Evidence map›Paper›PMID 27342958›Full record

SynthesisKidney international2016

APOL1 renal-risk variants associate with reduced cerebral white matter lesion volume and increased gray matter volume.

Barry I Freedman, Crystal A Gadegbeku, R Nick Bryan, Nicholette D Palmer, Pamela J Hicks, Lijun Ma, Michael V Rocco, S Carrie Smith, Jianzhao Xu, Christopher T Whitlow and 15 more

Open access · bronzeAbstract readMeta-Analysis
In one paragraph

Synthesis in Kidney international, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.3field-weighted citation impact, top 13% 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

14 citing papers in PubMed, 17 citations in OpenAlex.

  1. Trial
  2. Arteriosclerosis, thrombosis, and vascular biology · 2017
    Trial
  3. Article
  4. Article
  5. Review
  6. The metabolic effects of APOL1 in humans.Pflugers Archiv : European journal of physiology · 2023
    Review
  7. Review
  8. The Impact of APOL1 on Chronic Kidney Disease and Hypertension.Advances in chronic kidney disease · 2019
    Review
  9. Article
  10. Article
  11. Association BetweenJournal of the American Heart Association · 2017
    Article
  12. Hypertension in African Americans.Current cardiology reports · 2017
    Review
  13. APOL1 Gene Kidney Risk Variants and Cardiovascular Disease: Getting to the Heart of the Matter.American journal of kidney diseases : the official journal of the National Kidney Foundation · 2017
    Review
  14. Kidney international reports · 2017
    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

25 authors at 7 institutions in 1 country.

Barry I Freedman *Department of Internal Medicine, Section on Nephrology; Wake Forest School of Medicine, Winston-Salem, NC.
Crystal A Gadegbeku *Department of Medicine, Temple University School of Medicine, Philadelphia, PA.
R Nick Bryan *Department of Radiology, University of Pennsylvania, Philadelphia, PA.
Nicholette D PalmerCenters for Diabetes Research and Genomics and Personalized Medicine Research; Wake Forest School of Medicine, Winston-Salem, NC.
Pamela J HicksDepartment of Biochemistry; Wake Forest School of Medicine, Winston-Salem, NC.
Lijun MaDepartment of Internal Medicine, Section on Nephrology; Wake Forest School of Medicine, Winston-Salem, NC.
Michael V RoccoDepartment of Internal Medicine, Section on Nephrology; Wake Forest School of Medicine, Winston-Salem, NC.
S Carrie SmithDepartment of Biochemistry; Wake Forest School of Medicine, Winston-Salem, NC.
Jianzhao XuDepartment of Biochemistry; Wake Forest School of Medicine, Winston-Salem, NC.
Christopher T WhitlowDepartment of Radiologic Sciences, Advanced Neuroscience Imaging Research (ANSIR) Laboratory; Wake Forest School of Medicine, Winston-Salem, NC.
Benjamin C WagnerDepartment of Radiologic Sciences, Advanced Neuroscience Imaging Research (ANSIR) Laboratory; Wake Forest School of Medicine, Winston-Salem, NC.
Carl D LangefeldDivision of Public Health Sciences, Department of Biostatistical Sciences; Wake Forest School of Medicine, Winston-Salem, NC.
Amret T HawfieldDepartment of Internal Medicine, Section on Nephrology; Wake Forest School of Medicine, Winston-Salem, NC.
Jeffrey T BatesMichael E. DeBakey Veterans Administration Medical Center and Baylor College of Medicine, Houston, TX.
Alan J LernerDepartment of Neurology, Case Western Reserve University School of Medicine, Cleveland, OH.
Dominic S RajDepartment of Medicine, George Washington University, Washington, DC.
Mohammad S SadaghianiDepartment of Medicine, Temple University School of Medicine, Philadelphia, PA.
Robert D TotoDepartment of Internal Medicine, University of Texas, Southwestern Medical Center, Dallas, TX.
Jackson T WrightDepartment of Medicine, Case Western Reserve University School of Medicine, Cleveland, OH.
Donald W BowdenCenters for Diabetes Research and Genomics and Personalized Medicine Research; Wake Forest School of Medicine, Winston-Salem, NC.
Jeff D WilliamsonDepartment of Internal Medicine, Section on Gerontology and Geriatric Medicine; Wake Forest School of Medicine, Winston-Salem, NC.
Kaycee M SinkDepartment of Internal Medicine, Section on Gerontology and Geriatric Medicine; Wake Forest School of Medicine, Winston-Salem, NC.
Joseph A MaldjianDepartment of Radiologic Sciences, Advanced Neuroscience Imaging Research (ANSIR) Laboratory; Wake Forest School of Medicine, Winston-Salem, NC.
Nicholas M Pajewski *Division of Public Health Sciences, Department of Biostatistical Sciences; Wake Forest School of Medicine, Winston-Salem, NC.
Jasmin Divers *Division of Public Health Sciences, Department of Biostatistical Sciences; Wake Forest School of Medicine, Winston-Salem, NC.
Wake Forest University · USUniversity of Pennsylvania · USThe University of Texas Southwestern Medical Center · USUniversity School · USBaylor College of Medicine · USGeorge Washington University · USTemple University · US

