Chiara Cauzzo
Valentina Chiavaroli
Susanna Di Valerio
Francesco Chiarelli- 1Department of Pediatrics, University of Chieti, Chieti, Italy
- 2Neonatal Intensive Care Unit, Pescara Public Hospital, Pescara, Italy
There is increasing evidence of a strong association between intrauterine growth and subsequent development of chronic disease in adult life. Birth size and growth trajectory have been demonstrated to have an impact on cardio-metabolic health, both in childhood and adult life. Hence, careful observation of the children’s growth pattern, starting from the intrauterine period and the first years of life, should be emphasized to detect the possible onset of cardio-metabolic sequelae. This allows to intervene on them as soon as they are detected, first of all through lifestyle interventions, whose efficacy seems to be higher when they are started early. Recent papers suggest that prematurity may constitute an independent risk factor for the development of cardiovascular disease and metabolic syndrome, regardless of birth weight. The purpose of the present review is to examine and summarize the available knowledge about the dynamic association between intrauterine and postnatal growth and cardio-metabolic risk, from childhood to adulthood.
1 Introduction
The switch in the worldwide pattern of diseases from infectious illnesses towards chronic disorders has been of special concern for several decades in developed countries, but it is becoming relevant also in developing nations, which are facing an epidemiological transition towards an emerging epidemic of chronic diseases (1). Of note, it is becoming increasingly evident the strong connection between birth weight and subsequent development of chronic diseases in adult life (2–5). Namely, there is evidence from several studies that individuals born small for gestational age (SGA) are more likely to present cardio-metabolic complications in later life (6–8). Birth weight is not only determined by genetic factors, but it is also influenced by the prenatal environment (9, 10). It has been reported that unfavourable intrauterine environment and compromised fetal growth play a part in the development of atherosclerosis and adult cardiovascular disease (1). Therefore, greater attention should be given to a healthy lifestyle for women, especially in the months before conception and during pregnancy (11, 12). There is recent evidence that also prematurity may be an independent risk factor for the onset of cardiovascular disease and metabolic syndrome, regardless of birth weight (13).
While some studies indicate intrauterine undernutrition as the main factor in the determination of chronic disease, other authors highlight the crucial role of growth trajectory in the postnatal period as the most important determinant in later expression of chronic diseases, primarily cardiovascular and cerebrovascular (14–18). Likewise, careful observation of the children’s growth pattern, since the first years of life, should be emphasized. Furthermore, it is important to monitor the onset of the cardio-metabolic consequences linked to those growth patterns in order to promote strategies that contribute to health improvement (19, 20). The challenge is to intervene on cardio-metabolic risk factors as soon as they are detected, first of all through lifestyle interventions, whose efficacy seems to be higher when they are started early (21, 22).
Therefore, the purpose of the present review is to examine and abridge the available knowledge about the dynamic association between birth size as well as growth trajectory and cardio-metabolic risk in the subsequent extrauterine life, starting from childhood into adulthood.
An ample literature search was conducted through the main databases, including PubMed, UpToDate and Scopus, in order to examine the available data about definitions, pathogenesis, and consequences of being born SGA and/or preterm as well as the clinical management and approach to prevent and/or postpone future health problems. The following search terms were used: preterm birth, premature, SGA, birth size, cardio-metabolic risk, cardiovascular risk, diabetes and hypertension. Reference list of retrieved records was also checked out. The search was limited to the English language papers and was updated on May 1, 2023.
2 Definitions
The terms used in this review are the following: intrauterine growth restriction (IUGR), SGA, prematurity, low-, very low- and extremely low-birth weight (LBW), catch-up growth, overweight, obesity, and metabolic syndrome.
Overall, birth weight is influenced by a variety of determinants, including genetics, ethnicity, maternal nutrition before and during pregnancy, maternal obesity, smoking, and diabetes (23). The mechanisms responsible for impaired fetal growth can be classified as fetal, utero-placental, and maternal (such as malnutrition, low maternal body mass index (BMI) before pregnancy and insufficient gestational weight gain) (7, 24).
