scholarly journals Estimating the cumulative risk of postnatal depressive symptoms: the role of insomnia symptoms across pregnancy

Author(s):  
Johanna T. Pietikäinen ◽  
Tommi Härkänen ◽  
Päivi Polo-Kantola ◽  
Hasse Karlsson ◽  
Tiina Paunio ◽  
...  

Abstract Purpose Insomnia symptoms during late pregnancy are a known risk for postnatal depressive symptoms (PDS). However, the cumulative effect of various risk factors throughout pregnancy has not been explored. Our aim was to test how various insomnia symptoms (sleep latency, duration, quality, frequent night awakenings, early morning awakenings) and other risk factors (e.g., history of depression, symptoms of depression and anxiety, as well as sociodemographic factors) in early, mid-, and late pregnancy predict PDS. Methods Using data from the FinnBrain Birth Cohort Study and logistic regression analyses, we investigated the associations of distinct insomnia symptoms at gw 14, 24, and 34 with depressive symptoms (Edinburgh Postnatal Depression Scale score ≥ 11) 3 months postnatally. We also calculated separate and combined predictive models of PDS for each pregnancy time point and reported the odds ratios for each risk group. Results Of the 2224 women included in the study, 7.1% scored EPDS ≥ 11 3 months postnatally. Our predictive models indicated that sleep latency of ≥ 20 min, anxiety in early pregnancy, and insufficient sleep during late pregnancy predicted the risk of PDS. Furthermore, we found highly elevated odds ratios in early, mid-, and late pregnancy for women with multiple PDS risk factors. Conclusion Screening of long sleep latency and anxiety during early pregnancy, in addition to depression screening, could be advisable. Odds ratios of risk factor combinations demonstrate the magnitude of cumulating risk of PDS when multiple risk factors are present.

SLEEP ◽  
2021 ◽  
Vol 44 (Supplement_2) ◽  
pp. A259-A259
Author(s):  
Kathleen O’Hora ◽  
Mateo Lopez ◽  
Allison Morehouse ◽  
Andrea Cordero ◽  
Raquel Osorno ◽  
...  

Abstract Introduction The COVID-19 Pandemic and mitigation efforts have led to drastic increases in acute insomnia symptoms, which left untreated may contribute to increased risk for other negative mental health outcomes, including depression. However, the impact of treating acute insomnia symptoms on future depression outcomes remains unknown. Moreover, whether sleep improvements as a result of an insomnia treatment mediate subsequent reduction of depression symptoms similarly remains unknown. Methods At this writing, 44 individuals experiencing insomnia symptoms (Insomnia Severity Index; ISI ≥ 10) that began during the COVID-19 pandemic have been randomized to receive a brief, telehealth Cognitive Behavioral Therapy for Insomnia (CBTI) waitlist control. Treatment was delivered in 4 sessions over a 5-week period. CBTI is the gold-standard behavioral intervention for chronic insomnia and has been applied successfully via telemedicine. Outcome measures were depressive symptoms as measured by the Patient Health Questionnare-9 (PHQ-9) minus the sleep item and insomnia symptom severity as measured by the ISI. Both outcome measures were collected at baseline (week 0), throughout treatment phase (weeks 2–6), and at the post-treatment (week 7). Linear mixed models determined the impact of treatment on depression and insomnia symptom severity. Mediation was tested using the MacArthur framework. Results There was a significant Group x Time interaction, with CBTI leading to a greater rate of improvement in ISI (b = -1.14, p < 0.001) and PHQ-9 (b = -0.61, p = 0.002) than the control. Critically, the rate of improvement in insomnia symptoms to the last session of treatment, was associated with the subsequent improvement in depressive symptoms post-treatment (b = 2.06, p = 0.017). In contrast, depressive symptom improvement was not associated with insomnia symptom improvement (b = 4.28, p = 0.102). Conclusion This preliminary data suggests that brief CBTI can reduce pandemic onset insomnia and other depressive symptoms. The preliminary mediation results further suggest that sleep may be an important treatment target for reducing situational depressive symptoms and supports the need to examine the physiological mechanisms of sleep using high-density EEG in a larger sample. Support (if any):


