Abstract
Our review aimed to assess the effects of bariatric surgery-induced weight loss on ocular functions. We focused on retinochoroidal microcirculation, glaucomatous factors, and the condition of the eye surface pre- and postoperatively. The review covered 23 articles, including five case reports. Bariatric surgery positively impacts retinochoroidal microcirculation. The arterial perfusion and vascular density improve, venules constrict, and the arteriole-to-venule ratio increases. Weight loss positively correlates with intraocular pressure decrease. The impact of postoperative weight loss on the choroidal thickness (CT) and the retinal nerve fiber layer (RNFL) is still unclear. The correlation between ocular symptoms and hypovitaminosis A needs to be evaluated. Further research is required, especially regarding CT and RNFL, mainly focusing on long-term follow-up.
Similar content being viewed by others
Avoid common mistakes on your manuscript.
Introduction
Excess fat accumulation leads to common health consequences such as cardiovascular diseases, diabetes, and ophthalmic complications. Cataract, age-related maculopathy, diabetic retinopathy, and glaucomatous optic neuropathy are some obesity-related conditions. Early diagnostics and weight loss may stop or reverse obesity-induced changes [1].
This review aims to evaluate the impact of bariatric surgery-induced weight loss on ophthalmic parameters. We decided to focus on three significant aspects that might be useful in everyday practice: intraocular pressure (IOP) and retinal nerve fiber layer (RNFL), retinochoroidal microcirculation, and ocular surface. After bariatric surgery, we investigated the positive and negative ocular consequences of decreased body mass index (BMI).
IOP positively correlates with BMI [2]. Elevated IOP is the leading risk factor for glaucoma and glaucomatous optic neuropathy [3]. Other consequences of obesity are microvasculature alterations and endothelial dysfunction [4]. Retinal microvascular changes reflect the damage from obesity and related conditions and are crucial in obesity-related cardiovascular diseases [5].
Postoperative weight loss and fat malabsorption may cause deficiencies in fat-soluble vitamins [6, 7]. Vitamin A deficiency is especially problematic due to its crucial role in ocular surface and visual acuity [7-9].
Materials and Methods
We searched the PubMed electronic database from its inception to September 2022 and analyzed the available data on pre- and postoperative ocular changes in patients with extreme obesity. To be included in the study, ocular parameters had to be compared before and after bariatric surgery. We searched for the terms “bariatric,” “bariatric surgery,” “metabolic surgery,” and “gastric bypass” and for combinations of these terms with “ophthalmology,” “ocular,” and “ocular parameters.” After an initial analysis, we narrowed the search to the three most commonly studied areas—retinochoroidal microcirculation, glaucoma risk factors, and ocular surface. We reviewed the reference lists of relevant publications for additional references. The search was limited to English language articles. Studies on ocular surface condition were an exception. Because these changes were observed postoperatively, there were no retrospective studies comparing vitamin A levels before and after surgery. Twenty-three studies were included in this analysis, including five case reports. We presented all relevant data in five comprehensive tables.
Results
Retinochoroidal Microcirculation
As the insight into the fundus of the eye enables the examination of the retinal vascularity in vivo, it allows non-invasive observation and follow-up of post-bariatric surgery patients [4]. The results of postoperative changes in retinochoroidal microcirculation are summarized in Table 1.
Arteriole-to-Venule Ratio (AVR)
AVR indicates endothelial function and reflects even preclinical metabolic and cardiovascular risk in patients with obesity [10, 11]. AVR changes result from arterial narrowing, venular dilatation, or both. It decreases in the course of weight gain due to increased arteriolar resistance and systemic hypertension [12]. There are various methods to determine the AVR, including mean arteriole and venule width, the sum of widths of arterioles and venules, the sum of squares of widths of arterioles and venules, the central retinal artery equivalent (CRAE), and the central retinal venous equivalent (CRVE) [13, 14].
Digital fundus imaging was used in a study by Lammert et al. A significant dilatation of retinal arteries and decreased retinal vein calibers increased AVR. Moreover, the authors observed a significant increase in adiponectin, regardless of gender [15].