Although IUGR is often used as a synonym for SGA, this acronym refers to a condition where the fetus is not able to reach its growth potential because of underlying pathological conditions (7). Thus, the term IUGR should be used only in reference to the fetus and can be estimated from fetal sonographic measurements, through which a diminished growth velocity can be detected on serial ultrasounds (25). This growth pattern can be distinguished in early IUGR, when recognized before 32 weeks of gestation, and in late IUGR, if detected at 32 weeks of gestation or beyond (25). Many fetuses with IUGR may be born SGA, depending on timing of the intrauterine insult and its severity, but not all of them. On the other hand, many SGA newborns have not experienced IUGR (24, 26).
The term SGA is used to describe infants having a birth weight and/or length below the expected range for gestational age. While neonatologists tipically define SGA as a newborn with birth weight lower than the 10th percentile for gestational age (24), for pediatric endocrinologists SGA is defined as a birth weight and/or length at least 2 standard deviations (SDs) beneath the mean for gestational age and sex, derived from reference populations data (24, 27). Namely, the definition of the 10th percentile is relevant to evaluate morbidity and mortality in the neonatal period (24, 28), while the cut-off point of -2 SDs may help recognizing those infants who need careful and ongoing growth monitoring (22, 29). Infants can be subcategorized into the following three groups: SGA for weight, SGA for length and SGA for weight and length (26, 30). In order to obtain an accurate classification of SGA, it is recommended to use national growth charts or, as an alternative, the most appropriate ones for the region- and ethnic-specific population (26).
According to the World Health Organization (WHO), preterm birth is defined as a birth happening before 37 completed weeks of gestation, or less than 259 days after the first day of the last menstrual period preceding the pregnancy (31). Preterm birth can be further categorized into extremely preterm (< 28 weeks), very preterm (28 to < 32 weeks), and moderate (32 to < 34 weeks) to late preterm (34 to < 37 weeks) (32). The worldwide rate of preterm birth is about 11%, corresponding approximately to 15 million babies born preterm every year (32, 33). Preterm birth can be intended as an adverse pregnancy outcome (where the fetus is unable to achieve the growth potential inside maternal uterus) or a preferred outcome (where a miscarriage or non-viable prematurity has been avoided). Unfortunately, a proportion of babies can be born preterm even in low-risk pregnancies of healthy women (34).
WHO defines LBW as a weight at birth < 2500 g. This definition embraces both preterm infants who usually have appropriate size for their gestational age and infants born at term with poor birth weight (24). Very low- and extremely low-birth weight are specified as birth weight < 1500 and < 1000 g, respectively (22).
Catch-up growth is defined as an accelerated growth velocity in weight and/or height during early life that compensates the poor intrauterine growth in children born SGA. Indeed, approximately 90% of children born SGA undergo catch-up growth before the age of two (35, 36). This compensatory growth has been linked to positive effects in children born SGA, mainly on cognitive abilities and adult height (35). However, recent literature is increasingly focusing on the idea that growth patterns in the first years of life might influence long-term health (37–39). Catch-up growth, primarily in weight, has been proven to have an effect on cardio-metabolic risk factors, including overweight, obesity, and insulin resistance both in childhood and, to a greater extent, in adulthood, independently of birth weight (20, 35, 36). Rapid catch-up growth in the postnatal period is more common in newborns with LBW, which makes them more prone to chronic diseases in adult life (11). These findings underline the importance of a regular growth monitoring in these children.
WHO’s definition of overweight and obesity in children younger than 5 years refers to a weight-for-height index > 2 and 3 SDs above the WHO Child Growth Standards median, respectively. In older children and adolescents the definition is based on the BMI-for-age score, distinguishing overweight when > 1 and obesity when > 2 SDs over the WHO Growth Reference median. For adults, overweight and obesity are defined by WHO as a BMI ≥ 25 kg/m2 and 30 kg/m2, respectively (40).
