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1.
Cardiovasc Diabetol ; 23(1): 3, 2024 01 03.
Artigo em Inglês | MEDLINE | ID: mdl-38172813

RESUMO

BACKGROUND: The triglyceride-glucose (TyG) index has been proposed as a surrogate marker of insulin resistance. However, the relationship between the TyG index and central blood pressure (BP), has not been well studied in adults. METHODS: A total of 715 Chinese adult participants were enrolled in this study. Anthropometric and BP were assessed. The TyG index was calculated as ln[fasting triglycerides(mg/dL) × fasting glucose(mg/dL)/2]. Central BP was measured using SphygmoCor system. RESULTS: The participants were stratified into three groups based on the TyG index, and significant differences were observed in metabolic and cardiovascular parameters and the prevalence of hypertension among the groups. Both brachial (ß = 1.38, P = 0.0310; group highest vs. lowest, ß = 2.66, P = 0.0084) and aortic (ß = 2.38, P = 0.0002; group highest vs. lowest, ß = 3.96, P = 0.0001) diastolic BP were significantly and independently associated with the TyG index and increasing TyG index tertile. However, there was no independent association between the TyG index and systolic BP. A one-unit increase in the TyG index was associated with a 46% higher risk of hypertension (P = 0.0121), and compared with the lowest group, participants in the highest group had a 95% higher risk of hypertension (P = 0.0057). CONCLUSIONS: Our study demonstrates a significant and independent association between the TyG index and both brachial and aortic diastolic BP in Chinese adults. Furthermore, the TyG index was found to be an independent predictor of hypertension.


Assuntos
Hipertensão , Resistência à Insulina , Adulto , Humanos , Glucose/metabolismo , Glicemia/metabolismo , Triglicerídeos , Pressão Sanguínea , Hipertensão/diagnóstico , Hipertensão/epidemiologia , Biomarcadores , China/epidemiologia , Fatores de Risco
2.
Am J Primatol ; 84(7): e23394, 2022 07.
Artigo em Inglês | MEDLINE | ID: mdl-35612520

RESUMO

Adult males living in a one-male multi-female social group are expected to try to monopolize copulations with resident females to increase reproductive fitness. Gibbons have traditionally been described as living in monogamous groups, with the sole resident adult male assumed to sire all of the group's offspring. Here, we used microsatellite analyses and behavioral observations to examine rates of extra-group paternity (EGP) over 16 years in a population of crested gibbons (Nomascus concolor) that form stable and long-term one-male two-female social units. Forty percent of offspring (N = 14) were sired by extra-group males. To understand this high level of EGP, we tested whether inbreeding avoidance was related to EGP. Females who engaged in EGP did not show larger pairwise relatedness with their resident male compared to females who did not engage in EGP. Nevertheless, the standardized heterozygosity of EGP offspring was significantly higher than for offspring sired by the group's resident male. These results provide partial support for the inbreeding avoidance hypothesis. It appears that resident male crested gibbons are unable to monopolize resident females' matings. Our results indicate that long-term social partners are often distinct from sexual partners in this population. Clearly, the breeding system of crested gibbons is more flexible than previously thought, indicating a need for integrating long-term behavioral data and genetic research to re-evaluate gibbon social and sexual relationships derived from concepts of monogamy and pair-bonding.


Assuntos
Hylobates , Comportamento Sexual Animal , Animais , Feminino , Humanos , Endogamia , Masculino , Reprodução , Parceiros Sexuais
3.
Am J Primatol ; 80(9): e22922, 2018 09.
Artigo em Inglês | MEDLINE | ID: mdl-30281822