Agarwal et al. demonstrated no difference in AVR between patients with obesity who underwent bariatric surgery or conservative treatment (diet/exercise) [12]. Debourdeau et al. have detected factors predisposing to vein narrowing and increasing AVR. High baseline weight, male sex, and no diabetes history appeared to predispose to more significant improvement of the retinal microvasculature [16].
CRAE and CRVE give more repeatable and accurate results than separate measurements of the width of arterioles and veins of the retina. The SIVA software automatically identifies vessel types and calculates retinal microvascular parameters [5].
Choroidal Thickness (CT)
The CT reflects the total choroidal vasculature [12]. Patients with extreme obesity have decreased nitric oxide levels responsible for vasodilatation [17]. Moreover, a positive association between higher BMI and vasoconstrictor factors, endothelin-1 and angiotensin-II, has been found. It may result in a decrease in choroidal blood flow and CT lowering.
A study by Dogan et al. showed a statistically significant increase in subfoveal CT after bariatric surgery [18]. Agarwal et al. considered equal sample size allocation as Dogan et al., which allowed them to reach 95% confidence and 80% power [12]. They observed increased CT in patients with obesity compared to patients with normal BMI, although it did not reach statistical significance. In a study by Gonul et al., a significant decrease in the CT values gave the opposite results. It may result from the patient characteristics, gender distributions, follow up-period, or the OCT manufacturer [7].
Retinal Thickness
Postoperative changes in retinal thickness became an object of research in 2019. Posarelli et al. observed an inverse association between minimum foveal thickness (FT) values and BMI. Interestingly, the values of minimum FT remained within the normal limits after bariatric surgery [19].
Research by Laiginhas et al. highlighted that inner retinal layers are more vascularized than the outer layers; therefore, thickening of these layers might reflect the improved perfusion [20, 21].
Laiginhas et al. identified clinical predictors for retinal thickening after bariatric surgery. After the surgery, increased HbA1c and serum C-peptide drop were reportedly associated with retinal thickening in the foveal and parafoveal regions [4]. Brynskov et al., who conducted their study only on type 2 diabetic patients, confirmed that retinal thickness correlates inversely with HbA1c levels [22].
Vascular Density (VD)
Optical coherence tomography angiography (OCTA) is a new technology that provides non-invasive imaging and tracking of retinal capillaries. It allows the assessment and detection of retinal microvasculature abnormalities without requiring intravascular dyes in both superficial and deep vascular plexuses (SVP, DVP) and non-perfusion areas [23].
Agarwal et al. were the first to examine changes in SVP and DVP with OCTA before and after bariatric surgery. They obtained the capillary density index (CDI), the percentage of capillary density over the stromal area in a particular region. At the short, 3-month follow-up visit, no significant changes in CDI after surgery were observed [12].
Contrary to the previous study, El-Shazly et al. found a significant statistical increase in macular VD in the DVP 3 months after the bariatric surgery [21]. Their observation agreed with a study by Laiginhas et al., who reported a postoperative increase in perifoveal vascular density in the DVP [4]. Increased perfusion in the DVP is explained by its greater sensitivity than SVP [20].
Other Vascular Parameters
Researchers assessed other parameters related to microvascular changes in the eye before and after bariatric surgery. The smaller number of studies disabled the possibility of result comparison. Therefore, these data have been collected in this section.
Agrawal et al. proposed a new imaging tool to indicate the ratio of choroidal vessels to stroma—the choroidal vascularity index (CVI) [24]. CVI reflects the distinction between stromal and luminal vascular components [25]. In another study, Agarwal et al. analyzed the choroidovascular system and capillary density index (CDI), the ratio of the percentage of capillary density to the stromal area in both SVP and DVP. In this study, both groups noted no significant change in CVI and CDI [12].
SD-OCT was used to measure total macular volume (TMV) in the study by Dogan et al. Patients who underwent LSG presented a statistically significant increase in TMV postoperatively [18]. The authors did not explain their methods of TMV assessment, but in a study by Burkholder et al., TMV represented the sum of the volumes of the neural retina in the central 6 mm of the macula [26].
The foveal avascular zone (FAZ) is a circular capillary-free zone in the retina [27]. Microvascular diseases reflect in the increase in size and loss of round contour of FAZ. Increased FAZ circularity and decreased perimeter demonstrate the postoperative improvement in microvascular perfusion in the retina [4].
