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1.
Radiol Case Rep ; 18(12): 4435-4438, 2023 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-37823050

RESUMO

Sternal fractures are rare and are typically caused by major trauma such as motor vehicle collisions. However, sternal insufficiency fractures can occur with minimal to no trauma in patients with exaggerated thoracic kyphosis from multiple thoracic compression fractures, especially in the setting of osteoporosis. We describe a case of a sternal insufficiency fracture that presented as chest pain resembling a myocardial infarction. As sternal insufficiency fractures may vary in clinical presentation, this case demonstrates that radiologists should carefully evaluate the sternum, especially when risk factors are present. Furthermore, awareness and identification of these fractures can prevent unnecessary cardiac workups.

2.
Radiol Case Rep ; 16(10): 3134-3138, 2021 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-34457102

RESUMO

Ureterosciatic hernias are extremely rare, with fewer than 40 cases reported in the literature. We present a case of a patient with concurrent right ureterosciatic hernia (Lindbom hernia), ipsilateral bladder hernia, and appendix-containing inguinal hernia (Amyand hernia). These findings were discovered incidentally on imaging and the patient had no associated symptoms.

3.
Cell Rep ; 13(6): 1073-1080, 2015 Nov 10.
Artigo em Inglês | MEDLINE | ID: mdl-26526993

RESUMO

Brain-derived neurotrophic factor (BDNF) plays a key role in energy balance. In population studies, SNPs of the BDNF locus have been linked to obesity, but the mechanism by which these variants cause weight gain is unknown. Here, we examined human hypothalamic BDNF expression in association with 44 BDNF SNPs. We observed that the minor C allele of rs12291063 is associated with lower human ventromedial hypothalamic BDNF expression (p < 0.001) and greater adiposity in both adult and pediatric cohorts (p values < 0.05). We further demonstrated that the major T allele for rs12291063 possesses a binding capacity for the transcriptional regulator, heterogeneous nuclear ribonucleoprotein D0B, knockdown of which disrupts transactivation by the T allele. Binding and transactivation functions are both disrupted by substituting C for T. These findings provide a rationale for BDNF augmentation as a targeted treatment for obesity in individuals who have the rs12291063 CC genotype.


Assuntos
Fator Neurotrófico Derivado do Encéfalo/genética , Obesidade/genética , Polimorfismo de Nucleotídeo Único , Adolescente , Adulto , Fator Neurotrófico Derivado do Encéfalo/metabolismo , Estudos de Casos e Controles , Criança , Feminino , Células HEK293 , Ribonucleoproteína Nuclear Heterogênea D0 , Ribonucleoproteínas Nucleares Heterogêneas Grupo D/metabolismo , Humanos , Hipotálamo/metabolismo , Íntrons , Masculino , Pessoa de Meia-Idade , Ligação Proteica
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