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LL-37

Cathelicidin, hCAP-18, FALL-39, CAP-18

Quick Stats
Studies 2230
Trials 95
Score 1
2017 pubmed 28 citations

The Role of Biomarkers for the Diagnosis of Implant-Related Infections in Orthopaedics and Trauma.

Alvand. Abtin A; Rezapoor. Maryam M; Parvizi. Javad J

Key Findings

  • LL‑37 can be measured in synovial fluid and may help identify periprosthetic joint infections
  • Several other serum and synovial biomarkers (IL‑4, IL‑6, TNF‑α, procalcitonin, D‑dimer, HBD‑2/3, etc.) are also being studied for infection detection
  • Current diagnostic tests for implant infections are imperfect, so adding biomarker panels could improve accuracy

Practical Outcomes

  • For most biohackers this information isn’t directly useful unless you have a joint implant and suspect an infection. It doesn’t suggest a new supplement or protocol for longevity, metabolic health, or performance.

Summary

The paper talks about using blood and joint‑fluid markers, like the antimicrobial peptide LL‑37, to spot infections around joint implants. It’s mainly about diagnosing a specific medical problem, not about boosting health or performance.

Abstract

Diagnosis of implant-related (periprosthetic joint) infections poses a major challenge to infection disease physicians and orthopaedic surgeons. Conventional diagnostic tests continue to suffer from issues of accuracy and feasibility. Biomarkers are used throughout medicine for diagnostic and prognostic purposes, as they are able to objectively determine the presence of a disease or a biological state. There is increasing evidence to support the measurement of specific biomarkers in serum and/or synovial fluid of patients with suspected periprosthetic joint infections. Promising serum biomarkers include interleukin (IL)-4, IL-6, tumour necrosis factor (TNF)-α, procalcitonin, soluble intercellular adhesion molecule 1 (sICAM-1), and D-dimer. In addition to c-reactive protein and leucocyte esterase, promising biomarkers that can be measured in synovial fluid include antimicrobial proteins such as human β-defensin (HBD)-2 and human β-defensin (HBD)-3, and cathelicidin LL-37, as well as several interleukins such as IL-1β, IL-6, IL-8, IL-17, TNF- α, interferon-δ, and vascular endothelial growth factor.

Study Information

Provider

pubmed

Year

2017

DOI

10.1007/5584_2017_11

Citations

28

References

76