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1.
Curr Med Res Opin ; 38(5): 803-810, 2022 05.
Article in English | MEDLINE | ID: mdl-35225112

ABSTRACT

OBJECTIVE: This study aimed to evaluate the effectiveness of therapeutic lumbar drainage (LD) compared to therapeutic lumbar puncture (LP) for the management of intracranial hypertension (ICH) among HIV-positive patients with cryptococcal meningitis (CM). METHODS: The study was a multicenter prospective non-randomized interventional clinical trial. One hundred and sixteen HIV-associated CM patients were identified who presented with ICH (≥250 mmH2O). The LP group comprised 76 cases, while the LD group consisted of 40 cases. We compared mortality, intracranial pressure (ICP) normalization rate, and clinical symptom remission at 10 weeks, between the two groups. RESULTS: The cumulative mortality at week 10 was 22.4% in the LP group and 20% in the LD group (p = .927), without any significant difference in mortality between the two groups. Improvement after treatment at 2-weeks, ICP normalization, and headache reversal event occurrence in the two groups showed no significant difference (p > .05). The incidence of CSF Cryptococcus clearance at two weeks in the LD group was significantly higher than in the LP group (p < .05). The frequency of invasive lumbar therapeutic procedures in the LP group during the first week was higher than that of the LD group (p < .05). Localized infection at the puncture site occurred more frequently in the LD group than in the LP group (p < .05). CONCLUSION: For HIV-positive CM patients with an elevated ICP, LD and LP are comparably effective and safe options to normalize ICP. LP increases the frequency of invasive lumbar therapeutic procedures but does not incur more risk of infection events at the puncture site, while LD may accelerate CSF Cryptococcus clearance but may induce more frequent localized infection. TRIAL REGISTRATION: This study was registered as one of 12 trials under a general project at the Chinese Clinical Trial Registry (ChiCTR1900021195).


Subject(s)
HIV Infections , Intracranial Hypertension , Meningitis, Cryptococcal , Drainage/adverse effects , HIV Infections/complications , Humans , Intracranial Hypertension/etiology , Intracranial Hypertension/therapy , Meningitis, Cryptococcal/drug therapy , Meningitis, Cryptococcal/therapy , Prospective Studies , Spinal Puncture/adverse effects
2.
Gene ; 374: 10-8, 2006 Jun 07.
Article in English | MEDLINE | ID: mdl-16650944

ABSTRACT

Polydactyly is a common malformation of vertebrate limbs. Preaxial polydactyly (PPD) has been mapped in human, mouse and chicken to the syntenic region of human 7q36. Lmbr1 was thought as the critical candidate gene for human and mouse PPD. To understand the molecular mechanism underlying chicken polydactyly, we have cloned the open reading frame (ORF) of chicken Lmbr1, which contains 1467 nucleotides. Within this ORF, we found one short and one long splice forms. The short splice form has a complete deletion of exon 4. Six cSNPs were found in the chicken ORF, and two of these cSNPs, G797A and G1255A, lead to amino acid substitutions. However, G797A substitution had no significant association with polydactyly and the G1255A substitution had very low frequency in the population. The T1254C polymorphism in exon 13 was found to be strongly associated with polydactyly. Radiation hybrid mapping of a DNA fragment containing intron 13 of the chicken Lmbr1 assigned the gene to chromosome 2 between MCW071 (a marker within the EN2 gene) and ADL0270, a syntenic region to human 7q36.


Subject(s)
Chickens/genetics , Polydactyly/genetics , Polymorphism, Single Nucleotide , Alleles , Alternative Splicing , Amino Acid Substitution , Animals , Base Sequence , Chromosomes , Cloning, Molecular , Exons , Genetic Linkage , Introns , Membrane Proteins/genetics , Molecular Sequence Data , Open Reading Frames , Polydactyly/etiology , Polymorphism, Single-Stranded Conformational , Protein Isoforms/genetics , Protein Isoforms/metabolism , Radiation Hybrid Mapping
3.
Yi Chuan ; 26(3): 387-93, 2004 May.
Article in Chinese | MEDLINE | ID: mdl-15640026

ABSTRACT

Polydactyly is a common abnormal limb phenotype in vertebrate and there is similar limb phenotype among different species. Research shows that polydactyly has a similar development mechanism, and this kind of polydactyly character seems to be controlled by homologous genes among species. The latest research results on human and mouse further shows that PPD should be caused by the disruption of a long range cis-acting regulator for Shh within Lmbr1 intron. Here the development mechanism and related genes controlling polydactyly character of vertebrate are reviewed.


Subject(s)
Membrane Proteins/genetics , Polydactyly/genetics , Trans-Activators/genetics , Animals , Chromosomes, Human, Pair 2 , Chromosomes, Human, Pair 7 , Hedgehog Proteins , Homeodomain Proteins/genetics , Humans , Introns , Kruppel-Like Transcription Factors/genetics , Membrane Proteins/metabolism , Mutation , Nerve Tissue Proteins/genetics , Phenotype , Polydactyly/metabolism , Transcription Factors/genetics , Zinc Finger Protein Gli3
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