Funding

Phenotypic Diversity in COVID-19UL1TR001878 · NCATS · UNIVERSITY OF PENNSYLVANIA · PI FITZGERALD, GARRET A · 2016 to 2025
$102.4M
INSTITUTIONAL CLINICAL AND TRANSLATIONAL SCIENCE AWARDUL1RR024134 · NCRR · UNIVERSITY OF PENNSYLVANIA · PI FITZGERALD, GARRET A · 2006 to 2011
$70.4M
University of Pittsburgh Clinical and Translational Science InstituteUL1TR000005 · NCATS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI REIS, STEVEN E · 2012 to 2015
$50.8M
Clinical and Translational Science Collaborative of ClevelandUL1TR000439 · NCATS · CASE WESTERN RESERVE UNIVERSITY · PI KONSTAN, MICHAEL W. · 2012 to 2016
$50.0M
Michigan Institute for Clinical and Health Research (MCHR)UL1TR000433 · NCATS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI MASHOUR, GEORGE ALEXANDER · 2012 to 2016
$49.9M
The Vanderbilt Institute for Clinical and Translational Research (VICTR)UL1TR000445 · NCATS · VANDERBILT UNIVERSITY MEDICAL CENTER · PI BERNARD, GORDON RAPHAEL · 2012 to 2016
$41.4M
Institutional Clinical and Translational Science AwardUL1TR000003 · NCATS · UNIVERSITY OF PENNSYLVANIA · PI FITZGERALD, GARRET A · 2012 to 2015
$38.9M
Using social networks to map and evaluate team science across CTSA hubsUL1TR001427 · NCATS · UNIVERSITY OF FLORIDA · PI MITCHELL, DUANE A. · 2015 to 2024
$37.2M
Spectrum Stanford Center for clinical and Translational Research and EducationUL1TR001085 · NCATS · STANFORD UNIVERSITY · PI CULLEN, MARK RICHARD, GREENBERG, HARRY BERNARD · 2013 to 2017
$37.1M
WORKER PROTECTION AGAINST AIRBORNE INFLUENZA - A PILOT STUDYM01RR007122 · NCRR · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI HUNDLEY, WILLIAM GREGORY · 1992 to 2010
$35.2M
Wake Forest Clinical and Translational Science AwardUL1TR001420 · NCATS · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI ARD, JAMY D, FOLEY, KRISTIE L · 2015 to 2023
$32.3M
Tufts Clinical and Translational Research InstituteUL1TR001064 · NCATS · TUFTS UNIVERSITY BOSTON · PI SELKER, HARRY P. · 2013 to 2017
$26.4M
NCATS NIH HHS UL1 TR000002NCATS NIH HHS UL1 TR000003NCATS NIH HHS UL1 TR000005NCATS NIH HHS UL1 TR000050NCATS NIH HHS UL1 TR000064NCATS NIH HHS UL1 TR000073NCATS NIH HHS UL1 TR000075NCATS NIH HHS UL1 TR000093NCATS NIH HHS UL1 TR000105NCATS NIH HHS UL1 TR000433NCATS NIH HHS UL1 TR000439NCATS NIH HHS UL1 TR000445NCATS NIH HHS UL1 TR001064NCATS NIH HHS UL1 TR001070NCATS NIH HHS UL1 TR001085NCATS NIH HHS UL1 TR001420NCATS NIH HHS UL1 TR001427NCATS NIH HHS UL1 TR001878NCRR NIH HHS M01 RR007122NCRR NIH HHS UL1 RR024134NCRR NIH HHS UL1 RR025752NCRR NIH HHS UL1 RR025755NCRR NIH HHS UL1 RR025771NHLBI NIH HHS HHSN268200900040CNHLBI NIH HHS HHSN268200900046CNHLBI NIH HHS HHSN268200900047CNHLBI NIH HHS HHSN268200900048CNHLBI NIH HHS HHSN268200900049CNIDDK NIH HHS R01 DK071891NIGMS NIH HHS P30 GM103337NIMHD NIH HHS R01 MD009055NINDS NIH HHS R01 NS058700NINDS NIH HHS R01 NS075107
6 · The paper itself