Lastly, according to Cook’s criteria, metabolic syndrome is defined as the co-existence of three or more of the five following components: abdominal circumference ≥ 90th percentile, blood pressure ≥ 90th percentile, fasting glycemia ≥ 100 mg/dl, HDL cholesterol ≤ 40 mg/dl and triglycerides ≥ 110 mg/dl (41). In 2014 a definition of metabolic syndrome for prepubertal children was proposed by the IDEFICS study, which used values obtained from 18.745 European children to determine age-specific and sex-specific percentiles (height-specific when considering blood pressure), from which to establish cutoffs for the metabolic syndrome components in children with age between 2 and 11 years: waist circumference (≥ 90th percentile); triglycerides (≥ 90th percentile); HDL cholesterol (≤ 10th percentile); blood pressure (systolic ≥ 90th percentile or diastolic ≥ 90th percentile); glucose metabolism (insulin ≥ 90th percentile or fasting glucose ≥ 90th percentile). In accordance with this last definition, a careful and strict follow-up is required when three or more of the risk factors overcome the 90th percentile (≤ 10th percentile for HDL cholesterol); intervention is recommended if three or more risk factors exceed the 95th percentile (≤ 5th percentile for HDL cholesterol) (42, 43).
3 Pathogenesis of cardio-metabolic sequelae
There is evidence that birth size and growth trajectory can be related to an increased cardio-metabolic risk. Namely, a link has been shown with the following health issues: glucose-insulin metabolism derangement, overweight/obesity, blood pressure alterations, endothelial dysfunction, lipidic profile modifications, and metabolic syndrome (22) (Figure 1).
Figure 1 Cardio-metabolic consequences linked to intrauterine and postnatal growth.
Barker was the first epidemiologist who suggested the correlation between LBW and cardiovascular disease and metabolic syndrome in later life (22, 44). Several hypotheses have been proposed to clarify this unfavorable association. The “fetal origins hypothesis” was formulated as a theory for the origin of type 2 diabetes (T2D), suggesting that glucose and insulin metabolism are programmed already in fetal life by factors able to affect also fetal growth, primarily maternal nutrition (45). According to the “fetal insulin hypothesis” genetically determined insulin resistance results in an impaired insulin-mediated growth in the fetus and in the development of insulin resistance in adulthood. Therefore, LBW, insulin resistance, glucose intolerance, diabetes and hypertension could all be phenotypes of the same insulin-resistant genotype (46). Indeed, the correlation observed between monogenic diseases that alter glucose tolerance or increase insulin resistance with impaired fetal growth supports the previous theory (46, 47). Afterwards, the “thrifty phenotype hypothesis” proposed that when a fetus endures insufficient nutrition during gestation the growth and development of vital organs, such as the brain, is guaranteed at the expense of other “less noble” tissues, such as the muscle and the endocrine pancreas. Of importance, the metabolism is able to adapt to a condition of limited nutrition, being programmed to take advantage when facing similar conditions in postnatal life (48). This last hypothesis was extended by the “predictive adaptive response hypothesis”: the fetus dynamically interacts with the environment and adapts to it (“developmental plasticity”) in order to survive when exposed to hostile intrauterine conditions (3). However, this “metabolic programming” becomes unfavorable when the fetus is exposed to excessive nutrition postnatally (49). Lastly, in the “rapid catch-up growth hypothesis”, LBW itself is not seen as a risk factor for chronic diseases as only SGA newborns who experience a rapid catch-up growth during the first years of life show an increased cardio-metabolic risk (50–52). Thus, the “metabolic programming” for later diseases starts before birth and continues throughout childhood (53).
Epigenetic changes (e.g., DNA methylation, histone modification, and noncoding RNAs) have also been proven to exert a pivotal role in the development of cardio-metabolic diseases (54). A recent work hints that alterations at birth in DNA methylation of specific imprinted genes (e.g., PLAGL1, MEST, PEG10, and NNAT DMRs) are correlated with the risk of obesity at the age of 1 and 3 years (55), supporting the findings from a previous study in older children (56). In addition, birth weight has itself been linked to epigenetic modifications. Namely, DNA methylation at several CpG sites at birth has been associated with birth weight, and this association has been partly observed also in childhood (57).
