Madeleine Lenski
Michigan State University
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Developmental Medicine & Child Neurology | 2009
Peterson Haak; Madeleine Lenski; Mary Jo Cooley Hidecker; Min Li; Nigel Paneth
Cerebral palsy (CP), the most common major disabling motor disorder of childhood, is frequently thought of as a condition that affects only children. Deaths in children with CP, never common, have in recent years become very rare, unless the child is very severely and multiply disabled. Thus, virtually all children assigned the diagnosis of CP will survive into adulthood. Attention to the adult with CP has been sparse, and the evolution of the motor disorder as the individual moves through adolescence, young adulthood, middle age, and old age is not well understood. Nor do we know what happens to other functional domains, such as communication and eating behavior, in adults with CP. Although the brain injury that initially causes CP by definition does not progressively worsen through the lifetime, the effects of CP manifest differently throughout the lifespan. The aging process must inevitably interact with the motor disorder, but we lack systematic, large‐scale follow‐up studies of children with CP into adulthood and through adulthood with thorough assessments performed over time.
Developmental Medicine & Child Neurology | 2012
Mary Jo Cooley Hidecker; Nhan Thi Ho; Nancy Dodge; Edward A. Hurvitz; Jaime Slaughter; Marilyn Seif Workinger; Ray D. Kent; Peter Rosenbaum; Madeleine Lenski; Bridget M. Messaros; Suzette B Vanderbeek; Steven T. DeRoos; Nigel Paneth
Aim To investigate the relationships among the Gross Motor Function Classification System (GMFCS), Manual Ability Classification System (MACS), and Communication Function Classification System (CFCS) in children with cerebral palsy (CP).
American Journal of Obstetrics and Gynecology | 2017
Robert M. Joseph; Steven J. Korzeniewski; Elizabeth N. Allred; T. Michael O’Shea; Timothy Heeren; Jean A. Frazier; Janice Ware; Deborah Hirtz; Alan Leviton; Karl Kuban; Taryn Coster; Brandi Henson; Rachel Wilson; Kirsten McGhee; Patricia Lee; Aimee Asgarian; Anjali Sadhwani; Ellen C. Perrin; Emily Neger; Kathryn Mattern; Jenifer Walkowiak; Susan Barron; Lauren Venuti; Beth Powers; Ann Foley; Brian Dessureau; Molly Wood; Jill Damon-Minow; Richard A. Ehrenkranz; Jennifer Benjamin
Background: No prospective cohort study of high‐risk children has used rigorous exposure assessment and optimal diagnostic procedures to examine the perinatal antecedents of autism spectrum disorder separately among those with and without cognitive impairment. Objective: We sought to identify perinatal factors associated with increased risk for autism spectrum disorder with and without intellectual disability (intelligence quotient <70) in children born extremely preterm. Study Design: This prospective multicenter (14 institutions in 5 states) birth cohort study included children born at 23–27 weeks’ gestation in 2002 through 2004 who were evaluated for autism spectrum disorder and intellectual disability at age 10 years. Pregnancy information was obtained from medical records and by structured maternal interview. Cervical‐vaginal “infection” refers to maternal report of bacterial infection (n = 4), bacterial vaginosis (n = 30), yeast infection (n = 62), mixed infection (n = 4), or other/unspecified infection (n = 43; eg, chlamydia, trichomonas, or herpes). We do not know the extent to which infection per se was confirmed by microbial colonization. We use the terms “fetal growth restriction” and “small for gestational age” interchangeably in light of the ongoing challenge to discern pathologically from constitutionally small newborns. Severe fetal growth restriction was defined as a birthweight Z‐score for gestational age at delivery <–2 (ie, ≥2 SD below the median birthweight in a referent sample that excluded pregnancies delivered for preeclampsia or fetal indications). Participants were classified into 4 groups based on whether or not they met rigorous diagnostic criteria for autism spectrum disorder and intellectual disability (autism spectrum disorder+/intellectual disability–, autism spectrum disorder+/intellectual disability+, autism spectrum disorder–/intellectual disability+, and autism spectrum disorder–/intellectual disability–). Temporally ordered multinomial logistic regression models were used to examine