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CompletedNCT01862211PolygenUpdated Dec 19, 2025

Polygen Defi-Alpha: Genetic Polymorphisms Study in Children With Alpha-1 Antitrypsin Deficiency, Included in the DEFI-ALPHA Cohort

An interventional study of blood sampling in Children With a Deficiency of Alpha-1 Antitrypsin, sponsored by Hospices Civils de Lyon. Completed at 20 sites in France. Open to participants aged 7 Years and older. Per ClinicalTrials.gov, last updated 2025-12-19.

Sponsored by Hospices Civils de Lyon · Not applicable, Interventional, and Diagnostic

Phase
Not applicable
Study type
Interventional
Enrollment
296
Allocation
Non-randomized
Ages
7 Years and older
Sex
All
01

Study summary

The deficiency of alpha-1 antitrypsin (DA1AT) is a genetic disorder of variable clinical expression, initially described in adults with pulmonary emphysema patients. In children, it is the second cause of neonatal cholestasis after biliary atresia and is a common indication for liver transplantation.

Several genotypes for SERPINA1 gene coding for alpha-1 anti-trypsin were identified. The main ones are M / M, M / Z, M / S and Z / Z and each genotype is closely correlated with the concentration of blood A1AT. The estimate for France suggests a prevalence of genotype deficit Z / Z of the order of 1/6054, (9982 patients), which in 11% of cases, have liver disease (prolonged neonatal jaundice). Half of them will move towards the development of cirrhosis with portal hypertension, at worst liver transplantation.

Currently, we do not know what are the clinical and genetic factors that predispose a patient A1AT deficiency develop liver damage. Recent studies have led us to think that polymorphisms in the gene SERPINA1, as well as that of the alpha-mannosidase 1 endoplasmic reticulum (Erman gene) could be a predictive marker of liver complications. Another possible candidate gene is one of the importin beta (KPNB1), a protein involved in the elimination of misfolded proteins. These data lead us to propose the study of genetic polymorphisms.

The main objective of the study is to compare the allele frequencies of these polymorphisms between (i) a cohort of A1AT deficient patients and with hepatic symptoms (portal hypertension and its complications, severe liver failure leading to transplant or not, or an indication for liver transplantation) and (ii) a cohort of A1AT deficient patients without signs of hepatic call. To build this last cohort, we will include in the genetic study the family members of deficient patients, some of whom probably carrying a deficit genotype Z / Z but without any associated clinical manifestations. This will allow us to facilitate the establishment of genotype profiles / phenotype clearly identified, which then allow a more appropriate care for children who may have such a development, we will strive to achieve a haplotype interpretation of polymorphisms found.

This study will be conducted in association with the DEFI-ALPHA study to identify clinical and biological prognostic factors such as age at diagnosis, the diagnostic mode, the results of liver biopsy (when available), the clinical course, family history, the existence of IUGR and long-term treatment.

The secondary objectives of the study are :

  • The measurement and interpretation of serum IL-8 in A1AT-deficient patients. Indeed, one study showed a higher IL-8 in patients with ulcerative colitis compared with healthy patients' serum. These considerations led us to hypothesize that IL-8 may be a marker of liver disease in A1AT deficiency.
  • Preservation of blood samples for further study of other genes, which may be in the future suspected to be associated with the occurrence of liver complications. To this end, a DNA bank will be created. It will involve the children with a deficiency of alpha-1 antitrypsin and their family of 1st and 2nd degree in civil law (parents and siblings).

This study is a continuation of the cohort DEFI-ALPHA (descriptive study of a cohort of children with DA1AT) and sought to identify the clinical and biological factors such as age at diagnosis, diagnosis mode, the result sets of the liver biopsy (when available), clinical course, family history, the presence of IUGR and long-term treatment.

The only criterion for not-inclusion is, according to the subject, the lack of consent of the child and his parents, the lack of consent of the adult patient, or the lack of consent of the witness. Demographic and clinical history data (for parents and brothers/sisters showing no DA1AT) will be collected.

Currently, the cohort of patients with DA1AT is being set up in the framework of the "Cohort DEFI-ALPHA." This multicenter project is realized with the help of french pediatric hepatology centers that regularly follow patients DA1AT. Today, over 100 patients DA1AT have already been identified, and the collection of historical data has already begun on several centers since September 2009. This study is therefore a continuation of this work.

Over a period of 30 months, the total number of potentially includable subjects is estimated at about 400 in this study (100 patients and 300 related to the first degree such as parents, brothers and sisters).

This study will be promoted by the Hospices Civils de Lyon. Authorization of the competent authority and the ethical committee will be obtained as well as informed consent from families before blood sampling.

02

Conditions studied

  • Children With a Deficiency of Alpha-1 Antitrypsin

Keywords

  • alpha antitrypsin, hepatic disease, genetic, polymorphism
03

In context

Digestive System Diseases

613 studies on the registry are indexed under Digestive System Diseases; 117 are open to participants now.

