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This article discusses the variables that affect the diagnostic process in patients with a compromised dentition and addresses the clinical decision of whether to extract or maintain teeth. A decision tree algorithm is proposed to guide clinicians in planning complete arch rehabilitations.
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Importance: Obstructive sleep apnea (OSA) is a common condition in older adult (aged >65 years) populations, but more mechanistic research is needed to individualize treatments. Previous evidence has suggested an association between OSA and posttraumatic stress disorder (PTSD) but is limited by possible selection bias. High-quality research on this association with a careful evaluation of possible confounders may yield important mechanistic insight into both conditions and improve treatment efforts. Objective: To investigate the association of current PTSD symptoms and PTSD diagnosis with OSA. Design, Setting, and Participants: This cross-sectional study of twin pairs discordant for PTSD, which allows for adjustment for familial factors, was conducted using in-laboratory polysomnography from March 20, 2017, to June 3, 2019. The study sample comprised male veteran twins recruited from the Vietnam Era Twin Registry. The data analysis was performed between June 11, 2022, and January 30, 2023. Exposure: Symptoms of PTSD in twins who served in the Vietnam War. Diagnosis of PTSD was a secondary exposure. Main Outcomes and Measures: Obstructive sleep apnea was assessed using the apnea-hypopnea index (AHI) (≥4% oxygen saturation criterion as measured by events per hour) with overnight polysomnography. Symptoms of PTSD were assessed using the PTSD Checklist (PCL) and structured clinical interview for PTSD diagnosis. Results: A total of 181 male twins (mean [SD] age, 68.4 [2.0] years) including 66 pairs discordant for PTSD symptoms and 15 pairs discordant for a current PTSD diagnosis were evaluated. In models examining the PCL and OSA within pairs and adjusted for body mass index (BMI) and other sociodemographic, cardiovascular, and psychiatric risk factors (including depression), each 15-point increase in PCL was associated with a 4.6 (95% CI, 0.1-9.1) events-per-hour higher AHI. Current PTSD diagnosis was associated with an adjusted 10.5 (95% CI, 5.7-15.3) events-per-hour higher AHI per sleep-hour. Comparable standardized estimates of the association of PTSD symptoms and BMI with AHI per SD increase (1.9 events per hour; 95% CI, 0.5-3.3 events per hour) were found. Conclusions and Relevance: This cross-sectional study found an association between PTSD and sleep-disordered breathing. The findings have important public health implications and may also enhance understanding of the many factors that potentially affect OSA pathophysiology.
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Apnea Obstructiva del Sueño , Trastornos por Estrés Postraumático , Veteranos , Humanos , Trastornos por Estrés Postraumático/epidemiología , Masculino , Apnea Obstructiva del Sueño/epidemiología , Estudios Transversales , Anciano , Veteranos/estadística & datos numéricos , Veteranos/psicología , Persona de Mediana Edad , Guerra de Vietnam , Polisomnografía , Enfermedades en Gemelos/epidemiología , GemelosRESUMEN
BACKGROUND: Individuals with posttraumatic stress disorder (PTSD) face an increased risk of cardiovascular disease, but the mechanisms linking PTSD to cardiovascular disease remain incompletely understood. We used a co-twin control study design to test the hypothesis that individuals with PTSD exhibit augmented peripheral and systemic vasoconstriction during a personalized trauma recall task. METHODS: In 179 older male twins from the Vietnam Era Twin Registry, lifetime history of PTSD and current (last month) PTSD symptoms were assessed. Participants listened to neutral and personalized trauma scripts while peripheral vascular tone (Peripheral Arterial Tone ratio) and systemic vascular tone (e.g., total vascular conductance) were measured. Linear mixed-effect models were used to assess the within-pair relationship between PTSD and vascular tone indices. RESULTS: The mean age of participants was 68 years, and 19% had a history of PTSD. For the Peripheral Arterial Tone ratio analysis, 32 twins were discordant for a history of PTSD, and 46 were discordant for current PTSD symptoms. Compared with their brothers without PTSD, during trauma recall, participants with a history of PTSD had greater increases in peripheral (ß = -1.01, 95% CI [-1.72, -0.30]) and systemic (total vascular conductance: ß = -1.12, 95% CI [-1.97, -0.27]) vasoconstriction after adjusting for cardiovascular risk factors. Associations persisted after adjusting for antidepressant medication use and heart rate and blood pressure during the tasks. Analysis of current PTSD symptom severity showed consistent results. CONCLUSIONS: PTSD is associated with exaggerated peripheral and systemic vasoconstrictor responses to traumatic stress reminders, which may contribute to elevated risk of cardiovascular disease.