Overall, it can be assumed that the susceptibility to cardio-metabolic disease originates from a combination of both genetic and environmental factors.
4 Glucose-insulin metabolism derangement
The correlation between birth weight and increased risk of developing T2D has been demonstrated in both children and adults (58, 59) (Table 1). Namely, most of the studies reported an inverse relationship of birth weight with: i) fasting glucose and insulin levels; ii) glucose levels two hours after a glucose tolerance test; iii) prevalence of T2D; and iv) insulin resistance, regardless of sex. In addition, these relationships are present whether or not adjustment for current size was carried out, providing indirect support for the “fetal origins hypothesis” (45).
Table 1 Glucose-Insulin Metabolism Derangement.
It has been reported that children born SGA have an increased risk of T2D than peers born appropriate-for-gestational-age (AGA) since school-age (59). It is well known that overweight and obesity, mostly in combination with a central distribution of adipose tissue, are associated with hyperinsulinism (60, 61). Nevertheless, glucose metabolism has been found altered independently of fatness in children born SGA (62). Insulin sensitivity, assessed by intravenous glucose tolerance test, has been found lower in SGA children than AGA peers and, as a consequence, the former group compensate by almost tripling the acute insulin response in the attempt to maintain a normal glucose tolerance (62). In children with obesity, being born SGA increases insulin resistance when compared to being born AGA (63). Although several studies have observed an increase in insulin levels and greater insulin resistance in SGA children compared to AGA peers, not all of them have found a consensual increase in fasting glucose levels (64).
Besides birth weight, accelerated early weight gain also contributes to increase the risk of insulin resistance in childhood, with the long-term effects of insulin resistance extending into adulthood (65–69). As a matter of fact, rapid infancy weight gain has been shown to be a strong predictor of fat accumulation during adult life (70), while another study reported only a feeble effect of rapid infancy weight gain on insulin levels in young adulthood (69).
Greater insulin resistance has been found also in children born preterm (71). Namely, 7-year-old children born prematurely have been found to be more insulin-resistant than controls having the same age; the effect of prematurity was independent of intrauterine growth (71). Another study involving 6-year-old children born preterm showed increased basal insulin and C-peptide levels in those with birth weights lower than the 10th percentile (72). In a recent systematic review and meta-analysis, an association between preterm birth and higher homeostatic model assessment for insulin resistance (HOMA-IR) levels, a surrogate marker of insulin resistance, has been observed, together with increased fasting glucose and insulin levels. It was concluded that preterm birth is strongly related with many metabolic syndrome components and cardiovascular disease in adult life, although the results were not differentiated between individuals born AGA and those born SGA (73). It must be emphasized that infants born very preterm differ from full term ones in the postnatal growth curve, which shows an initial slowing of growth speed followed by a later catch-up growth (i.e. at approximately 4 years of age) (74, 75). Higher fasting concentrations of 32-33 split proinsulin, a marker of insulin resistance, have been reported in children born preterm aged 13–16 years with rapid postnatal weight gain compared to those without (76). In adults born prematurely, altered glucose tolerance test and increased risk for cardiovascular disease were reported when compared to adults born at term; however, it must be highlighted that the preterm group included subjects who were born SGA or with LBW (13). Another study, conducted in a quite wide population of individuals born very preterm, demonstrated that accelerated weight gain in the first three months of age predicted higher insulin levels at age 19, although the association was weak. Furthermore, fat accumulation strongly correlated with higher insulin and C-peptide levels as well as increased HOMA-IR at 19 years of age. The impact of adult fat accumulation on these parameters of insulin resistance was found to be conditioned by birth weight SDs (69). In accordance with the previous findings, it has been showed that HOMA-IR (77) was relatively high in men and women born very preterm and that these subjects, already at the age of 19 years, showed some centralization of fat distribution compared with a reference population (69).
