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1.
J Endocrinol Invest ; 47(11): 2671-2678, 2024 Nov.
Article in English | MEDLINE | ID: mdl-39141075

ABSTRACT

PURPOSE: Randomized controlled trials with tirzepatide (TZP) displayed unprecedented glucose and body weight lowering efficacy in individuals with type 2 diabetes and/or obesity and a safety profile similar to that of glucagon-like peptide-1 receptor agonists (GLP-1RA), mainly characterized by gastrointestinal (GI) adverse events (AE). Concerns on diabetic retinopathy, pancreato-biliary disorders, and medullary thyroid cancer were also addressed. We aimed to investigate whether the same safety issues emerged from the FDA Adverse Event Reporting System (FAERS) post-marketing surveillance database. METHODS: OpenVigil 2.1-MedDRA-v24 and AERSMine (data 2004Q1-2023Q3) were used to query the FAERS database. Reports of GI AE, diabetic retinopathy, pancreato-biliary disorders, and medullary thyroid cancer were investigated. The analysis was then filtered for age, gender, and designation as primary suspect. AE occurrence with TZP was compared to insulin, sodium-glucose cotransporter-2Ā inhibitors, metformin, and GLP-1RA. RESULTS: Disproportionate reporting of GI [i.e., nausea (ROR 4.01, 95% CI 3.85-4.19)] and pancreato-biliary disorders [i.e., pancreatitis (ROR 3.63, 95% CI 3.15-4.19)], diabetic retinopathy (ROR 4.14, 95% CI 2.34-7.30), and medullary thyroid cancer (ROR 13.67, 95% CI 4.35-42.96) was detected. TZP exhibited a similar risk of GI AE and medullary thyroid cancer and a lower risk of most pancreato-biliary AE and diabetic retinopathy vs. GLP-1RA. CONCLUSIONS: TZP was associated with an increased risk of specific AE. However, its safety profile was similar to that of GLP-1RA, without increased risk of pancreato-biliary AE, diabetic retinopathy, and medullary thyroid cancer.


Subject(s)
Adverse Drug Reaction Reporting Systems , Diabetes Mellitus, Type 2 , Pharmacovigilance , United States Food and Drug Administration , Humans , Adverse Drug Reaction Reporting Systems/statistics & numerical data , United States/epidemiology , Male , Female , Middle Aged , Diabetes Mellitus, Type 2/drug therapy , Diabetes Mellitus, Type 2/epidemiology , Databases, Factual , Hypoglycemic Agents/adverse effects , Aged , Adult , Drug-Related Side Effects and Adverse Reactions/epidemiology , Drug-Related Side Effects and Adverse Reactions/etiology , Thyroid Neoplasms , Carcinoma, Neuroendocrine
2.
J Endocrinol Invest ; 46(11): 2213-2236, 2023 Nov.
Article in English | MEDLINE | ID: mdl-37378828

ABSTRACT

BACKGROUND: Adaptive thermogenesis represents the main mechanism through which the body generates heat in response to external stimuli, a phenomenon that includes shivering and non-shivering thermogenesis. The non-shivering thermogenesis is mainly exploited by adipose tissue characterized by a brown aspect, which specializes in energy dissipation. A decreased amount of brown adipose tissue has been observed in ageing and chronic illnesses such as obesity, a worldwide health problem characterized by dysfunctional adipose tissue expansion and associated cardiometabolic complications. In the last decades, the discovery of a trans-differentiation mechanism ("browning") within white adipose tissue depots, leading to the generation of brown-like cells, allowed to explore new natural and synthetic compounds able to favour this process and thus enhance thermogenesis with the aim of counteracting obesity. Based on recent findings, brown adipose tissue-activating agents could represent another option in addition to appetite inhibitors and inhibitors of nutrient absorption for obesity treatment. PURPOSE: This review investigates the main molecules involved in the physiological (e.g. incretin hormones) and pharmacological (e.g. Ɵ3-adrenergic receptors agonists, thyroid receptor agonists, farnesoid X receptor agonists, glucagon-like peptide-1, and glucagon receptor agonists) modulation of adaptive thermogenesis and the signalling mechanisms involved.