Summary
Higher BMI is associated with narrower retinal arteriolar and wider venular calibers. These microcirculation changes contribute to cardiovascular and cerebrovascular diseases [28]. Examining retinal and choroidal vessels in vivo provides a window to the human microvasculature. It is a non-invasive procedure, does not expose the patient to radiation, and is not associated with side effects.
AVR was the first parameter to be studied in 2012 [15]. With the development of new technologies, it has become possible to explore new links between BMI and microcirculation. OCT quickly became an essential tool in retinal diagnosis, enabling choroidal thickness measurements and vascular density indices. OCT angiography gives an insight into the perfusion in retinal microvasculature. Postoperative AVR improvement, increased choroidal and retinal thickness in the macula, and increased macular VD in the DVP prove that obesity-induced microvasculature alterations might be reversible after weight loss. Current research focuses on advanced technologies, including software for automatic vessel density measurement in DVP and SVP. It may provide even better insight into the subclinical changes in patients with obesity before and after bariatric surgery.
Glaucoma
Glaucoma is an ocular disorder leading to optic neuropathy and the first cause of irreversible blindness worldwide. Increased IOP is a leading risk factor in the pathogenesis of glaucoma. IOP can be elevated mechanically with fat accumulated intraorbital and elevated pressure in episcleral veins. Disrupted vascular homeostasis and endothelial dysfunction are reasons for the vascular etiology of glaucomatous changes. Changes in the RNFL and visual fields are objective parameters used to diagnose and evaluate the progression. In the course of glaucoma, RNFL thinning is noticed during several years of observation [29].
IOP
Weight loss is positively correlated with IOP decrease when the surgery succeeds. Postoperative changes in IOP are summarized in Table 2.
In a study by Viljanen et al., IOP values significantly decreased postoperatively. Measurements obtained with the Pascal dynamic contour tonometer were higher than with the Goldmann applanation tonometer [30]. Burgansky-Eliash et al. and Shimonov et al. also observed a significant IOP decrease, where it remained reduced at the 1-year follow-up visit [31, 32]. In a study by Posarelli et al., authors demonstrated no compatibility between IOP values 3 months and 1 year postoperatively [19].
RNFL
Changes in RNFL after the bariatric surgery are presented in Table 3.
Posarelli et al. concluded that blood pressure is inversely related to RNFL thickness, supporting the assumption of vascular pathogenesis of RNFL changes in subjects with obesity [19]. After the bodyweight dropped, systolic blood pressure (SBP) significantly decreased. Postoperatively RNFL thickness increased significantly in the superior sector of both eyes and decreased in the nasal sector in the left eye.
Shimonov et al. presented contrary results. In their study, RNFL thickness was significantly reduced postoperatively. The authors hypothesize that postoperative decrease of fat tissue or vascular changes might impact RNFL [31]. Other authors gaunt no statistically significant differences in RNFL thickness [20, 30].
Summary
A positive correlation between IOP and BMI is indisputable. The lower the body weight after the bariatric surgery, the lower the risk of glaucoma. Although the authors agree on the outcome, the mechanism of these findings needs to be investigated. On the contrary, RNFL thickness measurements need to be evaluated in long-term analyses to receive more unanimous results.
Ocular Surface
Ocular Surface Condition
Dry eye is a multifactorial disease of the tears and ocular surface that results in symptoms of discomfort, visual disturbance, and tear film instability. The clinical evaluation includes Schirmer’s test I and BUT (break-up time), ocular surface staining through fluorescein and rose bengal, and OSDI (Ocular Surface Disease Index) questionnaire to evaluate subjective symptoms such as sensitivity to light, grittiness, or blurred vision [33].
The ocular surface condition following bariatric surgery is summarized in Table 4.
Brandão et al. studied a group of patients who underwent bariatric surgery. Postoperatively, most patients reported mild to severe dry eye symptoms. No statistically significant correlation was found between variables such as visual function, ocular surface condition, and vitamin A serum level. However, some limitations of this study, such as no pre-surgery database, small sample, poor sex diversification, and a relatively short observational period, are noticeable [34].