Some wide population studies showed that both SGA and preterm birth can be risk factors for T2D onset in children (78, 79). The query of whether adults born very preterm, especially if SGA at birth and subsequently becoming overweight, experience an early onset of T2D is still open and needs to be further evaluated (69, 80).
Of note, while preterm birth has been described as a risk factor for type 1 diabetes (79), being born SGA seems to have a protective effect on this disease onset (81). These observations suggest different repercussions of SGA and preterm birth on glucose-insulin metabolism (82).
Overall, as there is a tracking of glucose-insulin metabolism derangement from childhood to adulthood, healthcare professionals should promptly recognize glucose-insulin alterations in subjects born SGA and/or preterm, especially in presence of early weight gain.
5 Overweight and obesity
Overweight and obesity are clearly related to cardio-metabolic risk factors. Thus, early preventive strategies need to be applied given that worldwide the prevalence of overweight and obesity has remarkably increased in the pediatric population, even in early childhood, and many of these preschoolers maintain obesity also in adolescence and adulthood (19, 20) (Table 2).
Table 2 Overweight and obesity.
In 2018 a longitudinal study starting at birth and extended to the whole first decade of life analyzed the connection of birth weight and current size with cardio-metabolic risk factors. The main finding was that the impact of current body size on cardio-metabolic parameters amplified over the years, partially numbing the potential effect of birth weight. Indeed, obesity at 5 years of age was directly related to birth weight, increased by maternal obesity and partially mitigated by breastfeeding, whereas at 10 years of age maternal obesity was the only factor related to obesity in children (20).
Children born SGA have an increased risk for obesity already during childhood and adolescence (7, 83). As there is clear evidence that rapid early weight gain predisposes to visceral adiposity (22), it is mandatory to promptly recognize those children born SGA who experience rapid catch-up growth, as they can develop visceral adiposity since pre-pubertal stage, even without overweight (84).
Furthermore, a reduced total fat mass with a lower amount of subcutaneous fat has been observed in SGA children, determining an increased visceral to subcutaneous fat ratio (85, 86). The role of body composition in cardio-metabolic risk is a relevant point to be addressed. Indeed, considering that regional body fat distribution is a well-known determinant of cardiovascular risk, body composition has acquired a prognostic significance (87). Visceral adipose tissue has been associated with insulin resistance and metabolic syndrome in adults (88) and, compared to subcutaneous fat, visceral fat is related to a less favorable adipokyne and inflammatory profile, leading to a significant reduction in insulin sensitivity (88, 89). Several studies have associated visceral fat to insulin resistance and metabolic derangement both in children and adolescents (90–95). Studies examining subcutaneous adipose tissue independently of total and visceral adipose tissue in obese adolescents showed that its effect may be neutral or even protective towards insulin resistance (90, 95). Indeed, subcutaneous fat may behave as a buffer and prevent lipotoxicity in other tissues, in consonance with the “adipose tissue expandability” hypothesis (88, 89). All these observations underline the importance of considering the impact of body composition in the SGA group.
Of importance, overweight and obesity may develop later in those born SGA (96). Puberty is another time of substantial metabolic and hormonal modifications, which may magnify the metabolic abnormalities. This has remarkable implications for adolescents with obesity, as evidence shows puberty as one of the prominent risk factors for transition from metabolically healthy to unhealthy obesity (97, 98). Notably, many studies reported a strong association between LBW and overweight in adolescence (99), and the risk for obesity remains high even in adult life in individuals born SGA (7, 83).
A more rapid weight gain after preterm birth has been associated with altered body composition (higher fat mass percentage, fat mass index and waist circumference) in childhood (100).
In adults born preterm a higher percentage of total body fat mass and a greater risk for cardiovascular disease have been reported when compared to individuals born at term, although results were not differentiated between adults born SGA and those born AGA (13, 73).
