Gestational Diabetes Research Papers

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21. Berkowitz GS, Lapinski RH, Wein R, Lee D. Race/ethnicity and other risk factors for gestational diabetes. Am J Epidemiol. 1992;135:965–973.[PubMed]

22. Retnakaran R, Hanley AJ, Connelly PW, Sermer M, Zinman B. Ethnicity modifies the effect of obesity on insulin resistance in pregnancy: a comparison of Asian, South Asian, and Caucasian women. J Clin Endocrinol Metab. 2006;91:93–97.[PubMed]

23. Cypryk K, Szymczak W, Czupryniak L, Sobczak M, Lewiński A. Gestational diabetes mellitus - an analysis of risk factors. Endokrynol Pol. 2008;59:393–397.[PubMed]

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25. Sermer M, Naylor CD, Farine D, Kenshole AB, Ritchie JW, Gare DJ, Cohen HR, McArthur K, Holzapfel S, Biringer A. The Toronto Tri-Hospital Gestational Diabetes Project. A preliminary review. Diabetes Care. 1998;21 Suppl 2:B33–B42.[PubMed]

26. Callesen NF, Ringholm L, Stage E, Damm P, Mathiesen ER. Insulin requirements in type 1 diabetic pregnancy: do twin pregnant women require twice as much insulin as singleton pregnant women? Diabetes Care. 2012;35:1246–1248.[PMC free article][PubMed]

27. Hyperglycemia and Adverse Pregnancy Outcome (HAPO) Study Cooperative Research Group. Hyperglycemia and Adverse Pregnancy Outcome (HAPO) study: preeclampsia. Am J Obstet Gynecol. 2010;202:255.e1–255.e7.[PMC free article][PubMed]

28. Gorgal R, Gonçalves E, Barros M, Namora G, Magalhães A, Rodrigues T, Montenegro N. Gestational diabetes mellitus: a risk factor for non-elective cesarean section. J Obstet Gynaecol Res. 2012;38:154–159.[PubMed]

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30. O’Sullivan JB, Charles D, Mahan CM, Dandrow RV. Gestational diabetes and perinatal mortality rate. Am J Obstet Gynecol. 1973;116:901–904.[PubMed]

31. Crowther CA, Hiller JE, Moss JR, McPhee AJ, Jeffries WS, Robinson JS. Effect of treatment of gestational diabetes mellitus on pregnancy outcomes. N Engl J Med. 2005;352:2477–2486.[PubMed]

32. Jensen DM, Damm P, Sorensen B, Molsted-Pedersen L, Westergaard JG, Korsholm L, Ovesen P, Beck-Nielsen H. Proposed diagnostic thresholds for gestational diabetes mellitus according to a 75-g oral glucose tolerance test. Maternal and perinatal outcomes in 3260 Danish women. Diabet Med. 2003;20:51–57.[PubMed]

33. Metzger BE, Persson B, Lowe LP, Dyer AR, Cruickshank JK, Deerochanawong C, Halliday HL, Hennis AJ, Liley H, Ng PC, et al. Hyperglycemia and adverse pregnancy outcome study: neonatal glycemia. Pediatrics. 2010;126:e1545–e1552.[PubMed]

34. Bellamy L, Casas JP, Hingorani AD, Williams D. Type 2 diabetes mellitus after gestational diabetes: a systematic review and meta-analysis. Lancet. 2009;373:1773–1779.[PubMed]

35. Feig DS, Zinman B, Wang X, Hux JE. Risk of development of diabetes mellitus after diagnosis of gestational diabetes. CMAJ. 2008;179:229–234.[PMC free article][PubMed]

36. Lauenborg J, Hansen T, Jensen DM, Vestergaard H, Mølsted-Pedersen L, Hornnes P, Locht H, Pedersen O, Damm P. Increasing incidence of diabetes after gestational diabetes: a long-term follow-up in a Danish population. Diabetes Care. 2004;27:1194–1199.[PubMed]

37. Kim C, Newton KM, Knopp RH. Gestational diabetes and the incidence of type 2 diabetes: a systematic review. Diabetes Care. 2002;25:1862–1868.[PubMed]

