Periodontal Diseases Clinical Trial
Official title:
Relationship Between Hidradenitis Suppurativa and Periodontal Diseases
Hidradenitis suppurativa or Verneuil's disease (HS) is a neglected and often overlooked
chronic inflammatory skin disease. Nevertheless, it is frequent (1% of the general
population) and deeply affects quality of life in patients with moderate and severe forms of
HS. This disease is characterized by the occurrence of deep, recurrent and painful nodules,
progressing to abscess formation and suppuration. It is usually localized in the axillary,
inguinal and anogenital areas. The pathogenesis of HS remains partly unknown but is probably
multifactorial (inflammatory, genetic, infectious, etc.) and related to many risk factors
(mostly smoking and obesity). An association can be found with other inflammatory diseases
such as gastrointestinal and rheumatic diseases like Crohn's disease and spondylo-arthritis
respectively.
Periodontal diseases are a heterogeneous group of infectious diseases with an inflammatory
component. Their clinical expression results in more or less rapid destruction of tooth
supporting tissues. Without treatment, these lesions may progress ultimately to tooth
exfoliation, the rate of disease progression being unevenly distributed in the population.
Various epidemiological studies in France indicate that 12 to 13% of middle-aged adults have
severe periodontal damage. In addition, a recent study shows that while 50% of adults in
France are suffering from severe attachment loss, generalized forms are rare and about 10% of
individuals seem to require special care. The bacterial factor is the main etiological factor
of these diseases but their progression depends primarily on the host immune response and on
modifying factors (genetic, systemic, environmental and behavioural). Some of these factors
are identified such as uncontrolled diabetes, smoking, stress, etc.. Finally, it is well
established that periodontal disease may also trigger the development of some systemic
diseases such as diabetes.
Thus, many common etiopathogenic factors between HS and periodontal diseases such as
inflammatory components and tobacco are found. This is corroborated by observations collected
from some patients with HS complaining of oral pain exacerbated during acute flares of HS.
Hence the aim of this project is to clarify existing potential association between
Hidradenitis suppurativa and periodontal diseases using a multicenter cross-sectional
descriptive clinical approach.
One hundred patients with HS will be included in the departments of dermatology at the
University Hospital in Reims and at the Pasteur Institute in Paris. They will be compared
with one hundred patients without HS recruited from "general practice" consultations in the
departments of Odontology at the University Hospital in Reims and at Bretonneau Hospital in
Paris.
The severity of HS will be assessed with Hurley's score by the dermatologist. The periodontal
status will be evaluated with clinical indices and radiographical parameters by a
periodontist according to the "Armitage" classification of periodontal disease and to CDC-AA
case definitions updated in 2012. Meanwhile, human saliva is a biological fluid taken to
reflect the health status of an individual and is or may be used for diagnosis and prognosis
of some oral cancers, some systemic diseases (type 2 diabetes, sarcoidosis, etc.) or
periodontal diseases. The saliva will be collected and analysed by proteomics and
metabolomics techniques in order to identify biomarkers for diagnosis and prognostic of HS
associated or not to periodontal diseases.
These unpublished works could demonstrate a predisposition to develop periodontal disease in
a subgroup of HS patients and help to unravel new etiopathogenic mechanisms common to both
diseases as well as ultimately lead to early periodontal management in order to avoid disease
progression and tooth losses.
The principal hypothesis of this project is the existence of an association between
Hidradenitis suppurativa (HS) and periodontal diseases (PD).
The primary objective is to evaluate this association using a multicenter cross-sectional
clinical approach.
The secondary objectives are:
- To study the association between the severity of PD and the severity of HS.
- To search, using saliva collected from a population with clinical signs of HS and from
no HS population, proteomic and metabolomic biosignatures by liquid chromatography
tandem-mass spectrometry (LC-MS), by vibrational spectroscopies and by 1H-NMR
spectroscopy.
- To compare vibrational biosignatures from saliva from patients with and without HS and /
or MP to determine a unique salivary spectral profile of HS patients with and without
PD.
- To compare the relevance of vibrational spectroscopy versus that of LC-MS and LC-MS / MS
and 1H-NMR in the analysis of salivary markers identified from an overall non-targeted
spectroscopy profile.
- To analyse and to compare proteomic and metabolomic biosignatures of unstimulated saliva
samples depending on the severity of HS.
Will be included patients with HS (regardless of Hurley score) followed in the dermatology
department of Reims University Hospital or the Institut Pasteur in Paris, and patients
without HS from the service Odontology of the University Hospital of Reims or the Bretonneau
Hospital (Paris) (whatever the reason for consultation), even also from the dermatology
departments.
One hundred patients with HS will be included. At the same time, 100 patients without HS will
be also included. Subjects without HS will be matched to subjects with HS on age (± 5 years).
Given the percentage of non-HS patients for whom periodontal disease will be diagnosed
(approximately 40%), this included number of patients will demonstrate an odds ratio of 2.6
(ie a percentage of patients with periodontal disease of 63% in the group with HS) with an α
risk of 5% and a power of 90%.
The primary endpoint is the presence of periodontal disease in both patients with HS and
without HS.
Diagnostic of periodontal disease will be posed in consultation by a periodontist and will be
determined by clinical and radiographic assessments including in this research context:
i. Gingival bleeding (Bleeding on Probing, BOP) ii. Depth of periodontal pockets using a
calibrated periodontal probe iii. Clinical attachment loss iiii. Interproximal bone loss.
Bone loss will be taken in consideration when the distance between the alveolar ridge and the
cement-enamel junction will be ≥ 2mm. A digital orthopantomogram will be performed with or
without six retroalveolar X-rays of Ramfjord teeth.
Considering the bacterial etiology of periodontal diseases, it is important to note the
amount of dental plaque directly in relation with the oral hygiene level performed with the
dichotomous index "Plaque Control Record".
All these indexes will be assessed at six sites per tooth corresponding to a maximum of 168
values per patient. The third molar was excluded from analysis. The reliability of clinical
measurements intra and inter- periodontists was verified. In retrospect, the causes of tooth
loss will be sought.
The clinical diagnosis of HS will be based on the presence of recurrent abscesses in the
folds, which can be multi-site, with residual scars according to the diagnosis criteria of
European guidelines published in 2015.
Secondary endpoints
- The severity of HS will be based on the score of Hurley.
- The extent and severity of PD, their progression will be posed according to the
"consensus" classification of periodontal diseases (Armitage et al., 1999).
Periodontitis cases were defined according to CDC-AAP case definitions updated in 2012
(Eke et al., 2015).
- Semi-quantification and characterization of spectral biosignatures will be performed on
saliva samples from patients with HS and non-HS patients.
Thus, at least 5mL of unstimulated saliva will be collected from HS or non-HS patients. The
pH will be measured. They will be frozen at -80°C before analysis by liquid chromatography
tandem-mass spectrometry and vibrational spectroscopies and, at -20°C by 1H-NMR spectroscopy.
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