Given that overweight and obesity represent a risk for later cardio-metabolic disease (101), it is essential to carry a regular growth evaluation in these high-risk groups of children to guarantee early and appropriate interventions. As a matter of fact, counseling in nutrition, physical activity and sleep routine addressed to the whole family may improve their future cardio-metabolic health.
6 Blood pressure alterations
Unsatisfactory intrauterine growth has been correlated with elevated systolic blood pressure in children, adolescents, and adults (8) (Table 3). The relationship between birth weight and blood pressure in childhood may be partly explained by the effect of birth weight on childhood overweight (102), although many authors found an independent correlation between weight at birth and blood pressure during childhood and adolescence (103). Maternal preeclampsia has also been related to higher systolic and diastolic blood pressure in children, and being born SGA after a pre-eclamptic pregnancy increases the risk of developing hypertension in childhood and young adulthood (104, 105). Nevertheless, although at birth blood pressure is related to birth weight, overtime it becomes progressively more dependent on body size, while the impact of birth weight gradually reduces (106, 107). Indeed, current weight has been recognized as the main determinant of childhood hypertension. An early catch-up growth also amplifies the risk of hypertension with onset in childhood (8, 108). As elevated blood pressure in childhood rises the risk for cardiovascular disease in adulthood, it is crucial to provide proper interventions as soon as possible (109, 110).
Table 3 Blood Pressure Alterations.
Considering a more long-term risk, a population-based study including over 11.000 women who were born SGA found an increased risk of severe preeclampsia during future pregnancies (26, 111).
Of note, a recent study including toddlers born very preterm demonstrated a significant blood pressure increase in both systolic and diastolic mean values compared to a term-born cohort (112). The worrying detection of these alterations already during the toddler period could indicate an increased risk of cardiovascular diseases in adulthood for this population. Moreover, the blood pressure increase was even more meaningful in individuals born preterm who experienced rapid weight gain in early life (112). Indeed, children born preterm, especially those who experience a more rapid weight gain in childhood, have been found to have higher blood pressure in adolescence (100). In adults born preterm elevated arterial blood pressure and increased risk for cardiovascular disease have been observed when compared to individuals born at term (13).
7 Endothelial disfunction and lipidic profile modifications
Some authors have described an association between birth weight and impaired endothelial function in childhood (113, 114) and adulthood (115) (Table 4).
Table 4 Endothelial disfunction and lipidic profile modifications.
Prenatal growth restraint has been reported to result in cardiovascular remodeling. This may intensify the predisposition for future cardiovascular disease (116). Aortic and carotid intima-media thickness (IMT), which are markers of preclinical atherosclerosis, were found increased in SGA subjects both in childhood and young adulthood (117, 118). In SGA children, increased carotid IMT has been detected already at the age of 3-6 years (119). In a population comprehensive of SGA and AGA children, excessive weight gain between 3 and 6 years of age turned out to be an independent predictor of carotid IMT (119, 120). Obesity-related increase of carotid IMT has been reported since childhood and adolescence, and it persists in adulthood if obesity is not corrected on time (121).
Higher IMT has been associated also with preterm birth (73). In addition, homocysteine and heart-type fatty acid-binding protein, well known markers of myocardial and vascular impairment in adults (122, 123), have been found altered in preterm fetuses with IUGR (124). However, the significance of these markers in apparently healthy SGA infants with catch-up growth is still controversial (125, 126).
Dyslipidemia has an important impact on cardio-metabolic health (127), and many authors have tried to understand the effect of birth weight on lipid levels in childhood. Some studies suggested a relationship between being born SGA and an unfavorable lipid profile both in childhood and adolescence (128, 129). Besides, poor catch-up growth in height has been associated with high levels of total cholesterol in adolescence (129). LBW has been associated with onset of dyslipidemia also in adulthood (14).
A recent work described an association between preterm birth and total cholesterol levels in adult life, but results were not differentiated between those born AGA and SGA (73).
Beyond the effects of BMI percentile, children born preterm in the fifth grade had significantly higher triglycerides levels than peers born at term (128).
