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Table 5 Means for the assessment of intestinal permeability (biomarkers, histology)

From: Intestinal permeability – a new target for disease prevention and therapy

Means

Hu

An

Test molecules

Test site

Material needed

Disadvantages

In vivo – biomarkers of epithelial cell damage

Citrulline

x

x

endogenous ep product

small intestine

plasma

 

FABP

x

x

endogenous ep marker

site- specific

plasma

only in acute phase?

αGST

x

x

endogenous ep enzyme

n.a.

plasma, urine

only in acute phase?

Claudin-3

x

x

ep tight junction protein

n.a.

urine

limited data

In vivo – other biomarkers

Fecal calprotectin

x

(x)

neutrophil release product

colon

feces

unspecific marker of gut inflammation

α1-anti- trypsin test

x

(x)

endogenous amino acid

small intestine

feces/ serum

unclear specificity

sIgA

x

x

IgA (ELISA)

whole intestine

serum

low specificity

In vivo – histological approaches

Tight junction expression

x

x

RNA (qPCR), Western blot

site- specific

biopsies

invasive

Goblet cell analysis

x

x

histology

site- specific

biopsies

invasive

Shedding of epithelium

x

x

histology

site- specific

biopsies

invasive

Paneth cell loss**

x

x

histology

site- specific

biopsies

invasive

Defensins

  

RNA (qPCR), Western blot

site- specific

biopsies

invasive

Mucus analysis***

  

histology/ staining

site- specific

biopsies

invasive

  1. Abbreviations: αGST α-glutathione S-transferase, ep epithelial, FABP fatty acid binding protein, n.a. not applicable, qPCR qunatitative PCR, see also Abbreviations in Table 4. **Ref. Nr. 226; ***Ref. Nr. 227.