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1.
Eur J Dent Educ ; 21(2): 79-85, 2017 May.
Article in English | MEDLINE | ID: mdl-26764013

ABSTRACT

INTRODUCTION: Mandibular two-implant overdentures are considered the minimum standard of care for edentulous patients and provide an excellent performance, as well as satisfaction to the patients. Dental schools are required to promote the teaching of current treatment options in order to enable students to master state-of-the-art procedures. AIMS: The purpose of this study was to examine how the theoretical and practical aspects of mandibular two-implant overdentures are taught in dental schools in North America. METHODS: Data were collected via an online questionnaire that included questions regarding the theoretical and clinical courses, surgical procedure and imaging method. RESULTS: Of 75 schools, 36 responded to the survey. Almost all the schools teach the subject theoretically, but it is not mandatory for students to perform in most of the schools. Only a minority (23%) of the mandibular dentures made by students are implant-supported. Almost all of the schools (94%) use two implants to support overdentures, and Locator abutment is used almost exclusively. The prevalent imaging for the surgical procedure is CT scans, although 30% of the schools use panoramic radiograph. None of the schools loads the implants immediately after surgery. CONCLUSION: Some clear trends are apparent in the current survey: the use of two implants, no use of bar connectors and delayed loading of the implants. It is likely that graduates will not have sufficient clinical skills and will need continuing education to be familiar with the required procedures, both surgical and prosthetic.


Subject(s)
Dental Prosthesis, Implant-Supported , Denture, Overlay , Education, Dental , Humans , Mandible , North America , Schools, Dental , Surveys and Questionnaires
2.
Eur J Clin Microbiol Infect Dis ; 35(1): 149-54, 2016 Jan.
Article in English | MEDLINE | ID: mdl-26581423

ABSTRACT

Since 2013, four hospitals in northern Israel have been providing care for Syrian nationals, primarily those wounded in the ongoing civil war. We analyzed carbapenemase-producing Enterobacteriaceae (CPE) isolates obtained from these patients. Isolate identification was performed using the VITEK 2 system. Polymerase chain reaction (PCR) was performed for the presence of bla KPC, bla NDM, and bla OXA-48. Susceptibility testing and genotyping were performed on selected isolates. During the study period, 595 Syrian patients were hospitalized, most of them young men. Thirty-two confirmed CPE isolates were grown from cultures taken from 30 patients. All but five isolates were identified as Klebsiella pneumoniae and Escherichia coli. Nineteen isolates produced NDM and 13 produced OXA-48. Among a further 29 isolates tested, multilocus sequence typing (MLST) showed that ST278 and ST38 were the major sequence types among the NDM-producing K. pneumoniae and OXA-48-producing E. coli isolates, respectively. Most were resistant to all three carbapenems in use in Israel and to gentamicin, but susceptible to colistin and fosfomycin. The source for bacterial acquisition could not be determined; however, some patients admitted to different medical centers were found to carry the same sequence type. CPE containing bla NDM and bla OXA-48 were prevalent among Syrian wounded hospitalized patients in northern Israel. The finding of the same sequence type among patients at different medical centers implies a common, prehospital source for these patients. These findings have implications for public health throughout the region.


Subject(s)
Bacterial Proteins/genetics , Enterobacteriaceae Infections/microbiology , Enterobacteriaceae/enzymology , Wound Infection/microbiology , beta-Lactamases/genetics , Adolescent , Adult , Bacterial Typing Techniques , Enterobacteriaceae/classification , Enterobacteriaceae/genetics , Enterobacteriaceae/isolation & purification , Female , Genotype , Hospitals , Humans , Israel , Male , Middle Aged , Multilocus Sequence Typing , Polymerase Chain Reaction , Syria , Warfare , Young Adult
3.
Infant Ment Health J ; 36(3): 337-48, 2015.
Article in English | MEDLINE | ID: mdl-25941026

