Table of Contents Table of Contents
Previous Page  93 / 172 Next Page
Information
Show Menu
Previous Page 93 / 172 Next Page
Page Background

e154

Abstracts of the 22

nd

National Congress of Digestive Diseases / Digestive and Liver Disease 48S2 (2016) e67–e231

information on GFD received at the time of diagnosis and disease

duration.

Conclusions:

In our reality celiac patients seem to be well informed

about GFD. Frequently they unnecessarily avoid foods that are safe

because gluten free. We identified some categories of celiac patients

at risk of less knowledge of GFD who deserve special training and

attention.

P.06.3

FODMAPS FREE DIET: AN EFFECTIVE SOLUTION FOR

SYMPTOMATIC COELIAC PATIENTS ON GLUTEN FREE DIET

Imperatore N.*

1

, Rispo A.

1

, Capone P.

1

, Castiglione F.

1

, Gerbino N.

1

,

Lucci L.

2

, Accarino G.

2

, Caporaso N.

1

, Tortora R.

1

1

Gastroenterology “Federico II” University, Naples, Italy,

2

Nutrition

“Federico II” University, Naples, Italy

Background and aim:

Recent studies have shown high efficacy of

a FODMAPs free diet (FFD) in patients suffering from non-coeliac

wheat sensitive (NCWS) and irritable bowel syndrome (IBS), but

data on this kind of dietary approach in coeliac disease (CD) are

still scarce.

Aim:

to establish the efficacy of FFD in symptomatic CD

patients despite being on gluten free diet (GFD), also comparing this

outcome with that of subjects affected by IBS.

Material and methods:

From January 2016 to September 2016

we carried out an observational prospective study including all

consecutive adult CD patients (Group A) who were symptomatic

(abdominal pain, diarrhoea, bloating, constipation) despite

performing a strict GFD. Also, we enrolled all consecutive adult

IBS patients (Group B) referred to our general Ambulatory. We

administered a personalized FFD and 2 questionnaires (IBS-SSS with

a pain score from 0-minimum to 3-maximum, and SF-36 with 8

different domains) at the time of the first visit (T0), 1month after (T1)

and at 3 months (T3) from the beginning of FFD. Statistical analysis

included ANOVA test with and without covariates adjustment. All

results were considered significant with a p< 0.05.

Results:

Finally, 66 patients were enrolled (Group A: 23 vs Group B:

43). All CD patients were on GFD from at least 1 year and showed

negative EMA and anti-transglutamineases. No differences were

noted in terms of age and gender (P = NS). When analyzing the

IBS-SSS results, the symptomatic score dropped in both Groups

after starting FFD (Group A: 2.04 at T0, 1.26 at T1 and 1.09 at T3

(P < 0.01); Group B: 2.35 at T0, 1.42 at T1 and 1.07 at T3 (P < 0.01)).

However, no statistically significant differences were noted between

the two Groups (P = NS). When analyzing the results from SF-36, no

differences were noted between the two Groups, even though both

CD and IBS population significantly improved their own status with

the regards of the 8 domains of SF-36, both at T1 (P < 0.01) and at

T3 (P < 0.01).

Conclusions:

FFD leads to a significant improvement of

gastrointestinal symptoms in CD patients who were persistently

symptomatic despite GFD. GFD in association with FFD should be

considered a first-line therapy CD this population.

P.06.4

ADULT CELIAC PATIENTS ADHERENCE TO A FOLLOW-UP

PROGRAM IN THE FIRST YEAR OF GLUTEN-FREE DIET: A SINGLE

CENTER STUDY

Sacchi M.C., Galli G.*, Esposito G., Carabotti M., Lahner E.,

Annibale B.

University Sapienza, Roma, Italy

Background and aim:

Coeliac disease (CD) is an immune-mediated

enteropathy. The treatment for CD is a gluten-free diet (GFD), which

requires significant patient education, motivation and follow-up.

Usually celiac patients are not included in a standardized follow-up

neither for the first year, nor for the subsequent years. Aim of this

study was to assess the patients adherence to time-based protocol

in the first year of GFD and if clinical characteristics and histological

parameters could affect the adherence to follow-up.

Material and methods:

226 consecutive newly diagnosed out­

patients with biopsy-proven atrophic CD, diagnosed between 2002

and 2014 (median age 33yrs, 16-72; 79% female), were included.

Clinical data were collected using a structured clinical questionnaire,

including life style items, gastrointestinal symptoms, biochemical

values and histological score. Moreover each patient was instructed,

by a specific sheet, to follow a follow-up program that included

five items: after 3 months of GFD: 1) outpatient visit; after 1 year

of GFD: 2) serologic testing for specific antibody assay and 3)

nutritional parameters, 4) endoscopy with biopsy and 5) outpatient

visit including a validated questionnaire for GFD adherence. Full

adherence to the program was defined when patients underwent to

all five controls. Adherence >50% and <50% were defined when the

patients underwent at least three or four controls of five and at least

one or two of five, respectively. Statistical analysis was performed

using the Cochran-Armitage for trend in order to compare groups

with different adherence to the follow-up program.

Results:

41.9% of patients had full adherence to the program, while

23.6% did not undergo any control. A first degree familiarity for CD

positively affected the adherence to follow-up (p=0.04), and the

presence of symptoms at diagnosis affected it negatively (p=0.04).

Among patients with full adherence to the follow-up protocol 87,5%

had adequate compliance to GFD, while only 40% of patients with

<50% adherence to follow-up showed an adequate compliance to

diet (p=0.0001).

Conclusions:

This study showed that full adhesion to the follow-

up program in the first year of GFD in adult patients occurred in

only 41.9% of patients influencing positively the adherence to GFD. A

scheduled follow-up program should be proposed in the adult celiac

patients management.

P.06.5

HIGH SMAD7 IN REFRACTORY CELIAC DISEASE SUSTAINS

INFLAMMATORY CYTOKINE RESPONSE

Sedda S.*

1

, De Simone V.

1

, Marafini I.

1

, Paoluzi O.A.

1

, Colantoni A.

1

,

Ortenzi A.

1

, Giuffrida P.

2

, Di Sabatino A.

2

, Pallone F.

1

, Monteleone G.

1

1

University Tor Vergata, Rome, Italy,

2

University Of Pavia, Pavia, Italy

Background and aim:

Background. Refractory celiac disease (RCD)

is a severe form of celiac disease (CD) resistant to gluten-free diet

and associated with elevated risk of complications. Enhanced

production of inflammatory cytokines is supposed to contribute to

the RCD-associated lesions, even though it remains unclear if tissue

destructive inflammatory response is also sustained by defects in

counter-regulatory mechanisms. One such a mechanism could

involve transforming growth factor (TGF)

b

1, an immunesuppressive

cytokine that negatively regulates inflammatory responses in the

gut.

Aim. To determine whether RCD-related inflammation is marked by

elevated levels of Smad7, an intracellular inhibitor of TGF-

b

1 activity.

Material and methods:

Methods. Smad7 expression was evaluated

in duodenal biopsy samples of patients with RCD, patients with

active CD (ACD), patients with inactive CD (ICD), and normal

controls by western blotting, immunohistochemistry and RT-PCR. In

biopsy samples taken from the same groups of patients and controls,

TGF

b

1 and phosphorylated Smad2/3 were evaluated by ELISA and

immunohistochemistry respectively. Expression of proinflammatory

cytokines was assessed in RCD biopsy samples cultured with Smad7

sense or antisense oligonucleotide by RT-PCR.