On the contrary, Marques et al. noticed no dry eye symptoms in bariatric surgery patients. The fact that 20% of patients maintained a BMI > 35 mg/m2 postoperatively may have contributed to this [35]. Slater et al. had similar conclusions, with 27.3% of patients with postoperative BMI >35 kg/m2 [6].
Iqbal et al. focused on assessing confocal microscopy parameters such as corneal nerve fiber density (CNFD), corneal branch density (CNBD), corneal nerve fiber length (CNFL), and keratocyte density (KD) before and 12 months after bariatric surgery. CNFL, CNBD, and keratocyte density from all three stroma layers were significantly lower in patients with obesity compared to controls. Confocal microscopy parameters significantly improved 12 months after bariatric surgery [36].
Eckert et al. determined seven patients with decreased vitamin A levels (<38 ug/dl) out of 64 patients after Roux-en-Y gastric bypass surgery. They assessed the correlation between ocular symptoms, and vitamin A deficiency was assessed. Six of them presented decreased visual acuity (p = 0.05) and xerosis (<0.05), five had night vision deterioration (p = 0.08), and four patients suffered from eye pain or foreign body sensation (p = 0.16). However, further examination indicated meibomian gland dysfunction as a possible cause of dry eye symptoms [37].
Vitamin A Deficiency
Vitamin A is one of the fat-soluble vitamins that cannot be synthesized by the human body and must be ingested to preserve tissue storage. The role of vitamin A is essential for the maintenance of correct vision and ocular surface integrity [34].
The ocular surface evaluation, visual function, and vitamin A deficiency following bariatric surgery are summarized in Table 5. We present several case reports describing the long-term side effects of vitamin A deficiency.
Donaldson et al. described the case of a 41-year-old woman who had bariatric surgery 8 years before laser-assisted in situ keratomileuses and then developed corneal ulceration that required combined non-invasive and invasive treatment. The levels of vitamin A were less than 2 ug/dl at the time. Finally, this patient underwent a penetrating keratoplasty because of central corneal scarring [38].
Crum et al. reported Bitot’s spots, an ocular manifestation of a systemic disease due to severe hypovitaminosis A, after bariatric surgery in a woman who presented dryness and diminished night vision symptoms. Given the patient’s history of bariatric surgery, anemia, and vitamin D deficiency, further investigation into micronutrient levels indicated a severe vitamin A deficiency. Oral vitamin A supplementation in this patient resulted in the complete resolution of her symptoms within 2 months [39].
Fok et al. reported two cases of female patients who presented visual deterioration developed due to decreased vitamin A serum levels resulting from ceased or irregular supplementation of vitamin A after bariatric surgery. Intramuscular vitamin A injections and oral multivitamin supplementation significantly improved visual function [40].
Lee et al. presented a case report of a woman who suffered from severe bilateral dry eye and visual deterioration due to inadequate vitamin A supplementation for 18 months following a duodenal switch gastric bypass surgery. Almost complete resolution of symptoms and normalized vitamin A level were achieved 6 months after presentation [41].
Summary
Studies on ocular surface disturbances following bariatric surgery have many limitations, including small, poor sex-diversified samples without a control group. In most studies, no significant change in ocular surface parameters was observed. Clinical presentation of vitamin A deficiency may imply many different ocular morbidities. Ocular complications of hypovitaminosis A are potentially reversible; however, in some cases, the recovery was significant but incomplete. Vitamin A supplementation after bariatric surgery is crucial to prevent severe visual impairment. Long-term side effects of insufficient vitamin A supplementation and its influence on the ocular surface and vision are documented mainly by case reports.
Conclusions
To date, bariatric surgery is one of the most efficient methods to reach a stable body weight. As the BMI decreases, ocular changes occur. Almost all studies agree on the positive impact of weight loss following bariatric surgery on retinal microvasculature. Improved arterial perfusion, retinal venular narrowing, and an increase of AVR occur postoperatively. The thickening of the retina following surgery-induced weight loss is observed mainly in the foveal and parafoveal regions. Positive changes were noticed in vascular density, especially in the macular DVP. All authors agree that weight loss in patients with extreme obesity is conducive to IOP decrease, which lowers the risk of glaucoma.