ABSTRACT

The present study investigated maternal emotion regulation as mediating the association between maternal posttraumatic stress symptoms and children's emotional dysregulation in a community sample of 431 Israeli mothers and children exposed to trauma. Little is known about the specific pathways through which maternal posttraumatic symptoms and deficits in emotion regulation contribute to emotional dysregulation. Inspired by the intergenerational process of relational posttraumatic stress disorder (PTSD), in which posttraumatic distress is transmitted from mothers to children, we suggest an analogous concept of relational emotion regulation, by which maternal emotion regulation problems may contribute to child emotion regulation deficits. Child emotion regulation problems were measured using the Child Behavior Checklist-Dysregulation Profile (CBCL-DP; T.M. Achenbach & I. Rescorla, 2000), which is comprised of three subscales of the CBCL: Attention, Aggression, and Anxiety/Depression. Maternal PTSD symptoms were assessed by the Posttraumatic Diagnostic Scale (E.B. Foa, L. Cashman, L. Jaycox, & K. Perry, 1997) and maternal emotion regulation by the Difficulties in Emotion Regulation Scale (K.L. Gratz & L. Roemer, 2004). Results showed that the child's emotion regulation problems were associated with both maternal posttraumatic symptoms and maternal emotion dysregulation. Further, maternal emotion regulation mediated the association between maternal posttraumatic symptoms and the child's regulation deficits. These findings highlight the central role of mothers' emotion regulation skills in the aftermath of trauma as it relates to children's emotion regulation skills. The degree of mothers' regulatory skills in the context of posttraumatic stress symptoms reflects a key process through which the intergenerational transmission of trauma may occur. Study results have critical implications for planning and developing clinical interventions geared toward the treatment of families in the aftermath of trauma and, in particular, the enhancement of mothers' emotion regulation skills after trauma.


Subject(s)
Emotions , Mothers/psychology , Psychology, Child , Stress Disorders, Post-Traumatic , Child , Child Behavior Disorders , Child, Preschool , Female , Humans , Interviews as Topic , Israel , Mother-Child Relations , Violence
4.
Tech Coloproctol ; 18(6): 551-6, 2014 Jun.
Article in English | MEDLINE | ID: mdl-24287642

ABSTRACT

BACKGROUND: Colorectal stents have a proven role in colorectal cancer as palliative care or a bridge to surgery. However, their efficacy and anchoring to the tissue varies according to stent design with stent migration rates up to 50 %. We present preliminary in vivo results of a new end-luminal anchoring system for stent fixation to the rectal canal. The aim was to assess the efficacy and safety of the stent using the anchoring system while subjecting the device to daily abdominal pressures related to daily activities in a porcine animal model. METHODS: Ex vivo anatomical and physical studies were performed to improve the system's structure and safety. Four female pigs were followed for the acute and chronic (16 weeks) period. Two animals were euthanized and underwent en-bloc pelvic visceral excision and histopathological examination. Device fixation time, animal behavior, device patency, anoscopic examination and histopathological features were assessed. RESULTS: Mean anchoring time was 13.83 weeks (standard error ± 1.38 weeks). One of the animals experienced early device expulsion with no complications. No obstruction was noted in any of the animals. Macroscopic examination revealed mild focal submucosal scarring in one animal and a normal examination in the other. Hematoxylin and eosin staining revealed mucosal ulceration and mixed inflammatory cell infiltrate, with no signs of granulomata, foreign body giant cell reaction or microabscess formation. CONCLUSIONS: A novel fixation device designed for long-term intrarectal implantation was well tolerated and maintained anal canal patency without migration. Larger studies are needed before its implementation in humans.


Subject(s)
Rectum/surgery , Stents , Animals , Colorectal Neoplasms/complications , Colorectal Neoplasms/surgery , Disease Models, Animal , Female , Foreign-Body Migration , Intestinal Obstruction/etiology , Intestinal Obstruction/surgery , Prosthesis Design , Swine , Time Factors , Titanium
5.
Colorectal Dis ; 15(6): e317-22, 2013 Jun.
Article in English | MEDLINE | ID: mdl-23406371

ABSTRACT

AIM: The long-term effects of surgical and non-surgical factors on increased stool frequency and incontinence following anterior resection have been variably reported. We investigated the effects of surgical characteristics on symptoms at 1 month and more than 1 year postoperatively following anterior resection of the rectum. METHOD: In this retrospective study of patients who underwent anterior resection of the rectum during 2002-2006, patients were interviewed regarding symptoms at 1 month and more than 1 year postoperatively. Anterior resection of the rectum syndrome (ARRS) is more simply defined as incontinence and/or frequent bowel movements after surgery and graded as severe, moderate or mild. RESULTS: Of the 165 patients who underwent anterior resection for rectal cancer during the study period, 106 were included in the analysis. The median follow-up period was 3.4 years (range 13-72 months). ARRS had a high prevalence 1 month postoperatively (55.6%) but abated in over half the cases at 1 year postoperatively. The likelihood of development of early but not late ARRS was associated with the anastomotic level suggesting adaptation. ARRS and continence were unaffected by total mesorectal excision, the use of adjuvant radiation or chemotherapy, patient age or disease stage. CONCLUSION: The level of anastomosis in anterior resection of the rectum had a significant effect on the prevalence of ARRS using a new simpler definition 1 month after surgery but not 1 year or more postoperatively. Further data on neorectal reservoir reconstruction using the simpler ARRS definition are required.


