Evidence map›Paper›PMID 22068337›Full record

ReviewCurrent hypertension reports2012

Target organ damage in African American hypertension: role of APOL1.

Barry I Freedman, Mariana Murea

Open access · greenAbstract readReview
In one paragraph

Review in Current hypertension reports, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
3.7field-weighted citation impact, top 7% 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

31 citing papers in PubMed, 57 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Review
  5. Article
  6. Kidney disease and APOL1.Human molecular genetics · 2021
    Review
  7. Review
  8. Article
  9. Article
  10. Review
  11. Review
  12. Apolipoprotein L1 Variants and Blood Pressure Traits in African Americans.Journal of the American College of Cardiology · 2017
    Article
  13. Review
  14. Article
  15. Assessment and management of hypertension in transplant patients.Journal of the American Society of Nephrology : JASN · 2015
    Review
  16. Review
  17. Review
  18. Gene-gene and gene-environment interactions in apolipoprotein L1 gene-associated nephropathy.Clinical journal of the American Society of Nephrology : CJASN · 2014
    Review
  19. Neighborhood socioeconomic status, race, and mortality in young adult dialysis patients.Journal of the American Society of Nephrology : JASN · 2014
    Article
  20. Familial clustering of ESRD in the Norwegian population.Clinical journal of the American Society of Nephrology : CJASN · 2014
    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

2 authors at 1 institution in 1 country.

Barry I FreedmanSection on Nephrology, Wake Forest School of Medicine, Winston-Salem, NC 27157-1053, USA. bfreedma@wakehealth.edu
Mariana Murea
Wake Forest University · US

Funding

Genetic Analysis of African American Hypertensive End-Stage Renal DiseaseR01DK070941 · NIDDK · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI FREEDMAN, BARRY IRA · 2006 to 2015
$4.7M
Natural History of MYH9-Associated NephropathyR01DK084149 · NIDDK · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI FREEDMAN, BARRY IRA · 2009 to 2012
$2.3M
GENETIC ANALYSIS OF HUMAN HYPERTENSIVE ESRDR01HL056266 · NHLBI · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI FREEDMAN, BARRY IRA · 1997 to 2001
$466k
NHLBI NIH HHS R01 HL56266NIDDK NIH HHS R01 DK070941NIDDK NIH HHS R01 DK084149
6 · The paper itself

Abstract

Apolipoprotein L1 (APOL1) gene association studies and results of the African American Study of Kidney Disease and Hypertension are disproving the longstanding concept that mild to moderate essential hypertension contributes substantially to end-stage renal disease susceptibility in African Americans. APOL1 coding variants underlie a spectrum of kidney diseases, including that attributed to hypertension (labeled arteriolar or hypertensive nephrosclerosis), focal segmental glomerulosclerosis, and HIV-associated nephropathy. APOL1 nephropathy risk variants persist because of protection afforded from the parasite that causes African sleeping sickness. This breakthrough will lead to novel treatments for hypertensive African Americans with low-level proteinuria, for whom effective therapies are lacking. Furthermore, APOL1 nephropathy risk variants contribute to racially variable allograft survival rates after kidney transplantation and assist in detecting nondiabetic forms of nephropathy in African Americans with diabetes. Discovery of APOL1-associated nephropathy was a major success of the genetics revolution, demonstrating that secondary hypertension is typically present in nondiabetic African Americans with nephropathy.

Indexed as

HypertensionKidney Failure, ChronicKidney GlomerulusProteinuriaAngiotensin-Converting Enzyme InhibitorsApolipoprotein L1ApolipoproteinsBlack or African AmericanCohort StudiesFamily HealthGenetic Predisposition to DiseaseGenome-Wide Association StudyGlomerular Filtration RateHumansIntracellular Signaling Peptides and ProteinsLipoproteins, HDLAngiotensin-Converting Enzyme InhibitorsAPOL1 protein, humanApolipoprotein L1ApolipoproteinsIntracellular Signaling Peptides and ProteinsLipoproteins, HDLMembrane ProteinsMolecular Motor ProteinsMYH9 protein, humanMyosin Heavy ChainsNPHS2 protein

Identifiers

PMID22068337
PMCPMC3253170
OpenAlexW2087251832

What OpenQuestion holds

Textmetadata
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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.