8 Metabolic syndrome
A systematic review focusing on the relationship between LBW and rapid catch-up growth with metabolic syndrome displayed that, in the largest number of studies including SGA-born children, adolescents and adults, both LBW and catch-up growth were associated with some aspects of metabolic syndrome in subsequent life (11). However, it was unclear which one between LBW and catch-up growth played the dominant role in leading to metabolic syndrome (11, 130) (Table 5).
Table 5 Metabolic syndrome.
An adverse cardio-metabolic profile, defined on the basis of clinical and biochemical parameters (BMI; systolic blood pressure; HOMA-IR; triglycerides and triglycerides:HDL ratio), was detected in children born SGA compared to AGA peers, with a worsening of this profile during adolescence. These data suggest a progression of insulin resistance and the overall cardiovascular risk from childhood to adolescence in SGA population (131).
A recent study compared metabolic syndrome parameters between very preterm and term children who were born AGA (41). The main finding was that some parameters were altered already in prepubertal age: namely, the proportion of children with low HDL-cholesterol concentrations and elevated blood pressure was higher in the very preterm group. A similar distribution of overweight and obesity was observed in both very preterm and term children. It is important to notice that, even though the two groups had similar BMIs, a stronger association with metabolic syndrome parameters was found in infants born very preterm (41). Accelerated weight gain during the first years of life may be a critical contributor to the development of obesity later in life in children born preterm (132). In another study involving adults, blood pressure was shown to be altered in 57.5% of those born very preterm, and elevated blood pressure was the most prevalent parameter of metabolic syndrome in this group. In addition, the mean value of HDL-cholesterol was significantly lower in adults born very preterm than in peers born at term (133).
Animal studies showed that accelerated weight gain amplifies the risk of metabolic disease, even in the absence of intrauterine growth restriction, and the effects of LBW on adult phenotype can be reversed with prevention of postnatal acceleration in weight. These observations support the concept that accelerated postnatal weight gain is a key independent risk factor for subsequent metabolic disease (26, 134).
9 Clinical management
Recently, an international consensus guideline clarified the main aspects and indications for SGA-born patients management from infancy to early adulthood. In this document, the authors stress out that children born SGA should be monitored during their first years of life, initially by a neonatologist and afterwards by a pediatrician to carefully evaluate their growth and weight gain (26). Namely, it is crucial to prevent excessive postnatal weight gain given its association with a less favorable cardio-metabolic profile in adult life. To do so, the authors recommend to avoid additional nutrition for healthy infants in the first 6 months of life, unless they endure malnutrition (26) (Table 6).
Table 6 Clinical management recommendations.
Furthermore, in these guidelines a few high-risk populations are pointed out: very preterm or severely SGA-born children (birth weight and/or length < -3 SDs for gestational age), infants with complicated perinatal period, small head circumference, or with a syndrome causing growth impairment. These groups of children should be monitored more carefully, with shorter time intervals and early referred to a pediatric endocrinologist (26).
In the first two years of life, clinical management should focus on optimal nutrition to guarantee correct catch-up growth and to prevent excessive weight gain, as well as to exclude a possible genetic cause (26, 135). Recent works involving SGA-born children with a long-term follow-up agreed on the importance of breastfeeding in promoting adequate growth without causing unfavorable body composition or impaired insulin sensitivity and represent, therefore, the ideal nutrition for infants born SGA (26, 136, 137). Age-appropriate balanced diet containing macro- and micronutrients is recommended for optimal growth (26).
Early growth pattern evaluation is a crucial tool in the clinical management of these newborn and children. Weight, length, head circumference, and BMI should be monitored every 3 months during the first year of life, every 6 months in the second year of life, and afterwards once a year until the achievement of genetic target height. Growth parameters should be plotted on an appropriate growth chart and the obtained curve should be assessed (26).
