Increased Levels of Serum Glycosylated Hemoglobin are Associated with Depressive Symptoms in a Population with Cancer (≥49 Years): An Antidepressant-Stratified Analysis

Huang, Ying; Xu, Yilin; Liu, Anwen

doi:10.2147/cia.s294704

Cited by 2 publications

(1 citation statement)

References 40 publications

(48 reference statements)

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“…This process may alter the synthesis of gangliosides, impairing the physiological function of the brain [108]. Even though no literature data exposed a precise causal correlation between altered glycosylation processes and suicidal behavior, this pathway is implicated in several disease states including psychiatric and neurodegenerative disorders [109][110][111][112][113][114][115][116].…”

Section: Molecular Pathway Analysismentioning

confidence: 99%

Suicide Related Phenotypes in a Bipolar Sample: Genetic Underpinnings

Lybech

Calabrò

Briuglia

et al. 2021

Genes

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Suicide in Bipolar Disorder (BD) is a relevant clinical concern. Genetics may shape the individual risk for suicide behavior in BD, together with known clinical factors. The lack of consistent replication in BD may be associated with its multigenetic component. In the present contribution we analyzed a sample of BD individuals (from STEP-BD database) to identify the genetic variants potentially associated with three different suicide-related phenotypes: 1) a feeling that the life was not worth living; 2) fantasies about committing a violent suicide; 3) previous attempted suicide. The sample under analysis included 1115 BD individuals. None of the SNPs reached genome-wide significance. However, a trend of association was evidenced for rs2767403, an intron variant of AOPEP gene, in association with phenotype #1 (p = 5.977 × 10−6). The molecular pathway analysis showed a significant enrichment in all the investigated phenotypes on pathways related to post synaptic signaling, neurotransmission and neurodevelopment. Further, NOTCH signaling or the γ-aminobutyric acid (GABA) -ergic signaling were found to be associated with specific suicide-related phenotypes. The present investigation contributes to the hypothesis that the genetic architecture of suicide behaviors in BD is related to alteration of entire pathways rather than single genes. In particular, our molecular pathway analysis points on some specific molecular events that could be the focus of further research in this field.

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Section: Molecular Pathway Analysismentioning

confidence: 99%

Suicide Related Phenotypes in a Bipolar Sample: Genetic Underpinnings

Lybech

Calabrò

Briuglia

et al. 2021

Genes

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A Mathematical Model for Controlling Exchanged Spinor Waves between Hemoglobin, Tumor and T-Cells

Fioranelli

Sepehri²,

Roccia

et al. 2021

Mathematics

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To date, it is known that tumor cells respond to attacks of T-cells by producing some PD-1/PD-L1 and other connections. Unfortunately, medical methods for preventing these connections are expensive and sometimes non-effective. In this study, we suggest a new way for reducing these connections by producing some noise in the exchanged information between tumor cells, T-cells, hemoglobin, and controller cells such as those of the heart or brain. In this model, we assume that human cells use spinor waves for exchanging information because the velocity of exchanged information between two spinors, which are located a large distance apart, exceeds the velocity of light. In fact, two spinors could send and receive information from each other instantaneously. In this hypothesis, the DNAs within heart cells, brain cells or any controller are built from some spinors such as electrons, and by their motion, some waves are generated. These spinor waves are received by iron atoms and multi-gonal molecules within hemoglobin and other spinors within the blood vessels. The hemoglobin molecules are located on some blood cells, move along the blood vessels and pass on their information to cells, proteins and RNAs. The spins of the spinors within the hemoglobin and also the spins of the charges and ions within the blood vessels are entangled and could transmit any information between cells. Thus, when a tumor is formed, its spinor waves change, and are transmitted rapidly into the heart cells, brain cells and other controller cells. The heart, brain or other controller cells diagnose these quantum waves, and by using the entanglement between the spinors within the blood vessels and the hemoglobin, send some messages to the T-cells. These messages are received by tumor cells and they become ready to respond to attacks. To prevent the reception of information by tumor cells, we can make use of some extra cells or hemoglobin, which interact with spinors and hemoglobin around tumor cells and produce some noise. Science quantum spinor waves are minute and have minor power and intensity; we cannot detect them by our present electronic devices and for this reason, we suggest using biological cells. This is a hypothesis; however, if experiments show its validity, some types of cancers could be cured or controlled by this method. We formulate the model by considering quantum entanglement between spinors within biological systems. By changing any spin within this system, all spins change and consequently, information is transmitted immediately. Then, we add new spinors to this system mathematically, and show that this causes the correlations between the initial spinors to reduce. Thus, the spinors of the extra hemoglobin or cells could act like noise, and prevent reception of real information by tumor cells.

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Increased Levels of Serum Glycosylated Hemoglobin are Associated with Depressive Symptoms in a Population with Cancer (≥49 Years): An Antidepressant-Stratified Analysis

Cited by 2 publications

References 40 publications

Suicide Related Phenotypes in a Bipolar Sample: Genetic Underpinnings

Suicide Related Phenotypes in a Bipolar Sample: Genetic Underpinnings

A Mathematical Model for Controlling Exchanged Spinor Waves between Hemoglobin, Tumor and T-Cells

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