3.
J Biol Regul Homeost Agents ; 32(6 Suppl. 1): 15-21, 2018.
Article in English | MEDLINE | ID: mdl-30644276

ABSTRACT

Diabetic foot ulcers (DFUs) are one of the most serious and devastating complication of diabetes mellitus, affecting about 15% of diabetic patients. This review describes the innovative treatment options currently available in the treatment of non-healing DFUs. The use of Platelet-Rich-Plasma (PRP) is a safe and valid approach in the treatment of DFUs. However, the methods used to obtain and prepare autologous PRP vary between the studies, thus further evidences are eagerly awaited. Adipose tissue-derived mesenchymal stem cells (ADSCs) are a promising tool in the treatment of DFUs, but additional largescale and long-term follow-up clinical trials are needed. Bone marrow mesenchymal stem cells (BM-MSCs) transplantation, on the other hand, revealed effective in reducing incidents and improving the quality of life of patients with amputations. Autologous Peripheral Blood Mononuclear Cells (A-PBMNCs) showed a good efficacy in the treatment of diabetic patients with CLI, but further RCTs are awaited to best investigate this new therapeutic approach. Photobiomodulation (PBM) therapy revealed effective in the treatment of DFUs in two RCTs, but a standardization of therapeutic protocols as well as level-I studies are needed.


Subject(s)
Diabetic Foot/therapy , Leukocytes, Mononuclear , Platelet-Rich Plasma , Wound Healing , Humans , Mesenchymal Stem Cell Transplantation , Quality of Life
4.
Biochim Biophys Acta ; 1861(9 Pt A): 970-979, 2016 09.
Article in English | MEDLINE | ID: mdl-27233517

ABSTRACT

Brown spider phospholipases D from Loxosceles venoms are among the most widely studied toxins since they induce dermonecrosis, triggering inflammatory responses, increase vascular permeability, cause hemolysis, and renal failure. The catalytic (H12 and H47) and metal-ion binding (E32 and D34) residues in Loxosceles intermedia phospholipase D (LiRecDT1) were mutated to understand their roles in the observed activities. All mutants were identified using whole venom serum antibodies and a specific antibody to wild-type LiRecDT1, they were also analyzed by circular dichroism (CD) and differential scanning calorimetry (DSC). The phospholipase D activities of H12A, H47A, H12A-H47A, E32, D34 and E32A-D34A, such as vascular permeability, dermonecrosis, and hemolytic effects were inhibited. The mutant Y228A was equally detrimental to biochemical and biological effects of phospholipase D, suggesting an essential role of this residue in substrate recognition and binding. On the other hand, the mutant C53A-C201A reduced the enzyme's ability to hydrolyze phospholipids and promote dermonecrosis, hemolytic, and vascular effects. These results provide the basis understanding the importance of specific residues in the observed activities and contribute to the design of synthetic and specific inhibitors for Brown spider venom phospholipases D.


Subject(s)
Catalytic Domain/genetics , Phospholipase D/chemistry , Phospholipids/chemistry , Spider Venoms/enzymology , Animals , Brown Recluse Spider/chemistry , Brown Recluse Spider/enzymology , Capillary Permeability , Circular Dichroism , Hemolysis , Mutation , Phospholipase D/metabolism , Phospholipids/metabolism , Phosphoric Diester Hydrolases/chemistry , Spider Venoms/chemistry
5.
J Biol Regul Homeost Agents ; 30(3): 867-870, 2016.
Article in English | MEDLINE | ID: mdl-27655513

ABSTRACT

The association between thyroid disorders and musculoskeletal diseases has long been suspected, but it is still debated whether they have a role in the pathogenesis of shoulder diseases. In vivo and in vitro studies describe the role of thyroid hormones in bone, cartilage and tendon biology. Retrospective studies and case reports suggest that thyroid diseases should be considered as risk factors and hold prognostic value in some of the most common causes of shoulder pain. Thus, it is advisable to search for underlying thyroid disorders in these patients. The pathophysiologic mechanisms by which thyroid hormone imbalance affects the onset, progression and response to treatment of these diseases are yet to be thoroughly defined and demand further studies.


