Evidence map›Paper›PMID 39633562›Full record

ArticleHypertension (Dallas, Tex. : 1979)2025

Orthostatic and Standing Hypertension and Risk of Cardiovascular Disease.

Sean W Dooley, Fredrick Larbi Kwapong, Hannah Col, Ruth-Alma N Turkson-Ocran, Long H Ngo, Jennifer L Cluett, Kenneth J Mukamal, Lewis A Lipsitz, Mingyu Zhang, Natalie R Daya and 6 more

Abstract read
In one paragraph

Article in Hypertension (Dallas, Tex. : 1979), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

4 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Review
  3. Article
  4. 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

16 authors.

Sean W DooleyDivision of General Medicine, Department of Medicine, Beth Israel Deaconess Medical Center, Boston, MA (S.W.D., F.L.K., H.C., R.-A.N.T.-O., L.H.N., J.L.C., K.J.M., L.A.L., M.Z., S.P.J.).ORCID 0009-0003-9008-0322
Fredrick Larbi KwapongDivision of General Medicine, Department of Medicine, Beth Israel Deaconess Medical Center, Boston, MA (S.W.D., F.L.K., H.C., R.-A.N.T.-O., L.H.N., J.L.C., K.J.M., L.A.L., M.Z., S.P.J.).ORCID 0000-0002-5585-632X
Hannah ColDivision of General Medicine, Department of Medicine, Beth Israel Deaconess Medical Center, Boston, MA (S.W.D., F.L.K., H.C., R.-A.N.T.-O., L.H.N., J.L.C., K.J.M., L.A.L., M.Z., S.P.J.).
Ruth-Alma N Turkson-OcranDivision of General Medicine, Department of Medicine, Beth Israel Deaconess Medical Center, Boston, MA (S.W.D., F.L.K., H.C., R.-A.N.T.-O., L.H.N., J.L.C., K.J.M., L.A.L., M.Z., S.P.J.).ORCID 0000-0001-9932-052X
Long H NgoDivision of General Medicine, Department of Medicine, Beth Israel Deaconess Medical Center, Boston, MA (S.W.D., F.L.K., H.C., R.-A.N.T.-O., L.H.N., J.L.C., K.J.M., L.A.L., M.Z., S.P.J.).
Jennifer L CluettDivision of General Medicine, Department of Medicine, Beth Israel Deaconess Medical Center, Boston, MA (S.W.D., F.L.K., H.C., R.-A.N.T.-O., L.H.N., J.L.C., K.J.M., L.A.L., M.Z., S.P.J.).ORCID 0000-0002-5744-1099
Kenneth J MukamalDivision of General Medicine, Department of Medicine, Beth Israel Deaconess Medical Center, Boston, MA (S.W.D., F.L.K., H.C., R.-A.N.T.-O., L.H.N., J.L.C., K.J.M., L.A.L., M.Z., S.P.J.).ORCID 0000-0001-8450-6970
Lewis A LipsitzDivision of General Medicine, Department of Medicine, Beth Israel Deaconess Medical Center, Boston, MA (S.W.D., F.L.K., H.C., R.-A.N.T.-O., L.H.N., J.L.C., K.J.M., L.A.L., M.Z., S.P.J.).
Mingyu ZhangDivision of General Medicine, Department of Medicine, Beth Israel Deaconess Medical Center, Boston, MA (S.W.D., F.L.K., H.C., R.-A.N.T.-O., L.H.N., J.L.C., K.J.M., L.A.L., M.Z., S.P.J.).ORCID 0000-0003-3628-0983
Natalie R DayaDepartment of Epidemiology, Johns Hopkins University, Baltimore, MD (N.R.D., E.S.).ORCID 0000-0002-2257-0480
Elizabeth SelvinDepartment of Epidemiology, Johns Hopkins University, Baltimore, MD (N.R.D., E.S.).ORCID 0000-0002-3539-2070
Pamela L LutseyUniversity of Minnesota, Minneapolis (P.L.L.).ORCID 0000-0002-1572-1340
Josef CoreshDepartments of Population Health and Medicine, New York University Grossman School of Medicine, NY (J.C.).ORCID 0000-0002-4598-0669
Beverly Gwen WindhamUniversity of Mississippi, University, MS (B.G.W.).
Lynne E WagenknechtWake Forest University School of Medicine, Winston-Salem, NC (L.E.W.).ORCID 0000-0002-9980-0889
Stephen P JuraschekDivision of General Medicine, Department of Medicine, Beth Israel Deaconess Medical Center, Boston, MA (S.W.D., F.L.K., H.C., R.-A.N.T.-O., L.H.N., J.L.C., K.J.M., L.A.L., M.Z., S.P.J.).ORCID 0000-0003-4168-2696

