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1 0.16-0.64) compared with men with low CRF in midlife.
2 fitness had higher cognitive test scores at midlife.
3 ve effect of cardiorespiratory fitness as of midlife.
4 nd striatal neurons, as well as morbidity in midlife.
5 sk of hyperproliferative disease (cancer) by midlife.
6 le to costly health and social problems into midlife.
7 evaluate men with above-median PSA levels in midlife.
8 o middle adulthood and cognitive function at midlife.
9 it scores and cardiovascular disease risk at midlife.
10 ines, was associated with worse cognition in midlife.
11 with intellectual decline from childhood to midlife.
12 ed, executive function, and verbal memory in midlife.
13 gain are associated with adult body size in midlife.
14 s either before or after elective surgery in midlife.
15 Of these adults, 10.6% had FCR in midlife.
16 sess the effectiveness of dietary changes in midlife.
17 hood to middle age and cognitive function in midlife.
18 l adversity in childhood to lung function in midlife.
19 ically leading to end-stage renal disease in midlife.
20 risk factor for obesity-related disorders in midlife.
21 fspring BMI associations are maintained into midlife.
22 acetyl-aspartate/creatine (NAA/Cr) ratio, in midlife.
23 ts in humans and animals that are evident by midlife.
24 ly childhood growth with BMI in daughters at midlife.
25 reasing cardiovascular (CV) risk in women at midlife.
26 associated with better cognitive function in midlife.
27 high fat intake during both adolescence and midlife.
28 socioeconomic mobility between childhood and midlife.
29 cognitive sequelae of these risk factors in midlife.
30 al territory, and with increasing age during midlife.
31 edict more pronounced depressive symptoms in midlife.
32 ed ELS in relation to depressive symptoms in midlife.
33 father, and a sibling from childhood through midlife.
34 with other physical health problems in early midlife.
35 nd measured coronary artery calcium (CAC) in midlife.
36 es (ACEs) are associated with elevated AL in midlife.
39 in and resultant excess cholesterol that, by midlife, activates cholesterol transport from astrocytes
42 obe white matter volumes increase throughout midlife adulthood in humans, and this aspect of aging is
43 ood psychological health are associated with midlife affective and anxiety disorders and to examine s
45 later life with cardiorespiratory fitness in midlife after adjustment for cardiovascular risk factors
50 e hypothesis that reproductive senescence in midlife, although apparent in natural-fertility, natural
51 mine whether better cognitive functioning at midlife among more physically fit individuals reflects n
52 ust negative effect on HRQOL in women during midlife, an association not explained by VMS or sleep di
53 cells with a rapid decline in population at midlife and a concomitant increase in peripheral blood b
54 oid-beta1-42 levels were already frequent in midlife and APOE genotype strongly affects the levels of
57 n ICAD prevalence and the risk factors (both midlife and concurrent) associated with its development
58 relation between habitual dietary intake at midlife and incident PAD over approximately 20 y of foll
60 d whether low levels of social engagement in midlife and late life were associated with the risk of i
61 ritis is the most common health condition in midlife and late life, and heart disease is the leading
62 ighest quartile of social engagement at both midlife and late life, only decreased social engagement
64 [95% CI, 1.67-2.55]), whereas subjects with midlife and late-life symptoms had more than a 3-fold in
66 post-intervention surveys for this sample of midlife and older adults new to smartphone technology.
68 tigated whether duration of diabetes in late midlife and poor glycaemic control were associated with
70 s Risk in Communities (ARIC) participants in midlife and to explore associations between midlife vasc
71 ich women are at greatest stroke risk during midlife and to identify the safest formulation, dose, an
72 life and fish-oil consumption in early life, midlife, and late life with osteoporotic fracture risk.
75 ly recorded ELS, but not stressful events in midlife, and the mean BDI score (average of time 1 and t
76 panics; black non-Hispanics and Hispanics at midlife, and those aged 65 and above in every racial and
77 d with a 1.5- to 2-fold increase in risk for midlife anxiety and affective disorder (P<.05), whereas
78 prospectively examined shift-work history at midlife as associated with cognitive function among olde
79 nges in memory circuitry that occur in early midlife, as a function of sex and women's reproductive s
84 dy aims to examine the relationships between midlife body mass index (BMI) and (1) AAO of AD (2) seve
88 childhood SES affects health status through midlife but the effects may abate in late life; its effe
89 w that induction of mitochondrial fission in midlife, but not in early life, extends the health and l
90 een apoB in young adults and the presence of midlife CAC independent of baseline traditional CVD risk
92 ntia risk by examining its associations with midlife cognitive performance and cognitive decline from
94 m childhood/adolescence associate with worse midlife cognitive performance independent of adulthood e
95 ood were independently associated with worse midlife cognitive performance, especially memory and lea
102 ning, and TPI identified an increased BTP in midlife depressed patients, suggesting early and subtle
106 entia was increased by approximately 20% for midlife depressive symptoms only (hazard ratio, 1.19 [95
107 eported many risk factors for poor child and midlife development (e.g., low IQ, dropping out of schoo
108 r Foundation Research Networks on Successful Midlife Development and Socio-economic Status and Health
109 se mortality over a 10-year follow-up in the Midlife Development in the United States (MIDUS) cohort
110 everyday discrimination using the 1995-2004 Midlife Development in the United States cohort study (N
117 ical health shows stronger associations with midlife disorders, indicating a poorer prognosis for adu
121 rom demographics and the APOE genotype, only midlife dyslipidemia was associated with amyloid deposit
122 he early phase of the study corresponding to midlife, even when chronic/recurring, do not increase th
125 cancer, exploring the influence of early and midlife exposures will further advance our understanding
126 ting Drp1-mediated mitochondrial fission, in midlife, facilitates mitophagy and improves both mitocho
127 odds (95% confidence interval, 1.01-18.2) of midlife FCR in comparison with those low in all factors.