RESUMO

Gibbons are generally reported to live in small socially monogamous family groups in which both sexes disperse when they reach maturity. For the first time, we documented the dispersal pattern in a population of gibbons living in stable polygynous groups (Nomascus concolor) integrating 16 years' field observation and genetic information from fecal DNA. All subadult males except for one dispersed at 9.8 ± 1.4 years of age (range: 8-12, N = 10). The last male remained in his natal group and obtained the breeding position at age 11 by evicting the original dominant male. Females reached sexual maturity (as evidenced by the change in body color from black to yellow) at 8 years (N = 4). Three of them dispersed and one obtained a position as a breeding female and bred in her natal group. We also observed one female returning to her natal group with her infant after her presumed father was taken over by a neighboring male. We identified only three mtDNA haplotypes from 22 individuals at Dazhaizi. Individuals in one group shared the same haplotype, with only one exception. Genetic results showed that the two breeding females were mother-daughter pairs in all three study groups at the end of this study, implying some degree of female philopatry. We argue that in the case of black crested gibbons, dispersal decisions appear to represent highly opportunistic events in response to reproductive opportunities in their natal and neighboring groups.


Assuntos
Distribuição Animal , Hylobatidae/fisiologia , Animais , China , Feminino , Hylobatidae/genética , Masculino , Comportamento Sexual Animal
4.
Cureus ; 16(1): e52063, 2024 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-38344586

RESUMO

Hypokalemic Periodic Paralysis Type 2 (HOKPP2) is a rare autosomal dominant disorder characterized by recurrent episodes of muscle weakness, paralysis, and hypokalemia. In this case report, we present the clinical details of a 49-year-old female diagnosed with HOKPP2. Genetic testing revealed a heterozygous mutation in the Sodium Voltage-Gated Channel Alpha Subunit 4 (SCN4A) gene, confirming the diagnosis of HOKPP2. Management strategies, including potassium supplementation and lifestyle modifications, were implemented, resulting in a significant decrease in the frequency of symptomatic episodes. This case highlights the importance of considering HOKPP2 in patients with recurrent muscle weakness, particularly those with a familial history of similar symptoms. Furthermore, it underscores the crucial role of genetic testing in guiding patient management and facilitating genetic counseling.

5.
Int J Gen Med ; 16: 3491-3501, 2023.
Artigo em Inglês | MEDLINE | ID: mdl-37601803

RESUMO

Background: Non-valvular atrial fibrillation (NVAF) is associated with increased stroke in elderly populations, yet anticoagulant therapy is underutilized. We analyzed clinical characteristics and anticoagulation treatment rates of elderly NVAF patients hospitalized in Dali, China, to identify potential contributing factors. Methods: We collected data for 155 elderly patients with NVAF aged ≥60 years, from July 01, 2020, to December 31, 2021. We analyzed the awareness rate, clinical characteristics, and anticoagulant treatment rate of atrial fibrillation (AF), and identified factors influencing treatment. Patients were followed up one year after discharge to assess vital status, cardiovascular events, and anticoagulation therapy status. Results: Among 155 patients, 52.26% were female, and the average age was 75.77 years. The awareness rate of AF was 47.74% at admission, and only 21.94% received anticoagulant therapy. After discharge, the rate of anticoagulant therapy significantly increased to 70.97%, and 89.09% used new oral anticoagulants. Thromboembolic history and persistent AF predicted anticoagulant therapy at discharge, while male gender, previous bleeding history, and antiplatelet therapy predicted non-anticoagulant therapy. Out of 133 patients who completed a one-year follow-up, 23.31% died, 3.01% had strokes, and 3.01% experienced bleeding. Anticoagulant therapy decreased to 51.96% during the follow-up year. Conclusion: Our findings highlight the low awareness rate and anticoagulant treatment rate, and high mortality among elderly NVAF patients in Dali. The development of comprehensive intervention strategies is critical to standardize AF management and improve prognosis.