Subject(s)
Defecation/physiology , Fecal Incontinence/physiopathology , Postoperative Complications/physiopathology , Rectal Neoplasms/surgery , Rectum/surgery , Adult , Aged , Aged, 80 and over , Anastomosis, Surgical , Digestive System Surgical Procedures , Female , Follow-Up Studies , Humans , Male , Middle Aged , Retrospective Studies , Syndrome , Treatment Outcome
6.
Tech Coloproctol ; 17(1): 39-44, 2013 Feb.
Article in English | MEDLINE | ID: mdl-22936584

ABSTRACT

BACKGROUND: One of the most unpleasant and sometimes difficult elements of colonoscopic examination is the bowel preparation which is usually performed 6 or more hours prior to the examination ("early" preparation), causing many patients to refrain from undergoing this procedure. We present a novel technique for bowel preparation that begins approximately 30 min prior to the introduction of the colonoscope and eliminates the need for significant pre-procedure preparation. METHODS: The medical records of all consecutive patients who underwent colonoscopy without "early" preparation (CWEP) from May 2009 through June 2010 were retrospectively reviewed. The procedure was performed using a novel cleansing device, the "ColonoScoPrep™", with which the colon is prepared about half an hour prior to insertion of the colonoscope. The only medication required is two to three bisacodyl tablets the night before. The quality of bowel preparation was graded as excellent, good, satisfactory, or poor, and patient satisfaction was assessed according to a prospective protocol. RESULTS: During this period, 125 patients underwent CWEP. Of these, 110 (89.4 %) patients had an excellent or good preparation, permitting complete colonoscopic examination unimpeded by fecal matter. In 11 patients, preparation was satisfactory, in 2 it was poor and in 2, colonoscopy was not completed due to unsatisfactory preparation. None of the patients suffered from abdominal pain or cramps during or after the CWEP and none had post-colonoscopy diarrhea. All patients were satisfied with the procedure. CONCLUSIONS: Despite the fact that the study is retrospective, CWEP appears safe and easy to perform. A prospective study comparing conventional bowel preparation and CWEP is now underway.


Subject(s)
Colon , Colonoscopy/methods , Therapeutic Irrigation/instrumentation , Adult , Aged , Female , Humans , Male , Middle Aged , Operative Time , Patient Satisfaction , Retrospective Studies , Water/administration & dosage , Young Adult
7.
Tech Coloproctol ; 17(2): 151-62, 2013 Apr.
Article in English | MEDLINE | ID: mdl-23076289

ABSTRACT

Between 25 and 80% of patients undergoing a low or very low anterior resection will suffer postoperatively, from a constellation of symptoms including fecal urgency, frequent bowel movements, bowel fragmentation and incontinence, collectively referred to as the low anterior resection syndrome (LARS). The etiology of LARS is multifactorial with the potential of sphincter injury during anastomosis construction, alterations in anorectal physiology, the development of a pudendal neuropathy, and a lumbar plexopathy with exacerbation of symptoms if there is associated anastomotic sepsis or the use of adjuvant and neoadjuavnt therapies. The symptoms of LARS may be obviated in part by the construction of a neorectal reservoir which may take the form of a colonic J-pouch, a transverse coloplasty, or a side-to-end anastomosis. This review outlines the factors contributing to LARS symptomatology along with the short- and medium-term functional results of comparative trials with the different types of neorectal reconstructions.


Subject(s)
Colonic Neoplasms/surgery , Digestive System Surgical Procedures/adverse effects , Postoperative Complications/epidemiology , Rectal Neoplasms/surgery , Colonic Pouches , Fecal Incontinence/epidemiology , Fecal Incontinence/physiopathology , Flatulence/epidemiology , Humans , Postoperative Complications/physiopathology , Plastic Surgery Procedures , Recovery of Function , Syndrome
8.
Colorectal Dis ; 13(10): 1110-5, 2011 Oct.
Article in English | MEDLINE | ID: mdl-21040362

ABSTRACT

AIM: The study aimed to characterize the pathological and clinical response of rectal gastrointestinal stromal tumours (GISTs) to neoadjuvant Imatinib. METHOD: The medical records of patients with rectal GISTs who were diagnosed and treated in five medical centres in Israel between January 2002 and January 2009 were retrospectively examined. Twelve patients who fulfilled the inclusion criteria of nonmetastatic rectal GIST for which preoperative neoadjuvant treatment with Imatinib was considered were suitable for enrollment. RESULTS: Of the 12 patients, nine received neoadjuvant treatment with Imatinib. The three patients who had immediate surgery were excluded. There were five men and four women with a median age of 63 years and a median follow up of 32 months. All tumours were located in the lower two-thirds of the rectum. One patient had a complete clinical response, six had a partial response and two had stable disease. Seven patients subsequently underwent surgery; six had an R0 resection and one had an R1 resection. Three patients had recurrence. There was no disease-related mortality. The reduction in both tumour size and mitotic activity during preoperative Imatinib therapy was significant. CONCLUSION: Preoperative Imatinib therapy can shrink large rectal GISTs, improving the chances of successful radical surgery and decreasing the risk of considerable morbidity.


