Evidence map›Paper›PMID 18950909›Full record

ArticleAmerican journal of kidney diseases : the official journal of the National Kidney Foundation2009

Association of the Q121 variant of ENPP1 gene with decreased kidney function among patients with type 2 diabetes.

Salvatore De Cosmo, Antonio Minenna, Yuan-Yuan Zhang, Ryan Thompson, Robert Thompson, Giuseppe Miscio, Monica Vedovato, Anna Rauseo, Alois Saller, Sandra Mastroianno and 5 more

Erratum issuedOpen access · greenAbstract readMulticenter Study
In one paragraph

Article in American journal of kidney diseases : the official journal of the National Kidney Foundation, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 6 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed, 1 pooled it
1.3field-weighted citation impact, top 21% 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

6 citing papers in PubMed, 1 synthesis or guideline pooled it, 18 citations in OpenAlex.

  1. Pooled it
  2. The IRS1 G972R polymorphism and glomerular filtration rate in patients with type 2 diabetes of European ancestry.Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association · 2013
    Article
  3. The 9p21 coronary artery disease locus and kidney dysfunction in patients with Type 2 diabetes mellitus.Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association · 2012
    Article
  4. Article
  5. ENPP1/PC-1 K121Q and other predictors of posttransplant diabetes.Metabolic syndrome and related disorders · 2011
    Article
  6. Review
4 · The record

Corrections and comments

  • Erratum issued
    Thompson, Robert [corrected to Thompson, Ryan]
5 · Who and what money

Authors and funding

15 authors at 5 institutions in 2 countries.

Salvatore De CosmoUnit of Endocrinology, Scientific Institute Casa Sollievo della Sofferenza, San Giovanni Rotondo, Italy. sdecosm@tin.it
Antonio Minenna
Yuan-Yuan Zhang
Ryan Thompson
Robert Thompson
Giuseppe Miscio
Monica Vedovato
Anna Rauseo
Alois Saller
Sandra Mastroianno
Fabio Pellegrini
Roberto Trevisan
Paola Fioretto
Alessandro Doria
Vincenzo Trischitta
Casa Sollievo della Sofferenza · ITJoslin Diabetes Center · USUniversity of Padua · ITMario Negri Sud Foundation · ITSapienza University of Rome · IT

Funding

SPECIAL ASSAY COREP30DK036836 · NIDDK · JOSLIN DIABETES CENTER · PI JEAN E. SCHAFFER · 1986 to 2026
$50.5M
Variability in Adipokine Genes and AtherosclerosisR01HL073168 · NHLBI · JOSLIN DIABETES CENTER · PI DORIA, ALESSANDRO · 2003 to 2012
$5.8M
NHLBI NIH HHS HL73168NHLBI NIH HHS R01 HL073168NIDDK NIH HHS DK36836NIDDK NIH HHS P30 DK036836
6 · The paper itself

Abstract

backgroundInsulin resistance has a role in diabetic kidney complications. The K121Q (lysine to glutamine substitution at amino acid 121, encoded by single-nucleotide polymorphism rs1044498) variant of the ectonucleotide pyrophosphatase/phosphodiesterase gene (ENPP1) has been associated with insulin resistance and related vascular complications in patients with type 2 diabetes (T2D) in many, although not all, studies. This study investigated whether the ENPP1 Q121 variant modulates the risk of decreased glomerular filtration rate (GFR) in patients with T2D. STUDY

designCross-sectional study. SETTING &

participants2 diabetes units from Italy (in Gargano and Padua) and 1 from the United States (Boston, MA) recruited a total of 1,392 patients with T2D. PREDICTOR: The ENPP1 Q121 variant. MEASUREMENTS: Estimated GFR from serum creatinine, urinary albumin excretion, blood pressure, hemoglobin A(1c), triglycerides, total cholesterol, and high-density lipoprotein cholesterol. OUTCOMES: Decreased GFRs (ie, estimated GFR <60 mL/min/1.73 m(2)).

resultsIn the Gargano and Boston populations, according to the dominant model of inheritance, Q121 carriers (ie, individual with either KQ or QQ alleles) had an increased risk of decreased GFR: odds ratios (ORs) of 1.69 (95% confidence interval [CI], 1.1 to 2.6) and 1.50 (95% CI, 1.0 to 2.2), respectively. In the Padua set, the association was in the same direction, but did not reach formal statistical significance (OR, 1.77; 95% CI, 0.7 to 4.5). When the 3 studies were pooled, Q121 carriers showed an increased risk of decreased GFR (OR, 1.58; 95% CI, 1.2 to 2.1; P = 0.002). Also, pooled mean differences in absolute GFRs were different across genotype groups, with Q121 carriers showing lower GFRs compared with KK individuals (P = 0.04). LIMITATIONS: P values not approaching a genome-wide level of significance.

conclusionsOur data suggest that patients with T2D carrying the ENPP1 Q121 variant are at increased risk of decreased GFR.

Indexed as

Glomerular Filtration RatePolymorphism, Single NucleotideAlbuminuriaAmino Acid SubstitutionDiabetes Mellitus, Type 2FemaleHumansMaleMiddle AgedPhosphoric Diester HydrolasesPyrophosphatasesectonucleotide pyrophosphatase phosphodiesterase 1Phosphoric Diester HydrolasesPyrophosphatases

Identifiers

PMID18950909
PMCPMC2939986
OpenAlexW2004809259

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.