38. Lauenborg J, Grarup N, Damm P, Borch-Johnsen K, Jørgensen T, Pedersen O, Hansen T. Common type 2 diabetes risk gene variants associate with gestational diabetes. J Clin Endocrinol Metab. 2009;94:145–150.[PubMed]

39. Lacroix M, Kina E, Hivert MF. Maternal/fetal determinants of insulin resistance in women during pregnancy and in offspring over life. Curr Diab Rep. 2013;13:238–244.[PubMed]

40. Sullivan SD, Umans JG, Ratner R. Gestational diabetes: implications for cardiovascular health. Curr Diab Rep. 2012;12:43–52.[PubMed]

41. Lauenborg J, Mathiesen E, Hansen T, Glümer C, Jørgensen T, Borch-Johnsen K, Hornnes P, Pedersen O, Damm P. The prevalence of the metabolic syndrome in a danish population of women with previous gestational diabetes mellitus is three-fold higher than in the general population. J Clin Endocrinol Metab. 2005;90:4004–4010.[PubMed]

42. Retnakaran R, Qi Y, Connelly PW, Sermer M, Zinman B, Hanley AJ. Glucose intolerance in pregnancy and postpartum risk of metabolic syndrome in young women. J Clin Endocrinol Metab. 2010;95:670–677.[PMC free article][PubMed]

43. Shah BR, Retnakaran R, Booth GL. Increased risk of cardiovascular disease in young women following gestational diabetes mellitus. Diabetes Care. 2008;31:1668–1669.[PMC free article][PubMed]

44. Retnakaran R, Shah BR. Mild glucose intolerance in pregnancy and risk of cardiovascular disease: a population-based cohort study. CMAJ. 2009;181:371–376.[PMC free article][PubMed]

45. Plagemann A. Perinatal programming and functional teratogenesis: impact on body weight regulation and obesity. Physiol Behav. 2005;86:661–668.[PubMed]

46. Pedersen J. Weight and length at birth of infants of diabetic mothers. Acta Endocrinol (Copenh) 1954;16:330–342.[PubMed]

47. Freinkel N. Banting Lecture 1980. Of pregnancy and progeny. Diabetes. 1980;29:1023–1035.[PubMed]

48. Ornoy A. Prenatal origin of obesity and their complications: Gestational diabetes, maternal overweight and the paradoxical effects of fetal growth restriction and macrosomia. Reprod Toxicol. 2011;32:205–212.[PubMed]

49. Aerts L, Van Assche FA. Animal evidence for the transgenerational development of diabetes mellitus. Int J Biochem Cell Biol. 2006;38:894–903.[PubMed]

50. Dabelea D, Pettitt DJ. Intrauterine diabetic environment confers risks for type 2 diabetes mellitus and obesity in the offspring, in addition to genetic susceptibility. J Pediatr Endocrinol Metab. 2001;14:1085–1091.[PubMed]

51. Dabelea D, Hanson RL, Lindsay RS, Pettitt DJ, Imperatore G, Gabir MM, Roumain J, Bennett PH, Knowler WC. Intrauterine exposure to diabetes conveys risks for type 2 diabetes and obesity: a study of discordant sibships. Diabetes. 2000;49:2208–2211.[PubMed]

52. Clausen TD, Mathiesen ER, Hansen T, Pedersen O, Jensen DM, Lauenborg J, Damm P. High prevalence of type 2 diabetes and pre-diabetes in adult offspring of women with gestational diabetes mellitus or type 1 diabetes: the role of intrauterine hyperglycemia. Diabetes Care. 2008;31:340–346.[PubMed]

53. Plagemann A, Harder T, Kohlhoff R, Rohde W, Dörner G. Glucose tolerance and insulin secretion in children of mothers with pregestational IDDM or gestational diabetes. Diabetologia. 1997;40:1094–1100.[PubMed]

54. Silverman BL, Metzger BE, Cho NH, Loeb CA. Impaired glucose tolerance in adolescent offspring of diabetic mothers. Relationship to fetal hyperinsulinism. Diabetes Care. 1995;18:611–617.[PubMed]