Nevertheless, knowledge about ocular changes after bariatric surgeries is still limited. The impact of the postoperative weight loss on the thickness of the choroid and RNFL is yet unclear. Results in analyzed studies vary, sometimes due to different techniques of examination, patient characteristics, gender distributions, or follow up-period. Both CT and RNFL outcomes need to be evaluated in further research. There is little evidence that the ocular surface condition changes following bariatric surgery. The authors observed vitamin A deficiency in most of the studies. The correlation between ocular symptoms and vitamin A deficiency needs further assessment.
Discussed studies are not free of limitations. Firstly, they have relatively small sample sizes. Groups of up to 88 patients were examined pre- and postoperatively [16]. Secondly, the study populations were mainly women, so further studies are required to investigate gender differences. Moreover, most of the studies lack a comparator group. A longer follow-up would help assess the durability of ocular changes after bariatric surgery.
References
Cheung N, Wong TY. Obesity and eye diseases. Surv Ophthalmol. 2007;52(2):180–95. https://doi.org/10.1016/j.survophthal.2006.12.003.
Klein BE, Klein R, Linton KL. Intraocular pressure in an American community. The Beaver Dam Eye Study. Invest Ophthalmol Vis Sci. 1992;33(7):2224–8.
Teberik K, Eski M, Doğan S, Pehlivan M, Kaya M. Ocular abnormalities in morbid obesity. Arq Bras Oftalmol. 2019;82:1. https://doi.org/10.5935/0004-2749.20190007.
Laiginhas R, Guimarães M, Nora M, Chibante J, Falcão M. Gastric bypass improves microvascular perfusion in patients with obesity. Obes Surg. 2021;31(5):2080–6. https://doi.org/10.1007/s11695-021-05223-1.
Viljanen A, Soinio M, Cheung CY, et al. Effects of bariatric surgery on retinal microvascular architecture in obese patients. Int J Obes (Lond). 2019;43(9):1675–80. https://doi.org/10.1038/s41366-018-0242-7.
Slater GH, Ren CJ, Siegel N, et al. Serum fat-soluble vitamin deficiency and abnormal calcium metabolism after malabsorptive bariatric surgery. J Gastrointest Surg. 2004;8(1):48–55. https://doi.org/10.1016/j.gassur.2003.09.020.
Gonul S, Yilmaz H, Gedik S, Ozturk BT, Oflaz AB, Sahin M. Evaluation of the choroidal thickness and retinal nerve fiber layer and visual fields in morbid obesity: does bariatric surgery affect retinal structure and function? Indian J Ophthalmol. 2021;69(2):301–6. https://doi.org/10.4103/ijo.IJO_295_20.
Pless M, Litzel M, Fischli S, Helfenstein M, Job O. The ophthalmic complications of bariatric surgery: the role of vitamin A deficiency. Klinische Monatsblätter für Augenheilkunde. 2019;236(04):483–6. https://doi.org/10.1055/a-0831-2222.
Sajovic J, Meglič A, Glavač D, Markelj Š, Hawlina M, Fakin A. The role of vitamin A in retinal diseases. Int J Mol Sci. 2022;23(3):1014. https://doi.org/10.3390/ijms23031014.
Wong TY, Mitchell P. Hypertensive retinopathy. N Engl J Med. 2004;351(22):2310–7. https://doi.org/10.1056/NEJMra032865.
Wong TY, Islam FM, Klein R, et al. Retinal vascular caliber, cardiovascular risk factors, and inflammation: the multi-ethnic study of atherosclerosis (MESA). Invest Ophthalmol Vis Sci. 2006;47(6):2341–50. https://doi.org/10.1167/iovs.05-1539.
Agarwal A, Saini A, Mahajan S, et al. Effect of weight loss on the retinochoroidal structural alterations among patients with exogenous obesity. PLoS One. 2020;15(7):e0235926. https://doi.org/10.1371/journal.pone.0235926.
Cheung N, Wong T. The retinal arteriole to venule ratio: informative or deceptive? Graefes Arch Clin Exp Ophthalmol. 2007;245(8):1245–6. https://doi.org/10.1007/s00417-006-0486-0.
