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JUSTUS- LIEBIG UNIVERSITÄT GIESSEN Klinik und Poliklinik für Urologie und Kinderurologie Klinik und Poliklinik für Urologie und Kinderurologie Universitätsklinikum Gießen und Marburg GmbH - Standort Gießen - Justus-Liebig-Universität Gießen (Direktor: Prof. Dr. W. Weidner) The role of inflammatory response and pain pathways in prostatitis FME Wagenlehner
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Page 1: The role of inflammatory response and pain pathways in ...

JUSTUS- LIEBIGUNIVERSITÄTGIESSEN

Klinik und Poliklinik für Urologie und Kinderurologie

Klinik und Poliklinik für Urologie und KinderurologieUniversitätsklinikum Gießen und Marburg GmbH

- Standort Gießen -Justus-Liebig-Universität Gießen(Direktor: Prof. Dr. W. Weidner)

The role of inflammatory response andpain pathways in prostatitis

FME Wagenlehner

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1. Acute bacterial Prostatitis

2. Chronic bacterial Prostatitis

3. Chronic Pelvic Pain Syndrom (CPPS)

3a. inflammatory

3b. non-inflammatory

4. Asymptomatic Prostatitis

NIH-Classification of the Prostatitis syndrome

National Institutes of Health: Chronic Prostatitis Workshop, Bethesda, Maryland, USA, 7.-8. Dez. 1995

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1. Acute bacterial Prostatitis ∼ 0,1%

2. Chronic bacterial Prostatitis ∼ 1%

3. Chronic Pelvic Pain Syndrom (CPPS) ∼ 10%

3a. Inflammatory ∼ 2%

3b. non-inflammatory ∼ 8%

4. Asymptomatic Prostatitis ∼ 90%

NIH-Classification of the Prostatitis syndrome

National Institutes of Health: Chronic Prostatitis Workshop, Bethesda, Maryland, USA, 7.-8. Dez. 1995

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1. Acute bacterial Prostatitis ∼ 0,1%

2. Chronic bacterial Prostatitis ∼ 1%

3. Chronic Pelvic Pain Syndrom (CPPS) ∼ 10%

3a. inflammatory ∼ 2%

3b. non-inflammatory ∼ 8%

4. Asymptomatic Prostatitis ∼ 90%

NIH-Classification of the Prostatitis syndrome

National Institutes of Health: Chronic Prostatitis Workshop, Bethesda, Maryland, USA, 7.-8. Dez. 1995

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1. Acute bacterial Prostatitis ∼ 0,1%

2. Chronic bacterial Prostatitis ∼ 1%

3. Chronic Pelvic Pain Syndrom (CPPS) ∼ 10%

3a. inflammatory ∼ 2%

3b. non-inflammatory ∼ 8%

4. Asymptomatic Prostatitis ∼ 90%

NIH-Classification of the Prostatitis syndrome

National Institutes of Health: Chronic Prostatitis Workshop, Bethesda, Maryland, USA, 7.-8. Dez. 1995

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CP/CPPS and clinical characteristics

40Sexual

63Abdominal

68Urinary

82Pain

%/ 764Symptoms

Bartoletti R et al., 2007 (Italian Prostatitis Study Group)

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Pain

International Association for the study of pain, 1994

Unpleasant sensory and emotionalexperience associated with actual or

potential tissue damage, or described interms of such damage.

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Pain

Protective response to tissue injury

Persistent pain is maladaptive

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Chronic Pain

International Association for the study of pain, 1994

Pain that persists past the healing phasefollowing an injury.

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Pain

• Acute 0 – 7 days

• Subacute 7 days – 3 months

• Chronic > 3 months

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Pain characteristics

• Stimulus-evoked– Hyperalgesia (noxious stimulus)– Allodynia (non-noxious stimulus)

• Stimulus-independent– Burning– Paresthesia

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Pain pathophysiology

• Nociceptive– Associated with tissue damage

(inflammation)• Neuropathic

– Associated with lesions in the nervous system(peripheral/ central)

• Mixed– Nociceptive + neuropathic

EAU guidelines 2008

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Inflammation is the basic processwhereby tissues of the body

respond to injury

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Immune system: basic principles• Innate (natural) system

– Responses always to same extent– Recognizes a few (10³) highly

conserved structures• Cells

– Phagocytic cells• Neutrophils• Monocytes• Macrophages

– Cells with inflammatory mediators• Basophils• Mast cells• Eosinophils

– Natural killer cells• Molecular components

– Complement proteins– Acute-phase proteins– Cytokines

• Acquired (adaptive) system– Responses improved on repeated

exposure– Recognizes multiple antigens (>107)

• Cells– Antigen-presenting cells

• Dendritic cells• Macrophages• B-lymphocytes

– Antigen-specific cells• B-lymphocytes• T-lymphocytes

• Molecular components– Antibodies– Cytokines

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Thacker MA et al., 2007

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Mendell JR et al., NEJM 2003

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Apkarian AV et al. 2008

Chronic back pain

Post herpetic neuralgia

Pelvic pain (visceral pain)Osteoarthritis

Post herpetic neuralgia

Healthy acute pain

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Nerves in the prostate

Doll A., Barcelona

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Cytokines and chemokines in CPPS

• No correlation with most mediators• Macrophage inflammatory protein-1a (MIP-1a)

– Chemotactic and activating activity for macrophages– Elevated in rheumatoid arthritis, ulcerative colitis– role in inflammation-induced hyperalgesia

Desireddi NV, AJ Schaeffer et al., 2008

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MIP-1a levels in EPS

Desireddi NV, AJ Schaeffer et al., 2008

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CPSI pain score and MIP-1a

Desireddi NV, AJ Schaeffer et al., 2008

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Autoimmune prostatitis in mice

•Von Frey filaments•Stimulation 10x•Response frequency

Rudick CN et al., 2008

Rat prostate suspension

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Rudick CN et al., 2008

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Inflammation scores

Control mice Autoimmune prostatitis mice

Rudick CN et al., 2008

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Autoimmune prostatitis in mice

Rudick CN et al., 2008

Autoimmune prostatitis miceControl mice

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Increased prostate neurite density

Rudick CN et al., 2008

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Mast cells and nerves

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Bunnett NW 2006

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STIMULUS Mast CellsActivation

(Degranulation)

Cytokines PAR-2 Receptor

Pain spinal cord sensoricnerves(CGRP)

Aumüller and Meinhardt, 2002

Hypothesis of pain in CP/CPPS

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Conclusion

• Pain most important symptom in CP/CPPS• Prostate inflammation can cause chronic

pain• Inflammation needs further characterisation• Causes need further study• Potential therapeutic targets

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Liang R et al., 2007

Organ crosstalk

control

colitis

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Liang R et al., 2007

control colitis

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Thacker MA et al., 2007


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