Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 4 de 4
Filter
Add more filters










Database
Language
Publication year range
1.
J Endocrinol Invest ; 47(8): 1881-1886, 2024 Aug.
Article in English | MEDLINE | ID: mdl-38358463

ABSTRACT

PURPOSE: The differential diagnosis of lipodystrophy involves other disorders characterized by severe fat loss and may be sometimes challenging. Owing to the rarity of lipodystrophy, it is relevant to search for tools and assays that differentiate it from other diseases that may mimic it. We conducted a study on leptin and high molecular weight (HMW) adiponectin serum concentrations in a series of patients diagnosed with lipodystrophy and compared them with those found in anorexia nervosa, one of the illnesses that may be cause of a missed diagnosis of lipodystrophy. METHODS: Leptin and HMW adiponectin serum concentrations were measured in six patients diagnosed with generalized lipodystrophy (GL), six with progeroid syndromes (PS), 13 with familial partial lipodystrophy type 1 (FPLD1, Kobberling syndrome), 10 with familial partial lipodystrophy type 2 (FPLD2, Dunnigan syndrome), 18 with acquired partial lipodystrophy (APL) and 12 affected by anorexia nervosa (AN). Measurements were compared to those obtained in 12 normal weight healthy subjects. RESULTS: Serum leptin concentrations were reduced to a similar degree in GL, PS and AN, proportionally to the extent of fat loss. Serum concentrations of HMW adiponectin were found extremely low in patients with GL and PS, while comparable to normal weight subjects in patients with AN. CONCLUSION: Serum HMW adiponectin can be regarded as a useful tool to discriminate between generalized lipodystrophy syndromes (including PS) and AN.


Subject(s)
Adiponectin , Anorexia Nervosa , Leptin , Humans , Anorexia Nervosa/blood , Anorexia Nervosa/diagnosis , Adiponectin/blood , Female , Adult , Diagnosis, Differential , Adolescent , Leptin/blood , Male , Young Adult , Lipodystrophy, Congenital Generalized/blood , Lipodystrophy, Congenital Generalized/diagnosis , Lipodystrophy/blood , Lipodystrophy/diagnosis , Child , Biomarkers/blood , Middle Aged , Case-Control Studies
2.
J Endocrinol Invest ; 45(8): 1569-1575, 2022 Aug.
Article in English | MEDLINE | ID: mdl-35384599

ABSTRACT

PURPOSE: SARS-CoV-2 infection may cause varying degrees of cardiac injury and the presence of underlying cardiovascular morbidities contributes to the frequency and severity of occurrence of this complication. Lipodystrophy syndromes are frequently characterized by severe metabolic derangements that represent relevant cardiovascular risk factors. Besides causing lipodystrophy, mutations in the lamin A/C (LMNA) gene can lead to a wide spectrum of tissue-specific disorders including cardiac involvement. METHODS AND RESULTS: We herein examine the case of two patients affected by atypical progeroid syndrome and partial lipodystrophy due to a heterozygous missense LMNA mutation c.1045 C > T (p.R349W) who presented initially with mild COVID-19 and developed severe cardiovascular complications within few weeks of SARS-CoV-2 infection. Before being infected with SARS-CoV-2, our patients had cardiovascular morbidities (mild mitral regurgitation in one patient, ischemic heart disease with bifascicular block in the other patient) in adjunct to cardiovascular risk factors, but the SARS-CoV-2 infection contributed to quickly and significantly decompensate their balance. CONCLUSION: These findings warn that patients affected by LMNA p.R349W mutation and likely other LMNA mutations associated with cardiovascular morbidity should be considered at extremely elevated risk of post-acute cardiological manifestations and should therefore undergo a vigilant follow-up after SARS-CoV-2 infection. Both patients developed COVID-19 before the specific vaccination was available to them and this unfortunate situation should remark the importance of vaccination coverage against SARS-CoV-2 infection for all patients affected by lipodystrophy, especially those with underlying comorbidities.


Subject(s)
COVID-19 , Lipodystrophy , COVID-19/complications , Humans , Lamin Type A/genetics , Mutation , SARS-CoV-2/genetics
4.
J Clin Laser Med Surg ; 17(5): 217-22, 1999 Oct.
Article in English | MEDLINE | ID: mdl-11199826

ABSTRACT

OBJECTIVE: Demonstrate a new technique to increase the width of keratinized gingiva using a biological membrane material in place of donor tissue. SUMMARY BACKGROUND DATA: Most current surgical techniques require donor tissue as a graft to increase keratinized gingiva, which results in a second trauma site for the patient. METHODS: Using an Nd:YAG laser with contact tip. Laser energy at settings of 3.0-6.0 W continuous mode. Local anesthetic, lidocaine 2% and epinephrine 1:100,000, was administered. A mucogingival flap was made to the periosteum and reflected, followed by placement of a biological membrane, and sutured into place, over the surgical site. RESULTS: A total of 20 sites were treated on 20 different patients of 15 mandible and 5 maxillary sites. The average increase for all sites was 3.8 mm of keratinized gingiva per site. No adverse events (e.g., bleeding, allergic reactions, abscesses, or pain) after any of the treatments were noted during the entire observation. The treatment procedure led to significant improvements in width of gingiva. The 20 patients were pleased with this new technique using the Nd:YAG laser with contact tip. CONCLUSION: It may be concluded that the new procedure provides significant increase of keratinized gingiva with the advantage of minimal morbidity and pleasing cosmetic results. Further clinical studies are needed to compare traditional procedures with the laser augmentation technique.


Subject(s)
Gingiva/surgery , Laser Therapy , Periodontal Attachment Loss/surgery , Biocompatible Materials , Humans
SELECTION OF CITATIONS
SEARCH DETAIL
...