Evidence map›Paper›PMID 30173819›Full record

ArticleAmerican journal of human genetics2018

Fetal-Not Maternal-APOL1 Genotype Associated with Risk for Preeclampsia in Those with African Ancestry.

Kimberly J Reidy, Rebecca C Hjorten, Claire L Simpson, Avi Z Rosenberg, Stacy D Rosenblum, Csaba P Kovesdy, Frances A Tylavsky, Joseph Myrie, Bianca L Ruiz, Soulin Haque and 11 more

Open access · hybridAbstract read
In one paragraph

Article in American journal of human genetics, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed, 2 pooled it
12.0field-weighted citation impact, top 1% 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

45 citing papers in PubMed, 2 syntheses or guidelines pooled it, 75 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Update on APOL1 and chronic kidney diseases in children.Pediatric nephrology (Berlin, Germany) · 2026
    Review
  4. Article
  5. Blood pressure andClinical kidney journal · 2026
    Article
  6. Article
  7. Cardiovascular complications of pregnancy.The Journal of clinical investigation · 2026
    Review
  8. Review
  9. Article
  10. Review
  11. Review
  12. Review
  13. Kidney international reports · 2025
    Article
  14. Article
  15. Review
  16. Kidney disease and reproductive health.Nature reviews. Nephrology · 2025
    Review
  17. Review
  18. Preeclampsia in mice carrying fetuses with APOL1 risk variants.bioRxiv : the preprint server for biology · 2024
    Article
  19. Article
  20. 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

21 authors at 7 institutions in 1 country.

Kimberly J ReidyDepartment of Pediatrics, Division of Pediatric Nephrology, Children's Hospital at Montefiore, Albert Einstein College of Medicine, Bronx, NY 10461, USA.
Rebecca C HjortenDepartment of Pediatrics, Division of Pediatric Nephrology, Children's Hospital at Montefiore, Albert Einstein College of Medicine, Bronx, NY 10461, USA; Department of Pediatrics, Division of Nephrology and Hypertension, Cincinnati Children's Hospital, Cincinnati OH 45229, USA.
Claire L SimpsonDepartment of Genetics, Genomics and Informatics, University of Tennessee Health Science Center, Memphis, TN 38163, USA.
Avi Z RosenbergDepartment of Pathology, John's Hopkins University, Baltimore, MD 21218, USA.
Stacy D RosenblumDepartment of Pediatrics, Division of Neonatology, Children's Hospital at Montefiore, Albert Einstein College of Medicine, Bronx, NY 10461, USA.
Csaba P KovesdyDepartment of Medicine, Division of Nephrology, University of Tennessee Health Science Center, Memphis, TN 38163, USA.
Frances A TylavskyDepartment of Preventive Medicine, University of Tennessee Health Science Center, Memphis, TN 38163, USA.
Joseph MyrieDepartment of Pediatrics, Division of Pediatric Nephrology, Children's Hospital at Montefiore, Albert Einstein College of Medicine, Bronx, NY 10461, USA.
Bianca L RuizDepartment of Pediatrics, Division of Pediatric Nephrology, Children's Hospital at Montefiore, Albert Einstein College of Medicine, Bronx, NY 10461, USA.
Soulin HaqueDepartment of Pediatrics, Division of Pediatric Nephrology, Children's Hospital at Montefiore, Albert Einstein College of Medicine, Bronx, NY 10461, USA.
Khyobeni MozhuiDepartment of Genetics, Genomics and Informatics, University of Tennessee Health Science Center, Memphis, TN 38163, USA; Department of Preventive Medicine, University of Tennessee Health Science Center, Memphis, TN 38163, USA.
George W NelsonAdvanced Biomedical Computational Science, Biomedical Informatics & Data Science Program, Frederick National Laboratory for Cancer Research sponsored by the National Cancer Institute, Frederick, MD 21701, USA.
Victor A DavidBasic Research Laboratory, Center for Cancer Research, National Cancer Institute, Frederick, MD 21702, USA.
Xiaoping YangDepartment of Pathology, John's Hopkins University, Baltimore, MD 21218, USA.
Masako SuzukiDepartment of Genetics, Albert Einstein College of Medicine, Bronx, NY 10461, USA.
Jack JacobDepartment of Pathology, Albert Einstein College of Medicine, Bronx, NY 10461, USA.
Sandra E ReznikDepartments of Pathology and Obstetrics & Gynecology and Women's Health, Albert Einstein College of Medicine, Bronx, NY 10461, USA; Department of Pharmaceutical Sciences, St. John's University, Queens, NY 11439, USA.
Frederick J KaskelDepartment of Pediatrics, Division of Pediatric Nephrology, Children's Hospital at Montefiore, Albert Einstein College of Medicine, Bronx, NY 10461, USA.
Jeffrey B KoppKidney Disease Section, National Institute of Diabetes and Digestive and Kidney Disease, National Institutes of Health, Bethesda, MD 20814, USA.
Cheryl A WinklerBasic Research Laboratory, Molecular Genetic Epidemiology Section, Frederick National Laboratory for Cancer Research sponsored by the National Cancer Institute, Frederick, MD 21702, USA. Electronic address: winklerc@mail.nih.gov.
Robert L DavisCenter for Biomedical Informatics, Department of Pediatrics, University of Tennessee Health Science Center, Memphis, TN 38103, USA. Electronic address: rdavis88@uthsc.edu.
Albert Einstein College of Medicine · USUniversity of Tennessee Health Science Center · USChildren's Hospital at Montefiore · USFrederick National Laboratory for Cancer Research · USJohns Hopkins University · USCenter for Cancer Research · USNational Institutes of Health · US