Subject(s)
Hypothyroidism/complications , Shoulder Pain/etiology , Thyroid Hormones/physiology , Bursitis/etiology , Bursitis/physiopathology , Collagen/metabolism , Disease Susceptibility , Homeostasis , Humans , Hypothyroidism/physiopathology , Models, Biological , Osteoarthritis/etiology , Osteoarthritis/physiopathology , Risk Factors , Rotator Cuff Injuries/etiology , Rotator Cuff Injuries/physiopathology , Shoulder Impingement Syndrome/etiology , Shoulder Impingement Syndrome/physiopathology , Shoulder Joint/physiopathology , Shoulder Pain/physiopathology , Tendons/physiopathology , Tenocytes/metabolism
6.
Int J Biol Macromol ; 279(Pt 1): 134945, 2024 Nov.
Article in English | MEDLINE | ID: mdl-39182877

ABSTRACT

The Growth factor receptor-bound protein 2 (Grb2) participates in early signaling complexes and regulates tyrosine kinase-mediated signal transduction through a monomer-dimer equilibrium. Grb2 dimeric state inhibits signal transduction whereas the monomer promotes signaling downstream. Since Grb2 dimer KD is Ć¢ĀˆĀ¼0.8Ā ĀµM, studies focused on the monomer are still challenging and require mutations or interaction with phosphotyrosine peptides. However, these mutants were never characterized considering their effects on protein structure and dynamics in solution. Here, we present the biophysical characterization of Grb2Y160F, the first Grb2 mutant to induce protein monomerization without disrupting its native behavior in solution due to net charge modifications or interaction with peptides. We also identified that Grb2Y160F exists in a monomer-dimer equilibrium. Grb2Y160F ability to dimerize implies that different dimerization interfaces might regulate signaling pathways in distinct ways and raises an important question about the role of the Y160 residue in other dimerization interfaces.


Subject(s)
GRB2 Adaptor Protein , Mutation , Protein Multimerization , GRB2 Adaptor Protein/metabolism , GRB2 Adaptor Protein/chemistry , GRB2 Adaptor Protein/genetics , Humans , Models, Molecular , Protein Binding
7.
Int J Biol Macromol ; 83: 178-84, 2016 Feb.
Article in English | MEDLINE | ID: mdl-26592780

ABSTRACT

Southern bean mosaic virus (SBMV) RNA purified from infected plants was used for cloning the viral genome-linked protein (VPg) and was subsequently expressed in Escherichia coli. Circular dichroism (CD), dynamic light scattering (DLS) and saturation transfer difference (STD) by nuclear magnetic resonance (NMR) measurements were employed to determine the degree of monodispersity and to investigate the conformational changes in the absence and presence of trifluoroethanol (TFE) which indicated increased helical content with increasing concentration of TFE. 8-Anilino-1-naphthalenesulfonic acid (ANS) was used as a probe to compare the unfolding regions of the protein before and after addition of TFE. The results indicated that although the TFE concentration influences VPg folding, it does not play a role in nucleotide binding and that the local solvent hydrophobicity causes significant conformational changes.


Subject(s)
Fabaceae/virology , Plant Viruses/genetics , Plant Viruses/metabolism , Trifluoroethanol/metabolism , Trifluoroethanol/pharmacology , Viral Nonstructural Proteins/genetics , Viral Nonstructural Proteins/metabolism , Amino Acid Sequence , Gene Expression , Histidine , Molecular Sequence Data , Nucleotides/metabolism , Protein Binding , Protein Conformation/drug effects , Viral Nonstructural Proteins/chemistry
8.
Bone ; 17(4): 383-90, 1995 Oct.
Article in English | MEDLINE | ID: mdl-8573412

ABSTRACT

The main objective of this study was to determine the effect of daily oral alendronate treatment on bone mass in postmenopausal women affected by osteoporosis. The efficacy of intranasal salmon calcitonin was also examined. Nine centers in Italy enrolled 286 postmenopausal women between the ages of 48 and 76 with spinal bone mineral density > or = 2 SD below adult mean peak in the two-year, double-blind, randomized, placebo-controlled trial. Patients were randomized to one of four treatment arms: double-blind placebo, alendronate 10 mg/day, alendronate 20 mg/day, or open-label intranasal salmon calcitonin 100 IU/day; all patients received 500 mg Ca++ supplements. Bone mass was measured by dual-energy x-ray absorptiometry every six months for two years. Patients who received alendronate 10 or 20 mg experienced significant increases in bone mass at all sites measured. At the end of the second year, the mean percent changes, for alendronate 10 and 20 mg relative to placebo, were 5.2% and 7.3% at the lumbar spine, 3.8% and 4.6% at the femoral neck, and 7.1% and 7.5% at the trochanter, respectively. In contrast, intranasal salmon calcitonin failed to increase bone mineral mass significantly at any site. Both alendronate doses significantly decreased serum alkaline phosphatase, serum osteocalcin, and urinary pyridinolines, markers of bone turnover, whereas placebo and intranasal calcitonin did not. Alendronate was generally well tolerated and no serious adverse events were attributed to its use.(ABSTRACT TRUNCATED AT 250 WORDS)