55. Kelstrup L, Damm P, Mathiesen ER, Hansen T, Vaag AA, Pedersen O, Clausen TD. Insulin resistance and impaired pancreatic β-cell function in adult offspring of women with diabetes in pregnancy. J Clin Endocrinol Metab. 2013;98:3793–3801.[PMC free article][PubMed]

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57. Clausen TD, Mathiesen ER, Hansen T, Pedersen O, Jensen DM, Lauenborg J, Schmidt L, Damm P. Overweight and the metabolic syndrome in adult offspring of women with diet-treated gestational diabetes mellitus or type 1 diabetes. J Clin Endocrinol Metab. 2009;94:2464–2470.[PubMed]

58. Landon MB, Spong CY, Thom E, Carpenter MW, Ramin SM, Casey B, Wapner RJ, Varner MW, Rouse DJ, Thorp JM, et al. A multicenter, randomized trial of treatment for mild gestational diabetes. N Engl J Med. 2009;361:1339–1348.[PMC free article][PubMed]

59. Lapolla A, Dalfrà MG, Fedele D. Management of gestational diabetes mellitus. Diabetes Metab Syndr Obes. 2009;2:73–82.[PMC free article][PubMed]

60. Reader D, Splett P, Gunderson EP. Impact of gestational diabetes mellitus nutrition practice guidelines implemented by registered dietitians on pregnancy outcomes. J Am Diet Assoc. 2006;106:1426–1433.[PubMed]

61. Homko CJ, Reece EA. Insulins and oral hypoglycemic agents in pregnancy. J Matern Fetal Neonatal Med. 2006;19:679–686.[PubMed]

62. Rowan JA, Hague WM, Gao W, Battin MR, Moore MP. Metformin versus insulin for the treatment of gestational diabetes. N Engl J Med. 2008;358:2003–2015.[PubMed]

63. Langer O, Conway DL, Berkus MD, Xenakis EM, Gonzales O. A comparison of glyburide and insulin in women with gestational diabetes mellitus. N Engl J Med. 2000;343:1134–1138.[PubMed]

64. Dhulkotia JS, Ola B, Fraser R, Farrell T. Oral hypoglycemic agents vs insulin in management of gestational diabetes: a systematic review and metaanalysis. Am J Obstet Gynecol. 2010;203:457.e1–457.e9.[PubMed]

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1Department of Psychological Health and Territorial Sciences, “G. d’Annunzio” University of Chieti-Pescara, Chieti, Italy
2Psychiatric Research Unit, Psychiatric Centre North Zealand, Copenhagen University Hospital, Hillerød, Denmark
3Department of Medicine and Aging, “G. d’Annunzio” University of Chieti-Pescara, Chieti, Italy

Copyright © 2017 Daniela Marchetti et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Background and Objective. Diagnosis of Gestational Diabetes Mellitus (GDM) could significantly increase the likelihood of health problems concerning both potential risks for the mother, fetus, and child’s development and negative effects on maternal mental health above all in terms of a diminished Quality of Life (QoL). The current systematic review study is aimed at further contributing to an advancement of knowledge about the clinical link between GDM and QoL. Methods. According to PRISMA guidelines, PubMed, Web of Science, Scopus, and Cochrane databases were searched for studies aimed at evaluating and/or improving levels of QoL in women diagnosed with GDM. Results. Fifteen research studies were identified and qualitatively analyzed by summarizing results according to the following two topics: GDM and QoL and interventions on QoL in patients with GDM. Studies showed that, in women with GDM, QoL is significantly worse in both the short term and long term. However, improvements on QoL can be achieved through different intervention programs by enhancing positive diabetes-related self-management behaviors. Conclusion. Future studies are strongly recommended to further examine the impact of integrative programs, including telemedicine and educational interventions, on QoL of GDM patients by promoting their illness acceptance and healthy lifestyle behaviors.

1. Introduction

Gestational Diabetes Mellitus (GDM) is defined as “diabetes diagnosed in the second or third trimester of pregnancy that was not clearly overt diabetes prior to gestation” [1]. GDM is one of the most frequent metabolic diseases during pregnancy and approximately affects 7% (range: 2–18%) of all pregnancies [2–5]. This clinical condition potentially affects not only negative medical outcomes but also the mental health status with additional adverse consequences on psychological well-being and Quality of Life (QoL) [6, 7].

