Evidence map›Paper›PMID 23676986›Full record

ReviewThrombosis and haemostasis2013

Role of plasma kallikrein in diabetes and metabolism.

E P Feener, Q Zhou, W Fickweiler

Abstract readReview
In one paragraph

Review in Thrombosis and haemostasis, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed, 1 pooled it
2.7field-weighted citation impact, top 10% 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

26 citing papers in PubMed, 1 synthesis or guideline pooled it, 55 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Plasma NOTCH3 and the risk of cardiovascular recurrence in patients with ischemic stroke.QJM : monthly journal of the Association of Physicians · 2024
    Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. HDL and Surgery.Advances in experimental medicine and biology · 2022
    Article
  10. Article
  11. Article
  12. Theaflavin Chemistry and Its Health Benefits.Oxidative medicine and cellular longevity · 2021
    Review
  13. Article
  14. The role of inflammation in diabetic eye disease.Seminars in immunopathology · 2019
    Review
  15. Article
  16. Diabetic Microvascular Disease: An Endocrine Society Scientific Statement.The Journal of clinical endocrinology and metabolism · 2017
    Review
  17. Article
  18. Article
  19. Observational
  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

3 authors at 1 institution in 1 country.

E P FeenerEdward P. Feener, PhD, Joslin Diabetes Center, One Joslin Place, Boston, Massachusetts 02215, USA, Tel.: +1 617 309 2599, Fax: +1 617 309 2637, E-mail: edward.feener@joslin.harvard.edu.
Q Zhou
W Fickweiler
Joslin Diabetes Center · US

Funding

SPECIAL ASSAY COREP30DK036836 · NIDDK · JOSLIN DIABETES CENTER · PI ROHIT N. KULKARNI · 1986 to 2026
$50.5M
Role of the kallikrein-kinin system in diabetic retinopathyR01EY019029 · NEI · JOSLIN DIABETES CENTER · PI AIELLO, LLOYD P · 2008 to 2017
$3.8M
Role of Hyperglycemia in Intracerebral HemorrhageR01NS077006 · NINDS · JOSLIN DIABETES CENTER · PI RASK-MADSEN, CHRISTIAN · 2012 to 2016
$1.8M
NEI NIH HHS EY019029NEI NIH HHS R01 EY019029NIDDK NIH HHS DK36836NIDDK NIH HHS P30 DK036836NINDS NIH HHS NS077006NINDS NIH HHS R01 NS077006
6 · The paper itself

Abstract

Plasma kallikrein (PK) is a serine protease generated from plasma prekallikrein, an abundant circulating zymogen expressed by the Klkb1 gene. The physiological actions of PK have been primarily attributed to its production of bradykinin and activation of coagulation factor XII, which promotes inflammation and the intrinsic coagulation pathway. Recent genetic, molecular, and pharmacological studies of PK have provided further insight into its role in physiology and disease. Genetic analyses have revealed common Klkb1 variants that are association with blood metabolite levels, hypertension, and coagulation. Characterisation of animal models with Klkb1 deficiency and PK inhibition have demonstrated effects on inflammation, vascular function, blood pressure regulation, thrombosis, haemostasis, and metabolism. These reports have also identified a host of PK substrates and interactions, which suggest an expanded physiological role for this protease beyond the bradykinin system and coagulation. The review summarises the mechanisms that contribute to PK activation and its emerging role in diabetes and metabolism.

Indexed as

Gene Expression RegulationAdipogenesisAnimalsBlood CoagulationBlood PressureBradykininDiabetes MellitusFactor XIIGenetic VariationGlucoseHemostasisHumansHypertensionInflammationMicePlasma KallikreinBradykininFactor XIIGlucosePlasma KallikreinPrekallikrein

Identifiers

PMID23676986
PMCPMC3757113
OpenAlexW2047023619

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.