SLEEP ◽  
2021 ◽  
Vol 44 (Supplement_2) ◽  
pp. A73-A73
Author(s):  
Pablo Soto ◽  
Joseph Dzierzewski ◽  
Mayra Ramos ◽  
Natalie Dautovich ◽  
Rosalie Corona

Abstract Introduction An individual’s culture presents unique risk and protective factors related to sleep outcomes. Similarly, emerging adulthood also represents a unique developmental period as it relates to sleep. The study of cultural factors during emerging adulthood is critical for better understanding the development of sleep dysfunction in vulnerable segments of the population. The present study investigated the association between perceived discrimination and insomnia symptoms in Latinx emerging adults. We hypothesized that perceived discrimination would result in higher insomnia symptom presentation above and beyond anxiety and depressive symptoms. Methods Participants included 198 (73.7% female; mean age=18.96) college-aged individuals self-identifying as Hispanic/Latinx who completed an online survey that assessed perceived racial/ethnic discrimination (Everyday Discrimination Scale; EDS), anxiety symptoms (General Anxiety Disorder Scale; GAD-7), depression symptoms (Patient Health Questionnaire; PHQ-9), and insomnia symptoms (Insomnia Severity Index; ISI). A three-block hierarchical regression was used to assess the impact of perceived discrimination on the presentation of insomnia symptomology above and beyond demographic characteristics and anxiety and depressive symptoms. Results The final model significantly predicted insomnia symptom presentation, F(5, 191)=26.379, p<.001, R2=.408. When age and gender identity were entered into the model they did not significantly predict insomnia symptoms F(2, 194)=.199, p=.82, R2=.002. Blocks 2, anxiety and depression symptoms (∆R2=.388), and 3, perceived discrimination (∆R2=.018), accounted for significant change in variance. In the final model, perceived discrimination significantly predicted insomnia symptoms (β=.151) above and beyond age (β=.016), gender identity (β= -.085), anxiety (β= -.075), and depression (β=.621). Conclusion Results suggest that discrimination among Hispanic/Latinx emerging adults is a unique contributor that may explain some of the higher prevalence rates of insomnia symptomology in this segment of the population. As such, it would be beneficial to tailor existing approaches aimed at improving sleep outcomes by accounting for stressors that could result from or influence discrimination against the individual and incorporate other cultural factors into treatment protocols. Support (if any) National Institute on Aging (K23AG049955, PI: Dzierzewski).


2019 ◽  
Vol 38 (7) ◽  
pp. 545-567
Author(s):  
Hanne N⊘rr Fentz ◽  
Marianne Simonsen ◽  
Tea Trillingsgaard

Introduction: Paternal postnatal depression has significant negative consequences for the family and child. Still, only little attention has been paid to potential unique risk factors of depression in fathers and the theoretical grounding of such research is sparse. Method: This study examined prenatal risk factors derived from three theoretical models: the cognitive vulnerability-stress model, the interpersonal model, and the gender role risk model of paternal postnatal depression. The sample consisted of 211 expectant fathers, of whom 5.7% scored above the clinical cut-off on the Edinburgh Postnatal Depression Scale, and 235 mothers were included as a reference group. Participants filled in questionnaires during pregnancy and four months postpartum. Results: The study results suggest that prenatal depressive score is the strongest risk factor for both paternal and maternal postnatal depressive symptoms. In addition, childhood separation from parents, unemployment, financial strain, and doubts about having the child were unique risk factors for paternal depressive symptoms, while lower marital satisfaction was a unique risk factor for maternal depression. Discussion: These findings highlight that beyond the strong role of prenatal depressive symptoms for both genders, specific risk factors for father depression exist. This may be informative to health care professionals in increasing the reach and prevention of depression in new fathers.


2019 ◽  
Vol 249 ◽  
pp. 371-377 ◽  
Author(s):  
Deborah Da Costa ◽  
Coraline Danieli ◽  
Michal Abrahamowicz ◽  
Kaberi Dasgupta ◽  
Maida Sewitch ◽  
...  