Funding

Core-010UL1TR001073 · NCATS · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI KELLER, MARLA J, SHAMOON, HARRY · 2013 to 2017
$21.3M
Focal Segmental Glomerulosclerosis: Genetics & MechanismsZIADK043308 · NIDDK · NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES · PI KOPP, JEFFREY BURNETT · 2009 to 2024
$15.7M
Genetics of Renal Disease in African AmericansZIABC010022 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI WINKLER, CHERYL · 2009 to 2022
$8.9M
Focal segmental glomerulosclerosis: TreatmentZIADK043412 · NIDDK · NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES · PI KOPP, JEFFREY BURNETT · 2009 to 2024
$7.4M
DEVELOPMENTAL RENAL AND ELECTROLYTE PHYSIOLOGYT32DK007110 · NIDDK · YESHIVA UNIVERSITY · PI KASKEL, FREDERICK JEFFREY, MELAMED, MICHAL L · 1986 to 2021
$5.6M
RESEARCH TRAINING IN PEDIATRIC NEPHROLOGYT32DK007695 · NIDDK · CINCINNATI CHILDRENS HOSP MED CTR · PI DEVARAJAN, PRASAD · 1992 to 2023
$2.2M
Role of Par1 Polarity Proteins in Podocyte Development and Glomerular DiseaseK08DK091507 · NIDDK · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI REIDY, KIMBERLY JEAN · 2011 to 2015
$667k
NCATS NIH HHS UL1 TR001073NIDDK NIH HHS K08 DK091507NIDDK NIH HHS T32 DK007110NIDDK NIH HHS T32 DK007695
6 · The paper itself

Abstract

Black Americans are at increased risk for preeclampsia. Genetic variants in apolipoprotein L1 (APOL1) account for much of the increased risk for kidney disease in blacks. APOL1 is expressed in human placenta and transgenic mice expressing APOL1 develop preeclampsia. We evaluated the role of APOL1 variants in human preeclampsia. We determined maternal and fetal APOL1 genotypes in black women with preeclampsia in two populations. At Einstein Montefiore Center (EMC) Affiliated Hospitals, we studied 121 pregnancies in black women with preeclampsia. At University of Tennessee Health Science Center (UTHSC), we studied 93 pregnancies in black women with preeclampsia and 793 pregnancies without preeclampsia. We measured serum markers of preeclampsia soluble fms-like tyrosine kinase 1 (sFlt-1), placental growth factor (PlGF), and soluble endoglin (sEng). Fetal APOL1 high-risk (HR) genotype was associated with preeclampsia, with odds ratios at EMC and UTHSC of 1.84 (95% CI 1.11, 2.93) and 1.92 (95% CI 1.05, 3.49), respectively. Maternal APOL1 HR genotype was not associated with preeclampsia. Mothers with the fetal APOL1 HR genotype had more cerebral or visual disturbances (63% versus 37%, p = 0.04). In addition, fetal APOL1 HR genotype was associated with a higher sFLT-1/PlGF ratio at birth (p = 0.04). Fetal APOL1 high-risk genotype increases the risk for preeclampsia, likely by adversely affecting placental function. Further research is needed to assess whether APOL1 genetic testing can predict preeclampsia and improve pregnancy outcomes.

Indexed as

AdultApolipoprotein L1BiomarkersBlack or African AmericanCase-Control StudiesFemaleFetusGenetic TestingGenotypeHumansMothersPre-EclampsiaPregnancyRiskAPOL1 protein, humanApolipoprotein L1BiomarkersAfrican AmericanAPOL1fetal genotypehealth disparitypreeclampsiaprematurity

Identifiers

PMID30173819
PMCPMC6128247
OpenAlexW2888943797

What OpenQuestion holds

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LicenceCC BY-NC-ND
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.