Pregnancy is a particular time for all women. This condition becomes even more delicate when there is a diagnosis of GDM which makes necessary controls and therapies that will inevitably affect the woman’s life. GDM can lead to potential risks for the mother, fetus, and child’s development, as well as clinically relevant negative effects on maternal mental health, above all in terms of a diminished QoL [8, 9].

Health-related QoL was extensively accepted as a highly relevant outcome in different clinical trials [10]. QoL potentially operates as a unifying concept that comprises many domains such as general, physical, and psychological health, positive social relationships, environmental mastery, purpose in life, self-acceptance, autonomy, and personal growth factors [3, 11]. However, it may act by a core mechanism of subjective appraisal of own health status [12] resulting in specific diagnostic and therapeutic implications [13]. That is, QoL dimension can explain the different individual response to a standard medical treatment leading to an incomplete recovery in terms of health perception [14].

This concept was further highlighted by the World Health Organization criteria [15], which stressed the clinical relevance to promote the health status by not only treating physical symptoms but also instilling a positive mental state [16]. In this regard, the current systematic review study is aimed at further contributing to an advancement of knowledge about the clinical link between GDM and QoL.

2. Materials and Methods

2.1. Information Sources and Searches

According to Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines [17], a comprehensive electronic search strategy was used to identify peer-reviewed articles assessing QoL experienced by pregnant women diagnosed with GDM up to 19 October 2016. The following keywords were used: “gestational diabetes OR gestational hyperglycemia OR hyperglycemic pregnancy” combined using AND Boolean operator with “quality of life OR well-being”. After the initial search was performed, studies were screened for eligibility; their relevance was initially assessed using titles and abstracts and finally the full review of papers. Searching and eligibility of target responses were carried out independently by two investigators (DM and DC); any type of disagreements was resolved by consensus among these primary raters and a senior investigator (EV).

Electronic research-literature databases searched included PubMed, Web of Science, Scopus, and Cochrane databases. In order to detect any missed articles during the literature search, reference lists of candidate articles were reviewed for further studies not yet identified. For each excluded study, we determined which elements of the electronic search were not addressed.

2.2. Eligibility Criteria

Papers were eligible for inclusion if they were research reports in English language describing data on QoL domains in relation to GDM diagnosis during pregnancy. We focused on studies examining QoL in women with GDM directly or evaluating the link between QoL and well-being alternatively by specifically using measures testing QoL. Based on this inclusion criterion, we selected studies referring to QoL or well-being related to QoL by consequently excluding research reports assessing well-being through measures on negative mental health (i.e., depression, anxiety, bipolar mood, and distress) or by focusing on a medical definition of well-being (health status, wellness, physical health, etc.). Also studies aimed at evaluating the effectiveness of programs targeted for GDM patients providing effects on QoL were included.

We excluded peer-reviewed single-case studies, reviews, meta-analyses, letters to the editor and commentaries, conference abstracts, books, and papers that were clearly irrelevant. In order to generate conclusions specific to GDM, we excluded research reports aimed at addressing levels of QoL in diabetic patients, without reporting specific data for GDM subgroup (e.g., considering diabetic pregnant women those with preexisting diabetes and those receiving the first diagnosis of GDM during pregnancy). No limit was set with regard to publication date.

2.3. Analysis and Data Synthesis

The heterogeneous nature of the identified studies (in terms of design and measures) did not permit a formal meta-analysis. Hence, narrative synthesis approach was judged to be the most appropriate method for the review.

Studies were categorized based on the object of the study, differentiated as those that aimed at assessing association and those that evaluated interventions. Significant information for each study was summarized and compared.

3. Results

The search of PubMed, Web of Science, Scopus, and Cochrane databases, including additional manual search, initially provided a total of 906 articles, as shown in the PRISMA flowchart (see Figure 1). Fifteen research studies were identified as clearly relevant and qualitatively analyzed in the systematic review. Pertinent results were summarized according to the following two specific chapters: (a) GDM and QoL (Table 1) and (b) interventions on QoL in patients with GDM (Table 2). Criteria for the diagnosis of GDM used in reviewed studies are illustrated in Table 3. In all but two studies [9, 26], standardized measures of QoL were used (see Tables 1 and 2 for details).

