Evidence map›Paper›PMID 35947673›Full record

ArticleScience translational medicine2022

Neuroblastoma suppressor of tumorigenicity 1 is a circulating protein associated with progression to end-stage kidney disease in diabetes.

Hiroki Kobayashi, Helen C Looker, Eiichiro Satake, Francesca D'Addio, Jonathan M Wilson, Pierre Jean Saulnier, Zaipul I Md Dom, Kristina O'Neil, Katsuhito Ihara, Bozena Krolewski and 14 more

Open access · greenAbstract read
In one paragraph

Article in Science translational medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
6.5field-weighted citation impact, top 2% 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

29 citing papers in PubMed, 42 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

24 authors at 12 institutions in 4 countries.

Hiroki KobayashiSection on Genetics and Epidemiology, Research Division, Joslin Diabetes Center, Boston, MA 02215, USA.ORCID 0000-0002-9674-0374
Helen C LookerChronic Kidney Disease Section, National Institute of Diabetes and Digestive and Kidney Diseases, Phoenix, AZ 85014, USA.
Eiichiro SatakeSection on Genetics and Epidemiology, Research Division, Joslin Diabetes Center, Boston, MA 02215, USA.ORCID 0000-0002-9784-4423
Francesca D'AddioPediatric Clinical Research Center Romeo ed Enrica Invernizzi, DIBIC L. Sacco, Università di Milano and Endocrinology Division ASST Sacco-FBF, Milan 20121, Italy.ORCID 0000-0002-0345-0694
Jonathan M WilsonDiabetes and Complications Department, Lilly Research Laboratories, Eli Lilly and Company, Indianapolis, IN 46225, USA.ORCID 0000-0002-8648-600X
Pierre Jean SaulnierChronic Kidney Disease Section, National Institute of Diabetes and Digestive and Kidney Diseases, Phoenix, AZ 85014, USA.ORCID 0000-0003-1862-4252
Zaipul I Md DomSection on Genetics and Epidemiology, Research Division, Joslin Diabetes Center, Boston, MA 02215, USA.ORCID 0000-0003-3503-7391
Kristina O'NeilSection on Genetics and Epidemiology, Research Division, Joslin Diabetes Center, Boston, MA 02215, USA.ORCID 0000-0002-2020-8728
Katsuhito IharaSection on Genetics and Epidemiology, Research Division, Joslin Diabetes Center, Boston, MA 02215, USA.ORCID 0000-0001-9554-3646
Bozena KrolewskiSection on Genetics and Epidemiology, Research Division, Joslin Diabetes Center, Boston, MA 02215, USA.
Hannah S BadgerDiabetes and Complications Department, Lilly Research Laboratories, Eli Lilly and Company, Indianapolis, IN 46225, USA.ORCID 0000-0002-5566-3149
Adriana PetrazzuoloPediatric Clinical Research Center Romeo ed Enrica Invernizzi, DIBIC L. Sacco, Università di Milano and Endocrinology Division ASST Sacco-FBF, Milan 20121, Italy.ORCID 0000-0002-6549-7703
Domenico CorradiDepartment of Medicine and Surgery, Unit of Pathology, University of Parma, Parma 43126, Italy.ORCID 0000-0002-8836-4778
Andrzej GaleckiDepartment of Internal Medicine, Medical School, University of Michigan, Ann Arbor, MI 48109, USA.
Parker C WilsonDivision of Anatomic and Molecular Pathology, Department of Pathology and Immunology, Washington University in Saint Louis School of Medicine, St. Louis 63110, USA.ORCID 0000-0001-8647-9662
Behzad NajafianDepartment of Laboratory Medicine & Pathology, University of Washington, Seattle, WA 98109, USA.ORCID 0000-0002-0904-6721
Michael MauerDepartment of Pediatrics and Medicine, University of Minnesota, Minneapolis, MN 55455, USA.ORCID 0000-0001-7301-9616
Monika A NiewczasSection on Genetics and Epidemiology, Research Division, Joslin Diabetes Center, Boston, MA 02215, USA.ORCID 0000-0003-2371-595X
Alessandro DoriaSection on Genetics and Epidemiology, Research Division, Joslin Diabetes Center, Boston, MA 02215, USA.ORCID 0000-0002-3830-4304
Benjamin D HumphreysDivision of Nephrology, Department of Medicine, Washington University in Saint Louis School of Medicine, St. Louis, MO 63110, USA.ORCID 0000-0002-6420-8703
Kevin L DuffinDiabetes and Complications Department, Lilly Research Laboratories, Eli Lilly and Company, Indianapolis, IN 46225, USA.ORCID 0000-0002-1656-8982
Paolo FiorinaPediatric Clinical Research Center Romeo ed Enrica Invernizzi, DIBIC L. Sacco, Università di Milano and Endocrinology Division ASST Sacco-FBF, Milan 20121, Italy.ORCID 0000-0002-1093-7724
Robert G NelsonChronic Kidney Disease Section, National Institute of Diabetes and Digestive and Kidney Diseases, Phoenix, AZ 85014, USA.ORCID 0000-0001-7307-3786
Andrzej S KrolewskiSection on Genetics and Epidemiology, Research Division, Joslin Diabetes Center, Boston, MA 02215, USA.ORCID 0000-0002-1705-2953
Joslin Diabetes Center · USEli Lilly (United States) · USLuigi Sacco Hospital · ITNational Institute of Diabetes and Digestive and Kidney Diseases · USWashington University in St. Louis · USBoston Children's Hospital · USInserm · FRNihon University · JPUniversity of Michigan · USUniversity of Minnesota · USUniversity of Parma · ITUniversity of Washington · US