Subject(s)
Bone Density/drug effects , Calcitonin/pharmacology , Diphosphonates/pharmacology , Osteoporosis, Postmenopausal/drug therapy , Absorptiometry, Photon , Administration, Intranasal , Administration, Oral , Aged , Analysis of Variance , Biomarkers/blood , Biomarkers/urine , Bone and Bones/metabolism , Calcitonin/administration & dosage , Calcium, Dietary/administration & dosage , Diphosphonates/administration & dosage , Double-Blind Method , Female , Femur/drug effects , Femur Neck/drug effects , Humans , Italy , Longitudinal Studies , Lumbar Vertebrae/drug effects , Middle Aged , Osteoporosis, Postmenopausal/blood , Osteoporosis, Postmenopausal/urine , Patient Compliance
9.
Am J Med ; 83(5A): 66-71, 1987 Nov 20.
Article in English | MEDLINE | ID: mdl-3318442

ABSTRACT

In a double-blind study, the efficacy and tolerability of S-adenosylmethionine (SAMe) were evaluated in comparison with those of placebo and naproxen in the treatment of osteoarthritis of the hip, knee, spine, and hand. Thirty-three centers, 18 rheumatologic and 15 orthopedic, participated in this study. A total of 734 subjects, including 582 with coxarthrosis (hip osteoarthritis) or gonarthrosis (knee osteoarthritis), were enrolled. SAMe administered orally at a dose of 1,200 mg daily was shown to exert the same analgesic activity as naproxen at a dose of 750 mg daily. Both drugs were more effective than placebo (p less than 0.01). Tolerability of SAMe was significantly better than that of naproxen, both in terms of physicians' (p less than 0.025) and patients' (p less than 0.01) judgments and in terms of the number of patients with side effects (p less than 0.05). There was no difference between SAMe and placebo in the number of side effects. Ten patients in the SAMe group and 13 in the placebo group withdrew from the study because of intolerance to the drug.


Subject(s)
Anti-Inflammatory Agents, Non-Steroidal/therapeutic use , Naproxen/therapeutic use , Osteoarthritis/drug therapy , S-Adenosylmethionine/therapeutic use , Clinical Trials as Topic , Double-Blind Method , Female , Humans , Male , Middle Aged , Naproxen/adverse effects , Placebos/therapeutic use , Random Allocation , S-Adenosylmethionine/adverse effects
10.
Aliment Pharmacol Ther ; 1 Suppl 1: 540S-547S, 1987.
Article in English | MEDLINE | ID: mdl-2979702

ABSTRACT

The pathogenetic role of non-steroidal anti-inflammatory drugs (NSAIDs) in peptic ulcer disease is reviewed, on the basis of available experimental and epidemiological knowledge. In addition, original clinical data are provided concerning the prophylactic and therapeutic role of the H2-receptor antagonists ranitidine and cimetidine, and colloidal bismuth subcitrate, in the treatment of NSAID-associated peptic lesions in rheumatic patients.


