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Dive into the research topics where Joan R. Jacobs is active.

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Featured researches published by Joan R. Jacobs.


Journal of Pediatric Gastroenterology and Nutrition | 2003

Growth and Development of Premature Infants Fed Predominantly Human Milk, Predominantly Premature Infant Formula, or a Combination of Human Milk and Premature Formula

Deborah L O'Connor; Joan R. Jacobs; Robert T. Hall; David H. Adamkin; Nancy Auestad; Marcella Castillo; William E. Connor; Sonja L. Connor; Katherine A. Fitzgerald; Sharon Groh-Wargo; E. Eugenie Hartmann; Jeri S. Janowsky; Alan Lucas; Dean Margeson; Patricia Mena; Martha Neuringer; Gail Ross; Lynn T. Singer; Terence Stephenson; Joanne S. Szabo; Vance Zemon

Background In a recent meta-analysis, human milk feeding of low birth-weight (LBW) infants was associated with a 5.2 point improvement in IQ tests. However, in the studies in this meta-analysis, feeding regimens were used (unfortified human milk, term formula) that no longer represent recommended practice. Objective To compare the growth, in-hospital feeding tolerance, morbidity, and development (cognitive, motor, visual, and language) of LBW infants fed different amounts of human milk until term chronologic age (CA) with those of LBW infants fed nutrient-enriched formulas from first enteral feeding. Methods The data in this study were collected in a previous randomized controlled trial assessing the benefit of supplementing nutrient-enriched formulas for LBW infants with arachidonic acid and docosahexaenoic acid. Infants (n = 463, birth weight, 750–1,800 g) were enrolled from nurseries located in Chile, the United Kingdom, and the United States. If human milk was fed before hospital discharge, it was fortified (3,050–3,300 kJ/L, 22–24 kcal/oz). As infants were weaned from human milk, they were fed nutrient-enriched formula with or without arachidonic and docosahexaenoic acids (3,300 kJ/L before term, 3,050 kJ/L thereafter) until 12 months CA. Formula fed infants were given nutrient-enriched formula with or without added arachidonic and docosahexaenoic acids (3,300 kJ/L to term, 3,050 kJ/L thereafter) until 12 months CA. For the purposes of this evaluation, infants were categorized into four mutually exclusive feeding groups: 1) predominantly human milk fed until term CA (PHM-T, n = 43); 2) ≥ 50% energy from human milk before hospital discharge (≥ 50% HM, n = 98); 3) < 50% of energy from human milk before hospital discharge (< 50% HM, n = 203); or 4) predominantly formula fed until term CA (PFF-T, n = 119). Results PFF-T infants weighed approximately 500 g more at term CA than did PHM-T infants. This absolute difference persisted until 6 months CA. PFF-T infants were also longer (1.0–1.5 cm) and had larger head circumferences (0.3–1.1 cm) than both PHM-T and ≥ 50% HM infants at term CA. There was a positive association between duration of human milk feeding and the Bayley Mental Index at 12 months CA (P = 0.032 full and P = 0.073 reduced, statistical models) after controlling for the confounding variables of home environment and maternal intelligence. Infants with chronic lung disease fed ≥ 50% HM until term CA (n = 22) had a mean Bayley Motor Index about 11 points higher at 12 months CA compared with infants PFF-T (n = 24, P = 0.033 full model). Conclusion Our data suggest that, despite a slower early growth rate, human milk fed LBW infants have development at least comparable to that of infants fed nutrient-enriched formula. Exploratory analysis suggests that some subgroups of human milk fed LBW infants may have enhanced development, although this needs to be confirmed in future studies.


Pediatric Research | 2005

Body Composition in Preterm Infants Who Are Fed Long-Chain Polyunsaturated Fatty Acids: A Prospective, Randomized, Controlled Trial

Sharon Groh-Wargo; Joan R. Jacobs; Nancy Auestad; Deborah L O'Connor; John J. Moore; Edith Lerner