Hemminki V, Kähönen M, Tuomisto M, Turjanmaa V, Uusitalo H. Determination of retinal blood vessel diameters and arteriovenous ratios in systemic hypertension: comparison of different calculation formulae. Graefes Arch Clin Exp Ophthalmol. 2006;245(1):8–17. https://doi.org/10.1007/s00417-006-0358-7.
Lammert A, Hasenberg T, Kräupner C, Schnülle P, Hammes HP. Improved arteriole-to-venule ratio of retinal vessels resulting from bariatric surgery. Obesity (Silver Spring). 2012;20(11):2262–7. https://doi.org/10.1038/oby.2012.122.
Debourdeau E, Gardes G, Nocca D, et al. Longitudinal effect of bariatric surgery on retinal microcirculation and target organ damage: the BASTOD study. Obes Surg. 2022;32(7):1–10. https://doi.org/10.1007/s11695-022-06064-2.
Toda N, Okamura T. Obesity impairs vasodilatation and blood flow increase mediated by endothelial nitric oxide: an overview. J Clin Pharmacol. 2013;53(12):1228–39. https://doi.org/10.1002/jcph.179.
Dogan B, Dogan U, Erol MK, Habibi M, Bulbuller N. Optical coherence tomography parameters in morbidly obese patients who underwent laparoscopic sleeve gastrectomy. J Ophthalmol. 2016;2016:5302368. https://doi.org/10.1155/2016/5302368.
Posarelli C, Salvetti G, Piaggi P, et al. Ophthalmologic evaluation of severely obese patients undergoing bariatric surgery: a pilot, monocentric, prospective, open-label study. PLoS One. 2019;14(5):e0216351. https://doi.org/10.1371/journal.pone.0216351.
Laiginhas R, Guimarães M, Cardoso P, et al. Bariatric surgery induces retinal thickening without affecting the retinal nerve fiber layer independent of diabetic status. Obes Surg. 2020;30(12):4877–84. https://doi.org/10.1007/s11695-020-04904-7.
El-Shazly M, Salama M, Elessawy K. Changes in the macular vascular density after bariatric surgery measured by optical coherence tomography angiography. Clin Ophthalmol. 2021;15:3131–7. https://doi.org/10.2147/OPTH.S317965.
Brynskov T, Laugesen CS, Floyd AK, Sørensen TL. Thickening of inner retinal layers in the parafovea after bariatric surgery in patients with type 2 diabetes. Acta Ophthalmol. 2016;94(7):668–74. https://doi.org/10.1111/aos.13087.
Chu Z, Lin J, Gao C, et al. Quantitative assessment of the retinal microvasculature using optical coherence tomography angiography. J Biomed Opt. 2016;21(6):66008. https://doi.org/10.1117/1.JBO.21.6.066008.
Agrawal R, Gupta P, Tan KA, Cheung CM, Wong TY, Cheng CY. Choroidal vascularity index as a measure of vascular status of the choroid: measurements in healthy eyes from a population-based study. Sci Rep. 2016;6:21090. https://doi.org/10.1038/srep21090.
Iovino C, Pellegrini M, Bernabei F, et al. Choroidal vascularity index: an in-depth analysis of this novel optical coherence tomography parameter. J Clin Med. 2020;9(2):595. https://doi.org/10.3390/jcm9020595.
Burkholder BM, Osborne B, Loguidice MJ, et al. Macular volume determined by optical coherence tomography as a measure of neuronal loss in multiple sclerosis. Arch Neurol. 2009;66(11):1366–72. https://doi.org/10.1001/archneurol.2009.230.
Chui TY, Zhong Z, Song H, Burns SA. Foveal avascular zone and its relationship to foveal pit shape. Optom Vis Sci. 2012;89(5):602–10. https://doi.org/10.1097/OPX.0b013e3182504227.
Boillot A, Zoungas S, Mitchell P, et al. Obesity and the microvasculature: a systematic review and meta-analysis. PLoS One. 2013;8(2):e52708. https://doi.org/10.1371/journal.pone.0052708.
Medeiros FA, Alencar LM, Zangwill LM, Sample PA, Weinreb RN. The relationship between intraocular pressure and progressive retinal nerve fiber layer loss in glaucoma. Ophthalmology. 2009;116(6):1125-33.e333. https://doi.org/10.1016/j.ophtha.2008.12.062.
