Diabetes Mellitus, Type 2 Clinical Trial
Official title:
Human Polymorphonuclear Neutrophil (PMN) Cytosolic Signaling and Effector Functions in Patients With Diabetes Mellitus Type 2 and Periodontitis
White blood cell membrane and surface structures are affected by the metabolic disorders and
complications found in diabetes mellitus. Therefore, cellular activation, signal propagation,
intracellular signaling as well as bactericidal effector functions are altered.
When diabetic symptoms are corrected by the systemic intervention and treatment of the
patients (Anti-diabetic Therapy/ADT, i.e. anti-diabetic medication, diet and dietetic
supervision, physiotherapy and physical exercises), white blood cell functions will then
normalize and reach the functionality comparable to those cells derived from healthy
subjects.
Gum diseases like periodontitis have long been associated with and termed complications of
uncontrolled diabetes mellitus. Vice versa, after diabetic conditions are corrected,
periodontitis treatment will be proven effective, when oral hygiene regimen, full mouth
decontamination (FD, i.e. the oral use of topical antiseptics prior and after professional
mechanical tooth cleaning, tooth as well as root surface planing, polishing as well as gum
and soft tissue decontamination in combination with systemic antibiotics) are performed. To
reinforce gum healing, reinfection prevention (RP) as well as supportive periodontal therapy
(SPT) will be administered by dental professionals on an individual basis and a detailed
schedule.
If periodontal pockets critical for participant's self care are not eliminated by FD
including RP and SPT, and niches >5mm after 6 month persist, patients are informed and
offered surgical intervention as indicated for gum disease elimination.
Dental follow up exams will be offered to all participants.
Specific Aims
1. To investigate if cytosolic Ca2+- ( delta[Ca2+]i) and pH (delta_pHi) signaling responses
and bactericidal effector functions of PMN dependent upon the status of diabetic control
and are reduced or increased when compared to age and gender matched controls
2. To determine the biochemical basis for diabetic PMN alteration of motility as well as
bactericidal functions: production of superoxide and release of elastase, respectively
3. To characterize the molecular basis of the observed alterations in the regulation of
cytosolic calcium (delta[Ca2+]i) and pH (delta_pHi) exhibited by diabetic PMN
4. To investigate if the pre-activated state and altered bactericidal functionality of
diabetic PMN are reversed when the patients' glycemic control is normalized, blood
glucose levels as well as periodontal disease are corrected
5. To evaluate, if systemic and periodontal intervention can lead to clinical attachment
gain in patients with diabetes mellitus type 2
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