The objective of this study was to evaluate growth and body composition of premature infants who were fed formulas with arachidonic acid (ARA; 20:4n6) and docosahexaenoic acid (DHA; 22:6n3) to 1 y of gestation-corrected age (CA). Preterm infants (750–1800 g birth weight and <33 wk gestational age) were assigned within 72 h of first enteral feeding to one of three formulas: control (n = 22), DHA+ARA from fish/fungal oil [DHA+ARA(FF); n = 20], or DHA+ARA from egg/fish oil [DHA+ARA(EF); n = 18]. Human milk feeding was allowed on the basis of the mothers choice. Infants were fed breast milk and/or preterm formulas with or without 0.26% DHA and 0.42% ARA to term CA followed by breast milk or postdischarge preterm formulas with or without 0.16% DHA and 0.42% ARA to 12 mo CA. Body composition was measured by dual-energy x-ray absorptiometry. There were no significant differences among the three study groups at any time point in weight, length, or head circumference. Bone mineral content and bone mineral density did not differ among groups. At 12 mo CA, infants who were fed DHA+ARA-supplemented formulas had significantly greater lean body mass (p < 0.05) and significantly less fat mass (p < 0.05) than infants who were fed the unsupplemented control formula. The DHA+ARA-supplemented formulas supported normal growth and bone mineralization in premature infants who were born at <33 wk gestation. Preterm formulas that had DHA+ARA at the levels and ratios in this study and were fed to 1 y CA led to increased lean body mass and reduced fat mass by 1 y of age.


Journal of Pediatric Gastroenterology and Nutrition | 2002

Immune status of infants fed soy-based formulas with or without added nucleotides for 1 year: part 2: immune cell populations.

Christopher T. Cordle; Timothy R. Winship; Joseph P. Schaller; Debra J. Thomas; Rachael H. Buck; Karin M. Ostrom; Joan R. Jacobs; Mark M. Blatter; Sechin Cho; Willis M. Gooch; Larry K. Pickering

Background Infants fed a soy protein isolate–based formula have immunization responses similar to breast-fed infants. However, cellular aspects of the immunologic development of soy-fed infants have not been studied extensively. Nucleotides added to milk-based formula benefit infant immune status, but reports of the immunologic effects of adding nucleotides to soy-based formula are not available. This study examines immune cell populations of infants fed soy protein isolate formulas with and without added nucleotides for 1 year. Methods Newborn, term infants studied in a masked 12-month feeding trial were assigned randomly to soy formula groups with and without added nucleotides (n = 94, n = 92). A nonrandomized human milk/formula-fed cohort (n = 81), was concurrently enrolled. Blood samples were collected at 6, 7, and 12 months. Thirty-two immune cell populations were characterized using three-color flow cytometry. Cellular markers were chosen to assess general pediatric immune status, emphasizing maturation and activation of B, T, and NK lymphocytes. Results All cell populations, number and percentages, were within age-related normal ranges. The only significant difference found between soy formula and human milk/formula-fed infants was the percentage of CD57+ NK T cells at 12 months (human milk/formula > soy formula, P = 0.034). There were significant differences at some time points between human milk/formula-fed and nucleotide-supplemented soy formula–fed infants in populations of lymphocytes, eosinophils, total T, helper T, naive helper, memory/effector helper, CD57−T, and CD11b+CD8+NK cells. None of the cell populations differed between infants fed soy formula versus soy plus nucleotides. Conclusions Infants fed this commercial soy formula demonstrated immune cell status similar to human milk/formula-fed infants, consistent with normal immune system development. The addition of nucleotides to soy formula did not significantly change specific individual immune cell populations but tended to increase numbers and percentages of T cells and decreased numbers and percentages of NK cells.


Clinical Pediatrics | 2011

Lactose-Free Milk Protein-Based Infant Formula: Impact on Growth and Gastrointestinal Tolerance in Infants

John B. Lasekan; Joan R. Jacobs; Keith S. Reisinger; Michael B. Montalto; Mary P. Frantz; Mark M. Blatter

Lactose, the major carbohydrate in human milk and standard milk—based formulas, provides energy for growth in infants. The use of lactose-free milk protein—based infant formulas has increased in the United States. However, clinical studies of their impact on growth, safety, and gastrointestinal tolerance in infants are limited. Thus, a prospective, blinded, randomized clinical trial was conducted in healthy, normal-term infants fed an experimental lactose-free milk protein—based formula (NoLAC; n = 63) versus a standard commercial lactose-containing milk-based formula (LAC; n = 65) for 112 days. Growth (weight, length, and head circumference) was similar and normal in both groups (weight gain: NoLAC = 31.1 ± 0.9 g/day, LAC = 29.4 ± 0.9 g/day, mean ± SEM; P = .895). Serum biochemistries for both groups were within infants’ normal reference ranges. Both groups had comparable tolerance but the NoLAC group had softer stools and lower spit-ups. Thus, the study suggests that absence of lactose in milk-based formula does not adversely affect normal growth in term infants.