133 lder with high midlife fitness than with low midlife fitness in both men($7,569 vs. $12,811; p < 0.00
135 articipants aged 65 years or older with high midlife fitness than with low midlife fitness in both me
136 psychiatric symptoms typically occurring in midlife, followed by unremitting progression and eventua
137 o women never on HT, those taking HT only at midlife had a 26% decreased risk (multivariate adjusted
140 rt the hypothesis that shift-work history in midlife has long-term effects on cognition in older adul
142 m consequences of early adult overweight for midlife health and socioeconomic attainment using prospe
144 ean age 60 years) from the Melbourne Women's Midlife Health Project and included 17 early (perimenopa
145 ut it is unclear whether flavonoid intake in midlife helps to maintain good health and wellbeing in a
150 with late-life ICAD in blacks only, whereas midlife hypertension and hyperlipidemia were associated
151 2) of several variables except job score and midlife hypertension in predicting exceptional aging wit
153 k factors (eg, physical inactivity, smoking, midlife hypertension, midlife obesity, and diabetes) and
154 f an association with the disease (diabetes, midlife hypertension, midlife obesity, physical inactivi
155 ly modifiable risk factors for AD: diabetes, midlife hypertension, midlife obesity, smoking, depressi
156 relations between dietary intake of women at midlife in 1996-1997 and prevalence of physical function
157 were incrementally lower per MET achieved in midlife in men (6.8% decrease in costs per MET achieved;
158 ist actigraphy among 426 participants in the Midlife in the United States Study (31% AA; 69% EA; 61%
159 RIH2 mRNA levels significantly decrease from midlife in vastus lateralis muscles and highly correlate
160 ealth-related quality of life (HRQOL) during midlife in women when vasomotor symptoms (VMS) and sleep
164 th the hypothesis that migraine with aura in midlife is associated with late-life vascular disease in
165 These results suggest that increased BMI at midlife is associated with neuronal and/or myelin abnorm
166 st that avoidance of certain risk factors in midlife is associated with the probability of a long and
167 en and their clinicians that hysterectomy in midlife is unlikely to accelerate the CVD risk of women.
169 e find that short-term induction of Drp1, in midlife, is sufficient to improve organismal health and
172 Diabetes prevention and glucose control in midlife may protect against late-life cognitive decline.
174 he associations of overweight and obesity at midlife (mean age, 50 (standard deviation, 4.7) years) w
176 were to investigate the association between midlife MedDiet adherence and cognitive performance asse
178 nce or more per month (n = 3243), those with midlife migraine with aura (n = 361) had an increased ri
179 ogy and mortality in mammals when applied in midlife.Mitochondrial fission and fusion are important m
182 he most dramatic decreases in early-life and midlife mortality coincided with advances in medicine; c
189 f these results, gathered in a population of midlife northeast American adults, hold in the general p
192 the disease (diabetes, midlife hypertension, midlife obesity, physical inactivity, depression, smokin
193 tors for AD: diabetes, midlife hypertension, midlife obesity, smoking, depression, cognitive inactivi
194 ocioeconomic markers (height, education, and midlife occupation categorized as low, intermediate, and
196 was strongly associated with baseline PSA in midlife: odds ratios (95% CIs) comparing PSA in the > 90
197 These findings suggest that use of HT in midlife only may protect against cognitive impairment, w
198 ymptoms were present in 14.1% of subjects in midlife only, 9.2% in late life only, and 4.2% in both.
