scholarly journals Clinical Characteristics Associated With Stuttering Persistence: A Meta-Analysis

2020 ◽  
Vol 63 (9) ◽  
pp. 2995-3018
Author(s):  
Cara M. Singer ◽  
Alison Hessling ◽  
Ellen M. Kelly ◽  
Lisa Singer ◽  
Robin M. Jones

Purpose The purpose of this meta-analytic study was to identify clinical characteristics, defined as child factors that can be assessed by a speech-language pathologist as part of a routine speech-language evaluation that may differentiate children who persist in stuttering from children who eventually recover from stuttering. Clinical characteristics explored included sex, age at onset, family history of stuttering, stuttering frequency and severity, speech-language skills, and temperament. Method Studies were identified through electronic databases, journals, and reference lists of relevant reports (e.g., research articles). Eligible studies followed young children who stutter (i.e., under 6 years old) for at least 24 months, assessed a potential clinical marker at study entry, and determined talker group classification (i.e., persistent or recovered) at study completion. Sex and family history differences were estimated using risk ratios; all other differences were estimated using Hedges's g . Heterogeneity and methodological differences among studies were evaluated. Results Eleven studies (41 reports) met eligibility criteria. Persistent children were older at stuttering onset and exhibited higher frequencies of stuttering-like disfluencies, lower speech sound accuracy, and lower expressive and receptive language skills than recovered children. Males and children with a family history of stuttering were also more likely to persist. Conclusions Clinical characteristics were identified that are associated with increased risk for stuttering persistence. Future studies have the potential to translate these clinical characteristics into prognostic markers for stuttering persistence risk.

2020 ◽  
Vol 38 (15_suppl) ◽  
pp. e16729-e16729
Author(s):  
Bara El Kurdi ◽  
Adam Bataineh ◽  
Sumbal Babar ◽  
Mahmoud El Iskandarani ◽  
Mohammad Alomari ◽  
...  

e16729 Background: Pancreatic adenocarcinoma (PADC) remains one of the most fatal malignancies with poor outcomes and prognosis. Several risk factors have been associated with its development such as smoking, age, obesity, chronic pancreatitis, diabetes mellitus and a family history of PADC. Furthermore, recent pathologic studies demonstrated that fatty infiltration of the pancreas (FP) is positively correlated with PADC development. We sought to systematically review the literature and perform the first meta-analysis to study the risk of PADC among patients with FP. Methods: We conducted a systematic search of the Pubmed, EMBASE, and Cochrane databases from inception through November-2019 for studies correlating FP with PADC. Relevant data was extracted and analyzed using comprehensive meta-analysis software. Random-effects model was used for all variables. Heterogeneity was assessed using the I2 measure and Cochrane Q-statistic. Publication bias was assessed using Egger’s test. Meta regression models accounting for independent variables such as age, sex, smoking, family history of PADC, chronic pancreatitis and method of FP diagnosis were constructed to explain heterogeneity. Results: Five observational case-control studies published between 2014 and 2019 including a total of 761 patients (320 PADC patients and 441 controls) were included. FP was associated with increased PADC with an OR 4.6 (CI 2.4-8.9) compared to controls with a considerable heterogeneity (I2= 69%). Meta regression analysis accounting for modality used to diagnose FP was able to explain 100% of the noted heterogeneity. Conclusions: While we noted FP to be significantly associated with increased PADC, heterogeneity in FP diagnostic approach resulted in significant inter-study variation. A consensus on a clear definition of FP with a standardized diagnostic approach is needed to better appraise literature on this emerging disease entity. Further prospective studies are needed to validate our results and explore the possible role for PADC screening in FP in addition to known factors such as family history and new-onset diabetes mellitus.


2018 ◽  
Vol 2018 ◽  
pp. 1-7 ◽  
Author(s):  
Wei Di ◽  
Zhiyong Zeng ◽  
Jingyan Li ◽  
Xiaoling Liu ◽  
Minzhi Bo ◽  
...  

