted to determine if reduced 11β-HSD2 activity is also associated with having resistant HTN.

methodWe evaluated 55 consecutive patients with RHTN, defined as blood pressure (BP) ≥140/90 mm Hg despite using ≥3 antihypertensive medications including a diuretic, and 38 patients whose BP was controlled on ≤3 medications to serve as a non-RHTN comparator group. All patients underwent biochemical evaluation, including measurement of 24-hour urinary UFF/UFE.

resultsThe 2 study groups had similar demographic characteristics. Systolic, diastolic BP, and number of antihypertensive medications were greater in patients with uncontrolled RHTN vs. the control group (167.5 ± 28.2/91.2 ± 18.8 vs. 126.6 ± 11.4/77.8 ± 8.65 mm Hg and 4.31 ± 1.23 vs. 2.74 ± 0.6, respectively). The 24-hour UFF was 13.6 ± 11.8 vs. 14.3 ± 10.7 µg/24 h and UFE was 64.9 ± 36.3 vs. 76.1 ± 44 µg/24 h such that the UFF/UFE was 0.22 ± 0.16 vs. 0.19 ± 0.09 in RHTN vs. the control group. This ratio was not associated to age, race, gender, and body mass index.

conclusionAn elevated UFF/UFE was not present in this large cohort of patients with uncontrolled RHTN. This suggests that reduced conversion of cortisol to cortisone does not contribute to the development of RHTN.

Indexed as

Blood PressureDrug Resistance11-beta-Hydroxysteroid Dehydrogenase Type 2AdultAgedAntihypertensive AgentsBiomarkersCortisoneCross-Sectional StudiesDrug Therapy, CombinationFemaleHumansHydrocortisoneHypertensionMaleMiddle Aged11-beta-Hydroxysteroid Dehydrogenase Type 2Antihypertensive AgentsBiomarkersCortisoneHSD11B2 protein, humanHydrocortisone11-beta dehydrogenase type 2blood pressurecortisol/ cortisone ratiohypertensionresistant hypertension.

Identifiers

PMID28180242
PMCPMC5861581
OpenAlexW2586208538

What OpenQuestion holds

Textmetadata
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.