Viljanen A, Hannukainen JC, Soinio M, et al. The effect of bariatric surgery on intraocular pressure. Acta Ophthalmol. 2018;96(8):849–52. https://doi.org/10.1111/aos.13826.
Burgansky-Eliash Z, Achiron A, Hecht I, Shimonov M. Reduction of intraocular pressure after bariatric surgery. Acta Ophthalmol. 2018;96(5):e592–5. https://doi.org/10.1111/aos.13722.
Shimonov M, Hecht I, Yehezkeli V, Maharshak I, Achiron A, Burgansky-Eliash Z. Does bariatric surgery affect intraocular pressure? Obes Surg. 2020;30(10):3742–6. https://doi.org/10.1007/s11695-020-04714-x.
Golden MI, Meyer JJ, Patel BC. Dry eye syndrome. In: StatPearls. Treasure Island (FL): StatPearls Publishing; 2021.
Brandão LP, Vilar L, Cavalcanti BM, Brandão PH, Arantes TE, Campos JM. Serum levels of vitamin A, visual function and ocular surface after bariatric surgery. Arq Gastroenterol. 2017;54(1):65–9. https://doi.org/10.1590/S0004-2803.2017v54n1-13.
Marques NPN, Felberg S, Barros JN, Malheiros CA. Evaluation of the ocular surface following bariatric surgery. Arq Bras Oftalmol. 2017;80(4):247–51. https://doi.org/10.5935/0004-2749.20170060.
Iqbal Z, Kalteniece A, Ferdousi M, et al. Corneal keratocyte density and corneal nerves are reduced in patients with severe obesity and improve after bariatric surgery. Invest Ophthalmol Vis Sci. 2021;62(1):20. https://doi.org/10.1167/iovs.62.1.20.
Eckert MJ, Perry JT, Sohn VY, et al. Incidence of low vitamin A levels and ocular symptoms after Roux-en-Y gastric bypass. Surg Obes Relat Dis. 2010;6(6):653–7. https://doi.org/10.1016/j.soard.2010.02.044.
Donaldson KE, Fishler J. Corneal ulceration in a LASIK patient due to vitamin a deficiency after bariatric surgery. Cornea. 2012;31(12):1497–9. https://doi.org/10.1097/ICO.0b013e318243e4ac.
Crum AR, Srikumaran D, Woreta F. Bitot’s spots following bariatric surgery: an ocular manifestation of a systemic disease. Case Rep Ophthalmol. 2017;8(3):581–9. https://doi.org/10.1159/000485235.
Fok JS, Li JY, Yong TY. Visual deterioration caused by vitamin A deficiency in patients after bariatric surgery. Eat Weight Disord. 2012;17(2):e144–6. https://doi.org/10.1007/BF03325340.
Lee WB, Hamilton SM, Harris JP, Schwab IR. Ocular complications of hypovitaminosis A after bariatric surgery. Ophthalmology. 2005;112(6):1031–4. https://doi.org/10.1016/j.ophtha.2004.12.045.
Pless M, Litzel M, Fischli S, Helfenstein M, Job O. The Ophthalmic Complications of Bariatric Surgery: The Role of Vitamin A Deficiency. Klinische Monatsblätter für Augenheilkunde. 2019;236(04):483–6. https://doi.org/10.1055/a-0831-2222.
Author information
Authors and Affiliations
Corresponding author
Ethics declarations
Ethical Approval
This article does not contain any studies with human participants or animals performed by any of the authors.
Informed Consent
Informed consent does not apply.
Conflict of Interest
The authors declare no competing interests.
Additional information
Publisher’s Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Key Points
• Bariatric surgery positively impacts retinochoroidal circulation.
• Surgery-induced weight loss positively correlates with intraocular pressure drop.
• Postoperative fat malabsorption and vitamin A deficiency imply ocular complications.
Rights and permissions
Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
About this article
Cite this article
Marta, K., Katarzyna, C., Marta, K. et al. How Does Weight Loss After Bariatric Surgery Impact the Ocular Parameters? A Review. OBES SURG 33, 1916–1927 (2023). https://doi.org/10.1007/s11695-023-06607-1
Received:
Revised:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s11695-023-06607-1