6.
Sci Rep ; 11(1): 2374, 2021 01 27.
Artigo em Inglês | MEDLINE | ID: mdl-33504927

RESUMO

Klotho, an important anti-aging protein, may be related to elevated blood pressure (BP) and arterial stiffness. We aimed to investigate associations between the serum klotho concentration and peripheral/central BP and arterial stiffness based on the carotid-femoral pulse wave velocity (cfPWV) in a Chinese population. We invited all inhabitants aged ≥ 18 years in two Dali communities for participation. The SphygmoCor system was used to record radial arterial waveforms. Aortic waveforms were derived using a generalized transfer function. The central BP was assessed by calibrating the brachial BP, which was measured using an oscillometric device. The serum klotho concentration was measured using an enzyme-linked immunosorbent assay and logarithmically transformed. Of the 716 participants (mean age: 51.9 ± 12.6 years), 467 (65.2%) were women. The median serum klotho concentration was 381.8 pg/mL. The serum klotho concentration did not significantly differ between patients with and without hypertension (P > 0.05) and between those with and without arterial stiffness (cfPWV ≥ 10 m/s) (P > 0.05). After adjusting for confounders, the serum klotho concentration was not significantly associated with the peripheral or central BP (P > 0.05) and cfPWV (P > 0.05). Our data indicated that the serum klotho concentration was not associated with BP or cfPWV in the general Chinese population.


Assuntos
Biomarcadores , Pressão Sanguínea , Glucuronidase/sangue , Adulto , China/epidemiologia , Diabetes Mellitus/epidemiologia , Feminino , Humanos , Hipertensão/epidemiologia , Proteínas Klotho , Masculino , Pessoa de Meia-Idade , Vigilância em Saúde Pública , Análise de Onda de Pulso
7.
J Clin Hypertens (Greenwich) ; 23(2): 363-372, 2021 02.
Artigo em Inglês | MEDLINE | ID: mdl-33369115

RESUMO

Thyroid dysfunction plays a role in blood pressure (BP) regulation. However, the associations between thyroid function and BP and arterial stiffness in the general Chinese population without thyroid disease are unknown. This population-based cross-sectional study aimed to investigate the association between thyroid function and peripheral and central BP and arterial stiffness in Chinese individuals. After excluding those who had thyroid diseases or incomplete clinical measurements, this study included 691 participants. Of the participants, 444 (64.2%) were women and 215 (31.1%) had hypertension. After adjustment for covariates, serum FT3 was significantly associated with a higher pulse rate in both sexes. In men, each 2.72-fold increase in serum FT4 levels was associated with higher peripheral systolic BP (+10.82 mmHg, p = .005) and pulse pressure (+5.71 mmHg, p = .03). Each 2.72-fold increase in serum FT4 levels was associated with higher central systolic BP (+8.03 mmHg, p = .03) and pulse pressure (+3.89 mmHg, p = .05). In women, serum FT4 was only associated with a higher central pulse pressure (+2.96 mmHg, p = .04). After adjustment for covariates, serum FT4 was significantly associated with a faster cfPWV exclusively in men. Our study showed that serum FT4 is associated with higher peripheral and central BP and faster cfPWV in men, whereas serum FT3 is positively associated with a higher pulse rate in both sexes, indicating that the effects of thyroid function on BP and arterial stiffness are more significant in men than in women.


Assuntos
Hipertensão , Rigidez Vascular , Pressão Sanguínea , Estudos Transversais , Feminino , Humanos , Hipertensão/epidemiologia , Masculino , Hormônios Tireóideos
8.
Dongwuxue Yanjiu ; 33(E5-6): E104-10, 2012 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-23266981

RESUMO

The genus Trachypithecus is the most diverse langur taxon, distributed in southwestern China, south and southeastern Asia. In this study, we include 16 recognized Trachypithecus species to reconstruct the phylogeny with particular concern to the taxonomy of the three subspecies of T. phayrei using multiple genes. Our results support a sister-relationship between T. p. phayrei and T. p. shanicus. However, the mitochondrial CYT B gene supported T. p. crepuscula as a distinct species, but the nuclear PRM1 gene suggested a closer relationship between T. p. crepuscula and T. p. phayrei. The incongruence between nuclear and mitochondrial genes suggests that hybridization may have occurred, a fact that would benefit from re-examination using multiple unlinked nuclear genes.


Assuntos
Colobinae/classificação , Colobinae/genética , Evolução Molecular , Filogenia , Sequência de Aminoácidos , Animais , China , Citocromos b/química , Citocromos b/genética , Dados de Sequência Molecular , Alinhamento de Sequência
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