Subject(s)
Anti-Inflammatory Agents, Non-Steroidal/adverse effects , Peptic Ulcer/chemically induced , Animals , Humans , Peptic Ulcer/physiopathology , Rheumatic Diseases/complications , Rheumatic Diseases/drug therapy
11.
Aliment Pharmacol Ther ; 12(4): 343-7, 1998 Apr.
Article in English | MEDLINE | ID: mdl-9690723

ABSTRACT

AIM: To compare the efficacy of cimetidine and tripotassium dicitrato bismuthate (TDB) in arthritic patients who had developed gastric (GU) or duodenal (DU) ulceration while taking non-steroidal anti-inflammatory drugs (NSAIDs). METHODS: Eighty-six rheumatoid arthritis (RA) patients affected by endoscopically proven DU (n = 44) or GU (n = 42), and on chronic NSAID therapy which was not suspended during anti-ulcer therapy, were randomized to cimetidine (400 mg t.d.s.) or TDB (120 mg q.d.s.). A repeat endoscopy was planned after 4 weeks (and 8 weeks, in case of failed healing). The patients who were unhealed after 8 weeks of therapy were allocated to the alternative anti-ulcer drug for a further 8 weeks without interrupting the anti-inflammatory therapy. RESULTS: At week 4 of therapy. 14/24 (58%) DU and 9/20 (45%) GU patients treated with cimetidine were healed, compared with 12/20 (60%) and 10/22 (45%) TDB-treated patients (N.S.). At week 8 of therapy, the DU healing rates were 15/24 (63%) with cimetidine and 14/20 (70%) for TDB. The corresponding GU healing rates were 12/20 (60%) with cimetidine and 13/22 (60%) for TDB (N.S.). At week 16, complete healing with cimetidine was observed in 67% of DU and 57% of GU patients unhealed with TDB; the corresponding figures in the patients crossed to TDB were 83% for DU and 63% for GU patients (N.S. vs. cimetidine). CONCLUSIONS: No statistically significant difference was found between the healing activities of cimetidine and TDB in rheumatoid arthritis patients with peptic ulcer who did not interrupt their NSAID treatment for arthritis. This trial showed that the continued consumption of NSAIDs appears to slow the ulcer healing process, especially in GU patients.


Subject(s)
Anti-Inflammatory Agents, Non-Steroidal/adverse effects , Anti-Ulcer Agents/therapeutic use , Arthritis, Rheumatoid/drug therapy , Cimetidine/therapeutic use , Duodenal Ulcer/drug therapy , Organometallic Compounds/therapeutic use , Stomach Ulcer/drug therapy , Administration, Oral , Adult , Anti-Ulcer Agents/administration & dosage , Cimetidine/administration & dosage , Double-Blind Method , Duodenal Ulcer/chemically induced , Female , Humans , Male , Middle Aged , Organometallic Compounds/administration & dosage , Stomach Ulcer/chemically induced , Treatment Outcome
12.
J Am Geriatr Soc ; 38(9): 985-8, 1990 Sep.
Article in English | MEDLINE | ID: mdl-2212452

ABSTRACT

The clinical efficacy and gastroduodenal tolerability of imidazole salicylate (imidazole 2-hydroxybenzoate, ITF 182), a new synthetic drug with an anti-inflammatory action, was evaluated endoscopically in comparison with those of piroxicam in elderly patients suffering from osteoarthrosis. Of the 41 patients entering the trial, only 38 completed the protocol (6 men and 32 women; mean age, 71; range, 65-80 years). After upper gastrointestinal endoscopy for the purpose of excluding gastric and duodenal mucosal lesions, the patients were allocated at random, according to a double-blind, double-dummy protocol, to treatment either with imidazole salicylate 750 mg three times daily or with piroxicam 20 mg once daily for a period of 4 weeks. Imidazole salicylate proved active in controlling a number of the pain symptoms caused by arthrosis, although its efficacy was inferior to that of piroxicam. Grade 2 gastric mucosal lesions were detected in 1 of 20 patients (5%) treated with imidazole salicylate; lesions corresponding to grades 2, 3, and 4 were found in 6 of 18 (33%) of those treated with piroxicam (P = .034). Painful dyspepsia was reported by 15% of the patients in the imidazole salicylate group and by 28% of those in the piroxicam group. On the basis of these results and under the experimental conditions adopted in this trial, the authors concluded that imidazole salicylate is characterized by good gastric tolerability and can thus be used in the treatment of rheumatic diseases in the elderly.(ABSTRACT TRUNCATED AT 250 WORDS)


