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      Preterm Birth: Long Term Cardiovascular and Renal Consequences

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          Abstract

          Background:

          Cardiovascular and chronic kidney diseases are a part of non-communicable chronic diseases, the leading causes of premature death worldwide. They are recognized as having early origins through altered developmental programming, due to adverse environmental conditions during development. Preterm birth is such an adverse factor. Rates of preterm birth increased in the last decades, however, with the improvement in perinatal and neonatal care, a growing number of preterm born subjects has now entered adulthood. Clinical and experimental evidence suggests that preterm birth is associated with impaired or arrested structural or functional development of key or-gans/systems making preterm infants vulnerable to cardiovascular and chronic renal diseases at adult-hood. This review analyzes the evidence of such cardiovascular and renal changes, the role of perina-tal and neonatal factors such as antenatal steroids and potential pathogenic mechanisms, including de-velopmental programming and epigenetic alterations.

          Conclusion:

          Preterm born subjects are exposed to a significantly increased risk for altered cardio-vascular and renal functions at young adulthood. Adequate, specific follow-up measures remain to be determined. While antenatal steroids have considerably improved preterm birth outcomes, repeated therapy should be considered with caution, as antenatal steroids induce long-term cardio-vascular and metabolic alterations in animals’ models and their involvement in the accelerated cellular senescence observed in human studies cannot be excluded.

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          Most cited references78

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          Left ventricular hypertrophy: pathogenesis, detection, and prognosis.

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            Effect of fetal and child health on kidney development and long-term risk of hypertension and kidney disease.

            Developmental programming of non-communicable diseases is now an established paradigm. With respect to hypertension and chronic kidney disease, adverse events experienced in utero can affect development of the fetal kidney and reduce final nephron number. Low birthweight and prematurity are the most consistent clinical surrogates for a low nephron number and are associated with increased risk of hypertension, proteinuria, and kidney disease in later life. Rapid weight gain in childhood or adolescence further compounds these risks. Low birthweight, prematurity, and rapid childhood weight gain should alert clinicians to an individual's lifelong risk of hypertension and kidney disease, prompting education to minimise additional risk factors and ensuring follow-up. Birthweight and prematurity are affected substantially by maternal nutrition and health during pregnancy. Optimisation of maternal health and early childhood nutrition could, therefore, attenuate this programming cycle and reduce the global burden of hypertension and kidney disease in the future. Copyright © 2013 Elsevier Ltd. All rights reserved.
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              Is low birth weight an antecedent of CKD in later life? A systematic review of observational studies.

              There has been considerable interest in the hypothesis that low birth weight may be a marker of impaired nephrogenesis and that this is causally related to chronic kidney disease (CKD). Systematic review and meta-analysis of observational studies. Studies of the relationship between birth weight and CKD published before February 1, 2008, were identified by using electronic searches. All studies that had collected data for birth weight and kidney function at greater than 12 months of age were eligible for inclusion, except for studies of extremely low-birth-weight infants, very premature infants, or toxic exposure in utero. STUDY FACTOR: Birth weight. CKD defined as albuminuria, low estimated glomerular filtration rate (<60 mL/min/1.73 m(2) or < 10th centile for age/sex), or end-stage renal disease. We analyzed 31 relevant cohort or case-control studies with data for 49,376 individuals and data for 2,183,317 individuals from a single record-linkage study. Overall, 16 studies reported a significant association between low birth weight and risk of CKD and 16 observed a null result. The combination of weighted estimates from the 18 studies for which risk estimates were available (n = 46,249 plus 2,183,317 from the record linkage study) gave an overall odds ratio (OR) of 1.73 (95% confidence interval [CI], 1.44 to 2.08). Combined ORs were consistent in magnitude and direction for risks of albuminuria (OR, 1.81; 95% CI, 1.19 to 2.77), end-stage renal disease (OR, 1.58; 95% CI, 1.33 to 1.88), or low estimated glomerular filtration rate (OR, 1.79; 95% CI, 1.31 to 2.45). A reliance on published estimates and estimates provided on request rather than individual patient data and the possibility of reporting bias. Existing data indicate that low birth weight is associated with subsequent risk of CKD, although there is scope for additional well-designed population-based studies with accurate assessment of birth weight and kidney function and consideration of important confounders, including maternal and socioeconomic factors.
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                Author and article information

                Journal
                Curr Pediatr Rev
                Curr Pediatr Rev
                CPR
                Current Pediatric Reviews
                Bentham Science Publishers
                1573-3963
                1875-6336
                November 2018
                November 2018
                : 14
                : 4
                : 219-226
                Affiliations
                Division of Pediatrics and DOHaD Lab, CHUV-UNIL, Lausanne, CH, Switzerland; University of Lausanne, CH, Lausanne, , Switzerland; Médecine Néonatale, Hôpital La Conception, APHM, Aix-Marseille Université , Marseille, , France
                Author notes
                [* ]Address correspondence to this author at the Division of Pediatrics and DOHaD Lab, CHUV-UNIL, Lausanne, CH, Switzerland; Tel: +417955639 35; E-mail: Umberto.simeoni@ 123456chuv.ch
                Article
                CPR-14-219
                10.2174/1573396314666180813121652
                6416185
                30101715
                b9f5e54e-671d-4adf-9ce7-4dbb3cbe4354
                © 2018 Bentham Science Publishers

                This is an open access article licensed under the terms of the Creative Commons Attribution-Non-Commercial 4.0 International Public License (CC BY-NC 4.0) ( https://creativecommons.org/licenses/by-nc/4.0/legalcode), which permits unrestricted, non-commercial use, distribution and reproduction in any medium, provided the work is properly cited.

                History
                : 31 January 2018
                : 26 July 2018
                : 27 July 2018
                Categories
                Article

                Pediatrics
                preterm infant,small for gestational age,preeclampsia,antenatal glucocorticoids,nephron number,hypertension,cardiovascular disease,chronic kidney disease,dohad,programming,noncommunicable diseases,adult

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