Abstract

To assess apolipoprotein L1 gene (APOL1) renal-risk-variant effects on the brain, magnetic resonance imaging (MRI)-based cerebral volumes and cognitive function were assessed in 517 African American-Diabetes Heart Study (AA-DHS) Memory IN Diabetes (MIND) and 2568 hypertensive African American Systolic Blood Pressure Intervention Trial (SPRINT) participants without diabetes. Within these cohorts, 483 and 197 had cerebral MRI, respectively. AA-DHS participants were characterized as follows: 60.9% female, mean age of 58.6 years, diabetes duration 13.1 years, estimated glomerular filtration rate of 88.2 ml/min/1.73 m(2), and a median spot urine albumin to creatinine ratio of 10.0 mg/g. In additive genetic models adjusting for age, sex, ancestry, scanner, intracranial volume, body mass index, hemoglobin A1c, statins, nephropathy, smoking, hypertension, and cardiovascular disease, APOL1 renal-risk-variants were positively associated with gray matter volume (β = 3.4 × 10(-3)) and negatively associated with white matter lesion volume (β = -0.303) (an indicator of cerebral small vessel disease) and cerebrospinal fluid volume (β= -30707) (all significant), but not with white matter volume or cognitive function. Significant associations corresponding to adjusted effect sizes (β/SE) were observed with gray matter volume (0.16) and white matter lesion volume (-0.208), but not with cerebrospinal fluid volume (-0.251). Meta-analysis results with SPRINT Memory and Cognition in Decreased Hypertension (MIND) participants who had cerebral MRI were confirmatory. Thus, APOL1 renal-risk-variants are associated with larger gray matter volume and lower white matter lesion volume suggesting lower intracranial small vessel disease.

Indexed as

Apolipoprotein L1ApolipoproteinsBlack or African AmericanBlood PressureBrainCardiovascular DiseasesCerebral Small Vessel DiseasesCognitionDiabetes Mellitus, Type 2Glomerular Filtration RateGray MatterHumansHypertensionKidney DiseasesKidney Function TestsLipoproteins, HDLAPOL1 protein, humanApolipoprotein L1ApolipoproteinsLipoproteins, HDLAfrican AmericansAPOL1braincognitionhypertensionmagnetic resonance imagingtype 2 diabetes mellitus

Identifiers

PMID27342958
PMCPMC4946987
OpenAlexW2469911226

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

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.