Subject(s)
Antineoplastic Agents/therapeutic use , Gastrointestinal Stromal Tumors/drug therapy , Neoadjuvant Therapy , Piperazines/therapeutic use , Pyrimidines/therapeutic use , Rectal Neoplasms/drug therapy , Adult , Aged , Aged, 80 and over , Benzamides , Female , Gastrointestinal Stromal Tumors/mortality , Gastrointestinal Stromal Tumors/pathology , Gastrointestinal Stromal Tumors/surgery , Humans , Imatinib Mesylate , Male , Middle Aged , Rectal Neoplasms/mortality , Rectal Neoplasms/pathology , Rectal Neoplasms/surgery , Survival Rate
9.
Colorectal Dis ; 13(11): 1230-5, 2011 Nov.
Article in English | MEDLINE | ID: mdl-21689324

ABSTRACT

AIM: The study assessed the clinicopathological features and survival rates of inflammatory bowel disease (IBD) patients with colorectal carcinoma (CRC), which accounts for ∼ 15% of all IBD associated death. METHOD: The medical records of patients operated on for CRC in three institutions between 1992 and 2009 were reviewed, and those with Crohn's colitis (CC) and ulcerative colitis (UC) were identified. Data on age, gender, disease duration, colitis severity, surgical procedure, tumour stage and survival were retrieved. RESULTS: Fifty-three patients (40 UC and 13 CC, 27 men, mean age at operation 54 years) were found. All parameters were comparable between the groups. Mean disease duration before CRC was 22.7 years for UC and 16.6 years for CC patients (P = 0.04). CRC was diagnosed preoperatively in 43 (81%) patients. Twenty-eight patients had colon cancer, 23 had rectal cancer and two patients had more than one cancer. All malignancies were located in segments with colitis. Over one-half were diagnosed at an advanced stage (36% stage III; 17% stage IV). At a mean follow up of 56 ± 65 months, 60% were alive (54% disease free) and 40% were dead from cancer-related causes. The 5-year survival rate was 61% for the UC and 37% for the CC patients (P = NS). CONCLUSION: CRC in IBD patients is frequently diagnosed at an advanced stage, a factor that contributes to poor prognosis. The risk of CRC in CC patients is comparable to those with UC. Long-term surveillance is recommended for patients with long-standing CC and UC.


Subject(s)
Carcinoma/pathology , Colitis, Ulcerative/complications , Colonic Neoplasms/pathology , Crohn Disease/complications , Rectal Neoplasms/pathology , Adult , Aged , Aged, 80 and over , Carcinoma/complications , Carcinoma/therapy , Colonic Neoplasms/complications , Colonic Neoplasms/therapy , Disease-Free Survival , Female , Follow-Up Studies , Humans , Kaplan-Meier Estimate , Male , Middle Aged , Neoplasm Staging , Prognosis , Rectal Neoplasms/complications , Rectal Neoplasms/therapy , Retrospective Studies
10.
Colorectal Dis ; 12(4): 358-62, 2010 Apr.
Article in English | MEDLINE | ID: mdl-19220385

ABSTRACT

OBJECTIVE: Complex anal fistulas traverse a significant portion of the external sphincter muscle, making their treatment a surgical challenge. Several surgical options are used with conflicting results. The aim of this study was to analyse the results of permanent loose seton in the management of high anal fistulas in Crohn's disease (CD) patients and two-stage seton fistulotomy in patients without CD. METHOD: We retrospectively reviewed the clinical records of 77 patients with complex anal fistula treated by loose seton over a 4-year period, in two medical centres. Recorded parameters included demographics, medical history, type of fistula, disease duration, previous surgery, morbidity, recurrence and mortality. RESULTS: Sixty patients without CD underwent 107 fistula-related surgical procedures, and 17 CD patients underwent 29 procedures. Early postoperative complications were recorded in eight (10%) patients. Perioperative complications, mainly local sepsis or bleeding, were recorded in eight (10%) patients. Long-term complications were observed in nine non-CD and four CD patients. During a median follow-up period of 24 months, the recurrence rate was 40% in CD patients and 47% in patients without CD. Five patients (four non-CD patients and one CD patient) developed some degree of faecal incontinence. CONCLUSION: The fistula recurrence rate following two-stage seton fistulotomy in non-CD patients was high. In CD patients the use of permanent loose seton is effective in controlling local sepsis in about half of patients and has low rates of subsequent incontinence.