Numerous studies have investigated the relationship between theLRRK2G2385R variant and clinical characteristics in Parkinson’s disease (PD), but the results have been inconsistent. This study investigated whether theLRRK2G2385R variant was associated with a unique clinical phenotype of PD in the Asian population, using a meta-analysis. The PubMed, Web of Science, EMBASE, CNKI, and WANFANG databases were searched until September 2017. The strict selection criteria and exclusion criteria were determined, and mean differences (MD) or odds ratios (OR) with 95% confidence intervals (CI) were used to assess the strength of associations. Statistical analyses and graphics were performed using Review Manager 5.3. Sixteen related case-control studies were included in the meta-analysis. TheLRRK2G2385R carriers significantly more often presented a family history (OR: 1.98; 95% CI: 1.16−3.39;P=0.01) and had a longer disease duration (MD = 0.47, 95% CI: 0.01−0.93,P=0.04) and a higher MMSE score (MD = 1.02, 95% CI: 0.43–1.62P=0.0007) thanLRRK2G2385R noncarriers. There were no significant differences in sex distribution, age at onset, initial symptoms, motor symptoms, depression, levodopa-equivalent dose, and related complications betweenLRRK2G2385R-carrier andLRRK2G2385R-noncarrier PD patients. Our results suggested that most of the clinical characteristics of PD patients withLRRK2G2385R mutations are similar to those ofLRRK2G2385R noncarriers among Asian PD patients, except for the more common family history, relatively longer disease duration, and higher MMSE scores in the former group.


2010 ◽  
Vol 120 (1-3) ◽  
pp. 121-130 ◽  
Author(s):  
Michelle L. Esterberg ◽  
Hanan D. Trotman ◽  
Carrie Holtzman ◽  
Michael T. Compton ◽  
Elaine F. Walker

Author(s):  
Pattara Rattanawong ◽  
Jakrin Kewcharoen ◽  
Chanavuth Kanitsoraphan ◽  
Timothy Barry ◽  
Anusha Shanbhag ◽  
...  

Background Brugada syndrome is an inherited cardiac channelopathy associated with major arrhythmic events (MAEs). The presence of a positive family history of sudden cardiac death (SCD) as a risk predictor of MAE remains controversial. We aimed to examine the association between family history of SCD and MAEs stratified by age of SCD with a systematic review and meta‐analysis. Methods and Results We searched the databases of MEDLINE and EMBASE from January 1992 to January 2020. Data from each study were combined using the random‐effects model. Fitted metaregression was performed to evaluate the association between the age of SCD in families and the risk of MAE. Twenty‐two studies from 2004 to 2019 were included in this meta‐analysis involving 3386 patients with Brugada syndrome. The overall family history of SCD was not associated with increased risk of MAE in Brugada syndrome (pooled odds ratio [OR], 1.11; 95% CI, 0.82–1.51; P =0.489, I 2 =45.0%). However, a history of SCD in family members of age younger than 40 years of age did increase the risk of MAE by ≈2‐fold (pooled OR, 2.03; 95% CI, 1.11–3.73; P =0.022, I 2 =0.0%). When stratified by the age of cut point at 50, 45, 40, and 35 years old, a history of SCD in younger family member was significantly associated with a higher risk of MAE (pooled OR, 0.49, 1.30, 1.51, and 2.97, respectively; P =0.046). Conclusions A history of SCD among family members of age younger than 40 years was associated with a higher risk of MAE.


