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Factor VIII (Recombinate / rAHF, Baxter / rurioctocog alpha)

✓ Approved

Baxter International, Inc. · F8 · 重组蛋白

什么是 Factor VIII?

Factor VIII 是一种重组蛋白,由Baxter International, Inc.研发。该药已获批,用于治疗相关适应症,给药途径:Injectable (Others)、Intravenous (IV)。

药物档案

商品名Recombinate, rAHF, Baxter, rurioctocog alpha
公司Baxter International, Inc.
药物类别重组蛋白, 细胞治疗
分子靶点F8
给药途径Injectable (Others), Intravenous (IV)
状态Approved

作用机制

分子靶点

Factor VIII 作用于 1 个分子靶点:

F8coagulation factor VIII (AHF, FVIII)
需要更深入的分析?Noah AI 可解释复杂机制并与同类药物比较。

治疗适应症

Factor VIII 针对 1 个适应症,涉及 1 个治疗领域。

治疗领域疾病/病症分期
Congenital, familial and genetic disordersFactor VIII deficiency✓ Approved

相关研究文献

PubMedFrontiers in psychology2026-09-11

Turkish adaptation and psychometric validation of the Normative Male Alexithymia Scale-Brief Form (NMAS-BF) among male university students.

Özel İrem İ

Normative male alexithymia reflects masculinity-related difficulties in identifying and expressing emotions and is theoretically linked to restrictive emotionality within masculine socialization. Existing measures predominantly assess clinical levels of alexithymia and may fail to capture subclinical, culturally embedded patterns of emotional restriction associated with masculine socialization. This study aimed to adapt the Normative Male Alexithymia Scale-Brief Form (NMAS-BF) to Turkish language and culture and to evaluate its psychometric properties. A methodological study was conducted with Turkish male university students. Linguistic equivalence was examined in a bilingual sample (n = 46), followed by a pilot study (n = 30). Separate non-overlapping samples were used for exploratory factor analysis (n = 376) and confirmatory factor analysis (n = 376) to assess structural validity. Exploratory factor analysis was conducted using principal axis factoring. Internal consistency was evaluated using Cronbach's alpha, corrected item-total correlations, and alpha-if-item-deleted values. The Turkish version of the NMAS-BF demonstrated high internal consistency (α = 0.890), with corrected item-total correlations ranging from 0.617 to 0.770. Exploratory factor analysis using principal axis factoring supported a single-factor structure explaining approximately 58.09% of the common variance. Confirmatory factor analysis indicated good model fit for the one-factor model, χ2(9) = 20.66, χ2/df = 2.30, RMSEA = 0.059, CFI = 0.99, TLI/NNFI = 0.99, SRMR = 0.025, and GFI = 0.98. The findings provide initial evidence for the internal consistency and structural validity of the Turkish NMAS-BF among Turkish male university students. Beyond its psychometric properties, the scale provides a culturally adapted tool for examining masculinity-related emotional restriction within the context of Turkish masculine socialization. Future studies may use the Turkish NMAS-BF to investigate associations between emotional restriction, emotional awareness, emotional expression, and psychological functioning among more diverse samples of Turkish men.

PMID 42724141
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PubMedJournal of ultrasound in medicine : official journal of the American Institute of Ultrasound in Medicine2026-09-11

Nodule Morphology: A General Prognostic Factor or Treatment Strategy-Related Heterogeneity in Treatment Response?

Ni Handan H

PMID 42723267
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PubMedEuropean journal of oral sciences2026-09-11

Considerations on TNF-α inhibition in ligature-induced periodontitis mice with the Alzheimer's disease risk factor APOE4.

Ardila Carlos M CM, Pineda-Vélez Eliana E, Díaz-Laclaustra Alejandro I AI

PMID 42723487
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PubMedPersonality and mental health2026-09-11

Latent Structure and Incremental Validity of the Semi-Structured Interview for Personality Functioning DSM-5 (STiP-5.1) in a Lithuanian Adolescent Sample.