Subject(s)
Drainage/adverse effects , Fecal Incontinence/etiology , Rectal Fistula/surgery , Suture Techniques/adverse effects , Adolescent , Adult , Aged , Aged, 80 and over , Crohn Disease/complications , Drainage/methods , Female , Follow-Up Studies , Humans , Male , Middle Aged , Rectal Fistula/complications , Reoperation , Retrospective Studies , Young Adult
11.
Tech Coloproctol ; 14(3): 265-7, 2010 Sep.
Article in English | MEDLINE | ID: mdl-20585823

ABSTRACT

We report the case of a patient who developed a desmoid tumor following total proctocolectomy and J-pouch reconstruction that was unresponsive to any medical treatment. Based on estrogen receptor alpha (ERalpha) and progesterone receptor (PR) evaluation (ERalpha-negative, but PR-positive), treatment with mifepristone, a pure antiprogesterone drug, was initiated, and partial tumor regression was achieved.


Subject(s)
Adenomatous Polyposis Coli/surgery , Fibromatosis, Aggressive/drug therapy , Mifepristone/therapeutic use , Peritoneal Neoplasms/drug therapy , Vinblastine/therapeutic use , Adenomatous Polyposis Coli/diagnosis , Adult , Anastomosis, Surgical/methods , Disease Progression , Drug Therapy, Combination , Fatal Outcome , Fibromatosis, Aggressive/diagnosis , Humans , Imaging, Three-Dimensional , Male , Peritoneal Neoplasms/diagnostic imaging , Peritoneal Neoplasms/secondary , Proctocolectomy, Restorative/methods , Receptors, Progesterone/metabolism , Tomography, X-Ray Computed
12.
Epidemiol Psychiatr Sci ; 29: e153, 2020 Aug 12.
Article in English | MEDLINE | ID: mdl-32782057

ABSTRACT

AIMS: Epidemiological studies indicate that individuals with one type of mental disorder have an increased risk of subsequently developing other types of mental disorders. This study aimed to undertake a comprehensive analysis of pair-wise lifetime comorbidity across a range of common mental disorders based on a diverse range of population-based surveys. METHODS: The WHO World Mental Health (WMH) surveys assessed 145 990 adult respondents from 27 countries. Based on retrospectively-reported age-of-onset for 24 DSM-IV mental disorders, associations were examined between all 548 logically possible temporally-ordered disorder pairs. Overall and time-dependent hazard ratios (HRs) and 95% confidence intervals (CIs) were calculated using Cox proportional hazards models. Absolute risks were estimated using the product-limit method. Estimates were generated separately for men and women. RESULTS: Each prior lifetime mental disorder was associated with an increased risk of subsequent first onset of each other disorder. The median HR was 12.1 (mean = 14.4; range 5.2-110.8, interquartile range = 6.0-19.4). The HRs were most prominent between closely-related mental disorder types and in the first 1-2 years after the onset of the prior disorder. Although HRs declined with time since prior disorder, significantly elevated risk of subsequent comorbidity persisted for at least 15 years. Appreciable absolute risks of secondary disorders were found over time for many pairs. CONCLUSIONS: Survey data from a range of sites confirms that comorbidity between mental disorders is common. Understanding the risks of temporally secondary disorders may help design practical programs for primary prevention of secondary disorders.


Subject(s)
Mental Disorders/epidemiology , Adolescent , Adult , Aged , Comorbidity , Cross-Sectional Studies , Diagnostic and Statistical Manual of Mental Disorders , Female , Health Surveys , Humans , Male , Mental Disorders/classification , Middle Aged , Prevalence , Proportional Hazards Models , Psychotic Disorders/epidemiology , Retrospective Studies , Risk Factors , Young Adult
13.
Science ; 281(5383): 1674-7, 1998 Sep 11.
Article in English | MEDLINE | ID: mdl-9733514

ABSTRACT

The ATM protein, encoded by the gene responsible for the human genetic disorder ataxia telangiectasia (A-T), regulates several cellular responses to DNA breaks. ATM shares a phosphoinositide 3-kinase-related domain with several proteins, some of them protein kinases. A wortmannin-sensitive protein kinase activity was associated with endogenous or recombinant ATM and was abolished by structural ATM mutations. In vitro substrates included the translation repressor PHAS-I and the p53 protein. ATM phosphorylated p53 in vitro on a single residue, serine-15, which is phosphorylated in vivo in response to DNA damage. This activity was markedly enhanced within minutes after treatment of cells with a radiomimetic drug; the total amount of ATM remained unchanged. Various damage-induced responses may be activated by enhancement of the protein kinase activity of ATM.