Funding

CARDIOVASCULAR EPIDEMIOLOGY INSTITUTIONAL TRAININGT32HL007024 · NHLBI · JOHNS HOPKINS UNIVERSITY · PI Elizabeth Selvin · 1985 to 2026
$17.5M
THE ATHEROSCLEROSIS RISK IN COMMUNITIES (ARIC) STUDY - COORDINATING CENTER - TASK AREA B.2 AND B.375N92022D00001 · NHLBI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI COUPER, DAVID · 2022 to 2025
$13.7M
THE ATHEROSCLEROSIS RISK IN COMMUNITIES (ARIC) STUDY - FIELD CENTER - TASK ORDER 01, TASK AREA A75N92022D00003 · NHLBI · UNIVERSITY OF MINNESOTA · PI LUTSEY, PAMELA L. · 2022 to 2025
$5.1M
THE ATHEROSCLEROSIS RISK IN COMMUNITIES (ARIC) STUDY - FIELD CENTER - TASK ORDER 01, TASK AREA A75N92022D00005 · NHLBI · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI WAGENKNECHT, LYNNE E · 2022 to 2025
$5.0M
THE ATHEROSCLEROSIS RISK IN COMMUNITIES (ARIC) STUDY - FIELD CENTER - TASK ORDER 01, TASK AREA A75N92022D00004 · NHLBI · UNIVERSITY OF MISSISSIPPI MED CTR · PI WINDHAM, BEVERLY GWEN · 2022 to 2025
$4.8M
THE ATHEROSCLEROSIS RISK IN COMMUNITIES (ARIC) STUDY - FIELD CENTER - TASK ORDER 01, TASK AREA A75N92022D00002 · NHLBI · JOHNS HOPKINS UNIVERSITY · PI CORESH, JOSEF · 2022 to 2025
$4.7M
Prognostic Implications of Home-Based Blood Pressure Monitoring in Older AdultsR01HL158622 · NHLBI · BETH ISRAEL DEACONESS MEDICAL CENTER · PI JURASCHEK, STEPHEN P · 2021 to 2025
$4.5M
Clinical Implications of Blood Pressure Patterns Among Older AdultsR01HL153191 · NHLBI · BETH ISRAEL DEACONESS MEDICAL CENTER · PI JURASCHEK, STEPHEN P · 2021 to 2023
$2.3M
Non-esterified Fatty Acids and Chronic Pain in Older AdultsK24AG065525 · NIA · BETH ISRAEL DEACONESS MEDICAL CENTER · PI MUKAMAL, KENNETH JAY · 2020 to 2024
$1.0M
Mentoring and Research in Patient-Oriented Cardiovascular PharmacoepidemiologyK24HL159246 · NHLBI · UNIVERSITY OF MINNESOTA · PI PAMELA L. Lutsey · 2021 to 2026
$644k
Research and Mentoring in the Clinical Epidemiology of Cardiovascular Disease and Type 2 DiabetesK24HL152440 · NHLBI · JOHNS HOPKINS UNIVERSITY · PI SELVIN, ELIZABETH · 2020 to 2024
$612k
NHLBI NIH HHS 75N92022D00001NHLBI NIH HHS 75N92022D00002NHLBI NIH HHS 75N92022D00003NHLBI NIH HHS 75N92022D00004NHLBI NIH HHS 75N92022D00005NHLBI NIH HHS K24 HL152440NHLBI NIH HHS K24 HL159246NHLBI NIH HHS R01 HL153191NHLBI NIH HHS R01 HL158622NHLBI NIH HHS T32 HL007024NIA NIH HHS K24 AG065525
6 · The paper itself

Abstract

backgroundOrthostatic hypertension is an emerging risk factor for adverse events. Recent consensus statements combine an increase in blood pressure upon standing with standing hypertension, but whether these 2 components have similar risk associations with cardiovascular disease (CVD) is unknown.

methodsThe ARIC study (Atherosclerosis Risk in Communities) measured supine and standing blood pressure during visit 1 (1987-1989). We defined systolic orthostatic increase (a rise in systolic blood pressure [SBP] ≥20 mm Hg, standing minus supine blood pressure) and elevated standing SBP (standing SBP ≥140 mm Hg) to examine the new consensus statement definition (rise in SBP ≥20 mm Hg and standing SBP ≥140 mm Hg). We used Cox regression to examine associations with incident coronary heart disease, heart failure, stroke, fatal coronary heart disease, and all-cause mortality.

resultsOf 11 369 participants (56% female; 25% Black adults; mean age, 54 years) without CVD at baseline, 1.8% had systolic orthostatic increases, 20.1% had standing SBP ≥140 mm Hg, and 1.3% had systolic orthostatic increases with standing SBP ≥140 mm Hg. During up to 30 years of follow-up, orthostatic increases were not significantly associated with any of the adverse outcomes of interest, while standing SBP ≥140 mm Hg was significantly associated with all end points. In joint models comparing systolic orthostatic increases and standing SBP ≥140 mm Hg, standing SBP ≥140 mm Hg was significantly associated with a higher risk of CVD, and associations differed significantly from systolic orthostatic increases.

conclusionsUnlike systolic orthostatic increases, standing SBP ≥140 mm Hg was strongly associated with CVD outcomes and death. These differences in CVD risk raise important concerns about combining systolic orthostatic increases and standing SBP ≥140 mm Hg in a consensus definition for orthostatic hypertension.

Indexed as

Blood PressureCardiovascular DiseasesHypertensionStanding PositionBlood Pressure DeterminationFemaleFollow-Up StudiesHumansIncidenceMaleMiddle AgedRisk AssessmentRisk FactorsUnited Statesblood pressurecoronary diseaseheart failuremortalitystroke

Identifiers

PMID39633562
PMCPMC11781805

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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.