Circulation ◽  
2012 ◽  
Vol 125 (suppl_10) ◽  
Author(s):  
Michael A Grandner ◽  
Pinyo Rattanaumpawan ◽  
Michael L Perlis ◽  
Philip R Gehrman ◽  
Nicholas J Jackson ◽  
...  

Introduction: Insomnia is a highly prevalent sleep disorder known to independently affect the onset, course, and response to treatment for a number of psychiatric disorders. In particular, insomnia is associated with neuroendocrine stress system changes. Less is known about medical risks, though recent evidence implicates insomnia in hypertension, metabolic dysregulation, and inflammation. We hypothesized that insomnia is positively associated with hypertension and objectively-assessed risk factors. Methods: Data from the 2007-2008 NHANES (N=4,072) examined which risk factors were associated with insomnia symptoms and previous insomnia diagnosis. In addition to previous diagnosis, insomnia symptoms were sleep latency (mins), difficulty falling asleep, difficulty resuming sleep upon awakening, and early morning awakening. The latter three were coded as never, rarely, sometimes, often or almost always. Cardiometabolic risk factors included hypertension history, systolic and diastolic BP, pulse, and fasting triglycerides, cholesterol, insulin, glucose, HbA1c, and c-reactive protein (CRP). Weighted regression models explored relationships adjusted for age, sex, race/ethnicity, income, education, marital status, BMI, diet, exercise, and smoking. Results: Overall, a pattern emerged, such that all insomnia variables were associated with increased risk of hypertension. Further, diastolic BP, triglycerides, and HbA1c were all positively associated with several insomnia variables. Other risk factors (e.g., cholesterol, glucose, CRP) were only associated with one of the insomnia variables. See Table for specific results. Conclusion: Symptoms of insomnia were associated with hypertension and a number of objectively-assessed cardiometabolic risk factors, including some in domains not previously explored relative to insomnia (e.g., lipids, HbA1c). Future prospective studies will be needed to ascertain whether pre-existing insomnia is a risk factor for the onset of cardiometabolic dysfunction. Associations between insomnia variables and cardiometabolic risk factors Variable β SE Previous Insomnia Diagnosis Hypertension (OR) Systolic BP Diastolic BP Pulse Triglycerides (log) Cholesterol Insulin (log) Glucose (log) HbA1c (log) CRP (log) ** 3.027 1.888 0.036 0.502 0.993 1.504 1.001 0.973 *** 0.966 1.000 1.067 2.315 1.515 1.182 0.102 6.561 0.111 0.022 0.009 0.173 Sleep Latency (Minutes) Hypertension (OR) Systolic BP Diastolic BP Pulse Triglycerides (log) Cholesterol Insulin (log) Glucose (log) HbA1c (log) CRP (log) *** 1.008 0.011 † 0.019 * 0.029 * 1.001 * 0.093 1.001 1.000 1.000 * 1.003 0.002 0.015 0.011 0.012 0.001 0.042 0.001 0.0002 0.0001 0.001 Difficulty Falling Asleep (“Almost Always” vs “Never”) Hypertension (OR) Systolic BP Diastolic BP Pulse Triglycerides (log) Cholesterol Insulin (log) Glucose (log) HbA1c (log) CRP (log) * 2.076 † 2.111 *** 2.804 † 1.585 ** 1.115 4.426 1.054 * 0.969 * 0.987 1.107 0.394 1.168 0.841 0.935 0.043 3.400 0.079 0.015 0.006 0.088 Difficulty Resuming Sleep (“Almost Always” vs “Never”) Hypertension (OR) Systolic BP Diastolic BP Pulse Triglycerides (log) Cholesterol Insulin (log) Glucose (log) HbA1c (log) CRP (log) *** 2.132 0.877 *** 3.830 1.029 * 1.098 3.779 1.028 0.990 ** 0.979 1.074 0.417 1.148 0.796 0.987 0.044 3.310 0.075 0.015 0.008 0.089 Early Morning Awakening (“Almost Always” vs “Never”) Hypertension (OR) Systolic BP Diastolic BP Pulse Triglycerides (log) Cholesterol Insulin (log) Glucose (log) HbA1c (log) CRP (log) ** 1.817 1.645 * 2.205 0.252 0.996 0.030 0.995 0.974 0.988 1.039 0.361 1.256 0.928 1.058 0.040 3.460 0.085 0.016 0.009 0.091 † p<0.10; * p<0.05; ** p<0.01; *** p<0.001