Subject(s)
Anti-Inflammatory Agents, Non-Steroidal/therapeutic use , Imidazoles/therapeutic use , Osteoarthritis/drug therapy , Peptic Ulcer/chemically induced , Piroxicam/therapeutic use , Salicylates/therapeutic use , Activities of Daily Living , Aged , Consumer Behavior , Double-Blind Method , Endoscopy , Female , Humans , Imidazoles/administration & dosage , Imidazoles/adverse effects , Male , Osteoarthritis/physiopathology , Osteoarthritis/psychology , Peptic Ulcer/diagnosis , Peptic Ulcer/pathology , Piroxicam/administration & dosage , Piroxicam/adverse effects , Salicylates/administration & dosage , Salicylates/adverse effects
13.
J Neurosci Methods ; 134(1): 37-43, 2004 Mar 15.
Article in English | MEDLINE | ID: mdl-15102501

ABSTRACT

PURPOSE: The aim of this work is to provide information about the degree of inter-subject uniformity of location of innervation zone (IZ) in 13 superficial muscles of the lower limb. The availability of such information will allow researchers to standardize and optimize their electrode positioning procedure and to obtain accurate and repeatable estimates of surface electromyography (sEMG) signal amplitude, spectral variables and muscle fiber conduction velocity. METHODS: Surface EMG signals from gluteus maximus, gluteus medius, tensor faciae latae, biceps femoris, semitendinosus, vastus medialis obliquus, vastus lateralis, rectus femoris, tibialis anterior, peroneus longus, soleus, gastrocnemius medialis and lateralis muscles of ten healthy male subjects aged between 25 and 34 years (average = 29.2 years, S.D. = 2.5 years) were recorded to assess individual IZ location and signal quality. RESULTS: Tensor faciae latae, biceps femoris, semitendinosus, vastus lateralis, gastrocnemius medialis and lateralis showed a high level of both signal quality and IZ location uniformity. In contrast, rectus femoris, gluteus medius and peroneus longus were found to show poor results for both indexes. Gluteus maximus, vastus medialis obliquus and tibialis anterior were found to show high signal quality but low IZ location uniformity. Finally, soleus muscle was found to show low signal quality but high IZ location uniformity. CONCLUSIONS: This study identifies optimal electrode sites for muscles in the lower extremity by providing a standard landmarking technique for the localization of the IZ of each muscle so that surface EMG electrodes can be properly positioned between the IZ and a tendon.


Subject(s)
Lower Extremity/physiology , Muscle, Skeletal/physiology , Adult , Electrodes/standards , Electromyography/methods , Electromyography/standards , Humans , Male
14.
Clin Exp Rheumatol ; 19(1 Suppl 22): S17-20, 2001.
Article in English | MEDLINE | ID: mdl-11296544

ABSTRACT

OBJECTIVE: To define the optimal dose of nimesulide (NIM) for treating psoriatic arthritis. METHODS: Eighty patients entered a 4-week, double-dummy, randomised, controlled study. Each patient was allocated to one of the following treatment groups: NIM 100 mg/day, NIM 200 mg/day, NIM 400 mg/day, or placebo. Primary end points for arthritis assessment were the scores for tender and swollen joints, and the physician's and patient's global assessment of efficacy. RESULTS: 76/80 patients completed the study. NIM decreased the score for tender and swollen joints from baseline to the end swollen joints from baseline to the end of therapy (p < 0.05). Pain severity on a visual analogue scale (VAS) was reduced by NIM 200 mg (p = 0.03) or NIM 400 mg (p = 0.019) compared to placebo, as was morning stiffness (p = 0.038 and p = 0.008, respectively), but the trends with 100 mg were not statistically significant. The investigators and patients assessed the global efficacy of the NIM 200 and 400 mg/day groups as better than placebo or NIM 100 mg. Side effects were observed in 12 patients (15%) during treatment. They were mostly mild, only one patient withdrew from the study as a result, and the trend for a higher incidence with NIM was not statistically significant. The Psoriasis Area Severity Index (PASI) and the ESR did not show any significant changes. Patients in the placebo group took more paracetamol per day compared with those in the NIM groups (p = 0.007). CONCLUSIONS: Nimesulide 200 and 400 mg/day are effective and safe in psoriatic arthritis.