Subject(s)
Carrier Proteins , DNA Damage , Protein Kinases/metabolism , Protein Serine-Threonine Kinases , Proteins/metabolism , Tumor Suppressor Protein p53/metabolism , Adaptor Proteins, Signal Transducing , Androstadienes/pharmacology , Ataxia Telangiectasia/metabolism , Ataxia Telangiectasia Mutated Proteins , Cell Cycle Proteins , Cell Line , DNA-Binding Proteins , Enzyme Inhibitors/pharmacology , Humans , Mutation , Phosphatidylinositol 3-Kinases/chemistry , Phosphoproteins/metabolism , Phosphorylation , Protein Kinase Inhibitors , Protein Kinases/chemistry , Proteins/antagonists & inhibitors , Proteins/chemistry , Proteins/genetics , Recombinant Proteins/metabolism , Tumor Cells, Cultured , Tumor Suppressor Proteins , Wortmannin , Zinostatin/pharmacology
14.
Science ; 268(5218): 1749-53, 1995 Jun 23.
Article in English | MEDLINE | ID: mdl-7792600

ABSTRACT

A gene, ATM, that is mutated in the autosomal recessive disorder ataxia telangiectasia (AT) was identified by positional cloning on chromosome 11q22-23. AT is characterized by cerebellar degeneration, immunodeficiency, chromosomal instability, cancer predisposition, radiation sensitivity, and cell cycle abnormalities. The disease is genetically heterogeneous, with four complementation groups that have been suspected to represent different genes. ATM, which has a transcript of 12 kilobases, was found to be mutated in AT patients from all complementation groups, indicating that it is probably the sole gene responsible for this disorder. A partial ATM complementary DNA clone of 5.9 kilobases encoded a putative protein that is similar to several yeast and mammalian phosphatidylinositol-3' kinases that are involved in mitogenic signal transduction, meiotic recombination, and cell cycle control. The discovery of ATM should enhance understanding of AT and related syndromes and may allow the identification of AT heterozygotes, who are at increased risk of cancer.


Subject(s)
Ataxia Telangiectasia/genetics , Chromosomes, Human, Pair 11 , Phosphotransferases (Alcohol Group Acceptor)/genetics , Protein Serine-Threonine Kinases , Proteins/genetics , Amino Acid Sequence , Ataxia Telangiectasia Mutated Proteins , Cell Cycle , Cell Cycle Proteins , Chromosome Mapping , Chromosomes, Artificial, Yeast , Cloning, Molecular , DNA, Complementary/genetics , DNA-Binding Proteins , Female , Genetic Complementation Test , Genetic Predisposition to Disease , Heterozygote , Humans , Male , Meiosis , Molecular Sequence Data , Neoplasms/genetics , Nucleic Acid Hybridization , Phosphatidylinositol 3-Kinases , Phosphotransferases (Alcohol Group Acceptor)/chemistry , Phosphotransferases (Alcohol Group Acceptor)/physiology , Proteins/chemistry , Proteins/physiology , Radiation Tolerance , Sequence Deletion , Signal Transduction , Tumor Suppressor Proteins
15.
Tech Coloproctol ; 13(3): 201-4, 2009 Sep.
Article in English | MEDLINE | ID: mdl-19609485

ABSTRACT

AIM: The study was conducted to investigate the differences in clinical-pathological, ethnic, and demographic presentations and the expression of mismatch repair proteins in a cohort of young-onset (50 years) with colorectal cancer. MATERIALS AND METHODS: Clinical, demographic, and histopathological data of patients with colorectal cancer were collected retrospectively from medical records and pathology reports. RESULTS: Ninety patients, 50 years of age or younger with a mean age of 42 years were compared with a group of 190 patients above 50 years of 50 (see Table 1). Sixty percent of the young-onset patients were females, compared to 40% in the older age group (P = 0.02). Twenty-one percent of the young-onset patients were Arabs as compared to 2% of older-onset patients (P = 0.001). Younger patients displayed a higher percentage of mucinous cancers and a higher percentage of diagnosis at an advanced stage of disease; 40% of young-onset versus 31% of older-onset patients presented Duke's stages C and D (P = 0.02). CONCLUSIONS: Younger age of onset colorectal cancer in our cohort of Israeli patients is associated with higher percentage of Arab patients, mucinous cancers, female gender, and advanced stage at diagnosis.