the information conveyed by perinatal factors about increased risk for autism spectrum disorder and/or intellectual disability (autism spectrum disorder+/intellectual disability–, autism spectrum disorder+/intellectual disability+, and autism spectrum disorder–/intellectual disability+). Results: In all, 889 of 966 (92%) children recruited were assessed at age 10 years, of whom 857 (96%) were assessed for autism spectrum disorder; of these, 840 (98%) children were assessed for intellectual disability. Autism spectrum disorder+/intellectual disability– was diagnosed in 3.2% (27/840), autism spectrum disorder+/intellectual disability+ in 3.8% (32/840), and autism spectrum disorder–/intellectual disability+ in 8.5% (71/840). Maternal report of presumed cervical‐vaginal infection during pregnancy was associated with increased risk of autism spectrum disorder+/intellectual disability+ (odds ratio, 2.7; 95% confidence interval, 1.2–6.4). The lowest gestational age category (23–24 weeks) was associated with increased risk of autism spectrum disorder+/intellectual disability+ (odds ratio, 2.9; 95% confidence interval, 1.3–6.6) and autism spectrum disorder+/intellectual disability– (odds ratio, 4.4; 95% confidence interval, 1.7–11). Severe fetal growth restriction was strongly associated with increased risk for autism spectrum disorder+/intellectual disability– (odds ratio, 9.9; 95% confidence interval, 3.3–30), whereas peripartum maternal fever was uniquely associated with increased risk of autism spectrum disorder–/intellectual disability+ (odds ratio, 2.9; 95% confidence interval, 1.2–6.7). Conclusion: Our study confirms that low gestational age is associated with increased risk for autism spectrum disorder irrespective of intellectual ability, whereas severe fetal growth restriction is strongly associated with autism spectrum disorder without intellectual disability. Maternal report of cervical‐vaginal infection is associated with increased risk of autism spectrum disorder with intellectual disability, and peripartum maternal fever is associated with increased risk for intellectual disability without autism spectrum disorder.
The Journal of Pediatrics | 2017
H. Reeve Bright; Kikelomo Babata; Elizabeth N. Allred; Carmina Erdei; Karl Kuban; Robert M. Joseph; T. Michael O'Shea; Alan Leviton; Olaf Dammann; Janice Ware; Taryn Coster; Brandi Hanson; Rachel Wilson; Kirsten McGhee; Patricia Lee; Aimee Asgarian; Anjali Sadhwani; Ellen C. Perrin; Emily Neger; Kathryn Mattern; Jenifer Walkowiak; Susan Barron; Bhavesh Shah; Rachana Singh; Anne Smith; Deborah Klein; Susan McQuiston; Lauren Venuti; Beth Powers; Ann Foley
OBJECTIVE To evaluate the difference in 10-year neurocognitive outcomes between extremely low gestational age newborns without bacteremia and those with suspected or confirmed late-onset bacteremia. STUDY DESIGN Neurocognitive function was evaluated at 10 years of age in 889 children born at <28 weeks of gestation and followed from birth. Definite (culture-positive) late-onset bacteremia during postnatal weeks 2-4 was identified in 223 children, and 129 children had suspected bacteremia. RESULTS Infants with the lowest gestational age and birth weight z-score had the highest prevalence of definite and suspected late-onset bacteremia. Compared with peers with no or suspected bacteremia, infants with definite bacteremia performed worse on tests of general cognitive ability, language, academic achievement, and executive function, even after adjustment for potential confounders. Adjustment for low IQ attenuated the associations between bacteremia and all dysfunctions at age 10 years. Children with suspected bacteremia did not differ appreciably from those with no evidence of bacteremia. The motor domain was unaffected. CONCLUSIONS Extremely low gestational age newborns who had definite late bacteremia during postnatal weeks 2-4 are at heightened risk of neurocognitive limitations at age 10 years.
The Journal of Pediatrics | 2014
Changshuai Wei; Qing Lu; Sok Kean Khoo; Madeleine Lenski; Raina N. Fichorova; Alan Leviton; Nigel Paneth
We studied gene expression in 9 sets of paired newborn blood spots stored for 8-10 years in either the frozen state or the unfrozen state. Fewer genes were expressed in unfrozen spots, but the average correlation coefficient for overall gene expression comparing the frozen and unfrozen state was 0.771 (95% CI, 0.700-0.828).