Grigaitė Agnė A, Gaudiešiūtė Elena E, Hutsebaut Joost J, Barkauskienė Rasa R

As personality functioning has become central to contemporary conceptualizations of personality pathology, understanding its structure and optimal assessment has emerged as an important research priority, particularly in adolescence. This study examined the latent structure of the Semi-Structured Interview for Personality Functioning DSM-5 (STiP-5.1) and its incremental validity in predicting functional impairment beyond self-reported personality functioning. Participants were 178 adolescents aged 11-18 years, including a clinical sample (n = 104) and a community sample (n = 74). Confirmatory factor analyses (CFA) and bifactor modeling were used to evaluate the latent structure of the STiP-5.1. Hierarchical regression analyses examined whether clinician-rated personality functioning explained additional variance in functional impairment (WHODAS 2.0) beyond self-reported personality functioning assessed with the LoPF-Q 12-18 Short. The bifactor model demonstrated the best overall fit and supported the predominance of a strong general factor. Most reliable variance was attributable to this factor, whereas self- and interpersonal-specific factors contributed little unique variance. A four-factor CFA model also demonstrated excellent fit, supporting differentiation among identity, self-direction, empathy, and intimacy. Clinician-rated personality functioning explained additional variance in functional impairment beyond self-report measures. Self-functioning, particularly the element of self-direction, emerged as a unique predictor of functional impairment. Findings support a predominantly unidimensional conceptualization of personality functioning in adolescence while retaining clinically meaningful differentiation across LPFS domains and elements. The STiP-5.1 provides unique information beyond self-report assessment, supporting multimethod approaches to the assessment of personality functioning in adolescents.

PMID 42723530
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PubMedSpinal cord2026-09-11

A new self-efficacy scale for people with a spinal cord injury; The General and Spinal Cord Injury Specific Self-efficacy Scale (G-SCI-SeS).

van Diemen Tijn T, van Nes Ilse J W IJW, de Klerk Erik E, Scholten Eline W M EWM et al.

A longitudinal cohort. This study aimed to be the first validation of the General and Spinal Cord Injury Specific Self-efficacy Scale (G-SCI-SeS), designed to capture both trait-like (general) and state-like (disease or SCI-specific) dimensions of self-efficacy (SE). Participants were followed from post-acute rehabilitation up to five years after discharge in the Netherlands. In the latest follow-up of a longitudinal spinal cord injury cohort, the G-SCI-SeS was administered alongside a general SE scale, two disease-specific SE scales, a distress scale and a life satisfaction scale. Among 142 participants with complete data, confirmatory factor analyses supported a two-factor structure, which demonstrated superior fit compared to a one-factor model. Internal consistency was excellent for the total score and General SE subscale, and good for the SCI-specific subscale. No floor effects and minimal ceiling effects were observed. Score distributions were non-normal, with a tendency toward higher values for all SE scales. Intercorrelations between the G-SCI-SeS and other SE scales were strong, even where moderate correlations were hypothesized. The G-SCI-SeS demonstrated a robust two-factor structure and moderate-to-good construct validity. Strong correlations between trait and state SE measures may reflect convergence of these constructs in the chronic phase of SCI. Developed through an iterative process incorporating cognitive interviews, the G-SCI-SeS appears suitable for clinical and research use. Further studies should investigate other forms of validity and the sensitivity of the G-SCI-SeS to change from the sub-acute phase to the chronic phase.

PMID 42722708
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PubMedFrontiers in medicine2026-09-11

Dynamic analysis of 22 serum biomarkers following pneumothorax.

Chen Jirui J, Lyu Qiang Q, Wang Cheng C, Han Qianyu Q et al.

Pneumothorax is a common respiratory emergency. Current diagnosis primarily relies on imaging examinations, but these have insufficient sensitivity for early or occult cases, and there is a lack of highly specific molecular markers. Investigating the dynamic changes in serum biomarkers is of great significance for the early diagnosis and intervention of pneumothorax. A rat pneumothorax model was established. Serum was collected before modeling and at 1, 2, 6, 12, 24, and 48 h after modeling. Using pre-modeling rat serum marker levels as a baseline, 22 biomarkers (including inflammatory factors, fibrosis-related molecules, immunomodulatory molecules, and metabolic indicators) were detected using enzyme-linked immunosorbent assay (ELISA). Small animal ultrasound was used to verify model establishment. The rat pneumothorax model was successfully established, with ultrasound showing the loss of the lung sliding sign. The biomarkers exhibited four dynamic patterns: (1) Early rapid increase in pro-inflammatory factors (tumor necrosis factor-α, interleukin-1β, etc.); (2) Sustained or fluctuating increase in fibrosis-related molecules (transforming growth factor-β, collagen, etc.); (3) Sustained decrease in the anti-inflammatory factor interleukin-10; (4) Fluctuating changes in metabolic indicators and aquaporin markers (25-hydroxyvitamin D, aquaporin-4/5). Notably, to our knowledge, this study is the first to discover early, significant, and rapid increases in tartrate-resistant acid phosphatase (TRACP), intercellular adhesion molecule-1 (ICAM-1), and nuclear factor-κB (NF-κB) in a pneumothorax model, which may provide a basis for the early diagnosis of pneumothorax. This study systematically delineates the dynamic evolution patterns of multiple classes of serum biomarkers following pneumothorax. The novel finding of abnormal elevations in TRACP, ICAM-1, and NF-κB challenges traditional understanding of their functions and provides new potential candidate targets for the early diagnosis of pneumothorax.

PMID 42723924
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