200 y extensive loss of striatal neurons and the midlife onset of debilitating and progressive chorea, de
201 functioning in healthy menopausal women with midlife onset of executive difficulties include modulati
204 and women (n = 23) aged 45 to 65 years with midlife-onset major or minor depression participated in
205 Herein we describe Japanese siblings with a midlife-onset, slowly progressive type of cerebellar ata
206 dolescence (vs. less than daily), but not in midlife or currently, was associated with a 3.2-fold ris
209 ings The National Institute of Mental Health Midlife Outpatient Clinic in the National Institutes of
210 -up of 26.2 (standard deviation, 4.9) years, midlife overweight and obesity were not associated with
213 that childhood growth and development affect midlife performance; prevention of disability and frailt
215 Prostate-specific antigen (PSA) level in midlife predicted future prostate cancer (PCa) mortality
216 to determine if a baseline PSA level during midlife predicts lethal PCa in a US population with oppo
217 otein that promotes mitochondrial fission-in midlife, prolongs Drosophila lifespan and healthspan.
218 on-based sample of individuals with NAFLD in midlife, prospectively assessed alcohol use is not assoc
219 Risk-stratified screening on the basis of midlife PSA should be considered in men age 45 to 59 yea
221 is study, we investigated the association of midlife quality of close relationships with subsequent c
222 Cognitive impairment first appeared in the midlife range (9-12 months) and coincided and correlated
223 demographics, APOE, intellectual enrichment, midlife risk factors (physical inactivity, obesity, smok
225 1, and 134 had 2 or more; a higher number of midlife risk factors was associated with elevated amyloi
228 ted biomechanical exposure and job strain in midlife separately and jointly predicted back and degene
229 l health and prolong lifespan, and observe a midlife shift toward a more elongated mitochondrial morp
235 development, would be positively related to midlife standing balance and chair rising, independently
237 he same age (12 months of age; approximately midlife), sufficiently early to influence initial cognit
239 an and nonhuman primate data suggest that in midlife, the structural integrity of myelin sheaths begi
240 symptoms (hot flashes, night sweats) during midlife, their etiology and risk factors are incompletel
241 ly influence outcomes in young adulthood and midlife, this long-term prospective study examines the e
243 nteract with the psychosocial environment of midlife to contribute to perimenopausal depression risk.
244 ents in, ideal cardiovascular health through midlife to late life are associated with lower CVD preva
245 al and primary prevention efforts throughout midlife to late life as a potential intervention to decr
246 that increasing weight loss per decade from midlife to late life is a marker for MCI and may help id
247 life, only decreased social engagement from midlife to late life was associated with an increased ri
248 the relationship of CVHS attainment through midlife to late life with CVD prevalence and cardiovascu
250 percentile of education/occupation score and midlife to late-life cognitive activity), the onset of c
251 his, Apoe-deficient mice were exercised from midlife to old age and in contrast to wild-type (Apoe-su
252 Importantly, long-term aerobic exercise from midlife to old age prevented this age-related neurovascu
253 itive performance and cognitive decline from midlife to old age, including cognitive decline trajecto
254 n (SD) rate of weight change per decade from midlife to study entry was greater for participants who
255 and coincided and correlated primarily with midlife upregulation of genes associated with cholestero
256 is 6-year longitudinal cohort study of 1,903 midlife US women (2000-2006) asked whether symptoms nega
257 me observational studies have suggested that midlife use of HT may be beneficial; however, this has n
258 rowth factors with adult BMI in daughters at midlife using quantile, linear, and logistic regression
259 be examined, highlighting the importance of midlife vascular risk factor control in the prevention o
260 midlife and to explore associations between midlife vascular risk factors and 25-year dementia incid
263 cipants without dementia and with nonmissing midlife vascular risk factors at baseline (mean age, 52
264 Place of birth, race, educational level, and midlife vascular risk factors data were collected betwee
268 terol, and smoking associated inversely with midlife visual and episodic memory and visuospatial asso
271 s having cancer at Medicare age, high CRF in midlife was associated with an adjusted 32% (HR, 0.68; 9
272 s level in metabolic equivalents achieved in midlife was associated with approximately 20% lower risk
276 ithout an incident CV event, OSA assessed in midlife was independently associated with higher left ve
277 the AHEI-2010 (upper vs. lower quintiles) in midlife was related to 34% (95% CI, 9% to 66%; P for tre
278 cognitive function is limited, especially in midlife.We hypothesize that higher intake of these B vit
279 Intakes of 6 major flavonoid subclasses in midlife were ascertained on the basis of averaged intake
282 mance, associations with area deprivation in midlife were robust to adjustment for individual socioec
283 at 3 life stages (childhood, adulthood, and midlife) were used to derive a measure of cumulative SEP
284 with poor outcomes in young adulthood and in midlife, were largely unrelated to satisfaction with ret
286 Increasing evidence of associations from midlife will guide the shift to interventional studies f
287 e of optimal levels of these risk factors in midlife will reduce the burden of LV hypertrophy, and po
290 lly diverse community sample of nearly 3,300 midlife women enrolled in the longitudinal, multisite St
294 urinary incontinence in a diverse cohort of midlife women, the authors analyzed the baseline and fir
295 pattern of decreasing depressive symptoms in midlife women, with higher risk before and lower risk af
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