Table 1: Characteristics of included studies assessing the impact of GDM on Quality of Life.

Table 2: Characteristics of included studies assessing the impact of treatments on Quality of Life among GDM pregnant women.

Table 3: Diagnostic criteria for GDM of included studies.

Figure 1: Flowchart of the systematic search.

3.1. GDM and QoL

When combining an evaluation of levels of illness acceptance with an assessment of the QoL, Bień et al. [3] have found that illness acceptance was significantly correlated with all QoL related scores () with values ranging from 0.20 to 0.54. Similarly, GDM participants who did not report an individual illness interference with everyday life obtained significantly higher scores compared to those stating an illness limitation on specific QoL factors. That is, statistical differences between groups were observed on general QoL (), perceived general health (), and physical (), psychological (), and environmental () domains. Moreover, further examining QoL dimensions, the psychological domain was slightly worse than other QoL domains [3].

A similar study from Kopec et al. [19] evidenced that 171 respondents (i.e., 87.3% of the total sample specifically used for statistical analyses) reported a negative impact of GDM on their social life. Results also showed that higher levels of distress were significantly reported by women who tested glucose levels more frequently and those under treatment with insulin. In addition, patients perceiving insufficient information about their GDM symptoms reported higher levels of distress than those perceiving adequate information [19].

Another recent study from Danyliv et al. [18] compared levels of health-related QoL (HRQoL) of GDM patients with those of women with normal glucose tolerance (NGT) during pregnancy. They found significantly lower scores on HRQoL dimension for the group of GDM patients. However, when adjusting for the effects of other clinical covariates by performing a pooled multivariate analysis, the authors [18] showed that GDM per se did not influence HRQOL levels.

Similarly, a study of Dalfrà et al. [8] compared levels of QoL between GDM patients, pregnant women with type 1 diabetes, and healthy pregnant participants. GDM respondents scored significantly lower than healthy controls on the SF-36 general health perception subscale () as evaluated during pregnancy at the third trimester. Moreover, whereas the SF-36 domains of QoL significantly improved after delivery among all three groups, rates of the SF-36 general health perception subscale remained significantly lower in GDM patients than in healthy controls [8].

Results in contrast with aforementioned findings were obtained from a previous research study aimed at evaluating impact of GDM on HRQOL after delivery. The authors [21] revealed no statistically significant differences between GDM patients and the healthy control group on the HRQOL dimensions. Similar results were previously reported also by Mautner et al. [22]. Their study underlined no clinically relevant differences between women with GDM and the healthy control group as concerns HRQoL levels.

Different results were later obtained from Trutnovsky et al. [20] who demonstrated significantly diminished levels of QoL among GDM patients. Specifically, GDM participants showed, from mid to late pregnancy, a significant reduction of physical, psychological, social, and global scores on the World Health Organization Quality of Life subscales (WHOQOL-BREF).

Results in line with above reported data were addressed by Rumbold and Crowther [24] when evidencing that women positively screened for GDM showed lower health perceptions than those with negative screening (). However, these statistical differences between positive and negative screened women for GDM were not significant late in pregnancy [24].

Similar results were provided in a study from Kim et al. [23]. This research highlighted that women with a diagnosis of GDM were significantly more prone to report poor physical function and a worse self-rated health status compared to healthy pregnant women. The same result was further supported after delivery with a greater proportion of GDM pregnant women reporting a lower self-rated health status than healthy controls. In addition, self-rated health status further worsened in the third trimester among women with GDM compared to healthy pregnant women without GDM. Surprisingly, GDM clinical condition was not significantly associated with declines in any other SF-36 health status subscales in the third trimester [23].

Finally, Lapolla et al. [9] indirectly revealed a worsening level of QoL among GDM women when demonstrating that this diagnosis resulted in the development of anxiety symptoms.