2020 ◽  
Vol 79 (Suppl 1) ◽  
pp. 1205-1206
Author(s):  
T. Arkachaisri ◽  
K. L. Teh ◽  
Y. X. Book ◽  
L. Das

Background:ERA is the most common Juvenile Idiopathic Arthritis (JIA) subtype in Singapore (1), but less common in the West. Clinical characteristics and treatment of ERA in the region is not well-described thus impede the diagnosis and management plan which could lead to poorer outcomes.Objectives:To describe the clinical characteristics, joint manifestation and treatment of ERA in a large monocentric cohort in Singapore over 10-year periodMethods:Children diagnosed with ERA according to ILAR criteria with a minimum follow-up of 3-month duration were recruited from our registry, from 2009 to 2019, at KK Women’s and Children’s Hospital, Singapore. Nonparametric descriptive statistics including median (IQR) were used to described data. Kaplan-Meier survival analyses were used to estimate the probability of ever sacroiliitis development. Multivariate logistic and Cox regression analyses were used to determine predictors as appropriate. The significant level was set at < 0.05.Results:A cohort of 147 ERA out of 439 JIA patients (male 88%; Chinese 80%) were included. Median age at onset was 11.9 yrs (IQR9.4-14.0) and disease duration was 6.0 yrs (3.1-8.9). Median lag period was 2.9 mo (1.2-7.4). Family history of HLA-B27 related diseases was positive at 8%. Acute uveitis occurred only 3%. Joint distribution at diagnosis and cumulative involvement were shown in Fig 1. Hip, sacroiliac and knee were the three most common joints involved. 24% presented with enthesitis and Achilles tendon enthesis were the most common. Majority presented with pauciarthritis (84%) while 12% of patients had no peripheral joint involvement. 40% of patients presented with sacroiliitis (SIs) with 59% had bilateral involvement. Median duration to develop SIs was 7.6 mo (IQR 2.0-26.9). Probability of SIs development was 36%, 55% and 70% at 1, 5 and 10 yrs after onset, respectively. Interestingly, neg HLA-B27, female and older age at onset predicted SIs (p=0.001-0.044). Hip arthritis increased (p=0.043) but tarsitis decreased (p=0.031) the risk of SIs. Again, female, hip arthritis at diagnosis and neg HLA-B27 had a shorter time to SIs (p=0.004-0.007). Fig 2 showed medication used in our ERA cohort. Methotrexate (MTX) remained the most common DMARD used. However, 76% required anti-TNF therapy (aTNF) due to MTX failure. For SIs patients, 86% were on MTX but 85% of these, as compared to patients without axial disease, 60%, failed MTX. Only 10% of patients had aTNF without MTX.Fig 1.Proportion of joint involvement at onset and cumulative involvement during the course of disease (%)Fig 2.Proportion of medications used in ERA cohort during the course of disease (%)Conclusion:Our ERA cohort had less uveitis and family history of HLA-B27 associated diseases, but comparable gender and age at onset as compared to reports elsewhere(2). Up to 40% of our patients presented with SIs and/or enthesitis. Majority of SIs developed within the first 5 yrs (88%) for which over one-half developed within the first year. When considering only ERA patients, interestingly that female, neg HLA-B27 and older age increased risk of SIs development. 77% of patients were treated with MTX, but 76% of the patients required aTNF later. As for SIs, concurred with adult AS data, 85% failed MTX. About one-half of non-axial disease patients failed MTX which is less response rate as compared to other JIA subtypes.References:[1]Arkachaisri T, Tang SP, Daengsuwan T, Phongsamart G, Vilaiyuk S, Charuvanij S, et al. Paediatric rheumatology clinic population in Southeast Asia: are we different? Rheumatology. 2017;56(3):390-8.[2]Mistry RR, Patro P, Agarwal V, Misra DP. Enthesitis-related arthritis: current perspectives. Open access rheumatology: research and reviews. 2019;11:19-31.Disclosure of Interests:None declared


2001 ◽  
Vol 16 (3) ◽  
pp. 151-156 ◽  
Author(s):  
F. Limosin ◽  
P. Gorwood ◽  
J. Adès

SummaryPresence of a family history of alcoholism may predict clinical characteristics in affected subjects, such as an earlier age at onset. More frequent and severe social maladjustment and somatic complications are also regularly cited for familial alcoholism, although subject to many other confusing factors. We analysed the clinical specificities of 79 alcohol-dependent inpatients according to the absence versus presence of family history of alcoholism.Patients were evaluated for lifetime psychiatric morbidity with the Diagnostic Interview for Genetic Studies (DIGS), for somatic complications with a systematic screening list, and first-degree relatives (N  =  428) were assessed with the Family Inventory Schedule and Criteria (FISC).Age at onset and social complications were predicting familial versus sporadic alcoholism, even when considering censored data and/or interaction between variables. But differences became non-significant when excluding patients with antisocial personality.If age at onset effectively appears to be the most informative characteristic for predicting familial versus sporadic alcoholism, it seems that it may be necessary in future studies to systematically take into account antisocial personality diagnosis, because of a probable contamination.