This study's enrollment of 296 is above the median of 80 across 401 interventional studies indexed under Digestive System Diseases.

Browse Digestive System Diseases studies →

Lead sponsor

Hospices Civils de Lyon is the lead sponsor of 1,826 studies on the registry; 439 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
7 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Children included in the DefiAlpha cohort or adult aged under 18 years at the time of inclusion in the cohort Defi-Alpha, with a deficiency of of alpha-1 antitrypsin
  • Beneficiaries subjects of a social security system
  • Presence of a signed informed consent (patient or parents) at the time of inclusion

Exclusion criteria

Exclusion Criteria:

- Lack of consent

05

Study design

Phase
Not applicable
Primary purpose
Diagnostic
Allocation
Non-randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
296 participants (actual)

Study arms

  • Experimental
    members of family of children with a DA1AT

    Other: blood sampling

  • Experimental
    children with a DA1AT

    Other: blood sampling

Interventions

  • Otherblood sampling

    A blood sampling will be performed for the genetic analysis and the measurement of serum IL-8.

06

What researchers measure

Primary outcomes

  1. presence of mutations / polymorphisms in genes SERPINA1, Ermani and KPNB1 (with haplotype interpretation) in children with hepatic complications

    The main objective of the study is to compare the allele frequencies of these polymorphisms between (i) a cohort of A1AT deficient patients and with hepatic symptoms (portal hypertension and its complications, severe liver failure leading to transplant or not, or an indication for liver transplantation) and (ii) a cohort of A1AT deficient patients without signs of hepatic call.

    Time frame: 1 day

Secondary outcomes

  1. measurement and interpretation of serum IL-8

    The measurement and interpretation of serum IL-8 in A1AT-deficient patients. Indeed, one study showed a higher IL-8 in patients with ulcerative colitis compared with healthy patients' serum. These considerations led us to hypothesize that IL-8 may be a marker of liver disease in A1AT deficiency.

    Time frame: 1 day

  2. Identification of modifier genes or mutations responsible of hepatic complications

    Find genes responsible of hepatic complications in A1AT-deficient patients by sequencing whole exome

    Time frame: 1 year

07

Study locations

20 sites
  • CHU d'Amiens - Hopital Nord
    Amiens, France
  • CHU de BESANCON
    Besançon, France
  • Hôpital Pellegrin
    Bordeaux, France
  • Hôpital Femme Mère Enfant de Lyon
    Bron, France
  • CHU Estaing
    Clermont-Ferrand, France
  • Hôpital Couple Enfant
    La Tronche, France
  • CHG Le HAVRE
    Le Havre, France
  • AP-HP - Kremlin Bicêtre
    Le Kremlin-Bicêtre, France
  • Hôpital Jeanne de Flandre
    Lille, France
  • Hopital de la Timone
    Marseille, France
  • Hôpital Brabois Enfants
    Nancy, France
  • Hôpital Mère Enfant
    Nantes, France
  • AP-HP Hôpital Necker
    Paris, France
  • Hôpital Anne de Bretagne
    Rennes, France
  • Hôpital Charles Nicolle
    Rouen, France
  • Hôpital Nord
    Saint-Etienne, France
  • CH Saint Nazaire
    Saint-Nazaire, France
  • Hopital Hautepierre
    Strasbourg, France
  • Hôpital des Enfants
    Toulouse, France
  • Centre de Pédiatrie Gatien de Clocheville
    Tours, France
08

References and documents

Publications

  • Ruiz M, Lacaille F, Berthiller J, Joly P, Dumortier J, Aumar M, Bridoux-Henno L, Jacquemin E, Lamireau T, Broue P, Rivet C, Belmalih A, Restier L, Chapuis-Cellier C, Bouchecareilh M, Lachaux A; Groupe Francophone d'Hepatologie Gastroenterologie et Nutrition Pediatriques. Liver disease related to alpha1-antitrypsin deficiency in French children: The DEFI-ALPHA cohort. Liver Int. 2019 Jun;39(6):1136-1146. doi: 10.1111/liv.14035. Epub 2019 Feb 1. PubMed 30589493 ↗
  • Joly P, Ruiz M, Garin R, Karatas E, Lachaux A, Restier L, Belmalih A, Renoux C, Lombard C, Dechomet M, Bouchecareilh M. A Particular SORL1 Micro-haplotype May Prevent Severe Liver Disease in a French Cohort of Alpha 1-Antitrypsin-deficient Children. J Pediatr Gastroenterol Nutr. 2021 Sep 1;73(3):e68-e72. doi: 10.1097/MPG.0000000000003125. PubMed 33720088 ↗
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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Dec 19, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT01862211
Lead sponsor
Hospices Civils de Lyon
Responsible party
Sponsor
First posted
May 24, 2013
Start date
May 2013
Primary completion
Nov 2017
Completion
Nov 2017
Last update
Dec 19, 2025

Oversight

Data monitoring committee
No
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