Journal of Maternal-fetal & Neonatal Medicine | 2013
Jaime Slaughter; Changshuai Wei; Steven J. Korzeniewski; Qing Lu; John S. Beck; Sok Kean Khoo; Ariel Brovont; Joel Maurer; Denny R. Martin; Madeleine Lenski; Nigel Paneth
Abstract Objective: To examine the correlation in genes expressed in paired umbilical cord blood (UCB) and newborn blood (NB). Method: Total mRNA and mRNA of three gene sets (inflammatory, hypoxia, and thyroidal response) was assessed using microarray in UCB and NB spotted on Guthrie cards from 7 mother/infant pairs. Results: The average gene expression correlation between paired UCB and NB samples was 0.941 when all expressed genes were considered, and 0.949 for three selected gene sets. Conclusion: The high correlation of UCB and NB gene expression suggest that either source may be useful for examining gene expression in the perinatal period.
Developmental Medicine & Child Neurology | 2001
Madeleine Lenski; Shariff K Bishai; Nigel Paneth
‘Comparison of survival in cerebral palsy between countries.’ SIR–The authors of the paper ‘Life expectancy among people with cerebral palsy in Western Australia’1 (see pages 508–15, this issue), kindly allowed us use of their database in order to compare with the large Californian database.2, 3 We begin our comparison at age 5 years because measurements of intellectual level and severity of cerebral palsy (CP) in Western Australia are updated only until that age. Overall survival rate in the Western Australian population is 93% compared with 83% in California. This large disparity is not, however, due to differences in care in the two regions. It arises because the Californian data include nearly all the more severely affected individuals but comparatively fewer mild instances whereas the Western Australian database includes everyone with CP (most of whom are only mildly affected). For a valid comparison, we stratified the population into four intellectual levels (IQ<20; 20–34; 25–49; 50–69) and three severities of motor dysfunction (mild, moderate,and severe), creating 12 groups. When just one factor (severity or IQ) was controlled, the gap in survival rates narrowed considerably. When both were controlled, the survival curves became strikingly similar. Figure 1 illustrates two cases: severe impairment with IQ<20 and with IQ in the range 20–34. Data from the UK study by Hutton and coworkers4 of the ‘three severe disabilities’ group was compared to the Californian database in the same way and found to be remarkably similar. To our knowledge, this is the first controlled comparison of survival in CP between countries. Robert M Shavelle PhD MBA David J Straus PhD FASA Steven M Day MS MAT
Pediatric Neurology | 2017
Alan Leviton; Stephen R. Hooper; Scott J. Hunter; Megan Scott; Elizabeth N. Allred; Robert M. Joseph; T. Michael O'Shea; Karl Kuban; Janice Ware; Taryn Coster; Brandi Henson; Rachel Wilson; Kirsten McGhee; Patricia Lee; Aimee Asgarian; Anjali Sadhwani; Ellen C. Perrin; Emily Neger; Kathryn Mattern; Jenifer Walkowiak; Susan Barron; Jean A. Frazier; Lauren Venuti; Beth Powers; Ann Foley; Brian Dessureau; Molly Wood; Jill Damon-Minow; Richard A. Ehrenkranz; Jennifer Benjamin
BACKGROUND The incidence of attention deficit hyperactivity disorder is higher among children born very preterm than among children who are mature at birth. METHODS We studied 583 ten-year-old children who were born before 28 weeks of gestation whose IQ was above 84 and had a parent-completed Child Symptom Inventory-4, which allowed classification of the child as having or not having symptoms of attention deficit hyperactivity disorder. For 422 children, we also had a teacher report, and for 583 children, we also had a parent report of whether or not a physician made an attention deficit hyperactivity disorder diagnosis. RESULTS The risk profile of screening positive for attention deficit hyperactivity disorder based on a parents report differed from the risk profile based on the teachers report, whereas the risk profile according to a physician and according to any two observers closely resembled the parent-reported profile. Among the statistically significant risk factors were young maternal age (parent, physician, and two observers), maternal obesity (parent, physician, and two observers), maternal smoking (parent, physician, and two observers), magnesium given at delivery for seizure prophylaxis (parent and two observers), recovery of Mycoplasma sp. from the placenta (teacher and two observers), low gestational age (parent and two observers), low birth weight (teacher and physician), singleton (parent, physician, and two observers), male (parent, teacher, physician, and two observers), mechanical ventilation on postnatal day seven (physician), receipt of a sedative (parent and two observers), retinopathy of prematurity (parent), necrotizing enterocolitis (physician), antibiotic receipt (physician and two observers), and ventriculomegaly on brain scan (parent and two observers). CONCLUSIONS The multiplicity of risk factors identified can be subsumed as components of four broad themes: low socioeconomic state, immaturity or vulnerability, inflammation, and epigenetic phenomena.
