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Geng, X.-Y.

Publications and source records attributed to Geng, X.-Y..

2 recordsLinked to original sources

Neural variability reliably and selectively encodes pain discriminability

Neural activity varies dramatically across time. While such variability has been associated with cognition, its relationship with pain remains largely unexplored. Here, we systematically investigated the relationship between neural variability and pain, particularly pain discriminability, in five large electroencephalography (EEG) datasets (total N = 489), collected from healthy individuals (Datasets 1-4) and patients with postherpetic neuralgia (PHN; Dataset 5) who had received painful or nonpainful sensory stimuli. We found robust correlations between neural variability and interindividual pain discriminability. These correlations were (1) replicable in multiple datasets, (2) pain selective, as no significant correlations were observed in nonpain modalities, and (3) clinically relevant, as they were partly disrupted in patients with PHN. Importantly, variability and amplitude of EEG signals were mutually independent and had distinct temporal and oscillatory profiles in encoding pain discriminability. These findings demonstrate that neural variability is a replicable and selective indicator of pain discriminability above and beyond amplitude, thereby enhancing the understanding of neural encoding of pain discriminability and underscoring the value of neural variability in pain studies.

neuroscience↗

Identification of CFAP52 as a novel diagnostic target of male infertility with defects of sperm head-tail connection and flagella development

Male infertility is a worldwide population health concern. Asthenoteratozoospermia is a common cause of male infertility, but its etiology remains incompletely understood. No evidence indicates the relevance of CFAP52 mutations to human male infertility. Our whole-exome sequencing identified compound heterozygous mutations in CFAP52 recessively cosegregating with male infertility status in a non-consanguineous Chinese family. Spermatozoa of CFAP52-mutant patient mainly exhibited abnormal head-tail connection and deformed flagella. Cfap52-knockout mice resembled the human infertile phenotype, showing a mixed acephalic spermatozoa syndrome (ASS) and multiple morphological abnormalities of the sperm flagella (MMAF) phenotype. The ultrastructural analyses further revealed a failure of connecting piece formation and a serious disorder of 9+2 axoneme structure. CFAP52 interacts with a head-tail coupling regulator SPATA6 and is essential for its stability. Expression of microtubule inner proteins and radial spoke proteins were reduced after the CFAP52 deficiency. Moreover, CFAP52-associated male infertility in humans and mice could be overcome by ICSI. The study reveals a prominent role for CFAP52 in sperm development, suggesting that CFAP52 might be a novel diagnostic target for male infertility with defects of sperm head-tail connection and flagella development

genetics↗