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Recuerdo Mental , Trastornos por Estrés Postraumático , Vasoconstricción , Humanos , Masculino , Trastornos por Estrés Postraumático/fisiopatología , Vasoconstricción/fisiología , Recuerdo Mental/fisiología , Anciano , Persona de Mediana Edad , Sistema de RegistrosRESUMEN
BACKGROUND: Autonomic function can be measured noninvasively using heart rate variability (HRV), which indexes overall sympathovagal balance. Deceleration capacity (DC) of heart rate is a more specific metric of vagal modulation. Higher values of these measures have been associated with reduced mortality risk primarily in patients with cardiovascular disease, but their significance in community samples is less clear. METHODS AND RESULTS: This prospective twin study followed 501 members from the VET (Vietnam Era Twin) registry. At baseline, frequency domain HRV and DC were measured from 24-hour Holter ECGs. During an average 12-year follow-up, all-cause death was assessed via the National Death Index. Multivariable Cox frailty models with random effect for twin pair were used to examine the hazard ratios of death per 1-SD increase in log-transformed autonomic metrics. Both in the overall sample and comparing twins within pairs, higher values of low-frequency HRV and DC were significantly associated with lower hazards of all-cause death. In within-pair analysis, after adjusting for baseline factors, there was a 22% and 27% lower hazard of death per 1-SD increment in low-frequency HRV and DC, respectively. Higher low-frequency HRV and DC, measured during both daytime and nighttime, were associated with decreased hazard of death, but daytime measures showed numerically stronger associations. Results did not substantially vary by zygosity. CONCLUSIONS: Autonomic inflexibility, and especially vagal withdrawal, are important mechanistic pathways of general mortality risk, independent of familial and genetic factors.
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Veteranos , Humanos , Bradicardia , Desaceleración , Electrocardiografía Ambulatoria , Frecuencia Cardíaca/fisiología , Estudios ProspectivosRESUMEN
Fundamento: La depresión mayor (DM) y el trastorno de estrés postraumático (TEPT) se caracterizan por su elevada comorbilidad. No se ha cuantificado el grado hasta el cual una predisposición genética común explica la etiología de su asociación y tiene importantes implicaciones para la investigación y la prevención. Métodos: Este artículo presenta un análisis de los datos de 6.744 miembros del Vietnam Era Twin Registry. La DM y el TEPT se evaluaron mediante el Diagnostic Interview Schedule-III-R en 19911992. Se efectuó un modelado bivariante de gemelos para determinar la etiología genética y ambiental de la asociación DM-TEPT. Resultados: El modelo con el mejor ajuste de la asociación DM-TEPT incluyó una correlación genética sustancial (r = 0,77; IC95%, 0,50-1,00) y una correlación modesta ambiental específica individual (r = 0,34; IC del 95%, 0,190,48). Una predisposición genética común explicó el 62,5% de la comorbilidad DM-TEPT. Las influencias genéticas comunes a la DM explicaron el 15% de la varianza total en el riesgo de TEPT y el 58% de la varianza genética en el TEPT. Las influencias ambientales específicas individuales comunes a la DM solo explicaron el 11% de la varianza ambiental individual específica en el TEPT. Limitaciones: Los participantes del presente estudio eran veteranos de la guerra de Vietnam y los hallazgos no pueden generalizarse a civiles, mujeres u otras cohortes. Conclusiones: La comorbilidad DM-TEPT se explica en gran parte por influencias genéticas comunes. La superposición genética sustancial entre ambos implica que los genes involucrados en la etiología de la DM son potentes candidatos para el TEPT y al contrario. Las influencias ambientales en ambos explican un menor grado su covariación y parecen ser en su mayor parte específicas de trastorno. Se requiere más investigación para identificar los factores ambientales que influyen en el desarrollo de la DM comparado con el TEPT en el contexto de una predisposición genética común (AU)
Background: Major depression (MD) and posttraumatic stress disorder (PTSD) are highly comorbid. The degree to which a common genetic liability explains the etiology of the MD-PTSD association has not been quantified and has important implications or research and prevention. Methods: This paper presents an analysis of data from 6744 members of the Vietnam Era Twin Registry. MD and PTSD were assessed using the Diagnostic Interview Schedule-III-R in 199192. Bivariate twin modeling was conducted to determine the genetic and environmental etiology of the MD-PTSD association. Results: The best-fitting model for the MD-PTSD association included a substantial genetic correlation (r = 77; 95% CI, .501.00) and a modest individual-specific environmental correlation (r = .34; 95% CI, .1948). Common genetic liability explained 62.5% of MD-PTSD comorbidity. Genetic influences common to MD explained 15% of the total variance in risk for PTSD and 58% of the genetic variance in PTSD. Individual-specific environmental influences common to MD explained only 11% of the individualspecific environmental variance in PTSD. Limitations: Our participants were male Vietnam era veterans and our findings may not generalize to civilians, females or other cohorts. Conclusions: MD-PTSD comorbidity is largely explained by common genetic influences. Substantial genetic overlap between MD and PTSD implies that genes implicated in the etiology of MD are strong candidates for PTSD and vice versa. Environmental influences on MD and PTSD explain less of their covariation and appear to be largely disorder-specific. Research is needed to identify environmental factors that influence the development of MD versus PTSD in the context of common genetic liability (AU)