Evidence map›Paper›PMID 11932230›Full record

ReviewClinical microbiology reviews2002

Lung infections associated with cystic fibrosis.

Jeffrey B Lyczak, Carolyn L Cannon, Gerald B Pier

Abstract readHistorical ArticleReview
In one paragraph

Review in Clinical microbiology reviews, 2002. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 742 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
742citing papers in PubMed, 1 pooled it
33.0field-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

742 citing papers in PubMed, 1 synthesis or guideline pooled it, 1,610 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Infection and immunity · 2026
    Article
  4. Article
  5. NagX, a periplasmic β-Antimicrobial agents and chemotherapy · 2026
    Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Journal of bacteriology · 2026
    Article
  12. Article
  13. Review
  14. Article
  15. Factors governing the response ofFrontiers in cellular and infection microbiology · 2026
    Review
  16. Article
  17. Article
  18. Article
  19. Elevated glucose increasesInfection and immunity · 2025
    Article
  20. Article

682 more citing papers are in PubMed but not listed here.

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 2 institutions in 1 country.

Jeffrey B LyczakChanning Laboratory, Brigham and Women's Hospital, Harvard Medical School, Children's Hospital, Boston, MA 02115, USA.
Carolyn L Cannon
Gerald B Pier
Harvard University · USBrigham and Women's Hospital · US

Funding

CFTR AND INFECTION OF CYSTIC FIBROSIS PATIENTSR01HL058398 · NHLBI · BRIGHAM AND WOMEN'S HOSPITAL · PI PIER, GERALD B · 1997 to 2009
$3.4M
VIRULENCE AND IMMUNITY TO MUCOID P. AERUGINOSAR01AI048917 · NIAID · BRIGHAM AND WOMEN'S HOSPITAL · PI PIER, GERALD B · 2001 to 2009
$3.2M
INTERACTION OF P AERUGINOSA AND CFTR ON CORNEAL CELLSF32EY006805 · NEI · BRIGHAM AND WOMEN'S HOSPITAL · PI LYCZAK, JEFFREY B · 1996 to 1999
–
NEI NIH HHS EY 06805NEI NIH HHS F32 EY006805NHLBI NIH HHS HL 58398NHLBI NIH HHS R01 HL058398NIAID NIH HHS AI 48917NIAID NIH HHS R01 AI048917
6 · The paper itself

Abstract

While originally characterized as a collection of related syndromes, cystic fibrosis (CF) is now recognized as a single disease whose diverse symptoms stem from the wide tissue distribution of the gene product that is defective in CF, the ion channel and regulator, cystic fibrosis transmembrane conductance regulator (CFTR). Defective CFTR protein impacts the function of the pancreas and alters the consistency of mucosal secretions. The latter of these effects probably plays an important role in the defective resistance of CF patients to many pathogens. As the modalities of CF research have changed over the decades from empirical histological studies to include biophysical measurements of CFTR function, the clinical management of this disease has similarly evolved to effectively address the ever-changing spectrum of CF-related infectious diseases. These factors have led to the successful management of many CF-related infections with the notable exception of chronic lung infection with the gram-negative bacterium Pseudomonas aeruginosa. The virulence of P. aeruginosa stems from multiple bacterial attributes, including antibiotic resistance, the ability to utilize quorum-sensing signals to form biofilms, the destructive potential of a multitude of its microbial toxins, and the ability to acquire a mucoid phenotype, which renders this microbe resistant to both the innate and acquired immunologic defenses of the host.

Indexed as

Bacterial InfectionsCystic FibrosisCystic Fibrosis Transmembrane Conductance RegulatorHaemophilus influenzaeHistory, 20th CenturyHumansLungMutationPseudomonas aeruginosaStaphylococcus aureusCFTR protein, humanCystic Fibrosis Transmembrane Conductance Regulator

Identifiers

PMID11932230
PMCPMC118069
OpenAlexW2100619015

What OpenQuestion holds

Textmetadata
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.