Evidence map›Paper›PMID 20478485›Full record

ReviewGastroenterology clinics of North America2010

Targets for current pharmacologic therapy in cholesterol gallstone disease.

Agostino Di Ciaula, David Q H Wang, Helen H Wang, Leonilde Bonfrate, Piero Portincasa

Abstract readReview
In one paragraph

Review in Gastroenterology clinics of North America, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
4.8field-weighted citation impact, top 5% 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

24 citing papers in PubMed, 64 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. New insights into the role ofLiver research (Beijing, China) · 2017
    Article
  12. Article
  13. Article
  14. Review
  15. A novel therapeutic effect of statins on nephrogenic diabetes insipidus.Journal of cellular and molecular medicine · 2015
    Review
  16. Article
  17. Article
  18. Therapy of gallstone disease: What it was, what it is, what it will be.World journal of gastrointestinal pharmacology and therapeutics · 2012
    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

5 authors at 3 institutions in 2 countries.

Agostino Di CiaulaDivision of Internal Medicine, Hospital of Bisceglie, Bisceglie (Bari), Italy.
David Q H Wang
Helen H Wang
Leonilde Bonfrate
Piero Portincasa
Beth Israel Deaconess Medical Center · USHarvard University · USOspedale degli Infermi · IT

Funding

CHOLESTEROL HOMEOSTASIS IN THE INBRED MOUSE.R01DK054012 · NIDDK · BRIGHAM AND WOMEN'S HOSPITAL · PI WANG, DAVID Q · 1999 to 2008
$2.9M
The Role of Dysfunctional CCK-1R in CholelithogenesisR01DK073917 · NIDDK · SAINT LOUIS UNIVERSITY · PI WANG, DAVID Q · 2008 to 2011
$1.4M
GPR30 and Hepatic Cholesterol HomeostasisR01DK106249 · NIDDK · SAINT LOUIS UNIVERSITY · PI WANG, DAVID Q · 2015 to 2017
$1.0M
NIDDK NIH HHS DK54012NIDDK NIH HHS DK73917NIDDK NIH HHS R01 DK054012NIDDK NIH HHS R01 DK073917NIDDK NIH HHS R01 DK106249
6 · The paper itself

Abstract

Gallstone disease is a frequent condition throughout the world and, cholesterol stones are the most frequent form in Western countries. The standard treatment of symptomatic gallstone subjects is laparoscopic cholecystectomy. The selection of patients amenable for nonsurgical, medical therapy is of key importance; a careful analysis should consider the natural history of the disease and the overall costs of therapy. Only patients with mild symptoms and small, uncalcified cholesterol gallstones in a functioning gallbladder with a patent cystic duct are considered for oral litholysis by hydrophilic ursodeoxycholic acid, in the hope of achieving cholesterol desaturation of bile and progressive stone dissolution. Recent studies have raised the possibility that cholesterol-lowering agents that inhibit hepatic cholesterol synthesis (statins) or intestinal cholesterol absorption (ezetimibe), or drugs acting on specific nuclear receptors involved in cholesterol and bile acid homeostasis, may offer, alone or in combination, additional medical therapeutic tools for treating cholesterol gallstones. Recent perspectives on medical treatment of cholesterol gallstone disease are discussed in this article.

Indexed as

AzetidinesCholesterolCholinergic AntagonistsEzetimibeGallstonesHumansHydroxymethylglutaryl-CoA Reductase InhibitorsIntestinal AbsorptionTreatment OutcomeAzetidinesCholesterolCholinergic AntagonistsEzetimibeHydroxymethylglutaryl-CoA Reductase Inhibitors

Identifiers

PMID20478485
PMCPMC2915454
OpenAlexW2075895288

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.