In the following years of life, other than nutrition and growth, clinical management also focuses on pubertal onset and progression, and metabolic profile (26, 29). Metabolic parameters evaluation (fasting plasma glucose, oral glucose tolerance test, lipid profile) is not routinely indicated, but should be performed in children with overweight or obesity, family history of T2D, or clinical signs suggestive of a metabolic disease (26). Excessive weight gain (change in weight-for-length > 0.67 SDs), particularly in early childhood and during school years, should be avoided (35). It is essential to recommend a healthy lifestyle, comprehensive of a balanced diet and regular physical activity (26).
10 Supplementary considerations for economically developing nations
In developing nations approximately up to 50-60% of infants born SGA show satisfying catch-up growth in height and/or weight, and in these situations of poor nutrition and low protein dietary intake catch-up growth may be delayed up to the age of 5 years (138, 139).
Many factors may be involved in this negative outcome, primarily poor maternal nutrition, insufficient hygiene, infections, and low socioeconomic status (138). Therefore, in order to reduce SGA births in these countries and obtain a sufficient catch-up growth, it is crucial to improve nutrition, hygiene, and antenatal care during pregnancy, as well as to exclude subclinical hypothyroidism and to prevent and treat malaria where it is endemic (26).
Local reference growth charts should be used to monitor children born SGA (140). Given that many healthy children are below the 3rd percentile for both height and weight considering WHO charts and that this phenomenon is emphasized in SGA, clinician should focus on the whole growth trajectory rather than on a single height and/or weight evaluation (26, 140).
Therefore, close monitoring of the growth trajectory is mandatory to prevent on one hand failure to thrive and on the other excessive catch-up in weight. Breastfeeding has been related with less rapid catch-up and growth lower fasting insulin and glucose concentrations both in infancy and childhood (141), with a protective effect against later obesity in numerous studies (142–144). Hence, WHO recommends exclusive breastfeeding or standard formulas rather than nutrient-enriched formulas during the first 6 months of life. Nevertheless, in LBW infants living in extremely poor regions, the priority is the avoidance of malnutrition and failure to thrive (145).
11 Conclusions
This review highlights how alterations in intrauterine growth have been associated with long-term cardiovascular and metabolic consequences. Children born SGA, particularly if they have experienced accelerated catch-up in weight in early life and/or obesity in later life, are at risk for insulin resistance and central adiposity since early childhood (51, 146, 147). They are also at risk for cardiovascular dysfunctions in later life (146). Additionally, growth trajectory in the first period of life is important in establishing risk for cardio-metabolic health across the lifespan (148). Thus, a careful observation of the children’s growth pattern, since the intrauterine period and the first years of life, should be emphasized, together with appropriate family counseling (22, 149). Notably, a healthier lifestyle for women in their fertility age, primarily while pregnant, is highly important to promote the offspring’s future health and wellbeing (11, 12), with a special focus on the first thousand days of life (19, 20).
Author contributions
CC and VC: wrote the manuscript and were involved in literature search and drafting the paper. SV and FC: coordinated and approved the final version of the manuscript. The content has not been published or submitted for publication elsewhere.
Conflict of interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
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Keywords: intrauterine growth, small for gestational age, birth weight, preterm, cardiovascular risk
Citation: Cauzzo C, Chiavaroli V, Di Valerio S and Chiarelli F (2023) Birth size, growth trajectory and later cardio-metabolic risk. Front. Endocrinol. 14:1187261. doi: 10.3389/fendo.2023.1187261
Received: 15 March 2023; Accepted: 19 May 2023;
Published: 05 June 2023.
Edited by:
Anna Di Sessa, University of Campania Luigi Vanvitelli, ItalyReviewed by:
Justyna Czech-Kowalska, Children’s Memorial Health Institute (IPCZD), PolandBarbara Glowinska-Olszewska, Medical University of Bialystok, Poland
Copyright © 2023 Cauzzo, Chiavaroli, Di Valerio and Chiarelli. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Chiara Cauzzo, Y2hpYXJhLmNhdXp6b0B5YWhvby5pdA==
†These authors have contributed equally to this work and share first authorship