Pediatric Research | 1999

Growth, Tolerance, and Morbidity of Preterm Infants Fed Exclusively Human Milk, Exclusively Preterm Infant Formula, or a Combination of Human Milk and a Preterm Infant Formula until Term Corrected Age (CA)

Deborah L O'Connor; R T Hall; David H. Adamkin; William E. Connor; Alan Lucas; Sharon Groh-Wargo; Patricia Mena; Mirjana Nesin; Lynn T. Singer; J Szabo; Joan R. Jacobs; W Qiu; R L Tressler; Nancy Auestad

Growth, Tolerance, and Morbidity of Preterm Infants Fed Exclusively Human Milk, Exclusively Preterm Infant Formula, or a Combination of Human Milk and a Preterm Infant Formula until Term Corrected Age (CA)


Pediatric Research | 1999

Randomized Trial of Premature Infants Fed Human Milk and/or a Nutrient Enriched Formula with and without a Source of Arachidonic Acid (AA) and DocosahexaenoicAcid (DHA)

Deborah L O'Connor; R T Hall; David H. Adamkin; William E. Connor; Alan Lucas; Sharon Groh-Wargo; Patricia Mena; Mirjana Nesin; Lynn T. Singer; J Szabo; Joan R. Jacobs; W Qiu; R L Tressler; Nancy Auestad

Randomized Trial of Premature Infants Fed Human Milk and/or a Nutrient Enriched Formula with and without a Source of Arachidonic Acid (AA) and DocosahexaenoicAcid (DHA)


Pediatrics | 2001

Growth and development in preterm infants fed long-chain polyunsaturated fatty acids: A prospective, randomized controlled trial

Deborah L O'Connor; Robert T. Hall; David H. Adamkin; Nancy Auestad; Marcella Castillo; William E. Connor; Sonja L. Connor; Kathleen M. Fitzgerald; Sharon Groh-Wargo; E. Eugenie Hartmann; Joan R. Jacobs; Jeri S. Janowsky; Alan Lucas; Dean Margeson; Patricia Mena; Martha Neuringer; Mirjana Nesin; Lynn T. Singer; Terence Stephenson; Joanne S. Szabo; Vance Zemon


Pediatrics | 2001

Growth and Development in Term Infants Fed Long-Chain Polyunsaturated Fatty Acids: A Double-Masked, Randomized, Parallel, Prospective, Multivariate Study

Nancy Auestad; Robin Halter; Robert T. Hall; Mark Blatter; Margaret L. Bogle; Wesley Burks; Julie Reed Erickson; Kathleen M. Fitzgerald; Velma Dobson; Sheila M. Innis; Lynn T. Singer; Michael B. Montalto; Joan R. Jacobs; Wenzi Qiu; Marc H. Bornstein


Pediatrics | 2003

Visual, Cognitive, and Language Assessments at 39 Months: A Follow-up Study of Children Fed Formulas Containing Long-Chain Polyunsaturated Fatty Acids to 1 Year of Age

Nancy Auestad; David T. Scott; Jeri S. Janowsky; Cynthia Jacobsen; Robin E. Carroll; Michael B. Montalto; Robin Halter; Wenzi Qiu; Joan R. Jacobs; William E. Connor; Sonja L. Connor; James A. Taylor; Martha Neuringer; Kathleen M. Fitzgerald; Robert T. Hall


Pediatrics | 2001

Growth of Preterm Infants Fed Nutrient-Enriched or Term Formula After Hospital Discharge

Jane D. Carver; Paul Y. K. Wu; Robert T. Hall; Ekhard E. Ziegler; Roberto Sosa; Joan R. Jacobs; Geraldine E. Baggs; Nancy Auestad; Beate Lloyd

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Nancy Auestad

University of California

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Robert T. Hall

University of Colorado Denver

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Lynn T. Singer

Case Western Reserve University

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Martha Neuringer

Oregon National Primate Research Center

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