Subject(s)
Adenocarcinoma, Mucinous/epidemiology , Adenocarcinoma, Mucinous/pathology , Colorectal Neoplasms/epidemiology , Colorectal Neoplasms/pathology , Adenocarcinoma, Mucinous/therapy , Adolescent , Adult , Age Distribution , Age of Onset , Aged , Aged, 80 and over , Arabs/statistics & numerical data , Case-Control Studies , Chi-Square Distribution , Colorectal Neoplasms/therapy , Combined Modality Therapy , Female , Humans , Israel/epidemiology , Jews/statistics & numerical data , Male , Middle Aged , Neoplasm Staging , Probability , Prognosis , Retrospective Studies , Risk Assessment , Sex Distribution , Survival Analysis , Young Adult
16.
Rejuvenation Res ; 11(5): 903-13, 2008 Oct.
Article in English | MEDLINE | ID: mdl-18803478

ABSTRACT

Aging is often associated with a decline in hippocampus-dependent spatial memory. Here, we show that functional cell-mediated immunity is required for the maintenance of hippocampus-dependent spatial memory. Sudden imposition of immune compromise in young mice caused spatial memory impairment, whereas immune reconstitution reversed memory deficit in immune-deficient mice. Analysis of hippocampal gene expression suggested that immune-dependent spatial memory performance was associated with the expression of insulin-like growth factor (Igf1) and of genes encoding proteins related to presynaptic activity (Syt10, Cplx2). We further showed that memory loss in aged mice could be attributed to age-related attenuation of the immune response and could be reversed by immune system activation. Homeostatic-driven proliferation of lymphocytes, which expands the existing T cell repertoire, restored spatial memory deficits in aged mice. Thus, our results identify a novel function of the immune system in the maintenance of spatial memory and suggest an original approach for arresting or reversing age-associated memory loss.


Subject(s)
Aging/immunology , Aging/psychology , Memory Disorders/immunology , Aging/genetics , Animals , Base Sequence , Bone Marrow Transplantation/immunology , DNA Primers/genetics , Gene Expression , Hippocampus/immunology , Hippocampus/metabolism , Immunity, Cellular , Insulin-Like Growth Factor I/genetics , Male , Maze Learning/physiology , Memory Disorders/genetics , Memory Disorders/therapy , Mice , Mice, Inbred C57BL , Mice, SCID , Microglia/immunology , Nerve Tissue Proteins/genetics , Synaptotagmins/genetics
17.
Anxiety Stress Coping ; 31(4): 418-430, 2018 07.
Article in English | MEDLINE | ID: mdl-29649912

ABSTRACT

BACKGROUND AND OBJECTIVES: Posttraumatic stress disorder, a commonly researched mental health outcome associated with trauma, does not develop in the majority of survivors. More common trajectories of adaptation include resilience, and posttraumatic growth (PTG). The objectives of the current study were to: (1) describe posttrauma adaptation profiles in a sample of Israeli male military veterans (N = 448); and (2) to explore the protective factors that promote constructive PTG within two profiles of posttrauma adaptation. METHODS: The study used secondary data to estimate latent profile mixture models and a series of logistic regression analyses. RESULTS: Demographic controls, combat related variables, endorsement of coping strategies, and reports of improvement in social support were not significant predictors of constructive growth in the resilient class. However, those in the struggling growth subset of the sample who reported improvement in perceived social support increased the odds of reaching constructive growth. CONCLUSION: These findings highlight the importance of tailored clinical interventions that account for more complex profiles of posttrauma adaptation; and further, provide evidence that adaptation takes place over time. Finally, these findings call for future research to continue to explore the quality of PTG and the contexts in which protective factors promote positive adaptation.


Subject(s)
Adaptation, Psychological , Resilience, Psychological , Social Support , Stress Disorders, Post-Traumatic/psychology , Veterans/psychology , Adult , Humans , Israel , Male , Models, Psychological , Psychotherapy, Group , Stress Disorders, Post-Traumatic/therapy , Surveys and Questionnaires
18.
Cancer Res ; 49(9): 2495-501, 1989 May 01.
Article in English | MEDLINE | ID: mdl-2539904

ABSTRACT

Ataxia-telangiectasia (A-T) is a multisystem hereditary disease featuring neurodegeneration, immunodeficiency, extreme cancer proneness, chromosomal instability, and radiosensitivity. A-T is found in many ethnic groups, and is genetically heterogeneous: four complementation groups have been identified in A-T so far. Attempts to isolate the A-T gene are based in part on gene transfer experiments, using permanent A-T fibroblast lines, obtained by transformation with SV40. "Immortalization" of A-T primary diploid fibroblasts using SV40 is difficult, possibly because of the chromosomal instability of these cells. The number of currently available permanent A-T fibroblast lines is small, and not all of them have been assigned to specific complementation groups. Using the assay of X-ray induced inhibition of DNA synthesis, we have assigned the A-T strain AT22IJE to complementation group AB. Origin-defective SV40 was used to transfect these cells, and one transformant (AT22IJE-T), which survived crisis, was found to have the typical characteristics of permanent cell lines obtained in this way. "In-gel renaturation" analysis did not show any DNA amplification of high degree in AT22IJE-T. Cytogenetic analysis showed considerable chromosomal instability in the new cell line, and medium conditioned by these cells contained the clastogenic activity which is characteristic of the parental strain as well. Other parameters of the "cellular A-T phenotype" have also been retained in the immortalized cells: hypersensitivity to the lethal effects of X-rays and neocarzinostatin, as well as "radioresistant" DNA synthesis. However, the sensitivity of AT22IJE-T to both DNA-damaging agents is less pronounced than that of the parental cells. The capacity of the cells for uptake of foreign DNA was tested by introducing into them the plasmid pRSVneo, using three different transfection methods. Satisfactory frequency of G418-resistant transfectants (0.66%) was achieved using a protocol recently published by Chen and Okayama (Mol. Cell Biol., 7: 2745-2752, 1987), which was found to be superior to the traditional calcium phosphate transfection method and to the polybrene-based method.