Subject(s)
Anti-Inflammatory Agents, Non-Steroidal/therapeutic use , Arthritis, Psoriatic/drug therapy , Sulfonamides/therapeutic use , Abdominal Pain/chemically induced , Abdominal Pain/pathology , Arthritis, Psoriatic/physiopathology , Dose-Response Relationship, Drug , Double-Blind Method , Female , Humans , Joints/drug effects , Joints/physiopathology , Male , Middle Aged , Patient Satisfaction , Severity of Illness Index , Treatment Outcome
15.
Clin Exp Rheumatol ; 18(5): 571-7, 2000.
Article in English | MEDLINE | ID: mdl-11072596

ABSTRACT

OBJECTIVE: To evaluate the efficacy of oral chicken type II collagen (CII) in the treatment of rheumatoid arthritis (RA). METHODS: Sixty patients with clinically active RA of long duration (mean 7.2 +/- 5.5 years) were treated for 6 months with oral chicken CII at 0.25 mg/day (n = 31) or with placebo (n = 29) in a double-blind randomized study. RESULTS: The response rate to treatment of the collagen-treated group, based on the ACR 20% criteria, was higher than that of the control group but this difference was not statistically significant at any time. Intention-to-treat (ITT) analysis did not show statistically significant improvement in any of the several secondary outcome measures over the 6 months of the study in the collagen-treated patients in comparison with the placebo-treated group. However, in 2 collagen-treated patients we observed a clinical remission according to the criteria of the American Rheumatism Association. CONCLUSION: Our study seems to show that the oral treatment of RA patients with chicken CII is ineffective and results in only small and inconsistent benefits. Furthermore, our results raise the possibility that in a sub-group of patients oral collagen administration, usually considered devoid of harmful effects, may actually induce disease flares.


Subject(s)
Arthritis, Rheumatoid/drug therapy , Collagen/therapeutic use , Administration, Oral , Aged , Antibodies/analysis , Double-Blind Method , Female , Humans , Male , Middle Aged , Placebos , Treatment Failure
16.
J Bone Joint Surg Br ; 61-B(2): 169-71, 1979 May.
Article in English | MEDLINE | ID: mdl-438268

ABSTRACT

An electromyographic investigation of patients with subluxation of the patella has been carried out on the parts of the extensor apparatus which actively contribute to the alignment of the patella, both before and after the operation to correct this disorder. The electromyographic pictures have revealed a sharp fall in the activity of the vastus medialis, with full recovery to normal values after a corrective operation. Even if the aligning function of the patella is altered by a variety of factors, the present study confirms the importance of the vastus medialis in the pathogenesis of malalignment of the extensor mechanism.


Subject(s)
Joint Dislocations/diagnosis , Muscles/physiopathology , Patella/injuries , Adult , Electromyography , Female , Humans , Joint Dislocations/physiopathology , Knee Injuries/diagnosis , Knee Injuries/physiopathology , Leg , Male
17.
J Electromyogr Kinesiol ; 14(3): 325-31, 2004 Jun.
Article in English | MEDLINE | ID: mdl-15094146

ABSTRACT

BACKGROUND AND PURPOSE: This study aims to verify if amplitude and spectral characteristics of surface EMG signal are modified due to recording in a wet environment. METHODS: Isometric contractions of the biceps brachii muscle of ten subjects were performed in several different set-up combinations, both in dry (D) and in water from hydrotherapy pools (PW), with (PWM) or without moving the pool water and with (T) or without water-resistant adhesive taping. RESULTS: In PW condition the amplitude of the recorded signal is reduced to 5-10% of the corresponding signal recorded in D condition. In PWM the power spectrum is drastically reduced and altered by the water movement that introduces an increase of spectral power in the frequency range 0-20 Hz. The use of T modality allows to record signals with both amplitude and spectral frequencies comparable with those obtained in the D conditions. DISCUSSION AND CONCLUSION: This work demonstrates the need for water resistant taping when EMG signals are recorded in water. Signals recorded without such a protective film are strongly affected in their amplitude and frequency characteristics by the conductivity and the movement of water.


