Project description:IntroductionBiological age (BA) can represent the actual state of human aging more accurately than chronological age (CA).MethodsUsing hematological data from 112,925 participants in southwestern China, collected between 2015 and 2021, this study constructed BA predictors using 7 machine learning (ML) methods (tailored separately for male and female populations). This study then analyzed the association between BA acceleration and type 2 diabetes mellitus (T2DM) within this data using logistic regression. Additionally, it examined the impact of glycemic control on BA in individuals with diabetes.ResultsAmong all ML models, deep neural networks (DNN) delivered the best performance in male [mean absolute error (MAE)=6.89, r=0.75] and female subsets (MAE=6.86, r=0.74). BA acceleration showed positive correlations with T2DM in both male [odds ratio (OR): 2.22, 95% confidence interval (CI): 1.77-2.77] and female subsets (OR: 3.10, 95% CI: 2.16-4.46), while BA deceleration showed negative correlations in both male (OR: 0.32, 95% CI: 0.27-0.39) and female subsets (OR: 0.42, 95% CI: 0.33-0.53). Individuals with diabetes with normal fasting glucose had significantly lower BAs than those with impaired fasting glucose in all CA groups except for patients older than 80.DiscussionArtificial intelligence (AI)-based hematological BA predictors show promise as advanced tools for assessing aging in epidemiological studies. Implementing AI-based BA predictors in public health initiatives could facilitate proactive aging management and disease prevention.

| S-EPMC11561367 | biostudies-literature

In the Limelight: April 2021.

Project description: Not available

| S-EPMC8014236 | biostudies-literature

Rapid Increase in SARS-CoV-2 P.1 Lineage Leading to Codominance with B.1.1.7 Lineage, British Columbia, Canada, January-April 2021.

Project description:Several severe acute respiratory syndrome coronavirus 2 variants of concern (VOCs) emerged in late 2020; lineage B.1.1.7 initially dominated globally. However, lineages B.1.351 and P.1 represent potentially greater risk for transmission and immune escape. In British Columbia, Canada, B.1.1.7 and B.1.351 were first identified in December 2020 and P.1 in February 2021. We combined quantitative PCR and whole-genome sequencing to assess relative contribution of VOCs in nearly 67,000 infections during the first 16 weeks of 2021 in British Columbia. B.1.1.7 accounted for <10% of screened or sequenced specimens early on, increasing to >50% by week 8. P.1 accounted for <10% until week 10, increased rapidly to peak at week 12, and by week 13 codominated within 10% of rates of B.1.1.7. B.1.351 was a minority throughout. This rapid expansion of P.1 but suppression of B.1.351 expands our understanding of population-level VOC patterns and might provide clues to fitness determinants for emerging VOCs.

| S-EPMC8544957 | biostudies-literature

The SARS-CoV-2 B.1.351 lineage (VOC β) is outgrowing the B.1.1.7 lineage (VOC α) in some French regions in April 2021.

Project description:To assess SARS-CoV-2 variants spread, we analysed 36,590 variant-specific reverse-transcription-PCR tests performed on samples from 12 April-7 May 2021 in France. In this period, contrarily to January-March 2021, variants of concern (VOC) β (B.1.351 lineage) and/or γ (P.1 lineage) had a significant transmission advantage over VOC α (B.1.1.7 lineage) in Île-de-France (15.8%; 95% confidence interval (CI): 15.5-16.2) and Hauts-de-France (17.3%; 95% CI: 15.9-18.7) regions. This is consistent with VOC β's immune evasion abilities and high proportions of prior-SARS-CoV-2-infected persons in these regions.

| S-EPMC8193991 | biostudies-literature

Two Imported Cases of New Variant COVID-19 First Emerging from Brazil - Guangdong Province, China, April 30, 2021.

Project description: Not available

| S-EPMC8392982 | biostudies-literature

Candidate Multi-Epitope Vaccine against Corona B.1.617 Lineage: In Silico Approach.

Project description:Various mutations have accumulated since the first genome sequence of SARS-CoV2 in 2020. Mutants of the virus carrying the D614G and P681R mutations in the spike protein are increasingly becoming dominant all over the world. The two mutations increase the viral infectivity and severity of the disease. This report describes an in silico design of SARS-CoV-2 multi-epitope carrying the spike D614G and P681R mutations. The designed vaccine harbors the D614G mutation that increases viral infectivity, fitness, and the P681R mutation that enhances the cleavage of S to S1 and S2 subunits. The designed multi-epitope vaccine showed an antigenic property with a value of 0.67 and the immunogenicity of the predicted vaccine was calculated and yielded 3.4. The vaccine construct is predicted to be non-allergenic, thermostable and has hydrophilic nature. The combination of the selected CTL and HTL epitopes in the vaccine resulted in 96.85% population coverage globally. Stable interactions of the vaccine with Toll-Like Receptor 4 were tested by docking studies. The multi-epitope vaccine can be a good candidate against highly infecting SARS-CoV-2 variants.

| S-EPMC9694184 | biostudies-literature

A new species of <i>Nidirana</i> Dubois, 1992 (Anura, Ranidae) from Chongqing Municipality, China.

Project description:BackgroundThe Nidirana Dubois, 1992 exhibit a ubiquitous presence in East and Southeast Asia, spanning from Japan west to southern China and from northern Thailand to northern Vietnam and Laos in the south. The taxonomic categorisations pertaining to this genus continue to be a subject of debate, particularly with regard to those species that possess broad geographical distributions. In China, 18 species of Nidirana are currently recognised.New informationWe describe a new species of this genus from south-western China. Mitochondrial 16S and COⅠ gene phylogenetic analyses support the new species as an independent clade nested within the Nidirana. The new species is phylogenetically close to N.yaoica, with a genetic distance of 2.5% from its sister taxon. Morphologically, the new species can be distinguished from congeners by a combination of the following characteristics: males relatively small (SVL 41.8-43.3 mm); lateroventral grooves present on both fingers and toes; relative finger length Ⅱ < Ⅰ < Ⅳ < Ⅲ; tibio-tarsal articulation reaching to the level of the eye or nostril; a pair of external subgular vocal sacs in males; one single nuptial pad on the dorsal surface of the base of the first finger in males during the breeding season; webbing formula I 1/2 - 1 II 1/2 - 2 III 1 - 2½ IV 2 - 1V.

| S-EPMC10848812 | biostudies-literature