3.2. Interventions on QoL in Patients with GDM

When comparing QoL levels in GDM women attending different treatment programs (i.e., metformin alone, insulin alone, or a combination of both treatments), Latif et al. [25] showed that the negative influence on overall QoL was less with metformin compared to insulin. Nevertheless, the treatment combining metformin with insulin resulted in a greater negative impact on the QoL. Concerning the evaluation of treatment outcomes, Elnour et al. [28] observed statistically significant () improvements in the HRQoL among patients attending a pharmacological care program.

A study, testing the effect of a telemedicine intervention, by Dalfrà and colleagues [27] found a significant improvement of the SF-36 general health perception, energy/vitality, and mental health subscales among participants attending the intervention group. Similar results were later obtained from Petkova et al. [26]. They found a significant improvement in QoL of women with GDM involved in an intervention program aimed at educating about diet, exercise, self-monitoring, and insulin treatment.

Finally, Crowther et al. [29] randomly assigned women with GDM to a specific intervention group aimed to provide dietary advice, blood glucose monitoring, and insulin therapy. At three months after delivery, participants reported a significant improvement in their QoL by obtaining higher scores on the SF-36.

4. Discussion

QoL is a clinically relevant concept determining the individual evaluation of own health status. This subjective appraisal seems to act, above all physical and treatment components of diabetes during pregnancy, as a psychological factor affecting medical outcomes in GDM. Based on current research studies, we have found that QoL could be significantly compromised, both short term and long term, when women cope with pregnancy complicated by GDM. However, GDM per se does not seem to act as unique clinical variable negatively affecting different levels of QoL among women with GDM. That is, the relationship between GDM medical symptoms and QoL domains could be mediated by a complex interaction of several factors whose unifying psychological element can be identified through the concept of the illness experience [30]. The potential underlying psychological factor, operating as core variable to clinically explain the different QoL status among patients with GDM, may consist of the varying individual way to respond to own bodily symptoms. Such psychological component conceived as general health perception was originally investigated by Mechanic and Volkart [31]. In this regard, they provided a definition of “the ways in which symptoms may be differentially perceived, evaluated, and acted upon by different kinds of persons” [30]. A relatively recent review study of Lawrence [32] has further underlined how perceptions and expectations of women with GDM may significantly affect their psychological and behavioral response during and after pregnancy.

To the very best of our knowledge, this is the first review study systematically analyzing the impact of GDM and its symptoms on QoL levels. Indeed, only a previous recently published systematic review study, evaluating the health status and QoL in postpartum women, was fulfilled by Van Der Woude et al. [33]. However, the authors neglected the assessment of such psychological mechanisms in women with GDM.

Based on additional relevant results from a review study examining the influence of QoL in the treatment outcomes of diabetes [34], specific implications can be identified. The medical evaluation of GDM should comprise a clinically valid psychological assessment of QoL in order to attempt monitoring its potential effects on GDM prognosis from first diagnosis, during the treatment, and after delivery. Specifically, the gold standard should comprise self-rating scales as screening measures for identifying psychological comorbidities potentially leading to adverse and negative clinical consequences during diabetes [35].

As regards the intervention studies examining the impact of specific treatments on QoL dimensions among women with GDM, promising results were found. The five studies retrieved [25–29] clearly indicate the efficacy of different therapeutic programs to improve QoL by enhancing positive diabetes self-management behaviors such as balanced diet, exercise, self-monitoring, and insulin control. Despite this, much more studies are largely needed when taking into account heterogeneity in subjects and study design as well as the evidence that the control group and experimental group were not consistent across studies we have qualitatively examined.

Further research should be conducted to test the effect of integrative programs on QoL focusing on pharmacological care mixed up with advanced practices based on information and communication technologies (e.g., telemedicine and/or games for health) [36, 37]. In this regard, the major aim is to educate patients on healthier lifestyle habits (healthy diet and physical activity domains) [38, 39] and to facilitate the process of illness acceptance [40] after a diagnosis of GDM.

Finally, our review shows some noteworthy points: (1) the positive effect of a telemedicine intervention on both diabetes-related medical outcomes and general health perception, energy/vitality, and mental health; (2) a significant improvement in QoL of women with GDM attending an educational program. In the future, these considerations should be taken into account for the management of diabetes during pregnancy.

Competing Interests

The authors declare that they have no competing interests to disclose.

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