2018 ◽  
Author(s):  
◽  
Angela Maria Haeny

[ACCESS RESTRICTED TO THE UNIVERSITY OF MISSOURI AT AUTHOR'S REQUEST.] Extensive research provides evidence that people with a family history of alcoholism are at risk for developing alcohol use disorder (AUD). Similarly, people with impulsivity-related traits are at increased risk for developing alcohol problems. Importantly, research suggests that impulsivity mediates the relation between family history of alcoholism and the development of alcohol problems. However, impulsivity is a heterogenous construct and has been assessed with a myriad of measures. The present work is a quantitative synthesis of the literature on the relation between family history of alcoholism and impulsivity-related traits and that also examines various potential moderators of this association. Sixty-nine independent effect sizes from 65 studies (N = 11,127) qualified for the meta-analysis. The overall effect size was small-to-moderate (d = .32 [95% CI: 0.25, 0.39], k = 69), and was moderated by offspring age (Z = 3.73, p less than .001), with the effect size increasing with age. When examining specific facets of impulsivity, a small effect was found for harm avoidance (d = -.26 [95% CI: -.41, -.11], k = 10) and was moderated by family history density (Q (1) = 4.12, p = .04) such that the effect was much larger among those with more than one alcoholic family member (d = -.66 [95% CI: -1.10, -.22], k = 3). A small-to-moderate effect size was found for sensation seeking (d = .30 [95% CI: .21, .40], k = 29) and was moderated by age (Z = 3.09, p = .002), with the effect increasing with age. The effect sizes for all other facets of impulsivity were not significant. Notably, there were much fewer studies investigating other facets of impulsivity (e.g., reward dependence, lack of perseverance, lack of planning) compared to sensation seeking, limiting power to detect larger effect sizes. Findings from this review suggest the need for additional studies investigating the relation between specific facets of impulsivity (e.g., positive and negative urgency) and family history of alcoholism. In addition, this review suggests that, to some degree, we can identify phenotypic risk beyond mere family history status and, thus, inform the development of interventions for individuals with a family history of alcoholism, targeting the specific types of impulsivity manifested.


1988 ◽  
Vol 152 (4) ◽  
pp. 460-465 ◽  
Author(s):  
Miron Baron ◽  
Rhoda Gruen

The association between the familial risk for schizophrenia and season of birth was studied in 88 schizophrenic patients. An increased risk for schizophrenia and ‘spectrum’ disorders was demonstrated among the first-degree relatives of winter and spring-born schizophrenic patients. However, patients with a family history of schizophrenia and ‘spectrum’ disorders did not differ from patients with no family history with respect to season of birth. Season of birth was unrelated to the sex of the patient, birth order, age at onset, or clinical subtypes (paranoid vs non-paranoid, as defined by the RDC, and ‘narrow’ vs ‘broad’, as defined by Taylor & Abrams' 1975 criteria). The morbid-risk data support a ‘stress-diathesis' hypothesis whereby environmental factors (in this case a seasonally varying viral insult may be implicated) interact with genetic vulnerability to increase the risk for schizophrenia.


2010 ◽  
Vol 21 (12) ◽  
pp. 2287-2293 ◽  
Author(s):  
Janneke A. Wilschut ◽  
J. Dik F. Habbema ◽  
Scott D. Ramsey ◽  
Rob Boer ◽  
Caspar W. N. Looman ◽  
...  

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