SLEEP ◽  
2019 ◽  
Vol 43 (3) ◽  
Author(s):  
Ariel A Williamson ◽  
Jodi A Mindell

Abstract Study Objectives To examine associations between cumulative socio-demographic risk factors, sleep health habits, and sleep disorder symptoms in young children. Methods Two hundred five caregiver-child dyads (child mean age ± SD: 3.3 ± 1.1 years; 53.7% girls; 62.9% black, 22.4% non-Hispanic/Latinx white, 4.4% Hispanic/Latinx; 85.4% maternal caregiver reporter) completed caregiver-rated sleep measures (Brief Child Sleep Questionnaire [BCSQ]; Pediatric Sleep Questionnaire [PSQ] snoring subscale), which were used to generate indexes of poor sleep health habits, pediatric insomnia symptoms, and obstructive sleep apnea (OSA) symptoms. A cumulative risk index was created reflecting caregiver, family, and neighborhood risks. Results Overall, 84.5% of children had ≥ 1 poor sleep health habit, 62.9% had ≥ 1 insomnia symptom, and 40.0% had ≥ 1 OSA symptom. Poisson regression indicated that each increase in the number of cumulative risk factors was associated with a 10% increase in poor sleep health habits, a 9% increase in insomnia symptoms, and an 18% increase in OSA symptoms. Specific caregiver risks (depressive symptoms, lower educational attainment) and family risks (single caregiver, crowded home) were most predictive of poor sleep outcomes. Conclusions Poor sleep health habits and sleep disorder symptoms are highly prevalent in early childhood, particularly among families experiencing cumulative socio-demographic risks. Findings underscore the need for targeted screening and prevention for modifiable sleep behaviors and efforts to tailor such strategies for at-risk children and families, especially those living in crowded conditions, or with caregivers who are single or have a lower educational attainment or depressive symptoms.


2011 ◽  
Vol 26 (S2) ◽  
pp. 1873-1873
Author(s):  
A. Bowen ◽  
R. Bowen ◽  
N. Muhajarine

IntroductionPerinatal depression is an important problem with potentially deleterious health outcomes; however, we know little about the trajectories of depression and treatment.PurposeWe report the patterns of maternal depression and trajectories of treatment response in early and late pregnancy and during postpartum in 649 women recruited from the general population of pregnant women in Western Canada. Women who scored ≥ 12 on the Edinburgh Postnatal Depression Scale were classified as depressed.FindingsFifty-two percent of participants were primiparas, 90% were partnered, 83.3% Caucasian, 67% earn more than $40,000 per year, 90% completed high school, and 77% had planned pregnancy. The unadjusted prevalence of depression in early pregnancy (17 weeks) was 14%, late pregnancy (30 weeks) 11.5%, and postpartum (4.1 weeks) was 9.8%. All of the psychosocial factors measured - history of depression, mood instability, lack of social support, relationship problems, worry, and stressors heighten depression symptoms throughout parturition. Our practice of referring women who screened positive for depression changed prevalence rates of women who were depressed and in treatment. The number of women in treatment increased from 12.2% in early pregnancy to 24.8% at postpartum. Women were significantly more likely to get symptom relief counselling in pregnancy compared to psychotropic medication use in postpartum, with the exception of those women with history of depression and treatment engagement.SummaryIncreased understanding of the patterns and nature of maternal depression and treatment response is essential to early identification of women who are depressed and lead to treatment that is more effective.


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