Subject(s)
Bandages , Electrodes , Electromyography/instrumentation , Immersion , Muscle, Skeletal/physiology , Water , Adult , Artifacts , Electromyography/methods , Equipment Failure Analysis/methods , Humans , Isometric Contraction/physiology , Male , Reproducibility of Results , Sensitivity and Specificity
18.
Clin Rheumatol ; 2(4): 363-7, 1983 Dec.
Article in English | MEDLINE | ID: mdl-6678196

ABSTRACT

The efficacy and tolerability of Timegadine, a new antirheumatic agent, administered at a dose of 250 mg twice daily was evaluated in an open trial of 24 weeks' duration in 31 patients with active rheumatoid arthritis. The subjective and objective clinical parameters improved significantly from the 2nd to 6th week of treatment. For some of the parameters further improvement was observed during the continuation of the treatment. At 6 weeks the ESR was significantly decreased, and a further reduction of the ESR was seen with the continuation of the treatment. At the end of the treatment period other humoral parameters of the disease were significantly modified. Moreover, in 65% of the patients with seropositive rheumatoid arthritis a reduction of the rheumatoid factor titre by at least two dilutions was observed. Five of the 31 patients were withdrawn from treatment due to the appearance of side effects. Although the study was open and the number of patients relatively small, the observed changes in the laboratory parameters of disease activity encourage further investigations to assess the potential of Timegadine as a remissive drug.


Subject(s)
Anti-Inflammatory Agents/therapeutic use , Arthritis, Rheumatoid/drug therapy , Guanidines/therapeutic use , Adult , Aged , Arthritis, Rheumatoid/blood , Arthritis, Rheumatoid/immunology , Blood Sedimentation , Drug Tolerance , Evaluation Studies as Topic , Female , Humans , Male , Middle Aged
19.
J Electromyogr Kinesiol ; 10(5): 327-36, 2000 Oct.
Article in English | MEDLINE | ID: mdl-11018442

ABSTRACT

Surface EMG signals detected in dynamic conditions are affected by a number of artefacts. Among them geometrical factors play an important role. During movement the muscle slides with respect to the skin because of the variation of its length. Such a shift can considerably modify sEMG amplitude. The purpose of this work is to assess geometrical artefacts on sEMG during isometric contractions at different muscle lengths. The average rectified value (ARV) of 15 single differential signals was obtained by means of a linear array of 16 bar electrodes from the vastus medialis and lateralis muscles. The knee angle was changed from 75 degrees to 165 degrees in steps of 30 degrees and voluntary isometric contractions at a low, medium and high force level were performed for each angle. The ARV pattern was normalized with respect to the mean activity to compare signals from different joint angles. From the data collected it was possible to separate the geometrical changes from the changes due to different intensities of activation. In three out of five subjects, we found (within the resolution of our measures) a 1 cm shift for the vastus medialis muscle while no shift was observed for the other two subjects. For the vastus lateralis muscle a 1 cm shift was found in two out of four subjects. Such a shift produces the main contribution to geometrical artefacts. To avoid such artefacts the innervation zones should be located and the EMG electrodes should not be placed near them.


Subject(s)
Electromyography , Isometric Contraction/physiology , Leg/physiology , Muscle, Skeletal/physiology , Adult , Artifacts , Humans , Male , Mathematics , Signal Processing, Computer-Assisted
20.
J Int Med Res ; 25(6): 307-17, 1997.
Article in English | MEDLINE | ID: mdl-9427164

ABSTRACT

Rheumatoid arthritis is a chronic progressive disease causing substantial morbidity and mortality for which current treatments are largely unsatisfactory. Over the past 20 years we have developed a novel therapeutic approach based on the intra-articular administration of rifamycin. The published studies on rifamycin therapy of rheumatoid arthritis and other chronic arthritic disorders, mainly from our group, are reviewed. Our results indicate that intra-articular rifamycin is effective against active synovitis and can profitably be combined with any basic therapy with slow-acting antirheumatic drugs. There is good evidence that the development of new erosions can be prevented or delayed by this treatment and that the balance between side-effects (mainly local pain) and antiarthritic activity is very favourable in the long term. Our observations have led us to hypothesize a possible systemic effect of rifamycin injected multilocally in peripheral joints; we believe that the available data deserve further investigation by independent researchers.


Subject(s)
Arthritis, Rheumatoid/drug therapy , Rifamycins/therapeutic use , Arthritis, Rheumatoid/epidemiology , Arthritis, Rheumatoid/physiopathology , Humans , Injections, Intra-Articular , Knee Joint , Rifamycins/administration & dosage , Rifamycins/adverse effects
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