The Journal of Pediatrics | 2017
Elizabeth T. Jensen; Jelske W. van der Burg; Thomas M. O'Shea; Robert M. Joseph; Elizabeth N. Allred; Timothy Heeren; Alan Leviton; Karl Kuban; Bhavesh Shah; Rachana Singh; Anne Smith; Deborah Klein; Susan McQuiston; Julie Vanier Rollins; Laurie M. Douglass; Janice Ware; Taryn Coster; Brandi Henson; Rachel Wilson; Kirsten McGhee; Patricia Lee; Aimee Asgarian; Anjali Sadhwani; Ellen C. Perrin; Emily Neger; Kathryn Mattern; Jenifer Walkowiak; Susan Barron; Jean A. Frazier; Lauren Venuti
Objective To assess the association between maternal prepregnancy body mass index and adequacy of pregnancy weight gain in relation to neurocognitive function in school‐aged children born extremely preterm. Study design Study participants were 535 ten‐year‐old children enrolled previously in the prospective multicenter Extremely Low Gestational Age Newborns cohort study who were products of singleton pregnancies. Soon after delivery, mothers provided information about prepregnancy weight. Prepregnancy body mass index and adequacy of weight gain were characterized based on this information. Children underwent a neurocognitive evaluation at 10 years of age. Results Maternal prepregnancy obesity was associated with increased odds of a lower score for Differential Ability Scales‐II Verbal IQ, for Developmental Neuropsychological Assessment‐II measures of processing speed and visual fine motor control, and for Wechsler Individual Achievement Test‐III Spelling. Children born to mothers who gained an excessive amount of weight were at increased odds of a low score on the Oral and Written Language Scales Oral Expression assessment. Conversely, children whose mother did not gain an adequate amount of weight were at increased odds of a lower score on the Oral and Written Language Scales Oral Expression and Wechsler Individual Achievement Test‐III Word Reading assessments. Conclusion In this cohort of infants born extremely preterm, maternal obesity was associated with poorer performance on some assessments of neurocognitive function. Our findings are consistent with the observational and experimental literature and suggest that opportunities may exist to mitigate risk through education and behavioral intervention before pregnancy. (J Pediatr 2017;187:50‐7).
Journal of Child Neurology | 2016
Qing Li; Madeleine Lenski; Glenn Copeland; Stephen L. Kinsman; Matthew Francis; Russell S. Kirby; Nigel Paneth
We evaluated the recording of neonatal seizures in birth certificates, hospital discharge abstracts, and maternal interviews in 372 children, 198 of them with cerebral palsy, born in Michigan hospitals from 1993 to 2010. In birth certificates, we examined checkbox items “seizures” or “seizure or serious neurologic dysfunction”; in hospital discharge abstracts ICD-9-CM codes 779.0, 345.X, and 780.3; and in maternal interviews a history of seizures or convulsions on day 1 of life recalled 2-16 years later. In 27 neonates, 38 neonatal seizures were recorded in 1 or more sources, 17 in discharge abstracts, 20 in maternal interviews, but just 1 on a birth certificate. The kappa coefficient (κ) between interviews and discharge abstracts was moderate (κ = 0.55), and substantial (κ = 0.63) if mothers noted use of antiepileptics. Agreement was higher (κ = 0.71 vs κ = 0.29) in term births than in preterm births. Birth certificates significantly underreported neonatal seizures.