Evidence map›Paper›PMID 30383807›Full record

ArticlePloS one2018

The association of multiple anti-hypertensive medication classes with Alzheimer's disease incidence across sex, race, and ethnicity.

Douglas Barthold, Geoffrey Joyce, Whitney Wharton, Patrick Kehoe, Julie Zissimopoulos

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed, 2 pooled it
6.0field-weighted citation impact, top 3% 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

50 citing papers in PubMed, 2 syntheses or guidelines pooled it, 88 citations in OpenAlex.

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  19. The effect of race and co-morbidities on Alzheimer's disease based on Medicare data.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2023
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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

5 authors at 4 institutions in 2 countries.

Douglas BartholdComparative Health Outcomes, Policy, and Economics (CHOICE) Institute, Department of Pharmacy, University of Washington, Seattle, Washington, United States of America.ORCID 0000-0003-0511-5520
Geoffrey JoyceSchool of Pharmacy, Schaeffer Center for Health Policy and Economics, University of Southern California, Los Angeles, California, United States of America.
Whitney WhartonDepartment of Neurology, Emory University School of Medicine, Atlanta, Georgia, United States of America.
Patrick KehoeBristol Medical School, Translational Health Sciences, University of Bristol, Bristol, United Kingdom.
Julie ZissimopoulosPrice School of Public Policy, Schaeffer Center for Health Policy and Economics, University of Southern California, Los Angeles, California, United States of America.
University of Southern California · USEmory University · USUniversity of Bristol · GBUniversity of Washington · US

Funding

USC Resource Center for Minority Aging Research (US-RCMAR)P30AG043073 · NIA · UNIVERSITY OF SOUTHERN CALIFORNIA · PI EILEEN M CRIMMINS · 2012 to 2026
$10.1M
The Science of Medicare ReformRC4AG039036 · NIA · UNIVERSITY OF SOUTHERN CALIFORNIA · PI GARBER, ALAN MICHAEL, GOLDMAN, DANA P · 2010 to 2010
$5.5M
Reducing Racial and Ethnic Disparities in Alzheimer's Disease: Role of ACOsR01AG055401 · NIA · UNIVERSITY OF SOUTHERN CALIFORNIA · PI ZISSIMOPOULOS, JULIE M · 2017 to 2019
$2.8M
Value of Information Methods for NHLBI TrialsR01HL126804 · NHLBI · UNIVERSITY OF WASHINGTON · PI BASU, ANIRBAN · 2015 to 2018
$2.7M
Effectiveness of Gastric Sleeve vs. Gastric Bypass for Cardiovascular DiseaseR01HL130462 · NHLBI · KAISER FOUNDATION RESEARCH INSTITUTE · PI COLEMAN, KAREN JACQUELINE · 2016 to 2019
$2.7M
Preclinical Alzheimer's Disease Biomarkers: Effects of Midlife Vascular FactorsK01AG042498 · NIA · UNIVERSITY OF WISCONSIN-MADISON · PI WHARTON, WHITNEY LEE · 2013 to 2017
$617k
Systems Pharmacology for Predictive Alzheimer's Therapeutics: SysPharmRx-ADR34AG049652 · NIA · UNIVERSITY OF SOUTHERN CALIFORNIA · PI BRINTON, ROBERTA EILEEN · 2014 to 2014
$329k
Medical Research Council MC_PC_13088NHLBI NIH HHS R01 HL126804NHLBI NIH HHS R01 HL130462NIA NIH HHS K01 AG042498NIA NIH HHS P30 AG043073NIA NIH HHS R01 AG055401NIA NIH HHS R34 AG049652NIA NIH HHS RC4 AG039036
6 · The paper itself

Abstract

backgroundAntihypertensive treatments have been shown to reduce the risk of Alzheimer's disease (AD). The renin-angiotensin system (RAS) has been implicated in AD, and thus RAS-acting AHTs (angiotensin converting enzyme inhibitors (ACEIs), and angiotensin-II receptor blockers (ARBs)) may offer differential and additional protective benefits against AD compared with other AHTs, in addition to hypertension management.

methodsIn a retrospective cohort design, we examined the medical and pharmacy claims of a 20% sample of Medicare beneficiaries from 2007 to 2013, and compared rates of AD diagnosis for 1,343,334 users of six different AHT drug treatments, 65 years of age or older (4,215,338 person-years). We compared AD risk between RAS and non-RAS AHT drug users, and between ACEI users and ARB users, by sex and race/ethnicity. Models adjusted for age, socioeconomic status, underlying health, and comorbidities.

findingsRAS-acting AHTs were slightly more protective against onset of AD than non-RAS-acting AHTs for males, (male OR = 0.931 (CI: 0.895-0.969)), but not so for females (female OR = 0.985 (CI: 0.963-1.007)). Relative to other AHTs, ARBs were superior to ACEIs for both men (male ARB OR = 0.834 (CI: 0.788-0.884); male ACEI OR = 0.978 (CI: 0.939-1.019)) and women (female ARB OR = 0.941 (CI: 0.913-0.969); female ACEI OR = 1.022 (CI: 0.997-1.048)), but only in white men and white and black women. No association was shown for Hispanic men and women.

conclusionHypertension management treatments that include RAS-acting ARBs may, in addition to lowering blood pressure, reduce AD risk, particularly for white and black women and white men. Additional studies and clinical trials that include men and women from different racial and ethnic groups are needed to confirm these findings. Understanding the potentially beneficial effects of certain RAS-acting AHTs in high-risk populations is of great importance.

Indexed as

AgedAlzheimer DiseaseAntihypertensive AgentsFemaleHumansIncidenceMaleMedicareRetrospective StudiesRiskUnited StatesAntihypertensive Agents

Identifiers

PMID30383807
PMCPMC6211717
OpenAlexW2898855232

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.