Funding

SPECIAL ASSAY COREP30DK036836 · NIDDK · JOSLIN DIABETES CENTER · PI ROHIT N. KULKARNI · 1986 to 2026
$50.5M
Research Education CoreP30AG024824 · NIA · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Lona Mody, RAYMOND L YUNG · 2004 to 2026
$29.2M
Tumor necrosis factor superfamily of ligands and receptors in progressive renal decline in diabetesR01DK041526 · NIDDK · JOSLIN DIABETES CENTER · PI KROLEWSKI, ANDRZEJ S · 1990 to 2018
$7.8M
Development of Prognostic Algorithms to Identify Subjects at High Risk of ESKD in Type 2 DiabetesR01DK126799 · NIDDK · JOSLIN DIABETES CENTER · PI KROLEWSKI, ANDRZEJ S · 2021 to 2024
$2.7M
Understanding the role of the Complement Proteome in progressive Diabetic Kidney DiseaseR01DK123459 · NIDDK · JOSLIN DIABETES CENTER · PI NIEWCZAS, MONIKA ANNA · 2020 to 2024
$2.3M
The role of microRNAs in progressive renal decline in Type 1 diabetesR01DK110350 · NIDDK · UNIVERSITY OF UTAH · PI PEZZOLESI, MARCUS GUY · 2017 to 2021
$1.8M
The Single Cell Landscape of Early Human Diabetic NephropathyK08DK126847 · NIDDK · WASHINGTON UNIVERSITY · PI Parker C. Wilson · 2022 to 2026
$840k
NIA NIH HHS P30 AG024824NIDDK NIH HHS K08 DK126847NIDDK NIH HHS P30 DK036836NIDDK NIH HHS R01 DK041526NIDDK NIH HHS R01 DK110350NIDDK NIH HHS R01 DK123459NIDDK NIH HHS R01 DK126799
6 · The paper itself

Abstract

Circulating proteins associated with transforming growth factor-β (TGF-β) signaling are implicated in the development of diabetic kidney disease (DKD). It remains to be comprehensively examined which of these proteins are involved in the pathogenesis of DKD and its progression to end-stage kidney disease (ESKD) in humans. Using the SOMAscan proteomic platform, we measured concentrations of 25 TGF-β signaling family proteins in four different cohorts composed in total of 754 Caucasian or Pima Indian individuals with type 1 or type 2 diabetes. Of these 25 circulating proteins, we identified neuroblastoma suppressor of tumorigenicity 1 (NBL1, aliases DAN and DAND1), a small secreted protein known to inhibit members of the bone morphogenic protein family, to be most strongly and independently associated with progression to ESKD during 10-year follow-up in all cohorts. The extent of damage to podocytes and other glomerular structures measured morphometrically in 105 research kidney biopsies correlated strongly with circulating NBL1 concentrations. Also, in vitro exposure to NBL1 induced apoptosis in podocytes. In conclusion, circulating NBL1 may be involved in the disease process underlying progression to ESKD, and its concentration in circulation may identify subjects with diabetes at increased risk of progression to ESKD.

Indexed as

Diabetes Mellitus, Type 2Kidney Failure, ChronicNeuroblastomaCell Cycle ProteinsDisease ProgressionHumansProteomicsTransforming Growth Factor betaCell Cycle ProteinsNBL1 protein, humanTransforming Growth Factor beta

Identifiers

PMID35947673
PMCPMC9531292
OpenAlexW4292665401

What Socratic holds

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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 Socratic graph.