Subject(s)
Ataxia Telangiectasia/genetics , Cell Line , Chromosome Aberrations , DNA/biosynthesis , DNA Damage , Gene Amplification , Humans , Karyotyping , Simian virus 40/genetics , Transfection
19.
Oncogene ; 15(2): 159-67, 1997 Jul 10.
Article in English | MEDLINE | ID: mdl-9244351

ABSTRACT

Ataxia-telangiectasia (A-T) is an autosomal recessive disorder characterized by neurodegeneration, immunodeficiency, cancer predisposition, genome instability and radiation sensitivity. The cellular phenotype of A-T points to defects in signal transduction pathways involved in activation of cell cycle checkpoints by free radical damage, and other pathways that mediate the transmission of specific mitogenic stimuli. The product of the responsible gene, ATM, belongs to a family of large proteins that contribute to maintaining genome stability and cell cycle progression in various organisms. A recombinant vector that stably expresses a full-length ATM protein is a valuable tool for its functional analysis. We constructed and cloned a recombinant, full-length open reading frame of ATM using a combination of vectors and hosts that overcame an inherent instability of this sequence. Recombinant ATM was stably expressed in insect cells using a baculovirus vector, albeit at a low level, and in human A-T cells using an episomal expression vector. An amino-terminal FLAG epitope added to the protein allowed highly specific detection of the recombinant molecule by immunoblotting, immunoprecipitation and immunostaining, and its isolation using immunoaffinity. Similar to endogenous ATM, the recombinant protein is located mainly in the nucleus, with low levels in the cytoplasm. Ectopic expression of ATM in A-T cells restored normal sensitivity to ionizing radiation and the radiomimetic drug neocarzinostatin, and a normal pattern of post-irradiation DNA synthesis, which represents an S-phase checkpoint. These observations indicate that the recombinant, epitope-tagged protein is functional. Introduction into this molecule of a known A-T missense mutation, Glu2904Gly, resulted in apparent instability of the protein and inability to complement the A-T phenotype. These findings indicate that the physiological defects characteristic of A-T cells result from the absence of the ATM protein, and that this deficiency can be corrected by ectopic expression of this protein.


Subject(s)
Protein Serine-Threonine Kinases , Proteins/physiology , Animals , Ataxia Telangiectasia Mutated Proteins , Cell Cycle Proteins , Cell Line , Cloning, Molecular , DNA-Binding Proteins , Humans , Mutation , Open Reading Frames , Phenotype , Protein Biosynthesis , Proteins/analysis , Rabbits , Recombinant Proteins/analysis , Recombinant Proteins/biosynthesis , Spodoptera , Tumor Suppressor Proteins
20.
Am J Med Genet ; 43(6): 989-95, 1992 Aug 01.
Article in English | MEDLINE | ID: mdl-1415350

ABSTRACT

The Weissenbacher-Zweymüller syndrome (WZS) is defined as congenital neonatal rhizomelic dwarfism with metaphyseal widening of the long bones and vertebral coronal clefts. Catch-up growth after 2-3 years is one of the striking manifestations. It is generally thought that WZS is a neonatal expression of the Stickler syndrome, even though in the latter, myopia, retinal detachment and a progressive metaphyseal dysplasia are characteristics that are not found in WZS. A critical analysis of all published patients with WZS in addition to 5 patients in 3 new families, shows that the WZS is a distinct syndrome of delayed skeletal maturation, different from the Stickler syndrome, and inherited as an autosomal recessive trait. The recognition of its unique characteristics has important implications in genetic counseling.


Subject(s)
Bone Diseases, Developmental/genetics , Dwarfism/genetics , Bone Diseases, Developmental/congenital , Child , Child, Preschool , Dwarfism/congenital , Female , Genes, Recessive , Humans , Male , Phenotype , Syndrome
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